8-38682905-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38682905
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 38682905
    reference: chr 8
allele count: 1
allele frequency: 8.240218860212928e-6
allele num: 121356
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000522955
  gene symbol: TACC1
  hgvsc: ENST00000522955.1:n.1368+19C>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430959
  ensembl transcript: ENST00000520973
  gene symbol: TACC1
  hgvsc: ENST00000520973.1:c.867+19C>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430306
  ensembl transcript: ENST00000518809
  gene symbol: TACC1
  hgvsc: ENST00000518809.1:c.401+19C>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000429418
  ensembl transcript: ENST00000520611
  gene symbol: TACC1
  hgvsc: ENST00000520611.1:c.-234-1781C>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000473342
  ensembl transcript: ENST00000520340
  gene symbol: TACC1
  hgvsc: ENST00000520340.1:c.1344+19C>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000332794
  ensembl transcript: ENST00000330691
  gene symbol: TACC1
  hgvsc: ENST00000330691.6:c.174+19C>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000369263
  ensembl transcript: ENST00000379931
  gene symbol: TACC1
  hgvsc: ENST00000379931.3:c.1488+19C>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428450
  ensembl transcript: ENST00000520615
  gene symbol: TACC1
  hgvsc: ENST00000520615.1:c.867+19C>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428949
  ensembl transcript: ENST00000521050
  gene symbol: TACC1
  hgvsc: ENST00000521050.1:c.174+19C>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428687
  ensembl transcript: ENST00000519416
  gene symbol: TACC1
  hgvsc: ENST00000519416.1:c.864+19C>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000321703
  ensembl transcript: ENST00000317827
  gene symbol: TACC1
  hgvsc: ENST00000317827.4:c.1452+19C>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428466
  ensembl transcript: ENST00000521642
  gene symbol: TACC1
  hgvsc: ENST00000521642.1:c.138+19C>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428706
  ensembl transcript: ENST00000518415
  gene symbol: TACC1
  hgvsc: ENST00000518415.1:c.1317+19C>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000517336
  gene symbol: TACC1
  hgvsc: ENST00000517336.1:n.172+19C>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000276520
  ensembl transcript: ENST00000276520
  gene symbol: TACC1
  hgvsc: ENST00000276520.8:c.222+19C>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000523239
  gene symbol: TACC1
  hgvsc: ENST00000523239.1:n.94+19C>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000393647
  ensembl transcript: ENST00000443286
  gene symbol: TACC1
  hgvsc: ENST00000443286.2:c.1500+19C>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428253
  ensembl transcript: ENST00000521866
  gene symbol: TACC1
  hgvsc: ENST00000521866.1:c.812+19C>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000522752
  gene symbol: TACC1
  hgvsc: ENST00000522752.1:n.172+19C>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430355
  ensembl transcript: ENST00000522904
  gene symbol: TACC1
  hgvsc: ENST00000522904.1:c.1368+19C>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000327818
  ensembl transcript: ENST00000348567
  gene symbol: TACC1
  hgvsc: ENST00000348567.4:c.138+19C>G
  variant of: http://identifiers.org/hgnc/11522
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Other
population: African
population: East Asian
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: DP
site quality: ReadPosRankSum

8-38682907-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38682907
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 38682907
    reference: chr 8
allele count: 2
allele frequency: 1.647935137272997e-5
allele num: 121364
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000473342
  ensembl transcript: ENST00000520340
  gene symbol: TACC1
  hgvsc: ENST00000520340.1:c.1344+21A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428687
  ensembl transcript: ENST00000519416
  gene symbol: TACC1
  hgvsc: ENST00000519416.1:c.864+21A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428450
  ensembl transcript: ENST00000520615
  gene symbol: TACC1
  hgvsc: ENST00000520615.1:c.867+21A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430959
  ensembl transcript: ENST00000520973
  gene symbol: TACC1
  hgvsc: ENST00000520973.1:c.867+21A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430306
  ensembl transcript: ENST00000518809
  gene symbol: TACC1
  hgvsc: ENST00000518809.1:c.401+21A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000522955
  gene symbol: TACC1
  hgvsc: ENST00000522955.1:n.1368+21A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000517336
  gene symbol: TACC1
  hgvsc: ENST00000517336.1:n.172+21A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000369263
  ensembl transcript: ENST00000379931
  gene symbol: TACC1
  hgvsc: ENST00000379931.3:c.1488+21A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000393647
  ensembl transcript: ENST00000443286
  gene symbol: TACC1
  hgvsc: ENST00000443286.2:c.1500+21A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000523239
  gene symbol: TACC1
  hgvsc: ENST00000523239.1:n.94+21A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000321703
  ensembl transcript: ENST00000317827
  gene symbol: TACC1
  hgvsc: ENST00000317827.4:c.1452+21A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000327818
  ensembl transcript: ENST00000348567
  gene symbol: TACC1
  hgvsc: ENST00000348567.4:c.138+21A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428253
  ensembl transcript: ENST00000521866
  gene symbol: TACC1
  hgvsc: ENST00000521866.1:c.812+21A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428949
  ensembl transcript: ENST00000521050
  gene symbol: TACC1
  hgvsc: ENST00000521050.1:c.174+21A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430355
  ensembl transcript: ENST00000522904
  gene symbol: TACC1
  hgvsc: ENST00000522904.1:c.1368+21A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428706
  ensembl transcript: ENST00000518415
  gene symbol: TACC1
  hgvsc: ENST00000518415.1:c.1317+21A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000332794
  ensembl transcript: ENST00000330691
  gene symbol: TACC1
  hgvsc: ENST00000330691.6:c.174+21A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000276520
  ensembl transcript: ENST00000276520
  gene symbol: TACC1
  hgvsc: ENST00000276520.8:c.222+21A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000429418
  ensembl transcript: ENST00000520611
  gene symbol: TACC1
  hgvsc: ENST00000520611.1:c.-234-1779A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000522752
  gene symbol: TACC1
  hgvsc: ENST00000522752.1:n.172+21A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428466
  ensembl transcript: ENST00000521642
  gene symbol: TACC1
  hgvsc: ENST00000521642.1:c.138+21A>G
  variant of: http://identifiers.org/hgnc/11522
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
population: Latino
reference allele: A
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD

8-38682916-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38682916
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 38682916
    reference: chr 8
allele count: 1
allele frequency: 8.241169586787756e-6
allele num: 121342
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428466
  ensembl transcript: ENST00000521642
  gene symbol: TACC1
  hgvsc: ENST00000521642.1:c.138+30C>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000321703
  ensembl transcript: ENST00000317827
  gene symbol: TACC1
  hgvsc: ENST00000317827.4:c.1452+30C>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000522955
  gene symbol: TACC1
  hgvsc: ENST00000522955.1:n.1368+30C>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428253
  ensembl transcript: ENST00000521866
  gene symbol: TACC1
  hgvsc: ENST00000521866.1:c.812+30C>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000369263
  ensembl transcript: ENST00000379931
  gene symbol: TACC1
  hgvsc: ENST00000379931.3:c.1488+30C>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000429418
  ensembl transcript: ENST00000520611
  gene symbol: TACC1
  hgvsc: ENST00000520611.1:c.-234-1770C>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428949
  ensembl transcript: ENST00000521050
  gene symbol: TACC1
  hgvsc: ENST00000521050.1:c.174+30C>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430306
  ensembl transcript: ENST00000518809
  gene symbol: TACC1
  hgvsc: ENST00000518809.1:c.401+30C>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000517336
  gene symbol: TACC1
  hgvsc: ENST00000517336.1:n.172+30C>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430959
  ensembl transcript: ENST00000520973
  gene symbol: TACC1
  hgvsc: ENST00000520973.1:c.867+30C>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000522752
  gene symbol: TACC1
  hgvsc: ENST00000522752.1:n.172+30C>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000473342
  ensembl transcript: ENST00000520340
  gene symbol: TACC1
  hgvsc: ENST00000520340.1:c.1344+30C>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430355
  ensembl transcript: ENST00000522904
  gene symbol: TACC1
  hgvsc: ENST00000522904.1:c.1368+30C>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428687
  ensembl transcript: ENST00000519416
  gene symbol: TACC1
  hgvsc: ENST00000519416.1:c.864+30C>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428450
  ensembl transcript: ENST00000520615
  gene symbol: TACC1
  hgvsc: ENST00000520615.1:c.867+30C>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000332794
  ensembl transcript: ENST00000330691
  gene symbol: TACC1
  hgvsc: ENST00000330691.6:c.174+30C>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428706
  ensembl transcript: ENST00000518415
  gene symbol: TACC1
  hgvsc: ENST00000518415.1:c.1317+30C>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000276520
  ensembl transcript: ENST00000276520
  gene symbol: TACC1
  hgvsc: ENST00000276520.8:c.222+30C>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000327818
  ensembl transcript: ENST00000348567
  gene symbol: TACC1
  hgvsc: ENST00000348567.4:c.138+30C>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000393647
  ensembl transcript: ENST00000443286
  gene symbol: TACC1
  hgvsc: ENST00000443286.2:c.1500+30C>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000523239
  gene symbol: TACC1
  hgvsc: ENST00000523239.1:n.94+30C>T
  variant of: http://identifiers.org/hgnc/11522
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: DP

8-38682919-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38682919
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 38682919
    reference: chr 8
allele count: 1
allele frequency: 8.241305422778968e-6
allele num: 121340
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428450
  ensembl transcript: ENST00000520615
  gene symbol: TACC1
  hgvsc: ENST00000520615.1:c.867+33A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000522955
  gene symbol: TACC1
  hgvsc: ENST00000522955.1:n.1368+33A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428706
  ensembl transcript: ENST00000518415
  gene symbol: TACC1
  hgvsc: ENST00000518415.1:c.1317+33A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428949
  ensembl transcript: ENST00000521050
  gene symbol: TACC1
  hgvsc: ENST00000521050.1:c.174+33A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430306
  ensembl transcript: ENST00000518809
  gene symbol: TACC1
  hgvsc: ENST00000518809.1:c.401+33A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430355
  ensembl transcript: ENST00000522904
  gene symbol: TACC1
  hgvsc: ENST00000522904.1:c.1368+33A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000517336
  gene symbol: TACC1
  hgvsc: ENST00000517336.1:n.172+33A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000327818
  ensembl transcript: ENST00000348567
  gene symbol: TACC1
  hgvsc: ENST00000348567.4:c.138+33A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000429418
  ensembl transcript: ENST00000520611
  gene symbol: TACC1
  hgvsc: ENST00000520611.1:c.-234-1767A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000276520
  ensembl transcript: ENST00000276520
  gene symbol: TACC1
  hgvsc: ENST00000276520.8:c.222+33A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428687
  ensembl transcript: ENST00000519416
  gene symbol: TACC1
  hgvsc: ENST00000519416.1:c.864+33A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000393647
  ensembl transcript: ENST00000443286
  gene symbol: TACC1
  hgvsc: ENST00000443286.2:c.1500+33A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000321703
  ensembl transcript: ENST00000317827
  gene symbol: TACC1
  hgvsc: ENST00000317827.4:c.1452+33A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000523239
  gene symbol: TACC1
  hgvsc: ENST00000523239.1:n.94+33A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428466
  ensembl transcript: ENST00000521642
  gene symbol: TACC1
  hgvsc: ENST00000521642.1:c.138+33A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430959
  ensembl transcript: ENST00000520973
  gene symbol: TACC1
  hgvsc: ENST00000520973.1:c.867+33A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000332794
  ensembl transcript: ENST00000330691
  gene symbol: TACC1
  hgvsc: ENST00000330691.6:c.174+33A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428253
  ensembl transcript: ENST00000521866
  gene symbol: TACC1
  hgvsc: ENST00000521866.1:c.812+33A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000369263
  ensembl transcript: ENST00000379931
  gene symbol: TACC1
  hgvsc: ENST00000379931.3:c.1488+33A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000522752
  gene symbol: TACC1
  hgvsc: ENST00000522752.1:n.172+33A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000473342
  ensembl transcript: ENST00000520340
  gene symbol: TACC1
  hgvsc: ENST00000520340.1:c.1344+33A>G
  variant of: http://identifiers.org/hgnc/11522
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
reference allele: A
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum

8-38684638-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38684638
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 38684638
    reference: chr 8
allele count: 1
allele frequency: 8.739272542953525e-6
allele num: 114426
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000522955
  gene symbol: TACC1
  hgvsc: ENST00000522955.1:n.1369-48A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000473342
  ensembl transcript: ENST00000520340
  gene symbol: TACC1
  hgvsc: ENST00000520340.1:c.1345-48A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428949
  ensembl transcript: ENST00000521050
  gene symbol: TACC1
  hgvsc: ENST00000521050.1:c.175-48A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000429418
  ensembl transcript: ENST00000520611
  gene symbol: TACC1
  hgvsc: ENST00000520611.1:c.-234-48A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430959
  ensembl transcript: ENST00000520973
  gene symbol: TACC1
  hgvsc: ENST00000520973.1:c.868-48A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000327818
  ensembl transcript: ENST00000348567
  gene symbol: TACC1
  hgvsc: ENST00000348567.4:c.139-48A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430355
  ensembl transcript: ENST00000522904
  gene symbol: TACC1
  hgvsc: ENST00000522904.1:c.1369-48A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000522752
  gene symbol: TACC1
  hgvsc: ENST00000522752.1:n.173-48A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000517336
  gene symbol: TACC1
  hgvsc: ENST00000517336.1:n.173-48A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428253
  ensembl transcript: ENST00000521866
  gene symbol: TACC1
  hgvsc: ENST00000521866.1:c.813-48A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000321703
  ensembl transcript: ENST00000317827
  gene symbol: TACC1
  hgvsc: ENST00000317827.4:c.1453-48A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000393647
  ensembl transcript: ENST00000443286
  gene symbol: TACC1
  hgvsc: ENST00000443286.2:c.1501-48A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428466
  ensembl transcript: ENST00000521642
  gene symbol: TACC1
  hgvsc: ENST00000521642.1:c.139-48A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000369263
  ensembl transcript: ENST00000379931
  gene symbol: TACC1
  hgvsc: ENST00000379931.3:c.1489-48A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428450
  ensembl transcript: ENST00000520615
  gene symbol: TACC1
  hgvsc: ENST00000520615.1:c.868-48A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000523239
  gene symbol: TACC1
  hgvsc: ENST00000523239.1:n.95-48A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428706
  ensembl transcript: ENST00000518415
  gene symbol: TACC1
  hgvsc: ENST00000518415.1:c.1318-48A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000332794
  ensembl transcript: ENST00000330691
  gene symbol: TACC1
  hgvsc: ENST00000330691.6:c.175-48A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000276520
  ensembl transcript: ENST00000276520
  gene symbol: TACC1
  hgvsc: ENST00000276520.8:c.223-48A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428687
  ensembl transcript: ENST00000519416
  gene symbol: TACC1
  hgvsc: ENST00000519416.1:c.865-48A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430306
  ensembl transcript: ENST00000518809
  gene symbol: TACC1
  hgvsc: ENST00000518809.1:c.402-48A>G
  variant of: http://identifiers.org/hgnc/11522
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
population: Latino
population: Other
reference allele: A
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP

8-38684639-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38684639
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 38684639
    reference: chr 8
allele count: 1
allele frequency: 8.735302852949913e-6
allele num: 114478
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428450
  ensembl transcript: ENST00000520615
  gene symbol: TACC1
  hgvsc: ENST00000520615.1:c.868-47T>C
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000321703
  ensembl transcript: ENST00000317827
  gene symbol: TACC1
  hgvsc: ENST00000317827.4:c.1453-47T>C
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428466
  ensembl transcript: ENST00000521642
  gene symbol: TACC1
  hgvsc: ENST00000521642.1:c.139-47T>C
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000327818
  ensembl transcript: ENST00000348567
  gene symbol: TACC1
  hgvsc: ENST00000348567.4:c.139-47T>C
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000369263
  ensembl transcript: ENST00000379931
  gene symbol: TACC1
  hgvsc: ENST00000379931.3:c.1489-47T>C
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428706
  ensembl transcript: ENST00000518415
  gene symbol: TACC1
  hgvsc: ENST00000518415.1:c.1318-47T>C
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000332794
  ensembl transcript: ENST00000330691
  gene symbol: TACC1
  hgvsc: ENST00000330691.6:c.175-47T>C
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000522752
  gene symbol: TACC1
  hgvsc: ENST00000522752.1:n.173-47T>C
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000473342
  ensembl transcript: ENST00000520340
  gene symbol: TACC1
  hgvsc: ENST00000520340.1:c.1345-47T>C
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430355
  ensembl transcript: ENST00000522904
  gene symbol: TACC1
  hgvsc: ENST00000522904.1:c.1369-47T>C
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000522955
  gene symbol: TACC1
  hgvsc: ENST00000522955.1:n.1369-47T>C
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430306
  ensembl transcript: ENST00000518809
  gene symbol: TACC1
  hgvsc: ENST00000518809.1:c.402-47T>C
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000429418
  ensembl transcript: ENST00000520611
  gene symbol: TACC1
  hgvsc: ENST00000520611.1:c.-234-47T>C
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428949
  ensembl transcript: ENST00000521050
  gene symbol: TACC1
  hgvsc: ENST00000521050.1:c.175-47T>C
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428687
  ensembl transcript: ENST00000519416
  gene symbol: TACC1
  hgvsc: ENST00000519416.1:c.865-47T>C
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428253
  ensembl transcript: ENST00000521866
  gene symbol: TACC1
  hgvsc: ENST00000521866.1:c.813-47T>C
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000517336
  gene symbol: TACC1
  hgvsc: ENST00000517336.1:n.173-47T>C
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000523239
  gene symbol: TACC1
  hgvsc: ENST00000523239.1:n.95-47T>C
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000393647
  ensembl transcript: ENST00000443286
  gene symbol: TACC1
  hgvsc: ENST00000443286.2:c.1501-47T>C
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000276520
  ensembl transcript: ENST00000276520
  gene symbol: TACC1
  hgvsc: ENST00000276520.8:c.223-47T>C
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430959
  ensembl transcript: ENST00000520973
  gene symbol: TACC1
  hgvsc: ENST00000520973.1:c.868-47T>C
  variant of: http://identifiers.org/hgnc/11522
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Other
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
reference allele: T
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD

8-38684648-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38684648
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 38684648
    reference: chr 8
allele count: 1
allele frequency: 8.701402666109778e-6
allele num: 114924
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000473342
  ensembl transcript: ENST00000520340
  gene symbol: TACC1
  hgvsc: ENST00000520340.1:c.1345-38C>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428450
  ensembl transcript: ENST00000520615
  gene symbol: TACC1
  hgvsc: ENST00000520615.1:c.868-38C>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000522752
  gene symbol: TACC1
  hgvsc: ENST00000522752.1:n.173-38C>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000517336
  gene symbol: TACC1
  hgvsc: ENST00000517336.1:n.173-38C>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000327818
  ensembl transcript: ENST00000348567
  gene symbol: TACC1
  hgvsc: ENST00000348567.4:c.139-38C>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000429418
  ensembl transcript: ENST00000520611
  gene symbol: TACC1
  hgvsc: ENST00000520611.1:c.-234-38C>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430306
  ensembl transcript: ENST00000518809
  gene symbol: TACC1
  hgvsc: ENST00000518809.1:c.402-38C>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428687
  ensembl transcript: ENST00000519416
  gene symbol: TACC1
  hgvsc: ENST00000519416.1:c.865-38C>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430959
  ensembl transcript: ENST00000520973
  gene symbol: TACC1
  hgvsc: ENST00000520973.1:c.868-38C>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000393647
  ensembl transcript: ENST00000443286
  gene symbol: TACC1
  hgvsc: ENST00000443286.2:c.1501-38C>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428466
  ensembl transcript: ENST00000521642
  gene symbol: TACC1
  hgvsc: ENST00000521642.1:c.139-38C>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000369263
  ensembl transcript: ENST00000379931
  gene symbol: TACC1
  hgvsc: ENST00000379931.3:c.1489-38C>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000332794
  ensembl transcript: ENST00000330691
  gene symbol: TACC1
  hgvsc: ENST00000330691.6:c.175-38C>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428706
  ensembl transcript: ENST00000518415
  gene symbol: TACC1
  hgvsc: ENST00000518415.1:c.1318-38C>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000321703
  ensembl transcript: ENST00000317827
  gene symbol: TACC1
  hgvsc: ENST00000317827.4:c.1453-38C>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000276520
  ensembl transcript: ENST00000276520
  gene symbol: TACC1
  hgvsc: ENST00000276520.8:c.223-38C>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000523239
  gene symbol: TACC1
  hgvsc: ENST00000523239.1:n.95-38C>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428253
  ensembl transcript: ENST00000521866
  gene symbol: TACC1
  hgvsc: ENST00000521866.1:c.813-38C>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000522955
  gene symbol: TACC1
  hgvsc: ENST00000522955.1:n.1369-38C>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430355
  ensembl transcript: ENST00000522904
  gene symbol: TACC1
  hgvsc: ENST00000522904.1:c.1369-38C>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428949
  ensembl transcript: ENST00000521050
  gene symbol: TACC1
  hgvsc: ENST00000521050.1:c.175-38C>G
  variant of: http://identifiers.org/hgnc/11522
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: Other
reference allele: C
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff

8-38684658-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38684658
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 38684658
    reference: chr 8
allele count: 5
allele frequency: 4.319579791277904e-5
allele num: 115752
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000517336
  gene symbol: TACC1
  hgvsc: ENST00000517336.1:n.173-28G>A
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428687
  ensembl transcript: ENST00000519416
  gene symbol: TACC1
  hgvsc: ENST00000519416.1:c.865-28G>A
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000327818
  ensembl transcript: ENST00000348567
  gene symbol: TACC1
  hgvsc: ENST00000348567.4:c.139-28G>A
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428450
  ensembl transcript: ENST00000520615
  gene symbol: TACC1
  hgvsc: ENST00000520615.1:c.868-28G>A
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428253
  ensembl transcript: ENST00000521866
  gene symbol: TACC1
  hgvsc: ENST00000521866.1:c.813-28G>A
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430306
  ensembl transcript: ENST00000518809
  gene symbol: TACC1
  hgvsc: ENST00000518809.1:c.402-28G>A
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000332794
  ensembl transcript: ENST00000330691
  gene symbol: TACC1
  hgvsc: ENST00000330691.6:c.175-28G>A
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000473342
  ensembl transcript: ENST00000520340
  gene symbol: TACC1
  hgvsc: ENST00000520340.1:c.1345-28G>A
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428949
  ensembl transcript: ENST00000521050
  gene symbol: TACC1
  hgvsc: ENST00000521050.1:c.175-28G>A
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000369263
  ensembl transcript: ENST00000379931
  gene symbol: TACC1
  hgvsc: ENST00000379931.3:c.1489-28G>A
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000321703
  ensembl transcript: ENST00000317827
  gene symbol: TACC1
  hgvsc: ENST00000317827.4:c.1453-28G>A
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428706
  ensembl transcript: ENST00000518415
  gene symbol: TACC1
  hgvsc: ENST00000518415.1:c.1318-28G>A
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430355
  ensembl transcript: ENST00000522904
  gene symbol: TACC1
  hgvsc: ENST00000522904.1:c.1369-28G>A
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000393647
  ensembl transcript: ENST00000443286
  gene symbol: TACC1
  hgvsc: ENST00000443286.2:c.1501-28G>A
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430959
  ensembl transcript: ENST00000520973
  gene symbol: TACC1
  hgvsc: ENST00000520973.1:c.868-28G>A
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428466
  ensembl transcript: ENST00000521642
  gene symbol: TACC1
  hgvsc: ENST00000521642.1:c.139-28G>A
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000522752
  gene symbol: TACC1
  hgvsc: ENST00000522752.1:n.173-28G>A
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000429418
  ensembl transcript: ENST00000520611
  gene symbol: TACC1
  hgvsc: ENST00000520611.1:c.-234-28G>A
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000523239
  gene symbol: TACC1
  hgvsc: ENST00000523239.1:n.95-28G>A
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000522955
  gene symbol: TACC1
  hgvsc: ENST00000522955.1:n.1369-28G>A
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000276520
  ensembl transcript: ENST00000276520
  gene symbol: TACC1
  hgvsc: ENST00000276520.8:c.223-28G>A
  variant of: http://identifiers.org/hgnc/11522
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: East Asian
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum

8-38684661-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38684661
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 38684661
    reference: chr 8
allele count: 1
allele frequency: 8.612374259335814e-6
allele num: 116112
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430306
  ensembl transcript: ENST00000518809
  gene symbol: TACC1
  hgvsc: ENST00000518809.1:c.402-25G>A
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430355
  ensembl transcript: ENST00000522904
  gene symbol: TACC1
  hgvsc: ENST00000522904.1:c.1369-25G>A
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000522752
  gene symbol: TACC1
  hgvsc: ENST00000522752.1:n.173-25G>A
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428466
  ensembl transcript: ENST00000521642
  gene symbol: TACC1
  hgvsc: ENST00000521642.1:c.139-25G>A
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428450
  ensembl transcript: ENST00000520615
  gene symbol: TACC1
  hgvsc: ENST00000520615.1:c.868-25G>A
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428706
  ensembl transcript: ENST00000518415
  gene symbol: TACC1
  hgvsc: ENST00000518415.1:c.1318-25G>A
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000473342
  ensembl transcript: ENST00000520340
  gene symbol: TACC1
  hgvsc: ENST00000520340.1:c.1345-25G>A
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000522955
  gene symbol: TACC1
  hgvsc: ENST00000522955.1:n.1369-25G>A
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430959
  ensembl transcript: ENST00000520973
  gene symbol: TACC1
  hgvsc: ENST00000520973.1:c.868-25G>A
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000369263
  ensembl transcript: ENST00000379931
  gene symbol: TACC1
  hgvsc: ENST00000379931.3:c.1489-25G>A
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000517336
  gene symbol: TACC1
  hgvsc: ENST00000517336.1:n.173-25G>A
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428253
  ensembl transcript: ENST00000521866
  gene symbol: TACC1
  hgvsc: ENST00000521866.1:c.813-25G>A
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000327818
  ensembl transcript: ENST00000348567
  gene symbol: TACC1
  hgvsc: ENST00000348567.4:c.139-25G>A
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000429418
  ensembl transcript: ENST00000520611
  gene symbol: TACC1
  hgvsc: ENST00000520611.1:c.-234-25G>A
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000321703
  ensembl transcript: ENST00000317827
  gene symbol: TACC1
  hgvsc: ENST00000317827.4:c.1453-25G>A
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000393647
  ensembl transcript: ENST00000443286
  gene symbol: TACC1
  hgvsc: ENST00000443286.2:c.1501-25G>A
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428687
  ensembl transcript: ENST00000519416
  gene symbol: TACC1
  hgvsc: ENST00000519416.1:c.865-25G>A
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000276520
  ensembl transcript: ENST00000276520
  gene symbol: TACC1
  hgvsc: ENST00000276520.8:c.223-25G>A
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000332794
  ensembl transcript: ENST00000330691
  gene symbol: TACC1
  hgvsc: ENST00000330691.6:c.175-25G>A
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428949
  ensembl transcript: ENST00000521050
  gene symbol: TACC1
  hgvsc: ENST00000521050.1:c.175-25G>A
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000523239
  gene symbol: TACC1
  hgvsc: ENST00000523239.1:n.95-25G>A
  variant of: http://identifiers.org/hgnc/11522
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Latino
population: Other
population: South Asian
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum

8-38684662-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38684662
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 38684662
    reference: chr 8
allele count: 1
allele frequency: 8.600522911793038e-6
allele num: 116272
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000276520
  ensembl transcript: ENST00000276520
  gene symbol: TACC1
  hgvsc: ENST00000276520.8:c.223-24C>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428253
  ensembl transcript: ENST00000521866
  gene symbol: TACC1
  hgvsc: ENST00000521866.1:c.813-24C>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000393647
  ensembl transcript: ENST00000443286
  gene symbol: TACC1
  hgvsc: ENST00000443286.2:c.1501-24C>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430355
  ensembl transcript: ENST00000522904
  gene symbol: TACC1
  hgvsc: ENST00000522904.1:c.1369-24C>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000517336
  gene symbol: TACC1
  hgvsc: ENST00000517336.1:n.173-24C>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000369263
  ensembl transcript: ENST00000379931
  gene symbol: TACC1
  hgvsc: ENST00000379931.3:c.1489-24C>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430959
  ensembl transcript: ENST00000520973
  gene symbol: TACC1
  hgvsc: ENST00000520973.1:c.868-24C>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428706
  ensembl transcript: ENST00000518415
  gene symbol: TACC1
  hgvsc: ENST00000518415.1:c.1318-24C>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430306
  ensembl transcript: ENST00000518809
  gene symbol: TACC1
  hgvsc: ENST00000518809.1:c.402-24C>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000321703
  ensembl transcript: ENST00000317827
  gene symbol: TACC1
  hgvsc: ENST00000317827.4:c.1453-24C>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000522955
  gene symbol: TACC1
  hgvsc: ENST00000522955.1:n.1369-24C>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000332794
  ensembl transcript: ENST00000330691
  gene symbol: TACC1
  hgvsc: ENST00000330691.6:c.175-24C>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428450
  ensembl transcript: ENST00000520615
  gene symbol: TACC1
  hgvsc: ENST00000520615.1:c.868-24C>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000429418
  ensembl transcript: ENST00000520611
  gene symbol: TACC1
  hgvsc: ENST00000520611.1:c.-234-24C>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428466
  ensembl transcript: ENST00000521642
  gene symbol: TACC1
  hgvsc: ENST00000521642.1:c.139-24C>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000522752
  gene symbol: TACC1
  hgvsc: ENST00000522752.1:n.173-24C>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000523239
  gene symbol: TACC1
  hgvsc: ENST00000523239.1:n.95-24C>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000327818
  ensembl transcript: ENST00000348567
  gene symbol: TACC1
  hgvsc: ENST00000348567.4:c.139-24C>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428949
  ensembl transcript: ENST00000521050
  gene symbol: TACC1
  hgvsc: ENST00000521050.1:c.175-24C>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428687
  ensembl transcript: ENST00000519416
  gene symbol: TACC1
  hgvsc: ENST00000519416.1:c.865-24C>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000473342
  ensembl transcript: ENST00000520340
  gene symbol: TACC1
  hgvsc: ENST00000520340.1:c.1345-24C>T
  variant of: http://identifiers.org/hgnc/11522
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: Other
population: European (Finnish)
population: South Asian
reference allele: C
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: DP

8-38684665-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38684665
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 38684665
    reference: chr 8
allele count: 2
allele frequency: 1.712856702408277e-5
allele num: 116764
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000473342
  ensembl transcript: ENST00000520340
  gene symbol: TACC1
  hgvsc: ENST00000520340.1:c.1345-21C>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000321703
  ensembl transcript: ENST00000317827
  gene symbol: TACC1
  hgvsc: ENST00000317827.4:c.1453-21C>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428253
  ensembl transcript: ENST00000521866
  gene symbol: TACC1
  hgvsc: ENST00000521866.1:c.813-21C>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000393647
  ensembl transcript: ENST00000443286
  gene symbol: TACC1
  hgvsc: ENST00000443286.2:c.1501-21C>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428687
  ensembl transcript: ENST00000519416
  gene symbol: TACC1
  hgvsc: ENST00000519416.1:c.865-21C>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000522955
  gene symbol: TACC1
  hgvsc: ENST00000522955.1:n.1369-21C>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428466
  ensembl transcript: ENST00000521642
  gene symbol: TACC1
  hgvsc: ENST00000521642.1:c.139-21C>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000429418
  ensembl transcript: ENST00000520611
  gene symbol: TACC1
  hgvsc: ENST00000520611.1:c.-234-21C>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430306
  ensembl transcript: ENST00000518809
  gene symbol: TACC1
  hgvsc: ENST00000518809.1:c.402-21C>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430959
  ensembl transcript: ENST00000520973
  gene symbol: TACC1
  hgvsc: ENST00000520973.1:c.868-21C>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428450
  ensembl transcript: ENST00000520615
  gene symbol: TACC1
  hgvsc: ENST00000520615.1:c.868-21C>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000523239
  gene symbol: TACC1
  hgvsc: ENST00000523239.1:n.95-21C>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000517336
  gene symbol: TACC1
  hgvsc: ENST00000517336.1:n.173-21C>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000522752
  gene symbol: TACC1
  hgvsc: ENST00000522752.1:n.173-21C>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000369263
  ensembl transcript: ENST00000379931
  gene symbol: TACC1
  hgvsc: ENST00000379931.3:c.1489-21C>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000332794
  ensembl transcript: ENST00000330691
  gene symbol: TACC1
  hgvsc: ENST00000330691.6:c.175-21C>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000276520
  ensembl transcript: ENST00000276520
  gene symbol: TACC1
  hgvsc: ENST00000276520.8:c.223-21C>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000327818
  ensembl transcript: ENST00000348567
  gene symbol: TACC1
  hgvsc: ENST00000348567.4:c.139-21C>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430355
  ensembl transcript: ENST00000522904
  gene symbol: TACC1
  hgvsc: ENST00000522904.1:c.1369-21C>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428706
  ensembl transcript: ENST00000518415
  gene symbol: TACC1
  hgvsc: ENST00000518415.1:c.1318-21C>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428949
  ensembl transcript: ENST00000521050
  gene symbol: TACC1
  hgvsc: ENST00000521050.1:c.175-21C>T
  variant of: http://identifiers.org/hgnc/11522
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
population: European (Finnish)
population: Other
population: South Asian
reference allele: C
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD

8-38684674-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38684674
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 38684674
    reference: chr 8
allele count: 1
allele frequency: 8.456516591685553e-6
allele num: 118252
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000473342
  ensembl transcript: ENST00000520340
  gene symbol: TACC1
  hgvsc: ENST00000520340.1:c.1345-12T>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430959
  ensembl transcript: ENST00000520973
  gene symbol: TACC1
  hgvsc: ENST00000520973.1:c.868-12T>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428450
  ensembl transcript: ENST00000520615
  gene symbol: TACC1
  hgvsc: ENST00000520615.1:c.868-12T>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430355
  ensembl transcript: ENST00000522904
  gene symbol: TACC1
  hgvsc: ENST00000522904.1:c.1369-12T>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000522752
  gene symbol: TACC1
  hgvsc: ENST00000522752.1:n.173-12T>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000327818
  ensembl transcript: ENST00000348567
  gene symbol: TACC1
  hgvsc: ENST00000348567.4:c.139-12T>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428466
  ensembl transcript: ENST00000521642
  gene symbol: TACC1
  hgvsc: ENST00000521642.1:c.139-12T>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000522955
  gene symbol: TACC1
  hgvsc: ENST00000522955.1:n.1369-12T>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000332794
  ensembl transcript: ENST00000330691
  gene symbol: TACC1
  hgvsc: ENST00000330691.6:c.175-12T>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428706
  ensembl transcript: ENST00000518415
  gene symbol: TACC1
  hgvsc: ENST00000518415.1:c.1318-12T>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430306
  ensembl transcript: ENST00000518809
  gene symbol: TACC1
  hgvsc: ENST00000518809.1:c.402-12T>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000321703
  ensembl transcript: ENST00000317827
  gene symbol: TACC1
  hgvsc: ENST00000317827.4:c.1453-12T>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000517336
  gene symbol: TACC1
  hgvsc: ENST00000517336.1:n.173-12T>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428253
  ensembl transcript: ENST00000521866
  gene symbol: TACC1
  hgvsc: ENST00000521866.1:c.813-12T>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000523239
  gene symbol: TACC1
  hgvsc: ENST00000523239.1:n.95-12T>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000369263
  ensembl transcript: ENST00000379931
  gene symbol: TACC1
  hgvsc: ENST00000379931.3:c.1489-12T>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000393647
  ensembl transcript: ENST00000443286
  gene symbol: TACC1
  hgvsc: ENST00000443286.2:c.1501-12T>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000276520
  ensembl transcript: ENST00000276520
  gene symbol: TACC1
  hgvsc: ENST00000276520.8:c.223-12T>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428949
  ensembl transcript: ENST00000521050
  gene symbol: TACC1
  hgvsc: ENST00000521050.1:c.175-12T>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428687
  ensembl transcript: ENST00000519416
  gene symbol: TACC1
  hgvsc: ENST00000519416.1:c.865-12T>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000429418
  ensembl transcript: ENST00000520611
  gene symbol: TACC1
  hgvsc: ENST00000520611.1:c.-234-12T>G
  variant of: http://identifiers.org/hgnc/11522
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Other
population: African
population: European (Finnish)
reference allele: T
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum

8-38684681-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38684681
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 38684681
    reference: chr 8
allele count: 1
allele frequency: 8.389965601141035e-6
allele num: 119190
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428949
  ensembl transcript: ENST00000521050
  gene symbol: TACC1
  hgvsc: ENST00000521050.1:c.175-5C>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000393647
  ensembl transcript: ENST00000443286
  gene symbol: TACC1
  hgvsc: ENST00000443286.2:c.1501-5C>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428687
  ensembl transcript: ENST00000519416
  gene symbol: TACC1
  hgvsc: ENST00000519416.1:c.865-5C>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428450
  ensembl transcript: ENST00000520615
  gene symbol: TACC1
  hgvsc: ENST00000520615.1:c.868-5C>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430355
  ensembl transcript: ENST00000522904
  gene symbol: TACC1
  hgvsc: ENST00000522904.1:c.1369-5C>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000321703
  ensembl transcript: ENST00000317827
  gene symbol: TACC1
  hgvsc: ENST00000317827.4:c.1453-5C>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000327818
  ensembl transcript: ENST00000348567
  gene symbol: TACC1
  hgvsc: ENST00000348567.4:c.139-5C>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430306
  ensembl transcript: ENST00000518809
  gene symbol: TACC1
  hgvsc: ENST00000518809.1:c.402-5C>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000473342
  ensembl transcript: ENST00000520340
  gene symbol: TACC1
  hgvsc: ENST00000520340.1:c.1345-5C>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428253
  ensembl transcript: ENST00000521866
  gene symbol: TACC1
  hgvsc: ENST00000521866.1:c.813-5C>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430959
  ensembl transcript: ENST00000520973
  gene symbol: TACC1
  hgvsc: ENST00000520973.1:c.868-5C>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428466
  ensembl transcript: ENST00000521642
  gene symbol: TACC1
  hgvsc: ENST00000521642.1:c.139-5C>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000523239
  gene symbol: TACC1
  hgvsc: ENST00000523239.1:n.95-5C>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000369263
  ensembl transcript: ENST00000379931
  gene symbol: TACC1
  hgvsc: ENST00000379931.3:c.1489-5C>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000517336
  gene symbol: TACC1
  hgvsc: ENST00000517336.1:n.173-5C>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000429418
  ensembl transcript: ENST00000520611
  gene symbol: TACC1
  hgvsc: ENST00000520611.1:c.-234-5C>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428706
  ensembl transcript: ENST00000518415
  gene symbol: TACC1
  hgvsc: ENST00000518415.1:c.1318-5C>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000332794
  ensembl transcript: ENST00000330691
  gene symbol: TACC1
  hgvsc: ENST00000330691.6:c.175-5C>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000522955
  gene symbol: TACC1
  hgvsc: ENST00000522955.1:n.1369-5C>T
  variant of: http://identifiers.org/hgnc/11522
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: c.1453-5C>T
num of homozygotes: 0
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: QD
site quality: FS
site quality: InbreedingCoeff

8-38684686-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38684686
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 38684686
    reference: chr 8
allele count: 1
allele frequency: 8.346548702111677e-6
allele num: 119810
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000522955
  gene symbol: TACC1
  hgvsc: ENST00000522955.1:n.1369G>A
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428706
  ensembl transcript: ENST00000518415
  gene symbol: TACC1
  hgvsc: ENST00000518415.1:c.1318G>A
  hgvsp: ENSP00000428706.1:p.Asp440Asn
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000429418
  ensembl transcript: ENST00000520611
  gene symbol: TACC1
  hgvsc: ENST00000520611.1:c.-234G>A
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000369263
  ensembl transcript: ENST00000379931
  gene symbol: TACC1
  hgvsc: ENST00000379931.3:c.1489G>A
  hgvsp: ENSP00000369263.3:p.Asp497Asn
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428450
  ensembl transcript: ENST00000520615
  gene symbol: TACC1
  hgvsc: ENST00000520615.1:c.868G>A
  hgvsp: ENSP00000428450.1:p.Asp290Asn
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000393647
  ensembl transcript: ENST00000443286
  gene symbol: TACC1
  hgvsc: ENST00000443286.2:c.1501G>A
  hgvsp: ENSP00000393647.2:p.Asp501Asn
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428687
  ensembl transcript: ENST00000519416
  gene symbol: TACC1
  hgvsc: ENST00000519416.1:c.865G>A
  hgvsp: ENSP00000428687.1:p.Asp289Asn
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428253
  ensembl transcript: ENST00000521866
  gene symbol: TACC1
  hgvsc: ENST00000521866.1:c.813G>A
  hgvsp: ENSP00000428253.1:p.Asp272Asn
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000276520
  ensembl transcript: ENST00000276520
  gene symbol: TACC1
  hgvsc: ENST00000276520.8:c.223G>A
  hgvsp: ENSP00000276520.8:p.Asp75Asn
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430355
  ensembl transcript: ENST00000522904
  gene symbol: TACC1
  hgvsc: ENST00000522904.1:c.1369G>A
  hgvsp: ENSP00000430355.1:p.Asp457Asn
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430959
  ensembl transcript: ENST00000520973
  gene symbol: TACC1
  hgvsc: ENST00000520973.1:c.868G>A
  hgvsp: ENSP00000430959.1:p.Asp290Asn
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428949
  ensembl transcript: ENST00000521050
  gene symbol: TACC1
  hgvsc: ENST00000521050.1:c.175G>A
  hgvsp: ENSP00000428949.1:p.Asp59Asn
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428466
  ensembl transcript: ENST00000521642
  gene symbol: TACC1
  hgvsc: ENST00000521642.1:c.139G>A
  hgvsp: ENSP00000428466.1:p.Asp47Asn
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000321703
  ensembl transcript: ENST00000317827
  gene symbol: TACC1
  hgvsc: ENST00000317827.4:c.1453G>A
  hgvsp: ENSP00000321703.4:p.Asp485Asn
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000473342
  ensembl transcript: ENST00000520340
  gene symbol: TACC1
  hgvsc: ENST00000520340.1:c.1345G>A
  hgvsp: ENSP00000473342.1:p.Asp449Asn
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000517336
  gene symbol: TACC1
  hgvsc: ENST00000517336.1:n.173G>A
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000327818
  ensembl transcript: ENST00000348567
  gene symbol: TACC1
  hgvsc: ENST00000348567.4:c.139G>A
  hgvsp: ENSP00000327818.5:p.Asp47Asn
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430306
  ensembl transcript: ENST00000518809
  gene symbol: TACC1
  hgvsc: ENST00000518809.1:c.402G>A
  hgvsp: ENSP00000430306.1:p.Asp135Asn
  variant of: http://identifiers.org/hgnc/11522
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Asp485Asn
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff

8-38684688-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38684688
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 38684688
    reference: chr 8
allele count: 2
allele frequency: 1.66602802259134e-5
allele num: 120046
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000369263
  ensembl transcript: ENST00000379931
  gene symbol: TACC1
  hgvsc: ENST00000379931.3:c.1491T>G
  hgvsp: ENSP00000369263.3:p.Asp497Glu
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000517336
  gene symbol: TACC1
  hgvsc: ENST00000517336.1:n.175T>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430959
  ensembl transcript: ENST00000520973
  gene symbol: TACC1
  hgvsc: ENST00000520973.1:c.870T>G
  hgvsp: ENSP00000430959.1:p.Asp290Glu
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428450
  ensembl transcript: ENST00000520615
  gene symbol: TACC1
  hgvsc: ENST00000520615.1:c.870T>G
  hgvsp: ENSP00000428450.1:p.Asp290Glu
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430306
  ensembl transcript: ENST00000518809
  gene symbol: TACC1
  hgvsc: ENST00000518809.1:c.404T>G
  hgvsp: ENSP00000430306.1:p.Asp135Glu
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430355
  ensembl transcript: ENST00000522904
  gene symbol: TACC1
  hgvsc: ENST00000522904.1:c.1371T>G
  hgvsp: ENSP00000430355.1:p.Asp457Glu
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000393647
  ensembl transcript: ENST00000443286
  gene symbol: TACC1
  hgvsc: ENST00000443286.2:c.1503T>G
  hgvsp: ENSP00000393647.2:p.Asp501Glu
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428706
  ensembl transcript: ENST00000518415
  gene symbol: TACC1
  hgvsc: ENST00000518415.1:c.1320T>G
  hgvsp: ENSP00000428706.1:p.Asp440Glu
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000321703
  ensembl transcript: ENST00000317827
  gene symbol: TACC1
  hgvsc: ENST00000317827.4:c.1455T>G
  hgvsp: ENSP00000321703.4:p.Asp485Glu
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000332794
  ensembl transcript: ENST00000330691
  gene symbol: TACC1
  hgvsc: ENST00000330691.6:c.177T>G
  hgvsp: ENSP00000332794.6:p.Asp59Glu
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428949
  ensembl transcript: ENST00000521050
  gene symbol: TACC1
  hgvsc: ENST00000521050.1:c.177T>G
  hgvsp: ENSP00000428949.1:p.Asp59Glu
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000473342
  ensembl transcript: ENST00000520340
  gene symbol: TACC1
  hgvsc: ENST00000520340.1:c.1347T>G
  hgvsp: ENSP00000473342.1:p.Asp449Glu
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428253
  ensembl transcript: ENST00000521866
  gene symbol: TACC1
  hgvsc: ENST00000521866.1:c.815T>G
  hgvsp: ENSP00000428253.1:p.Asp272Glu
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000429418
  ensembl transcript: ENST00000520611
  gene symbol: TACC1
  hgvsc: ENST00000520611.1:c.-232T>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000523239
  gene symbol: TACC1
  hgvsc: ENST00000523239.1:n.97T>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428466
  ensembl transcript: ENST00000521642
  gene symbol: TACC1
  hgvsc: ENST00000521642.1:c.141T>G
  hgvsp: ENSP00000428466.1:p.Asp47Glu
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000522752
  gene symbol: TACC1
  hgvsc: ENST00000522752.1:n.175T>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000522955
  gene symbol: TACC1
  hgvsc: ENST00000522955.1:n.1371T>G
  variant of: http://identifiers.org/hgnc/11522
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Asp485Glu
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Other
population: African
population: South Asian
population: Latino
population: European (Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: QD

8-38684695-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38684695
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 38684695
    reference: chr 8
allele count: 4
allele frequency: 3.316749585406302e-5
allele num: 120600
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428466
  ensembl transcript: ENST00000521642
  gene symbol: TACC1
  hgvsc: ENST00000521642.1:c.148G>A
  hgvsp: ENSP00000428466.1:p.Ala50Thr
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000321703
  ensembl transcript: ENST00000317827
  gene symbol: TACC1
  hgvsc: ENST00000317827.4:c.1462G>A
  hgvsp: ENSP00000321703.4:p.Ala488Thr
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428687
  ensembl transcript: ENST00000519416
  gene symbol: TACC1
  hgvsc: ENST00000519416.1:c.874G>A
  hgvsp: ENSP00000428687.1:p.Ala292Thr
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000276520
  ensembl transcript: ENST00000276520
  gene symbol: TACC1
  hgvsc: ENST00000276520.8:c.232G>A
  hgvsp: ENSP00000276520.8:p.Ala78Thr
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428253
  ensembl transcript: ENST00000521866
  gene symbol: TACC1
  hgvsc: ENST00000521866.1:c.822G>A
  hgvsp: ENSP00000428253.1:p.Ala275Thr
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000523239
  gene symbol: TACC1
  hgvsc: ENST00000523239.1:n.104G>A
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000517336
  gene symbol: TACC1
  hgvsc: ENST00000517336.1:n.182G>A
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000369263
  ensembl transcript: ENST00000379931
  gene symbol: TACC1
  hgvsc: ENST00000379931.3:c.1498G>A
  hgvsp: ENSP00000369263.3:p.Ala500Thr
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428450
  ensembl transcript: ENST00000520615
  gene symbol: TACC1
  hgvsc: ENST00000520615.1:c.877G>A
  hgvsp: ENSP00000428450.1:p.Ala293Thr
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428949
  ensembl transcript: ENST00000521050
  gene symbol: TACC1
  hgvsc: ENST00000521050.1:c.184G>A
  hgvsp: ENSP00000428949.1:p.Ala62Thr
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430959
  ensembl transcript: ENST00000520973
  gene symbol: TACC1
  hgvsc: ENST00000520973.1:c.877G>A
  hgvsp: ENSP00000430959.1:p.Ala293Thr
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428706
  ensembl transcript: ENST00000518415
  gene symbol: TACC1
  hgvsc: ENST00000518415.1:c.1327G>A
  hgvsp: ENSP00000428706.1:p.Ala443Thr
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430306
  ensembl transcript: ENST00000518809
  gene symbol: TACC1
  hgvsc: ENST00000518809.1:c.411G>A
  hgvsp: ENSP00000430306.1:p.Ala138Thr
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000429418
  ensembl transcript: ENST00000520611
  gene symbol: TACC1
  hgvsc: ENST00000520611.1:c.-225G>A
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000522752
  gene symbol: TACC1
  hgvsc: ENST00000522752.1:n.182G>A
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000522955
  gene symbol: TACC1
  hgvsc: ENST00000522955.1:n.1378G>A
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000327818
  ensembl transcript: ENST00000348567
  gene symbol: TACC1
  hgvsc: ENST00000348567.4:c.148G>A
  hgvsp: ENSP00000327818.5:p.Ala50Thr
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000473342
  ensembl transcript: ENST00000520340
  gene symbol: TACC1
  hgvsc: ENST00000520340.1:c.1354G>A
  hgvsp: ENSP00000473342.1:p.Ala452Thr
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000332794
  ensembl transcript: ENST00000330691
  gene symbol: TACC1
  hgvsc: ENST00000330691.6:c.184G>A
  hgvsp: ENSP00000332794.6:p.Ala62Thr
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430355
  ensembl transcript: ENST00000522904
  gene symbol: TACC1
  hgvsc: ENST00000522904.1:c.1378G>A
  hgvsp: ENSP00000430355.1:p.Ala460Thr
  variant of: http://identifiers.org/hgnc/11522
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Ala488Thr
num of homozygotes: 0
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum

8-38684696-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38684696
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 38684696
    reference: chr 8
allele count: 3
allele frequency: 2.486737400530504e-5
allele num: 120640
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428450
  ensembl transcript: ENST00000520615
  gene symbol: TACC1
  hgvsc: ENST00000520615.1:c.878C>T
  hgvsp: ENSP00000428450.1:p.Ala293Val
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000393647
  ensembl transcript: ENST00000443286
  gene symbol: TACC1
  hgvsc: ENST00000443286.2:c.1511C>T
  hgvsp: ENSP00000393647.2:p.Ala504Val
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000321703
  ensembl transcript: ENST00000317827
  gene symbol: TACC1
  hgvsc: ENST00000317827.4:c.1463C>T
  hgvsp: ENSP00000321703.4:p.Ala488Val
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000369263
  ensembl transcript: ENST00000379931
  gene symbol: TACC1
  hgvsc: ENST00000379931.3:c.1499C>T
  hgvsp: ENSP00000369263.3:p.Ala500Val
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000522752
  gene symbol: TACC1
  hgvsc: ENST00000522752.1:n.183C>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000429418
  ensembl transcript: ENST00000520611
  gene symbol: TACC1
  hgvsc: ENST00000520611.1:c.-224C>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428466
  ensembl transcript: ENST00000521642
  gene symbol: TACC1
  hgvsc: ENST00000521642.1:c.149C>T
  hgvsp: ENSP00000428466.1:p.Ala50Val
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000332794
  ensembl transcript: ENST00000330691
  gene symbol: TACC1
  hgvsc: ENST00000330691.6:c.185C>T
  hgvsp: ENSP00000332794.6:p.Ala62Val
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428253
  ensembl transcript: ENST00000521866
  gene symbol: TACC1
  hgvsc: ENST00000521866.1:c.823C>T
  hgvsp: ENSP00000428253.1:p.Ala275Val
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430355
  ensembl transcript: ENST00000522904
  gene symbol: TACC1
  hgvsc: ENST00000522904.1:c.1379C>T
  hgvsp: ENSP00000430355.1:p.Ala460Val
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428949
  ensembl transcript: ENST00000521050
  gene symbol: TACC1
  hgvsc: ENST00000521050.1:c.185C>T
  hgvsp: ENSP00000428949.1:p.Ala62Val
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000473342
  ensembl transcript: ENST00000520340
  gene symbol: TACC1
  hgvsc: ENST00000520340.1:c.1355C>T
  hgvsp: ENSP00000473342.1:p.Ala452Val
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430306
  ensembl transcript: ENST00000518809
  gene symbol: TACC1
  hgvsc: ENST00000518809.1:c.412C>T
  hgvsp: ENSP00000430306.1:p.Ala138Val
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430959
  ensembl transcript: ENST00000520973
  gene symbol: TACC1
  hgvsc: ENST00000520973.1:c.878C>T
  hgvsp: ENSP00000430959.1:p.Ala293Val
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000327818
  ensembl transcript: ENST00000348567
  gene symbol: TACC1
  hgvsc: ENST00000348567.4:c.149C>T
  hgvsp: ENSP00000327818.5:p.Ala50Val
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428687
  ensembl transcript: ENST00000519416
  gene symbol: TACC1
  hgvsc: ENST00000519416.1:c.875C>T
  hgvsp: ENSP00000428687.1:p.Ala292Val
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000517336
  gene symbol: TACC1
  hgvsc: ENST00000517336.1:n.183C>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000523239
  gene symbol: TACC1
  hgvsc: ENST00000523239.1:n.105C>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428706
  ensembl transcript: ENST00000518415
  gene symbol: TACC1
  hgvsc: ENST00000518415.1:c.1328C>T
  hgvsp: ENSP00000428706.1:p.Ala443Val
  variant of: http://identifiers.org/hgnc/11522
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Ala488Val
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: DP

8-38684698-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38684698
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 38684698
    reference: chr 8
allele count: 1
allele frequency: 8.280202036929701e-6
allele num: 120770
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428706
  ensembl transcript: ENST00000518415
  gene symbol: TACC1
  hgvsc: ENST00000518415.1:c.1330G>A
  hgvsp: ENSP00000428706.1:p.Val444Met
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000523239
  gene symbol: TACC1
  hgvsc: ENST00000523239.1:n.107G>A
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428687
  ensembl transcript: ENST00000519416
  gene symbol: TACC1
  hgvsc: ENST00000519416.1:c.877G>A
  hgvsp: ENSP00000428687.1:p.Val293Met
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430959
  ensembl transcript: ENST00000520973
  gene symbol: TACC1
  hgvsc: ENST00000520973.1:c.880G>A
  hgvsp: ENSP00000430959.1:p.Val294Met
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428949
  ensembl transcript: ENST00000521050
  gene symbol: TACC1
  hgvsc: ENST00000521050.1:c.187G>A
  hgvsp: ENSP00000428949.1:p.Val63Met
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000473342
  ensembl transcript: ENST00000520340
  gene symbol: TACC1
  hgvsc: ENST00000520340.1:c.1357G>A
  hgvsp: ENSP00000473342.1:p.Val453Met
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000321703
  ensembl transcript: ENST00000317827
  gene symbol: TACC1
  hgvsc: ENST00000317827.4:c.1465G>A
  hgvsp: ENSP00000321703.4:p.Val489Met
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430355
  ensembl transcript: ENST00000522904
  gene symbol: TACC1
  hgvsc: ENST00000522904.1:c.1381G>A
  hgvsp: ENSP00000430355.1:p.Val461Met
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000327818
  ensembl transcript: ENST00000348567
  gene symbol: TACC1
  hgvsc: ENST00000348567.4:c.151G>A
  hgvsp: ENSP00000327818.5:p.Val51Met
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428253
  ensembl transcript: ENST00000521866
  gene symbol: TACC1
  hgvsc: ENST00000521866.1:c.825G>A
  hgvsp: ENSP00000428253.1:p.Val276Met
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000369263
  ensembl transcript: ENST00000379931
  gene symbol: TACC1
  hgvsc: ENST00000379931.3:c.1501G>A
  hgvsp: ENSP00000369263.3:p.Val501Met
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430306
  ensembl transcript: ENST00000518809
  gene symbol: TACC1
  hgvsc: ENST00000518809.1:c.414G>A
  hgvsp: ENSP00000430306.1:p.Val139Met
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000276520
  ensembl transcript: ENST00000276520
  gene symbol: TACC1
  hgvsc: ENST00000276520.8:c.235G>A
  hgvsp: ENSP00000276520.8:p.Val79Met
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000332794
  ensembl transcript: ENST00000330691
  gene symbol: TACC1
  hgvsc: ENST00000330691.6:c.187G>A
  hgvsp: ENSP00000332794.6:p.Val63Met
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428450
  ensembl transcript: ENST00000520615
  gene symbol: TACC1
  hgvsc: ENST00000520615.1:c.880G>A
  hgvsp: ENSP00000428450.1:p.Val294Met
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000522752
  gene symbol: TACC1
  hgvsc: ENST00000522752.1:n.185G>A
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000393647
  ensembl transcript: ENST00000443286
  gene symbol: TACC1
  hgvsc: ENST00000443286.2:c.1513G>A
  hgvsp: ENSP00000393647.2:p.Val505Met
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000517336
  gene symbol: TACC1
  hgvsc: ENST00000517336.1:n.185G>A
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000522955
  gene symbol: TACC1
  hgvsc: ENST00000522955.1:n.1381G>A
  variant of: http://identifiers.org/hgnc/11522
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Val489Met
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

8-38684700-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38684700
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 38684700
    reference: chr 8
allele count: 4
allele frequency: 3.309723969020984e-5
allele num: 120856
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428949
  ensembl transcript: ENST00000521050
  gene symbol: TACC1
  hgvsc: ENST00000521050.1:c.189G>T
  hgvsp: ENST00000521050.1:c.189G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430355
  ensembl transcript: ENST00000522904
  gene symbol: TACC1
  hgvsc: ENST00000522904.1:c.1383G>T
  hgvsp: ENST00000522904.1:c.1383G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000473342
  ensembl transcript: ENST00000520340
  gene symbol: TACC1
  hgvsc: ENST00000520340.1:c.1359G>T
  hgvsp: ENST00000520340.1:c.1359G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430306
  ensembl transcript: ENST00000518809
  gene symbol: TACC1
  hgvsc: ENST00000518809.1:c.416G>T
  hgvsp: ENST00000518809.1:c.416G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000332794
  ensembl transcript: ENST00000330691
  gene symbol: TACC1
  hgvsc: ENST00000330691.6:c.189G>T
  hgvsp: ENST00000330691.6:c.189G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000522752
  gene symbol: TACC1
  hgvsc: ENST00000522752.1:n.187G>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428687
  ensembl transcript: ENST00000519416
  gene symbol: TACC1
  hgvsc: ENST00000519416.1:c.879G>T
  hgvsp: ENST00000519416.1:c.879G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428466
  ensembl transcript: ENST00000521642
  gene symbol: TACC1
  hgvsc: ENST00000521642.1:c.153G>T
  hgvsp: ENST00000521642.1:c.153G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000276520
  ensembl transcript: ENST00000276520
  gene symbol: TACC1
  hgvsc: ENST00000276520.8:c.237G>T
  hgvsp: ENST00000276520.8:c.237G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000523239
  gene symbol: TACC1
  hgvsc: ENST00000523239.1:n.109G>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430959
  ensembl transcript: ENST00000520973
  gene symbol: TACC1
  hgvsc: ENST00000520973.1:c.882G>T
  hgvsp: ENST00000520973.1:c.882G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000327818
  ensembl transcript: ENST00000348567
  gene symbol: TACC1
  hgvsc: ENST00000348567.4:c.153G>T
  hgvsp: ENST00000348567.4:c.153G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000393647
  ensembl transcript: ENST00000443286
  gene symbol: TACC1
  hgvsc: ENST00000443286.2:c.1515G>T
  hgvsp: ENST00000443286.2:c.1515G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000429418
  ensembl transcript: ENST00000520611
  gene symbol: TACC1
  hgvsc: ENST00000520611.1:c.-220G>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428450
  ensembl transcript: ENST00000520615
  gene symbol: TACC1
  hgvsc: ENST00000520615.1:c.882G>T
  hgvsp: ENST00000520615.1:c.882G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000321703
  ensembl transcript: ENST00000317827
  gene symbol: TACC1
  hgvsc: ENST00000317827.4:c.1467G>T
  hgvsp: ENST00000317827.4:c.1467G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000517336
  gene symbol: TACC1
  hgvsc: ENST00000517336.1:n.187G>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428253
  ensembl transcript: ENST00000521866
  gene symbol: TACC1
  hgvsc: ENST00000521866.1:c.827G>T
  hgvsp: ENST00000521866.1:c.827G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000522955
  gene symbol: TACC1
  hgvsc: ENST00000522955.1:n.1383G>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000369263
  ensembl transcript: ENST00000379931
  gene symbol: TACC1
  hgvsc: ENST00000379931.3:c.1503G>T
  hgvsp: ENST00000379931.3:c.1503G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/11522
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Val489Val
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum

8-38684710-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38684710
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 38684710
    reference: chr 8
allele count: 1
allele frequency: 8.252459232851389e-6
allele num: 121176
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430959
  ensembl transcript: ENST00000520973
  gene symbol: TACC1
  hgvsc: ENST00000520973.1:c.892A>G
  hgvsp: ENSP00000430959.1:p.Ile298Val
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430306
  ensembl transcript: ENST00000518809
  gene symbol: TACC1
  hgvsc: ENST00000518809.1:c.426A>G
  hgvsp: ENSP00000430306.1:p.Ile143Val
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428706
  ensembl transcript: ENST00000518415
  gene symbol: TACC1
  hgvsc: ENST00000518415.1:c.1342A>G
  hgvsp: ENSP00000428706.1:p.Ile448Val
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428466
  ensembl transcript: ENST00000521642
  gene symbol: TACC1
  hgvsc: ENST00000521642.1:c.163A>G
  hgvsp: ENSP00000428466.1:p.Ile55Val
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428450
  ensembl transcript: ENST00000520615
  gene symbol: TACC1
  hgvsc: ENST00000520615.1:c.892A>G
  hgvsp: ENSP00000428450.1:p.Ile298Val
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000276520
  ensembl transcript: ENST00000276520
  gene symbol: TACC1
  hgvsc: ENST00000276520.8:c.247A>G
  hgvsp: ENSP00000276520.8:p.Ile83Val
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000369263
  ensembl transcript: ENST00000379931
  gene symbol: TACC1
  hgvsc: ENST00000379931.3:c.1513A>G
  hgvsp: ENSP00000369263.3:p.Ile505Val
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000429418
  ensembl transcript: ENST00000520611
  gene symbol: TACC1
  hgvsc: ENST00000520611.1:c.-210A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000523239
  gene symbol: TACC1
  hgvsc: ENST00000523239.1:n.119A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000517336
  gene symbol: TACC1
  hgvsc: ENST00000517336.1:n.197A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428687
  ensembl transcript: ENST00000519416
  gene symbol: TACC1
  hgvsc: ENST00000519416.1:c.889A>G
  hgvsp: ENSP00000428687.1:p.Ile297Val
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428253
  ensembl transcript: ENST00000521866
  gene symbol: TACC1
  hgvsc: ENST00000521866.1:c.837A>G
  hgvsp: ENSP00000428253.1:p.Ile280Val
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000321703
  ensembl transcript: ENST00000317827
  gene symbol: TACC1
  hgvsc: ENST00000317827.4:c.1477A>G
  hgvsp: ENSP00000321703.4:p.Ile493Val
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000473342
  ensembl transcript: ENST00000520340
  gene symbol: TACC1
  hgvsc: ENST00000520340.1:c.1369A>G
  hgvsp: ENSP00000473342.1:p.Ile457Val
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428949
  ensembl transcript: ENST00000521050
  gene symbol: TACC1
  hgvsc: ENST00000521050.1:c.199A>G
  hgvsp: ENSP00000428949.1:p.Ile67Val
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000522752
  gene symbol: TACC1
  hgvsc: ENST00000522752.1:n.197A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000327818
  ensembl transcript: ENST00000348567
  gene symbol: TACC1
  hgvsc: ENST00000348567.4:c.163A>G
  hgvsp: ENSP00000327818.5:p.Ile55Val
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000393647
  ensembl transcript: ENST00000443286
  gene symbol: TACC1
  hgvsc: ENST00000443286.2:c.1525A>G
  hgvsp: ENSP00000393647.2:p.Ile509Val
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000522955
  gene symbol: TACC1
  hgvsc: ENST00000522955.1:n.1393A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430355
  ensembl transcript: ENST00000522904
  gene symbol: TACC1
  hgvsc: ENST00000522904.1:c.1393A>G
  hgvsp: ENSP00000430355.1:p.Ile465Val
  variant of: http://identifiers.org/hgnc/11522
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Ile493Val
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: Other
reference allele: A
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD

8-38684713-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38684713
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 38684713
    reference: chr 8
allele count: 1
allele frequency: 8.248919391559706e-6
allele num: 121228
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428253
  ensembl transcript: ENST00000521866
  gene symbol: TACC1
  hgvsc: ENST00000521866.1:c.840T>C
  hgvsp: ENSP00000428253.1:p.Ser281Pro
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428949
  ensembl transcript: ENST00000521050
  gene symbol: TACC1
  hgvsc: ENST00000521050.1:c.202T>C
  hgvsp: ENSP00000428949.1:p.Ser68Pro
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000321703
  ensembl transcript: ENST00000317827
  gene symbol: TACC1
  hgvsc: ENST00000317827.4:c.1480T>C
  hgvsp: ENSP00000321703.4:p.Ser494Pro
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000523239
  gene symbol: TACC1
  hgvsc: ENST00000523239.1:n.122T>C
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430306
  ensembl transcript: ENST00000518809
  gene symbol: TACC1
  hgvsc: ENST00000518809.1:c.429T>C
  hgvsp: ENSP00000430306.1:p.Ser144Pro
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428466
  ensembl transcript: ENST00000521642
  gene symbol: TACC1
  hgvsc: ENST00000521642.1:c.166T>C
  hgvsp: ENSP00000428466.1:p.Ser56Pro
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000473342
  ensembl transcript: ENST00000520340
  gene symbol: TACC1
  hgvsc: ENST00000520340.1:c.1372T>C
  hgvsp: ENSP00000473342.1:p.Ser458Pro
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000276520
  ensembl transcript: ENST00000276520
  gene symbol: TACC1
  hgvsc: ENST00000276520.8:c.250T>C
  hgvsp: ENSP00000276520.8:p.Ser84Pro
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000393647
  ensembl transcript: ENST00000443286
  gene symbol: TACC1
  hgvsc: ENST00000443286.2:c.1528T>C
  hgvsp: ENSP00000393647.2:p.Ser510Pro
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430355
  ensembl transcript: ENST00000522904
  gene symbol: TACC1
  hgvsc: ENST00000522904.1:c.1396T>C
  hgvsp: ENSP00000430355.1:p.Ser466Pro
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428450
  ensembl transcript: ENST00000520615
  gene symbol: TACC1
  hgvsc: ENST00000520615.1:c.895T>C
  hgvsp: ENSP00000428450.1:p.Ser299Pro
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000369263
  ensembl transcript: ENST00000379931
  gene symbol: TACC1
  hgvsc: ENST00000379931.3:c.1516T>C
  hgvsp: ENSP00000369263.3:p.Ser506Pro
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428687
  ensembl transcript: ENST00000519416
  gene symbol: TACC1
  hgvsc: ENST00000519416.1:c.892T>C
  hgvsp: ENSP00000428687.1:p.Ser298Pro
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000517336
  gene symbol: TACC1
  hgvsc: ENST00000517336.1:n.200T>C
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000522955
  gene symbol: TACC1
  hgvsc: ENST00000522955.1:n.1396T>C
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430959
  ensembl transcript: ENST00000520973
  gene symbol: TACC1
  hgvsc: ENST00000520973.1:c.895T>C
  hgvsp: ENSP00000430959.1:p.Ser299Pro
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000522752
  gene symbol: TACC1
  hgvsc: ENST00000522752.1:n.200T>C
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000332794
  ensembl transcript: ENST00000330691
  gene symbol: TACC1
  hgvsc: ENST00000330691.6:c.202T>C
  hgvsp: ENSP00000332794.6:p.Ser68Pro
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428706
  ensembl transcript: ENST00000518415
  gene symbol: TACC1
  hgvsc: ENST00000518415.1:c.1345T>C
  hgvsp: ENSP00000428706.1:p.Ser449Pro
  variant of: http://identifiers.org/hgnc/11522
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Ser494Pro
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
reference allele: T
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: VQSLOD

8-38684726-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38684726
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 38684726
    reference: chr 8
allele count: 1
allele frequency: 8.241577108195424e-6
allele num: 121336
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430959
  ensembl transcript: ENST00000520973
  gene symbol: TACC1
  hgvsc: ENST00000520973.1:c.908A>G
  hgvsp: ENSP00000430959.1:p.Asn303Ser
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000517336
  gene symbol: TACC1
  hgvsc: ENST00000517336.1:n.213A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000321703
  ensembl transcript: ENST00000317827
  gene symbol: TACC1
  hgvsc: ENST00000317827.4:c.1493A>G
  hgvsp: ENSP00000321703.4:p.Asn498Ser
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000473342
  ensembl transcript: ENST00000520340
  gene symbol: TACC1
  hgvsc: ENST00000520340.1:c.1385A>G
  hgvsp: ENSP00000473342.1:p.Asn462Ser
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000393647
  ensembl transcript: ENST00000443286
  gene symbol: TACC1
  hgvsc: ENST00000443286.2:c.1541A>G
  hgvsp: ENSP00000393647.2:p.Asn514Ser
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000429418
  ensembl transcript: ENST00000520611
  gene symbol: TACC1
  hgvsc: ENST00000520611.1:c.-194A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428687
  ensembl transcript: ENST00000519416
  gene symbol: TACC1
  hgvsc: ENST00000519416.1:c.905A>G
  hgvsp: ENSP00000428687.1:p.Asn302Ser
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000327818
  ensembl transcript: ENST00000348567
  gene symbol: TACC1
  hgvsc: ENST00000348567.4:c.179A>G
  hgvsp: ENSP00000327818.5:p.Asn60Ser
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430355
  ensembl transcript: ENST00000522904
  gene symbol: TACC1
  hgvsc: ENST00000522904.1:c.1409A>G
  hgvsp: ENSP00000430355.1:p.Asn470Ser
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428450
  ensembl transcript: ENST00000520615
  gene symbol: TACC1
  hgvsc: ENST00000520615.1:c.908A>G
  hgvsp: ENSP00000428450.1:p.Asn303Ser
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000369263
  ensembl transcript: ENST00000379931
  gene symbol: TACC1
  hgvsc: ENST00000379931.3:c.1529A>G
  hgvsp: ENSP00000369263.3:p.Asn510Ser
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428706
  ensembl transcript: ENST00000518415
  gene symbol: TACC1
  hgvsc: ENST00000518415.1:c.1358A>G
  hgvsp: ENSP00000428706.1:p.Asn453Ser
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000523239
  gene symbol: TACC1
  hgvsc: ENST00000523239.1:n.135A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428949
  ensembl transcript: ENST00000521050
  gene symbol: TACC1
  hgvsc: ENST00000521050.1:c.215A>G
  hgvsp: ENSP00000428949.1:p.Asn72Ser
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428466
  ensembl transcript: ENST00000521642
  gene symbol: TACC1
  hgvsc: ENST00000521642.1:c.179A>G
  hgvsp: ENSP00000428466.1:p.Asn60Ser
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000522752
  gene symbol: TACC1
  hgvsc: ENST00000522752.1:n.213A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000276520
  ensembl transcript: ENST00000276520
  gene symbol: TACC1
  hgvsc: ENST00000276520.8:c.263A>G
  hgvsp: ENSP00000276520.8:p.Asn88Ser
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000522955
  gene symbol: TACC1
  hgvsc: ENST00000522955.1:n.1409A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430306
  ensembl transcript: ENST00000518809
  gene symbol: TACC1
  hgvsc: ENST00000518809.1:c.442A>G
  hgvsp: ENSP00000430306.1:p.Asn148Ser
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000332794
  ensembl transcript: ENST00000330691
  gene symbol: TACC1
  hgvsc: ENST00000330691.6:c.215A>G
  hgvsp: ENSP00000332794.6:p.Asn72Ser
  variant of: http://identifiers.org/hgnc/11522
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Asn498Ser
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
reference allele: A
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: ClippingRankSum

8-38684729-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38684729
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 38684729
    reference: chr 8
allele count: 2
allele frequency: 1.648233917357551e-5
allele num: 121342
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000321703
  ensembl transcript: ENST00000317827
  gene symbol: TACC1
  hgvsc: ENST00000317827.4:c.1496G>C
  hgvsp: ENSP00000321703.4:p.Arg499Thr
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000369263
  ensembl transcript: ENST00000379931
  gene symbol: TACC1
  hgvsc: ENST00000379931.3:c.1532G>C
  hgvsp: ENSP00000369263.3:p.Arg511Thr
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000393647
  ensembl transcript: ENST00000443286
  gene symbol: TACC1
  hgvsc: ENST00000443286.2:c.1544G>C
  hgvsp: ENSP00000393647.2:p.Arg515Thr
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000327818
  ensembl transcript: ENST00000348567
  gene symbol: TACC1
  hgvsc: ENST00000348567.4:c.182G>C
  hgvsp: ENSP00000327818.5:p.Arg61Thr
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428949
  ensembl transcript: ENST00000521050
  gene symbol: TACC1
  hgvsc: ENST00000521050.1:c.218G>C
  hgvsp: ENSP00000428949.1:p.Arg73Thr
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428450
  ensembl transcript: ENST00000520615
  gene symbol: TACC1
  hgvsc: ENST00000520615.1:c.911G>C
  hgvsp: ENSP00000428450.1:p.Arg304Thr
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428253
  ensembl transcript: ENST00000521866
  gene symbol: TACC1
  hgvsc: ENST00000521866.1:c.856G>C
  hgvsp: ENSP00000428253.1:p.Arg286Thr
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430959
  ensembl transcript: ENST00000520973
  gene symbol: TACC1
  hgvsc: ENST00000520973.1:c.911G>C
  hgvsp: ENSP00000430959.1:p.Arg304Thr
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000429418
  ensembl transcript: ENST00000520611
  gene symbol: TACC1
  hgvsc: ENST00000520611.1:c.-191G>C
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428706
  ensembl transcript: ENST00000518415
  gene symbol: TACC1
  hgvsc: ENST00000518415.1:c.1361G>C
  hgvsp: ENSP00000428706.1:p.Arg454Thr
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000517336
  gene symbol: TACC1
  hgvsc: ENST00000517336.1:n.216G>C
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000473342
  ensembl transcript: ENST00000520340
  gene symbol: TACC1
  hgvsc: ENST00000520340.1:c.1388G>C
  hgvsp: ENSP00000473342.1:p.Arg463Thr
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430306
  ensembl transcript: ENST00000518809
  gene symbol: TACC1
  hgvsc: ENST00000518809.1:c.445G>C
  hgvsp: ENSP00000430306.1:p.Arg149Thr
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000276520
  ensembl transcript: ENST00000276520
  gene symbol: TACC1
  hgvsc: ENST00000276520.8:c.266G>C
  hgvsp: ENSP00000276520.8:p.Arg89Thr
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428466
  ensembl transcript: ENST00000521642
  gene symbol: TACC1
  hgvsc: ENST00000521642.1:c.182G>C
  hgvsp: ENSP00000428466.1:p.Arg61Thr
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000522955
  gene symbol: TACC1
  hgvsc: ENST00000522955.1:n.1412G>C
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428687
  ensembl transcript: ENST00000519416
  gene symbol: TACC1
  hgvsc: ENST00000519416.1:c.908G>C
  hgvsp: ENSP00000428687.1:p.Arg303Thr
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000332794
  ensembl transcript: ENST00000330691
  gene symbol: TACC1
  hgvsc: ENST00000330691.6:c.218G>C
  hgvsp: ENSP00000332794.6:p.Arg73Thr
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000522752
  gene symbol: TACC1
  hgvsc: ENST00000522752.1:n.216G>C
  variant of: http://identifiers.org/hgnc/11522
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Arg499Thr
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum

8-38684730-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38684730
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 38684730
    reference: chr 8
allele count: 2
allele frequency: 1.648206751054852e-5
allele num: 121344
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428466
  ensembl transcript: ENST00000521642
  gene symbol: TACC1
  hgvsc: ENST00000521642.1:c.183G>A
  hgvsp: ENST00000521642.1:c.183G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000332794
  ensembl transcript: ENST00000330691
  gene symbol: TACC1
  hgvsc: ENST00000330691.6:c.219G>A
  hgvsp: ENST00000330691.6:c.219G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428253
  ensembl transcript: ENST00000521866
  gene symbol: TACC1
  hgvsc: ENST00000521866.1:c.857G>A
  hgvsp: ENST00000521866.1:c.857G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000327818
  ensembl transcript: ENST00000348567
  gene symbol: TACC1
  hgvsc: ENST00000348567.4:c.183G>A
  hgvsp: ENST00000348567.4:c.183G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428949
  ensembl transcript: ENST00000521050
  gene symbol: TACC1
  hgvsc: ENST00000521050.1:c.219G>A
  hgvsp: ENST00000521050.1:c.219G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428706
  ensembl transcript: ENST00000518415
  gene symbol: TACC1
  hgvsc: ENST00000518415.1:c.1362G>A
  hgvsp: ENST00000518415.1:c.1362G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430306
  ensembl transcript: ENST00000518809
  gene symbol: TACC1
  hgvsc: ENST00000518809.1:c.446G>A
  hgvsp: ENST00000518809.1:c.446G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428450
  ensembl transcript: ENST00000520615
  gene symbol: TACC1
  hgvsc: ENST00000520615.1:c.912G>A
  hgvsp: ENST00000520615.1:c.912G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000276520
  ensembl transcript: ENST00000276520
  gene symbol: TACC1
  hgvsc: ENST00000276520.8:c.267G>A
  hgvsp: ENST00000276520.8:c.267G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430959
  ensembl transcript: ENST00000520973
  gene symbol: TACC1
  hgvsc: ENST00000520973.1:c.912G>A
  hgvsp: ENST00000520973.1:c.912G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000321703
  ensembl transcript: ENST00000317827
  gene symbol: TACC1
  hgvsc: ENST00000317827.4:c.1497G>A
  hgvsp: ENST00000317827.4:c.1497G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000523239
  gene symbol: TACC1
  hgvsc: ENST00000523239.1:n.139G>A
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000522752
  gene symbol: TACC1
  hgvsc: ENST00000522752.1:n.217G>A
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000393647
  ensembl transcript: ENST00000443286
  gene symbol: TACC1
  hgvsc: ENST00000443286.2:c.1545G>A
  hgvsp: ENST00000443286.2:c.1545G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430355
  ensembl transcript: ENST00000522904
  gene symbol: TACC1
  hgvsc: ENST00000522904.1:c.1413G>A
  hgvsp: ENST00000522904.1:c.1413G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000369263
  ensembl transcript: ENST00000379931
  gene symbol: TACC1
  hgvsc: ENST00000379931.3:c.1533G>A
  hgvsp: ENST00000379931.3:c.1533G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000522955
  gene symbol: TACC1
  hgvsc: ENST00000522955.1:n.1413G>A
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428687
  ensembl transcript: ENST00000519416
  gene symbol: TACC1
  hgvsc: ENST00000519416.1:c.909G>A
  hgvsp: ENST00000519416.1:c.909G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000429418
  ensembl transcript: ENST00000520611
  gene symbol: TACC1
  hgvsc: ENST00000520611.1:c.-190G>A
  variant of: http://identifiers.org/hgnc/11522
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Arg499Arg
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
population: European (Finnish)
reference allele: G
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum

8-38684731-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38684731
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 38684731
    reference: chr 8
allele count: 1
allele frequency: 8.240626287597857e-6
allele num: 121350
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000369263
  ensembl transcript: ENST00000379931
  gene symbol: TACC1
  hgvsc: ENST00000379931.3:c.1534G>T
  hgvsp: ENSP00000369263.3:p.Asp512Tyr
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000517336
  gene symbol: TACC1
  hgvsc: ENST00000517336.1:n.218G>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000523239
  gene symbol: TACC1
  hgvsc: ENST00000523239.1:n.140G>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000321703
  ensembl transcript: ENST00000317827
  gene symbol: TACC1
  hgvsc: ENST00000317827.4:c.1498G>T
  hgvsp: ENSP00000321703.4:p.Asp500Tyr
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428450
  ensembl transcript: ENST00000520615
  gene symbol: TACC1
  hgvsc: ENST00000520615.1:c.913G>T
  hgvsp: ENSP00000428450.1:p.Asp305Tyr
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000332794
  ensembl transcript: ENST00000330691
  gene symbol: TACC1
  hgvsc: ENST00000330691.6:c.220G>T
  hgvsp: ENSP00000332794.6:p.Asp74Tyr
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428466
  ensembl transcript: ENST00000521642
  gene symbol: TACC1
  hgvsc: ENST00000521642.1:c.184G>T
  hgvsp: ENSP00000428466.1:p.Asp62Tyr
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000393647
  ensembl transcript: ENST00000443286
  gene symbol: TACC1
  hgvsc: ENST00000443286.2:c.1546G>T
  hgvsp: ENSP00000393647.2:p.Asp516Tyr
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000522955
  gene symbol: TACC1
  hgvsc: ENST00000522955.1:n.1414G>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000327818
  ensembl transcript: ENST00000348567
  gene symbol: TACC1
  hgvsc: ENST00000348567.4:c.184G>T
  hgvsp: ENSP00000327818.5:p.Asp62Tyr
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430306
  ensembl transcript: ENST00000518809
  gene symbol: TACC1
  hgvsc: ENST00000518809.1:c.447G>T
  hgvsp: ENSP00000430306.1:p.Asp150Tyr
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000429418
  ensembl transcript: ENST00000520611
  gene symbol: TACC1
  hgvsc: ENST00000520611.1:c.-189G>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000276520
  ensembl transcript: ENST00000276520
  gene symbol: TACC1
  hgvsc: ENST00000276520.8:c.268G>T
  hgvsp: ENSP00000276520.8:p.Asp90Tyr
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428706
  ensembl transcript: ENST00000518415
  gene symbol: TACC1
  hgvsc: ENST00000518415.1:c.1363G>T
  hgvsp: ENSP00000428706.1:p.Asp455Tyr
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000473342
  ensembl transcript: ENST00000520340
  gene symbol: TACC1
  hgvsc: ENST00000520340.1:c.1390G>T
  hgvsp: ENSP00000473342.1:p.Asp464Tyr
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428949
  ensembl transcript: ENST00000521050
  gene symbol: TACC1
  hgvsc: ENST00000521050.1:c.220G>T
  hgvsp: ENSP00000428949.1:p.Asp74Tyr
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430959
  ensembl transcript: ENST00000520973
  gene symbol: TACC1
  hgvsc: ENST00000520973.1:c.913G>T
  hgvsp: ENSP00000430959.1:p.Asp305Tyr
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428253
  ensembl transcript: ENST00000521866
  gene symbol: TACC1
  hgvsc: ENST00000521866.1:c.858G>T
  hgvsp: ENSP00000428253.1:p.Asp287Tyr
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430355
  ensembl transcript: ENST00000522904
  gene symbol: TACC1
  hgvsc: ENST00000522904.1:c.1414G>T
  hgvsp: ENSP00000430355.1:p.Asp472Tyr
  variant of: http://identifiers.org/hgnc/11522
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Asp500Tyr
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
reference allele: G
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD

8-38684732-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38684732
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 38684732
    reference: chr 8
allele count: 1
allele frequency: 8.240490473993011e-6
allele num: 121352
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000321703
  ensembl transcript: ENST00000317827
  gene symbol: TACC1
  hgvsc: ENST00000317827.4:c.1499A>G
  hgvsp: ENSP00000321703.4:p.Asp500Gly
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000393647
  ensembl transcript: ENST00000443286
  gene symbol: TACC1
  hgvsc: ENST00000443286.2:c.1547A>G
  hgvsp: ENSP00000393647.2:p.Asp516Gly
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000332794
  ensembl transcript: ENST00000330691
  gene symbol: TACC1
  hgvsc: ENST00000330691.6:c.221A>G
  hgvsp: ENSP00000332794.6:p.Asp74Gly
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000327818
  ensembl transcript: ENST00000348567
  gene symbol: TACC1
  hgvsc: ENST00000348567.4:c.185A>G
  hgvsp: ENSP00000327818.5:p.Asp62Gly
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428687
  ensembl transcript: ENST00000519416
  gene symbol: TACC1
  hgvsc: ENST00000519416.1:c.911A>G
  hgvsp: ENSP00000428687.1:p.Asp304Gly
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428450
  ensembl transcript: ENST00000520615
  gene symbol: TACC1
  hgvsc: ENST00000520615.1:c.914A>G
  hgvsp: ENSP00000428450.1:p.Asp305Gly
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000523239
  gene symbol: TACC1
  hgvsc: ENST00000523239.1:n.141A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428949
  ensembl transcript: ENST00000521050
  gene symbol: TACC1
  hgvsc: ENST00000521050.1:c.221A>G
  hgvsp: ENSP00000428949.1:p.Asp74Gly
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000369263
  ensembl transcript: ENST00000379931
  gene symbol: TACC1
  hgvsc: ENST00000379931.3:c.1535A>G
  hgvsp: ENSP00000369263.3:p.Asp512Gly
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428466
  ensembl transcript: ENST00000521642
  gene symbol: TACC1
  hgvsc: ENST00000521642.1:c.185A>G
  hgvsp: ENSP00000428466.1:p.Asp62Gly
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000517336
  gene symbol: TACC1
  hgvsc: ENST00000517336.1:n.219A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430959
  ensembl transcript: ENST00000520973
  gene symbol: TACC1
  hgvsc: ENST00000520973.1:c.914A>G
  hgvsp: ENSP00000430959.1:p.Asp305Gly
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428706
  ensembl transcript: ENST00000518415
  gene symbol: TACC1
  hgvsc: ENST00000518415.1:c.1364A>G
  hgvsp: ENSP00000428706.1:p.Asp455Gly
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000276520
  ensembl transcript: ENST00000276520
  gene symbol: TACC1
  hgvsc: ENST00000276520.8:c.269A>G
  hgvsp: ENSP00000276520.8:p.Asp90Gly
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000522955
  gene symbol: TACC1
  hgvsc: ENST00000522955.1:n.1415A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430306
  ensembl transcript: ENST00000518809
  gene symbol: TACC1
  hgvsc: ENST00000518809.1:c.448A>G
  hgvsp: ENSP00000430306.1:p.Asp150Gly
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428253
  ensembl transcript: ENST00000521866
  gene symbol: TACC1
  hgvsc: ENST00000521866.1:c.859A>G
  hgvsp: ENSP00000428253.1:p.Asp287Gly
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000522752
  gene symbol: TACC1
  hgvsc: ENST00000522752.1:n.219A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000473342
  ensembl transcript: ENST00000520340
  gene symbol: TACC1
  hgvsc: ENST00000520340.1:c.1391A>G
  hgvsp: ENSP00000473342.1:p.Asp464Gly
  variant of: http://identifiers.org/hgnc/11522
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Asp500Gly
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: Other
reference allele: A
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum

8-38684736-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38684736
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 38684736
    reference: chr 8
allele count: 2
allele frequency: 1.647989452867502e-5
allele num: 121360
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000517336
  gene symbol: TACC1
  hgvsc: ENST00000517336.1:n.223C>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000369263
  ensembl transcript: ENST00000379931
  gene symbol: TACC1
  hgvsc: ENST00000379931.3:c.1539C>G
  hgvsp: ENST00000379931.3:c.1539C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428450
  ensembl transcript: ENST00000520615
  gene symbol: TACC1
  hgvsc: ENST00000520615.1:c.918C>G
  hgvsp: ENST00000520615.1:c.918C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428706
  ensembl transcript: ENST00000518415
  gene symbol: TACC1
  hgvsc: ENST00000518415.1:c.1368C>G
  hgvsp: ENST00000518415.1:c.1368C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430355
  ensembl transcript: ENST00000522904
  gene symbol: TACC1
  hgvsc: ENST00000522904.1:c.1419C>G
  hgvsp: ENST00000522904.1:c.1419C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430959
  ensembl transcript: ENST00000520973
  gene symbol: TACC1
  hgvsc: ENST00000520973.1:c.918C>G
  hgvsp: ENST00000520973.1:c.918C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000393647
  ensembl transcript: ENST00000443286
  gene symbol: TACC1
  hgvsc: ENST00000443286.2:c.1551C>G
  hgvsp: ENST00000443286.2:c.1551C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000321703
  ensembl transcript: ENST00000317827
  gene symbol: TACC1
  hgvsc: ENST00000317827.4:c.1503C>G
  hgvsp: ENST00000317827.4:c.1503C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428253
  ensembl transcript: ENST00000521866
  gene symbol: TACC1
  hgvsc: ENST00000521866.1:c.863C>G
  hgvsp: ENST00000521866.1:c.863C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428949
  ensembl transcript: ENST00000521050
  gene symbol: TACC1
  hgvsc: ENST00000521050.1:c.225C>G
  hgvsp: ENST00000521050.1:c.225C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000523239
  gene symbol: TACC1
  hgvsc: ENST00000523239.1:n.145C>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000276520
  ensembl transcript: ENST00000276520
  gene symbol: TACC1
  hgvsc: ENST00000276520.8:c.273C>G
  hgvsp: ENST00000276520.8:c.273C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000522955
  gene symbol: TACC1
  hgvsc: ENST00000522955.1:n.1419C>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000429418
  ensembl transcript: ENST00000520611
  gene symbol: TACC1
  hgvsc: ENST00000520611.1:c.-184C>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430306
  ensembl transcript: ENST00000518809
  gene symbol: TACC1
  hgvsc: ENST00000518809.1:c.452C>G
  hgvsp: ENST00000518809.1:c.452C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000473342
  ensembl transcript: ENST00000520340
  gene symbol: TACC1
  hgvsc: ENST00000520340.1:c.1395C>G
  hgvsp: ENST00000520340.1:c.1395C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000327818
  ensembl transcript: ENST00000348567
  gene symbol: TACC1
  hgvsc: ENST00000348567.4:c.189C>G
  hgvsp: ENST00000348567.4:c.189C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000332794
  ensembl transcript: ENST00000330691
  gene symbol: TACC1
  hgvsc: ENST00000330691.6:c.225C>G
  hgvsp: ENST00000330691.6:c.225C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428687
  ensembl transcript: ENST00000519416
  gene symbol: TACC1
  hgvsc: ENST00000519416.1:c.915C>G
  hgvsp: ENST00000519416.1:c.915C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/11522
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Gly501Gly
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: DP

8-38684741-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38684741
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 38684741
    reference: chr 8
allele count: 1
allele frequency: 8.239132584121543e-6
allele num: 121372
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428706
  ensembl transcript: ENST00000518415
  gene symbol: TACC1
  hgvsc: ENST00000518415.1:c.1373C>G
  hgvsp: ENSP00000428706.1:p.Ala458Gly
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000332794
  ensembl transcript: ENST00000330691
  gene symbol: TACC1
  hgvsc: ENST00000330691.6:c.230C>G
  hgvsp: ENSP00000332794.6:p.Ala77Gly
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428450
  ensembl transcript: ENST00000520615
  gene symbol: TACC1
  hgvsc: ENST00000520615.1:c.923C>G
  hgvsp: ENSP00000428450.1:p.Ala308Gly
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428466
  ensembl transcript: ENST00000521642
  gene symbol: TACC1
  hgvsc: ENST00000521642.1:c.194C>G
  hgvsp: ENSP00000428466.1:p.Ala65Gly
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000473342
  ensembl transcript: ENST00000520340
  gene symbol: TACC1
  hgvsc: ENST00000520340.1:c.1400C>G
  hgvsp: ENSP00000473342.1:p.Ala467Gly
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000393647
  ensembl transcript: ENST00000443286
  gene symbol: TACC1
  hgvsc: ENST00000443286.2:c.1556C>G
  hgvsp: ENSP00000393647.2:p.Ala519Gly
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428949
  ensembl transcript: ENST00000521050
  gene symbol: TACC1
  hgvsc: ENST00000521050.1:c.230C>G
  hgvsp: ENSP00000428949.1:p.Ala77Gly
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430959
  ensembl transcript: ENST00000520973
  gene symbol: TACC1
  hgvsc: ENST00000520973.1:c.923C>G
  hgvsp: ENSP00000430959.1:p.Ala308Gly
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000523239
  gene symbol: TACC1
  hgvsc: ENST00000523239.1:n.150C>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430306
  ensembl transcript: ENST00000518809
  gene symbol: TACC1
  hgvsc: ENST00000518809.1:c.457C>G
  hgvsp: ENSP00000430306.1:p.Ala153Gly
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000276520
  ensembl transcript: ENST00000276520
  gene symbol: TACC1
  hgvsc: ENST00000276520.8:c.278C>G
  hgvsp: ENSP00000276520.8:p.Ala93Gly
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000327818
  ensembl transcript: ENST00000348567
  gene symbol: TACC1
  hgvsc: ENST00000348567.4:c.194C>G
  hgvsp: ENSP00000327818.5:p.Ala65Gly
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000321703
  ensembl transcript: ENST00000317827
  gene symbol: TACC1
  hgvsc: ENST00000317827.4:c.1508C>G
  hgvsp: ENSP00000321703.4:p.Ala503Gly
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430355
  ensembl transcript: ENST00000522904
  gene symbol: TACC1
  hgvsc: ENST00000522904.1:c.1424C>G
  hgvsp: ENSP00000430355.1:p.Ala475Gly
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000522955
  gene symbol: TACC1
  hgvsc: ENST00000522955.1:n.1424C>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000517336
  gene symbol: TACC1
  hgvsc: ENST00000517336.1:n.228C>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000369263
  ensembl transcript: ENST00000379931
  gene symbol: TACC1
  hgvsc: ENST00000379931.3:c.1544C>G
  hgvsp: ENSP00000369263.3:p.Ala515Gly
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428687
  ensembl transcript: ENST00000519416
  gene symbol: TACC1
  hgvsc: ENST00000519416.1:c.920C>G
  hgvsp: ENSP00000428687.1:p.Ala307Gly
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000429418
  ensembl transcript: ENST00000520611
  gene symbol: TACC1
  hgvsc: ENST00000520611.1:c.-179C>G
  variant of: http://identifiers.org/hgnc/11522
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Ala503Gly
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: QD

8-38684761-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38684761
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 38684761
    reference: chr 8
allele count: 1
allele frequency: 8.238453806989504e-6
allele num: 121382
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000276520
  ensembl transcript: ENST00000276520
  gene symbol: TACC1
  hgvsc: ENST00000276520.8:c.298G>A
  hgvsp: ENSP00000276520.8:p.Ala100Thr
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428949
  ensembl transcript: ENST00000521050
  gene symbol: TACC1
  hgvsc: ENST00000521050.1:c.250G>A
  hgvsp: ENSP00000428949.1:p.Ala84Thr
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000321703
  ensembl transcript: ENST00000317827
  gene symbol: TACC1
  hgvsc: ENST00000317827.4:c.1528G>A
  hgvsp: ENSP00000321703.4:p.Ala510Thr
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430306
  ensembl transcript: ENST00000518809
  gene symbol: TACC1
  hgvsc: ENST00000518809.1:c.477G>A
  hgvsp: ENSP00000430306.1:p.Ala160Thr
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000522752
  gene symbol: TACC1
  hgvsc: ENST00000522752.1:n.248G>A
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000369263
  ensembl transcript: ENST00000379931
  gene symbol: TACC1
  hgvsc: ENST00000379931.3:c.1564G>A
  hgvsp: ENSP00000369263.3:p.Ala522Thr
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430959
  ensembl transcript: ENST00000520973
  gene symbol: TACC1
  hgvsc: ENST00000520973.1:c.943G>A
  hgvsp: ENSP00000430959.1:p.Ala315Thr
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430355
  ensembl transcript: ENST00000522904
  gene symbol: TACC1
  hgvsc: ENST00000522904.1:c.1444G>A
  hgvsp: ENSP00000430355.1:p.Ala482Thr
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000332794
  ensembl transcript: ENST00000330691
  gene symbol: TACC1
  hgvsc: ENST00000330691.6:c.250G>A
  hgvsp: ENSP00000332794.6:p.Ala84Thr
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000393647
  ensembl transcript: ENST00000443286
  gene symbol: TACC1
  hgvsc: ENST00000443286.2:c.1576G>A
  hgvsp: ENSP00000393647.2:p.Ala526Thr
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000429418
  ensembl transcript: ENST00000520611
  gene symbol: TACC1
  hgvsc: ENST00000520611.1:c.-159G>A
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428687
  ensembl transcript: ENST00000519416
  gene symbol: TACC1
  hgvsc: ENST00000519416.1:c.940G>A
  hgvsp: ENSP00000428687.1:p.Ala314Thr
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428253
  ensembl transcript: ENST00000521866
  gene symbol: TACC1
  hgvsc: ENST00000521866.1:c.888G>A
  hgvsp: ENSP00000428253.1:p.Ala297Thr
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000517336
  gene symbol: TACC1
  hgvsc: ENST00000517336.1:n.248G>A
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428466
  ensembl transcript: ENST00000521642
  gene symbol: TACC1
  hgvsc: ENST00000521642.1:c.214G>A
  hgvsp: ENSP00000428466.1:p.Ala72Thr
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000522955
  gene symbol: TACC1
  hgvsc: ENST00000522955.1:n.1444G>A
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000473342
  ensembl transcript: ENST00000520340
  gene symbol: TACC1
  hgvsc: ENST00000520340.1:c.1420G>A
  hgvsp: ENSP00000473342.1:p.Ala474Thr
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428450
  ensembl transcript: ENST00000520615
  gene symbol: TACC1
  hgvsc: ENST00000520615.1:c.943G>A
  hgvsp: ENSP00000428450.1:p.Ala315Thr
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428706
  ensembl transcript: ENST00000518415
  gene symbol: TACC1
  hgvsc: ENST00000518415.1:c.1393G>A
  hgvsp: ENSP00000428706.1:p.Ala465Thr
  variant of: http://identifiers.org/hgnc/11522
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Ala510Thr
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: South Asian
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQ

8-38684765-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38684765
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 38684765
    reference: chr 8
allele count: 20
allele frequency: 1.647717910693689e-4
allele num: 121380
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000276520
  ensembl transcript: ENST00000276520
  gene symbol: TACC1
  hgvsc: ENST00000276520.8:c.302C>T
  hgvsp: ENSP00000276520.8:p.Ser101Phe
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000473342
  ensembl transcript: ENST00000520340
  gene symbol: TACC1
  hgvsc: ENST00000520340.1:c.1424C>T
  hgvsp: ENSP00000473342.1:p.Ser475Phe
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430355
  ensembl transcript: ENST00000522904
  gene symbol: TACC1
  hgvsc: ENST00000522904.1:c.1448C>T
  hgvsp: ENSP00000430355.1:p.Ser483Phe
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000332794
  ensembl transcript: ENST00000330691
  gene symbol: TACC1
  hgvsc: ENST00000330691.6:c.254C>T
  hgvsp: ENSP00000332794.6:p.Ser85Phe
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428706
  ensembl transcript: ENST00000518415
  gene symbol: TACC1
  hgvsc: ENST00000518415.1:c.1397C>T
  hgvsp: ENSP00000428706.1:p.Ser466Phe
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428466
  ensembl transcript: ENST00000521642
  gene symbol: TACC1
  hgvsc: ENST00000521642.1:c.218C>T
  hgvsp: ENSP00000428466.1:p.Ser73Phe
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000517336
  gene symbol: TACC1
  hgvsc: ENST00000517336.1:n.252C>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000321703
  ensembl transcript: ENST00000317827
  gene symbol: TACC1
  hgvsc: ENST00000317827.4:c.1532C>T
  hgvsp: ENSP00000321703.4:p.Ser511Phe
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428253
  ensembl transcript: ENST00000521866
  gene symbol: TACC1
  hgvsc: ENST00000521866.1:c.892C>T
  hgvsp: ENSP00000428253.1:p.Ser298Phe
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430959
  ensembl transcript: ENST00000520973
  gene symbol: TACC1
  hgvsc: ENST00000520973.1:c.947C>T
  hgvsp: ENSP00000430959.1:p.Ser316Phe
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428450
  ensembl transcript: ENST00000520615
  gene symbol: TACC1
  hgvsc: ENST00000520615.1:c.947C>T
  hgvsp: ENSP00000428450.1:p.Ser316Phe
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000523239
  gene symbol: TACC1
  hgvsc: ENST00000523239.1:n.174C>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000429418
  ensembl transcript: ENST00000520611
  gene symbol: TACC1
  hgvsc: ENST00000520611.1:c.-155C>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000369263
  ensembl transcript: ENST00000379931
  gene symbol: TACC1
  hgvsc: ENST00000379931.3:c.1568C>T
  hgvsp: ENSP00000369263.3:p.Ser523Phe
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430306
  ensembl transcript: ENST00000518809
  gene symbol: TACC1
  hgvsc: ENST00000518809.1:c.481C>T
  hgvsp: ENSP00000430306.1:p.Ser161Phe
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428687
  ensembl transcript: ENST00000519416
  gene symbol: TACC1
  hgvsc: ENST00000519416.1:c.944C>T
  hgvsp: ENSP00000428687.1:p.Ser315Phe
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428949
  ensembl transcript: ENST00000521050
  gene symbol: TACC1
  hgvsc: ENST00000521050.1:c.254C>T
  hgvsp: ENSP00000428949.1:p.Ser85Phe
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000327818
  ensembl transcript: ENST00000348567
  gene symbol: TACC1
  hgvsc: ENST00000348567.4:c.218C>T
  hgvsp: ENSP00000327818.5:p.Ser73Phe
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000393647
  ensembl transcript: ENST00000443286
  gene symbol: TACC1
  hgvsc: ENST00000443286.2:c.1580C>T
  hgvsp: ENSP00000393647.2:p.Ser527Phe
  variant of: http://identifiers.org/hgnc/11522
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Ser511Phe
num of homozygotes: 1
population: East Asian
population: Latino
population: Other
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff

8-38684768-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38684768
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 38684768
    reference: chr 8
allele count: 1
allele frequency: 8.238589553468446e-6
allele num: 121380
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000321703
  ensembl transcript: ENST00000317827
  gene symbol: TACC1
  hgvsc: ENST00000317827.4:c.1535C>T
  hgvsp: ENSP00000321703.4:p.Thr512Met
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428949
  ensembl transcript: ENST00000521050
  gene symbol: TACC1
  hgvsc: ENST00000521050.1:c.257C>T
  hgvsp: ENSP00000428949.1:p.Thr86Met
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000473342
  ensembl transcript: ENST00000520340
  gene symbol: TACC1
  hgvsc: ENST00000520340.1:c.1427C>T
  hgvsp: ENSP00000473342.1:p.Thr476Met
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000517336
  gene symbol: TACC1
  hgvsc: ENST00000517336.1:n.255C>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430306
  ensembl transcript: ENST00000518809
  gene symbol: TACC1
  hgvsc: ENST00000518809.1:c.484C>T
  hgvsp: ENSP00000430306.1:p.Thr162Met
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430959
  ensembl transcript: ENST00000520973
  gene symbol: TACC1
  hgvsc: ENST00000520973.1:c.950C>T
  hgvsp: ENSP00000430959.1:p.Thr317Met
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430355
  ensembl transcript: ENST00000522904
  gene symbol: TACC1
  hgvsc: ENST00000522904.1:c.1451C>T
  hgvsp: ENSP00000430355.1:p.Thr484Met
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428450
  ensembl transcript: ENST00000520615
  gene symbol: TACC1
  hgvsc: ENST00000520615.1:c.950C>T
  hgvsp: ENSP00000428450.1:p.Thr317Met
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000276520
  ensembl transcript: ENST00000276520
  gene symbol: TACC1
  hgvsc: ENST00000276520.8:c.305C>T
  hgvsp: ENSP00000276520.8:p.Thr102Met
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428687
  ensembl transcript: ENST00000519416
  gene symbol: TACC1
  hgvsc: ENST00000519416.1:c.947C>T
  hgvsp: ENSP00000428687.1:p.Thr316Met
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000393647
  ensembl transcript: ENST00000443286
  gene symbol: TACC1
  hgvsc: ENST00000443286.2:c.1583C>T
  hgvsp: ENSP00000393647.2:p.Thr528Met
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000429418
  ensembl transcript: ENST00000520611
  gene symbol: TACC1
  hgvsc: ENST00000520611.1:c.-152C>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428706
  ensembl transcript: ENST00000518415
  gene symbol: TACC1
  hgvsc: ENST00000518415.1:c.1400C>T
  hgvsp: ENSP00000428706.1:p.Thr467Met
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000522955
  gene symbol: TACC1
  hgvsc: ENST00000522955.1:n.1451C>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000369263
  ensembl transcript: ENST00000379931
  gene symbol: TACC1
  hgvsc: ENST00000379931.3:c.1571C>T
  hgvsp: ENSP00000369263.3:p.Thr524Met
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000522752
  gene symbol: TACC1
  hgvsc: ENST00000522752.1:n.255C>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000327818
  ensembl transcript: ENST00000348567
  gene symbol: TACC1
  hgvsc: ENST00000348567.4:c.221C>T
  hgvsp: ENSP00000327818.5:p.Thr74Met
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000332794
  ensembl transcript: ENST00000330691
  gene symbol: TACC1
  hgvsc: ENST00000330691.6:c.257C>T
  hgvsp: ENSP00000332794.6:p.Thr86Met
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428253
  ensembl transcript: ENST00000521866
  gene symbol: TACC1
  hgvsc: ENST00000521866.1:c.895C>T
  hgvsp: ENSP00000428253.1:p.Thr299Met
  variant of: http://identifiers.org/hgnc/11522
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Thr512Met
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: Other
population: South Asian
population: European (Non-Finnish)
population: African
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP

8-38684769-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38684769
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 38684769
    reference: chr 8
allele count: 2
allele frequency: 1.647799363949445e-5
allele num: 121374
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430306
  ensembl transcript: ENST00000518809
  gene symbol: TACC1
  hgvsc: ENST00000518809.1:c.485G>A
  hgvsp: ENST00000518809.1:c.485G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000393647
  ensembl transcript: ENST00000443286
  gene symbol: TACC1
  hgvsc: ENST00000443286.2:c.1584G>A
  hgvsp: ENST00000443286.2:c.1584G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000523239
  gene symbol: TACC1
  hgvsc: ENST00000523239.1:n.178G>A
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000369263
  ensembl transcript: ENST00000379931
  gene symbol: TACC1
  hgvsc: ENST00000379931.3:c.1572G>A
  hgvsp: ENST00000379931.3:c.1572G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430959
  ensembl transcript: ENST00000520973
  gene symbol: TACC1
  hgvsc: ENST00000520973.1:c.951G>A
  hgvsp: ENST00000520973.1:c.951G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000332794
  ensembl transcript: ENST00000330691
  gene symbol: TACC1
  hgvsc: ENST00000330691.6:c.258G>A
  hgvsp: ENST00000330691.6:c.258G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428687
  ensembl transcript: ENST00000519416
  gene symbol: TACC1
  hgvsc: ENST00000519416.1:c.948G>A
  hgvsp: ENST00000519416.1:c.948G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430355
  ensembl transcript: ENST00000522904
  gene symbol: TACC1
  hgvsc: ENST00000522904.1:c.1452G>A
  hgvsp: ENST00000522904.1:c.1452G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000429418
  ensembl transcript: ENST00000520611
  gene symbol: TACC1
  hgvsc: ENST00000520611.1:c.-151G>A
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428466
  ensembl transcript: ENST00000521642
  gene symbol: TACC1
  hgvsc: ENST00000521642.1:c.222G>A
  hgvsp: ENST00000521642.1:c.222G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000276520
  ensembl transcript: ENST00000276520
  gene symbol: TACC1
  hgvsc: ENST00000276520.8:c.306G>A
  hgvsp: ENST00000276520.8:c.306G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000473342
  ensembl transcript: ENST00000520340
  gene symbol: TACC1
  hgvsc: ENST00000520340.1:c.1428G>A
  hgvsp: ENST00000520340.1:c.1428G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428253
  ensembl transcript: ENST00000521866
  gene symbol: TACC1
  hgvsc: ENST00000521866.1:c.896G>A
  hgvsp: ENST00000521866.1:c.896G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428949
  ensembl transcript: ENST00000521050
  gene symbol: TACC1
  hgvsc: ENST00000521050.1:c.258G>A
  hgvsp: ENST00000521050.1:c.258G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428450
  ensembl transcript: ENST00000520615
  gene symbol: TACC1
  hgvsc: ENST00000520615.1:c.951G>A
  hgvsp: ENST00000520615.1:c.951G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000321703
  ensembl transcript: ENST00000317827
  gene symbol: TACC1
  hgvsc: ENST00000317827.4:c.1536G>A
  hgvsp: ENST00000317827.4:c.1536G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428706
  ensembl transcript: ENST00000518415
  gene symbol: TACC1
  hgvsc: ENST00000518415.1:c.1401G>A
  hgvsp: ENST00000518415.1:c.1401G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000327818
  ensembl transcript: ENST00000348567
  gene symbol: TACC1
  hgvsc: ENST00000348567.4:c.222G>A
  hgvsp: ENST00000348567.4:c.222G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000522955
  gene symbol: TACC1
  hgvsc: ENST00000522955.1:n.1452G>A
  variant of: http://identifiers.org/hgnc/11522
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Thr512Thr
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: South Asian
reference allele: G
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD

8-38684797-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38684797
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 38684797
    reference: chr 8
allele count: 6
allele frequency: 4.943072284193702e-5
allele num: 121382
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428450
  ensembl transcript: ENST00000520615
  gene symbol: TACC1
  hgvsc: ENST00000520615.1:c.979G>A
  hgvsp: ENSP00000428450.1:p.Glu327Lys
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000332794
  ensembl transcript: ENST00000330691
  gene symbol: TACC1
  hgvsc: ENST00000330691.6:c.286G>A
  hgvsp: ENSP00000332794.6:p.Glu96Lys
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430306
  ensembl transcript: ENST00000518809
  gene symbol: TACC1
  hgvsc: ENST00000518809.1:c.513G>A
  hgvsp: ENSP00000430306.1:p.Glu172Lys
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428706
  ensembl transcript: ENST00000518415
  gene symbol: TACC1
  hgvsc: ENST00000518415.1:c.1429G>A
  hgvsp: ENSP00000428706.1:p.Glu477Lys
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430959
  ensembl transcript: ENST00000520973
  gene symbol: TACC1
  hgvsc: ENST00000520973.1:c.979G>A
  hgvsp: ENSP00000430959.1:p.Glu327Lys
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000523239
  gene symbol: TACC1
  hgvsc: ENST00000523239.1:n.206G>A
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000473342
  ensembl transcript: ENST00000520340
  gene symbol: TACC1
  hgvsc: ENST00000520340.1:c.1456G>A
  hgvsp: ENSP00000473342.1:p.Glu486Lys
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000429418
  ensembl transcript: ENST00000520611
  gene symbol: TACC1
  hgvsc: ENST00000520611.1:c.-123G>A
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000517336
  gene symbol: TACC1
  hgvsc: ENST00000517336.1:n.284G>A
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000369263
  ensembl transcript: ENST00000379931
  gene symbol: TACC1
  hgvsc: ENST00000379931.3:c.1600G>A
  hgvsp: ENSP00000369263.3:p.Glu534Lys
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428949
  ensembl transcript: ENST00000521050
  gene symbol: TACC1
  hgvsc: ENST00000521050.1:c.286G>A
  hgvsp: ENSP00000428949.1:p.Glu96Lys
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430355
  ensembl transcript: ENST00000522904
  gene symbol: TACC1
  hgvsc: ENST00000522904.1:c.1480G>A
  hgvsp: ENSP00000430355.1:p.Glu494Lys
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000321703
  ensembl transcript: ENST00000317827
  gene symbol: TACC1
  hgvsc: ENST00000317827.4:c.1564G>A
  hgvsp: ENSP00000321703.4:p.Glu522Lys
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000522752
  gene symbol: TACC1
  hgvsc: ENST00000522752.1:n.284G>A
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000327818
  ensembl transcript: ENST00000348567
  gene symbol: TACC1
  hgvsc: ENST00000348567.4:c.250G>A
  hgvsp: ENSP00000327818.5:p.Glu84Lys
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428687
  ensembl transcript: ENST00000519416
  gene symbol: TACC1
  hgvsc: ENST00000519416.1:c.976G>A
  hgvsp: ENSP00000428687.1:p.Glu326Lys
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000393647
  ensembl transcript: ENST00000443286
  gene symbol: TACC1
  hgvsc: ENST00000443286.2:c.1612G>A
  hgvsp: ENSP00000393647.2:p.Glu538Lys
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000522955
  gene symbol: TACC1
  hgvsc: ENST00000522955.1:n.1480G>A
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000276520
  ensembl transcript: ENST00000276520
  gene symbol: TACC1
  hgvsc: ENST00000276520.8:c.334G>A
  hgvsp: ENSP00000276520.8:p.Glu112Lys
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428253
  ensembl transcript: ENST00000521866
  gene symbol: TACC1
  hgvsc: ENST00000521866.1:c.924G>A
  hgvsp: ENSP00000428253.1:p.Glu309Lys
  variant of: http://identifiers.org/hgnc/11522
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Glu522Lys
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: African
population: Other
reference allele: G
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD

8-38684802-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38684802
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 38684802
    reference: chr 8
allele count: 1
allele frequency: 8.238453806989504e-6
allele num: 121382
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000429418
  ensembl transcript: ENST00000520611
  gene symbol: TACC1
  hgvsc: ENST00000520611.1:c.-118G>A
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000327818
  ensembl transcript: ENST00000348567
  gene symbol: TACC1
  hgvsc: ENST00000348567.4:c.255G>A
  hgvsp: ENST00000348567.4:c.255G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430306
  ensembl transcript: ENST00000518809
  gene symbol: TACC1
  hgvsc: ENST00000518809.1:c.518G>A
  hgvsp: ENST00000518809.1:c.518G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430959
  ensembl transcript: ENST00000520973
  gene symbol: TACC1
  hgvsc: ENST00000520973.1:c.984G>A
  hgvsp: ENST00000520973.1:c.984G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000332794
  ensembl transcript: ENST00000330691
  gene symbol: TACC1
  hgvsc: ENST00000330691.6:c.291G>A
  hgvsp: ENST00000330691.6:c.291G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000369263
  ensembl transcript: ENST00000379931
  gene symbol: TACC1
  hgvsc: ENST00000379931.3:c.1605G>A
  hgvsp: ENST00000379931.3:c.1605G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428706
  ensembl transcript: ENST00000518415
  gene symbol: TACC1
  hgvsc: ENST00000518415.1:c.1434G>A
  hgvsp: ENST00000518415.1:c.1434G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428253
  ensembl transcript: ENST00000521866
  gene symbol: TACC1
  hgvsc: ENST00000521866.1:c.929G>A
  hgvsp: ENST00000521866.1:c.929G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428949
  ensembl transcript: ENST00000521050
  gene symbol: TACC1
  hgvsc: ENST00000521050.1:c.291G>A
  hgvsp: ENST00000521050.1:c.291G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000517336
  gene symbol: TACC1
  hgvsc: ENST00000517336.1:n.289G>A
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000393647
  ensembl transcript: ENST00000443286
  gene symbol: TACC1
  hgvsc: ENST00000443286.2:c.1617G>A
  hgvsp: ENST00000443286.2:c.1617G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428466
  ensembl transcript: ENST00000521642
  gene symbol: TACC1
  hgvsc: ENST00000521642.1:c.255G>A
  hgvsp: ENST00000521642.1:c.255G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000473342
  ensembl transcript: ENST00000520340
  gene symbol: TACC1
  hgvsc: ENST00000520340.1:c.1461G>A
  hgvsp: ENST00000520340.1:c.1461G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428450
  ensembl transcript: ENST00000520615
  gene symbol: TACC1
  hgvsc: ENST00000520615.1:c.984G>A
  hgvsp: ENST00000520615.1:c.984G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000276520
  ensembl transcript: ENST00000276520
  gene symbol: TACC1
  hgvsc: ENST00000276520.8:c.339G>A
  hgvsp: ENST00000276520.8:c.339G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000523239
  gene symbol: TACC1
  hgvsc: ENST00000523239.1:n.211G>A
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428687
  ensembl transcript: ENST00000519416
  gene symbol: TACC1
  hgvsc: ENST00000519416.1:c.981G>A
  hgvsp: ENST00000519416.1:c.981G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000522955
  gene symbol: TACC1
  hgvsc: ENST00000522955.1:n.1485G>A
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000321703
  ensembl transcript: ENST00000317827
  gene symbol: TACC1
  hgvsc: ENST00000317827.4:c.1569G>A
  hgvsp: ENST00000317827.4:c.1569G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11522
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Val523Val
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: MQRankSum

8-38684805-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38684805
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 38684805
    reference: chr 8
allele count: 1
allele frequency: 8.238589553468446e-6
allele num: 121380
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428450
  ensembl transcript: ENST00000520615
  gene symbol: TACC1
  hgvsc: ENST00000520615.1:c.987A>T
  hgvsp: ENSP00000428450.1:p.Lys329Asn
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000276520
  ensembl transcript: ENST00000276520
  gene symbol: TACC1
  hgvsc: ENST00000276520.8:c.342A>T
  hgvsp: ENSP00000276520.8:p.Lys114Asn
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430959
  ensembl transcript: ENST00000520973
  gene symbol: TACC1
  hgvsc: ENST00000520973.1:c.987A>T
  hgvsp: ENSP00000430959.1:p.Lys329Asn
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000321703
  ensembl transcript: ENST00000317827
  gene symbol: TACC1
  hgvsc: ENST00000317827.4:c.1572A>T
  hgvsp: ENSP00000321703.4:p.Lys524Asn
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428706
  ensembl transcript: ENST00000518415
  gene symbol: TACC1
  hgvsc: ENST00000518415.1:c.1437A>T
  hgvsp: ENSP00000428706.1:p.Lys479Asn
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428253
  ensembl transcript: ENST00000521866
  gene symbol: TACC1
  hgvsc: ENST00000521866.1:c.932A>T
  hgvsp: ENSP00000428253.1:p.Lys311Asn
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000393647
  ensembl transcript: ENST00000443286
  gene symbol: TACC1
  hgvsc: ENST00000443286.2:c.1620A>T
  hgvsp: ENSP00000393647.2:p.Lys540Asn
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000369263
  ensembl transcript: ENST00000379931
  gene symbol: TACC1
  hgvsc: ENST00000379931.3:c.1608A>T
  hgvsp: ENSP00000369263.3:p.Lys536Asn
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428949
  ensembl transcript: ENST00000521050
  gene symbol: TACC1
  hgvsc: ENST00000521050.1:c.294A>T
  hgvsp: ENSP00000428949.1:p.Lys98Asn
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000327818
  ensembl transcript: ENST00000348567
  gene symbol: TACC1
  hgvsc: ENST00000348567.4:c.258A>T
  hgvsp: ENSP00000327818.5:p.Lys86Asn
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430355
  ensembl transcript: ENST00000522904
  gene symbol: TACC1
  hgvsc: ENST00000522904.1:c.1488A>T
  hgvsp: ENSP00000430355.1:p.Lys496Asn
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430306
  ensembl transcript: ENST00000518809
  gene symbol: TACC1
  hgvsc: ENST00000518809.1:c.521A>T
  hgvsp: ENSP00000430306.1:p.Lys174Asn
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000429418
  ensembl transcript: ENST00000520611
  gene symbol: TACC1
  hgvsc: ENST00000520611.1:c.-115A>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000332794
  ensembl transcript: ENST00000330691
  gene symbol: TACC1
  hgvsc: ENST00000330691.6:c.294A>T
  hgvsp: ENSP00000332794.6:p.Lys98Asn
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000473342
  ensembl transcript: ENST00000520340
  gene symbol: TACC1
  hgvsc: ENST00000520340.1:c.1464A>T
  hgvsp: ENSP00000473342.1:p.Lys488Asn
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000523239
  gene symbol: TACC1
  hgvsc: ENST00000523239.1:n.214A>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000522955
  gene symbol: TACC1
  hgvsc: ENST00000522955.1:n.1488A>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428687
  ensembl transcript: ENST00000519416
  gene symbol: TACC1
  hgvsc: ENST00000519416.1:c.984A>T
  hgvsp: ENSP00000428687.1:p.Lys328Asn
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428466
  ensembl transcript: ENST00000521642
  gene symbol: TACC1
  hgvsc: ENST00000521642.1:c.258A>T
  hgvsp: ENSP00000428466.1:p.Lys86Asn
  variant of: http://identifiers.org/hgnc/11522
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Lys524Asn
num of homozygotes: 0
population: African
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: East Asian
reference allele: A
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: FS

8-38684806-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38684806
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 38684806
    reference: chr 8
allele count: 1
allele frequency: 8.238453806989504e-6
allele num: 121382
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428466
  ensembl transcript: ENST00000521642
  gene symbol: TACC1
  hgvsc: ENST00000521642.1:c.259G>C
  hgvsp: ENSP00000428466.1:p.Gly87Arg
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000517336
  gene symbol: TACC1
  hgvsc: ENST00000517336.1:n.293G>C
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430306
  ensembl transcript: ENST00000518809
  gene symbol: TACC1
  hgvsc: ENST00000518809.1:c.522G>C
  hgvsp: ENSP00000430306.1:p.Gly175Arg
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000327818
  ensembl transcript: ENST00000348567
  gene symbol: TACC1
  hgvsc: ENST00000348567.4:c.259G>C
  hgvsp: ENSP00000327818.5:p.Gly87Arg
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000429418
  ensembl transcript: ENST00000520611
  gene symbol: TACC1
  hgvsc: ENST00000520611.1:c.-114G>C
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428949
  ensembl transcript: ENST00000521050
  gene symbol: TACC1
  hgvsc: ENST00000521050.1:c.295G>C
  hgvsp: ENSP00000428949.1:p.Gly99Arg
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000369263
  ensembl transcript: ENST00000379931
  gene symbol: TACC1
  hgvsc: ENST00000379931.3:c.1609G>C
  hgvsp: ENSP00000369263.3:p.Gly537Arg
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000321703
  ensembl transcript: ENST00000317827
  gene symbol: TACC1
  hgvsc: ENST00000317827.4:c.1573G>C
  hgvsp: ENSP00000321703.4:p.Gly525Arg
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000332794
  ensembl transcript: ENST00000330691
  gene symbol: TACC1
  hgvsc: ENST00000330691.6:c.295G>C
  hgvsp: ENSP00000332794.6:p.Gly99Arg
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000393647
  ensembl transcript: ENST00000443286
  gene symbol: TACC1
  hgvsc: ENST00000443286.2:c.1621G>C
  hgvsp: ENSP00000393647.2:p.Gly541Arg
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430355
  ensembl transcript: ENST00000522904
  gene symbol: TACC1
  hgvsc: ENST00000522904.1:c.1489G>C
  hgvsp: ENSP00000430355.1:p.Gly497Arg
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000522752
  gene symbol: TACC1
  hgvsc: ENST00000522752.1:n.293G>C
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428450
  ensembl transcript: ENST00000520615
  gene symbol: TACC1
  hgvsc: ENST00000520615.1:c.988G>C
  hgvsp: ENSP00000428450.1:p.Gly330Arg
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428706
  ensembl transcript: ENST00000518415
  gene symbol: TACC1
  hgvsc: ENST00000518415.1:c.1438G>C
  hgvsp: ENSP00000428706.1:p.Gly480Arg
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428253
  ensembl transcript: ENST00000521866
  gene symbol: TACC1
  hgvsc: ENST00000521866.1:c.933G>C
  hgvsp: ENSP00000428253.1:p.Gly312Arg
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000473342
  ensembl transcript: ENST00000520340
  gene symbol: TACC1
  hgvsc: ENST00000520340.1:c.1465G>C
  hgvsp: ENSP00000473342.1:p.Gly489Arg
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430959
  ensembl transcript: ENST00000520973
  gene symbol: TACC1
  hgvsc: ENST00000520973.1:c.988G>C
  hgvsp: ENSP00000430959.1:p.Gly330Arg
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000276520
  ensembl transcript: ENST00000276520
  gene symbol: TACC1
  hgvsc: ENST00000276520.8:c.343G>C
  hgvsp: ENSP00000276520.8:p.Gly115Arg
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428687
  ensembl transcript: ENST00000519416
  gene symbol: TACC1
  hgvsc: ENST00000519416.1:c.985G>C
  hgvsp: ENSP00000428687.1:p.Gly329Arg
  variant of: http://identifiers.org/hgnc/11522
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Gly525Arg
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: Other
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum

8-38684809-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38684809
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 38684809
    reference: chr 8
allele count: 2
allele frequency: 1.647772211969417e-5
allele num: 121376
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000332794
  ensembl transcript: ENST00000330691
  gene symbol: TACC1
  hgvsc: ENST00000330691.6:c.298G>A
  hgvsp: ENSP00000332794.6:p.Glu100Lys
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000276520
  ensembl transcript: ENST00000276520
  gene symbol: TACC1
  hgvsc: ENST00000276520.8:c.346G>A
  hgvsp: ENSP00000276520.8:p.Glu116Lys
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000522955
  gene symbol: TACC1
  hgvsc: ENST00000522955.1:n.1492G>A
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428687
  ensembl transcript: ENST00000519416
  gene symbol: TACC1
  hgvsc: ENST00000519416.1:c.988G>A
  hgvsp: ENSP00000428687.1:p.Glu330Lys
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430306
  ensembl transcript: ENST00000518809
  gene symbol: TACC1
  hgvsc: ENST00000518809.1:c.525G>A
  hgvsp: ENSP00000430306.1:p.Glu176Lys
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000393647
  ensembl transcript: ENST00000443286
  gene symbol: TACC1
  hgvsc: ENST00000443286.2:c.1621+3G>A
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000522752
  gene symbol: TACC1
  hgvsc: ENST00000522752.1:n.293+3G>A
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000321703
  ensembl transcript: ENST00000317827
  gene symbol: TACC1
  hgvsc: ENST00000317827.4:c.1576G>A
  hgvsp: ENSP00000321703.4:p.Glu526Lys
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428466
  ensembl transcript: ENST00000521642
  gene symbol: TACC1
  hgvsc: ENST00000521642.1:c.262G>A
  hgvsp: ENSP00000428466.1:p.Glu88Lys
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430959
  ensembl transcript: ENST00000520973
  gene symbol: TACC1
  hgvsc: ENST00000520973.1:c.988+3G>A
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430355
  ensembl transcript: ENST00000522904
  gene symbol: TACC1
  hgvsc: ENST00000522904.1:c.1489+3G>A
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000327818
  ensembl transcript: ENST00000348567
  gene symbol: TACC1
  hgvsc: ENST00000348567.4:c.262G>A
  hgvsp: ENSP00000327818.5:p.Glu88Lys
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428450
  ensembl transcript: ENST00000520615
  gene symbol: TACC1
  hgvsc: ENST00000520615.1:c.991G>A
  hgvsp: ENSP00000428450.1:p.Glu331Lys
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428949
  ensembl transcript: ENST00000521050
  gene symbol: TACC1
  hgvsc: ENST00000521050.1:c.298G>A
  hgvsp: ENSP00000428949.1:p.Glu100Lys
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428253
  ensembl transcript: ENST00000521866
  gene symbol: TACC1
  hgvsc: ENST00000521866.1:c.933+3G>A
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000369263
  ensembl transcript: ENST00000379931
  gene symbol: TACC1
  hgvsc: ENST00000379931.3:c.1612G>A
  hgvsp: ENSP00000369263.3:p.Glu538Lys
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000429418
  ensembl transcript: ENST00000520611
  gene symbol: TACC1
  hgvsc: ENST00000520611.1:c.-111G>A
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000473342
  ensembl transcript: ENST00000520340
  gene symbol: TACC1
  hgvsc: ENST00000520340.1:c.1465+3G>A
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428706
  ensembl transcript: ENST00000518415
  gene symbol: TACC1
  hgvsc: ENST00000518415.1:c.1438+3G>A
  variant of: http://identifiers.org/hgnc/11522
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Glu526Lys
num of homozygotes: 1
population: African
population: South Asian
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: MQ
site quality: DP

8-38684814-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38684814
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 38684814
    reference: chr 8
allele count: 1
allele frequency: 8.238861059847087e-6
allele num: 121376
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428450
  ensembl transcript: ENST00000520615
  gene symbol: TACC1
  hgvsc: ENST00000520615.1:c.996A>G
  hgvsp: ENST00000520615.1:c.996A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430959
  ensembl transcript: ENST00000520973
  gene symbol: TACC1
  hgvsc: ENST00000520973.1:c.988+8A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428253
  ensembl transcript: ENST00000521866
  gene symbol: TACC1
  hgvsc: ENST00000521866.1:c.933+8A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428706
  ensembl transcript: ENST00000518415
  gene symbol: TACC1
  hgvsc: ENST00000518415.1:c.1438+8A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000332794
  ensembl transcript: ENST00000330691
  gene symbol: TACC1
  hgvsc: ENST00000330691.6:c.303A>G
  hgvsp: ENST00000330691.6:c.303A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428687
  ensembl transcript: ENST00000519416
  gene symbol: TACC1
  hgvsc: ENST00000519416.1:c.993A>G
  hgvsp: ENST00000519416.1:c.993A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000327818
  ensembl transcript: ENST00000348567
  gene symbol: TACC1
  hgvsc: ENST00000348567.4:c.267A>G
  hgvsp: ENST00000348567.4:c.267A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000522752
  gene symbol: TACC1
  hgvsc: ENST00000522752.1:n.293+8A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000321703
  ensembl transcript: ENST00000317827
  gene symbol: TACC1
  hgvsc: ENST00000317827.4:c.1581A>G
  hgvsp: ENST00000317827.4:c.1581A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428949
  ensembl transcript: ENST00000521050
  gene symbol: TACC1
  hgvsc: ENST00000521050.1:c.303A>G
  hgvsp: ENST00000521050.1:c.303A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430355
  ensembl transcript: ENST00000522904
  gene symbol: TACC1
  hgvsc: ENST00000522904.1:c.1489+8A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000393647
  ensembl transcript: ENST00000443286
  gene symbol: TACC1
  hgvsc: ENST00000443286.2:c.1621+8A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430306
  ensembl transcript: ENST00000518809
  gene symbol: TACC1
  hgvsc: ENST00000518809.1:c.530A>G
  hgvsp: ENST00000518809.1:c.530A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000369263
  ensembl transcript: ENST00000379931
  gene symbol: TACC1
  hgvsc: ENST00000379931.3:c.1617A>G
  hgvsp: ENST00000379931.3:c.1617A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000523239
  gene symbol: TACC1
  hgvsc: ENST00000523239.1:n.223A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000473342
  ensembl transcript: ENST00000520340
  gene symbol: TACC1
  hgvsc: ENST00000520340.1:c.1465+8A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428466
  ensembl transcript: ENST00000521642
  gene symbol: TACC1
  hgvsc: ENST00000521642.1:c.267A>G
  hgvsp: ENST00000521642.1:c.267A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000276520
  ensembl transcript: ENST00000276520
  gene symbol: TACC1
  hgvsc: ENST00000276520.8:c.351A>G
  hgvsp: ENST00000276520.8:c.351A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000429418
  ensembl transcript: ENST00000520611
  gene symbol: TACC1
  hgvsc: ENST00000520611.1:c.-106A>G
  variant of: http://identifiers.org/hgnc/11522
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: c.1489+8A>G
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: Other
population: European (Finnish)
population: South Asian
reference allele: A
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: DP

http://identifiers.org/exac.variant/8-38684824-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38684824
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 38684824
    reference: chr 8
allele count: 3
allele frequency: 2.471699045924168e-5
allele num: 121374
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000473342
  ensembl transcript: ENST00000520340
  gene symbol: TACC1
  hgvsc: ENST00000520340.1:c.1465+18C>A
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000369263
  ensembl transcript: ENST00000379931
  gene symbol: TACC1
  hgvsc: ENST00000379931.3:c.1627C>A
  hgvsp: ENSP00000369263.3:p.Leu543Met
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000321703
  ensembl transcript: ENST00000317827
  gene symbol: TACC1
  hgvsc: ENST00000317827.4:c.1591C>A
  hgvsp: ENSP00000321703.4:p.Leu531Met
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000523239
  gene symbol: TACC1
  hgvsc: ENST00000523239.1:n.233C>A
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000429418
  ensembl transcript: ENST00000520611
  gene symbol: TACC1
  hgvsc: ENST00000520611.1:c.-96C>A
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430355
  ensembl transcript: ENST00000522904
  gene symbol: TACC1
  hgvsc: ENST00000522904.1:c.1489+18C>A
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428253
  ensembl transcript: ENST00000521866
  gene symbol: TACC1
  hgvsc: ENST00000521866.1:c.933+18C>A
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428706
  ensembl transcript: ENST00000518415
  gene symbol: TACC1
  hgvsc: ENST00000518415.1:c.1438+18C>A
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000522752
  gene symbol: TACC1
  hgvsc: ENST00000522752.1:n.293+18C>A
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430959
  ensembl transcript: ENST00000520973
  gene symbol: TACC1
  hgvsc: ENST00000520973.1:c.988+18C>A
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000393647
  ensembl transcript: ENST00000443286
  gene symbol: TACC1
  hgvsc: ENST00000443286.2:c.1621+18C>A
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000276520
  ensembl transcript: ENST00000276520
  gene symbol: TACC1
  hgvsc: ENST00000276520.8:c.361C>A
  hgvsp: ENSP00000276520.8:p.Leu121Met
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000327818
  ensembl transcript: ENST00000348567
  gene symbol: TACC1
  hgvsc: ENST00000348567.4:c.277C>A
  hgvsp: ENSP00000327818.5:p.Leu93Met
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428450
  ensembl transcript: ENST00000520615
  gene symbol: TACC1
  hgvsc: ENST00000520615.1:c.1006C>A
  hgvsp: ENSP00000428450.1:p.Leu336Met
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428687
  ensembl transcript: ENST00000519416
  gene symbol: TACC1
  hgvsc: ENST00000519416.1:c.1003C>A
  hgvsp: ENSP00000428687.1:p.Leu335Met
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428466
  ensembl transcript: ENST00000521642
  gene symbol: TACC1
  hgvsc: ENST00000521642.1:c.277C>A
  hgvsp: ENSP00000428466.1:p.Leu93Met
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428949
  ensembl transcript: ENST00000521050
  gene symbol: TACC1
  hgvsc: ENST00000521050.1:c.313C>A
  hgvsp: ENSP00000428949.1:p.Leu105Met
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430306
  ensembl transcript: ENST00000518809
  gene symbol: TACC1
  hgvsc: ENST00000518809.1:c.540C>A
  hgvsp: ENSP00000430306.1:p.Leu181Met
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000522955
  gene symbol: TACC1
  hgvsc: ENST00000522955.1:n.1507C>A
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000332794
  ensembl transcript: ENST00000330691
  gene symbol: TACC1
  hgvsc: ENST00000330691.6:c.313C>A
  hgvsp: ENSP00000332794.6:p.Leu105Met
  variant of: http://identifiers.org/hgnc/11522
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Leu531Met
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Other
population: African
reference allele: C
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ

8-38684828-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38684828
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 38684828
    reference: chr 8
allele count: 3
allele frequency: 2.471739775236463e-5
allele num: 121372
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430355
  ensembl transcript: ENST00000522904
  gene symbol: TACC1
  hgvsc: ENST00000522904.1:c.1489+22A>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000523239
  gene symbol: TACC1
  hgvsc: ENST00000523239.1:n.237A>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000321703
  ensembl transcript: ENST00000317827
  gene symbol: TACC1
  hgvsc: ENST00000317827.4:c.1595A>T
  hgvsp: ENSP00000321703.4:p.Glu532Val
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000473342
  ensembl transcript: ENST00000520340
  gene symbol: TACC1
  hgvsc: ENST00000520340.1:c.1465+22A>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428687
  ensembl transcript: ENST00000519416
  gene symbol: TACC1
  hgvsc: ENST00000519416.1:c.1007A>T
  hgvsp: ENSP00000428687.1:p.Glu336Val
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428253
  ensembl transcript: ENST00000521866
  gene symbol: TACC1
  hgvsc: ENST00000521866.1:c.933+22A>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000276520
  ensembl transcript: ENST00000276520
  gene symbol: TACC1
  hgvsc: ENST00000276520.8:c.365A>T
  hgvsp: ENSP00000276520.8:p.Glu122Val
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000327818
  ensembl transcript: ENST00000348567
  gene symbol: TACC1
  hgvsc: ENST00000348567.4:c.281A>T
  hgvsp: ENSP00000327818.5:p.Glu94Val
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000369263
  ensembl transcript: ENST00000379931
  gene symbol: TACC1
  hgvsc: ENST00000379931.3:c.1631A>T
  hgvsp: ENSP00000369263.3:p.Glu544Val
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000522752
  gene symbol: TACC1
  hgvsc: ENST00000522752.1:n.293+22A>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428706
  ensembl transcript: ENST00000518415
  gene symbol: TACC1
  hgvsc: ENST00000518415.1:c.1438+22A>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428450
  ensembl transcript: ENST00000520615
  gene symbol: TACC1
  hgvsc: ENST00000520615.1:c.1010A>T
  hgvsp: ENSP00000428450.1:p.Glu337Val
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430306
  ensembl transcript: ENST00000518809
  gene symbol: TACC1
  hgvsc: ENST00000518809.1:c.544A>T
  hgvsp: ENSP00000430306.1:p.Glu182Val
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000393647
  ensembl transcript: ENST00000443286
  gene symbol: TACC1
  hgvsc: ENST00000443286.2:c.1621+22A>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000332794
  ensembl transcript: ENST00000330691
  gene symbol: TACC1
  hgvsc: ENST00000330691.6:c.317A>T
  hgvsp: ENSP00000332794.6:p.Glu106Val
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428466
  ensembl transcript: ENST00000521642
  gene symbol: TACC1
  hgvsc: ENST00000521642.1:c.281A>T
  hgvsp: ENSP00000428466.1:p.Glu94Val
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000522955
  gene symbol: TACC1
  hgvsc: ENST00000522955.1:n.1511A>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000429418
  ensembl transcript: ENST00000520611
  gene symbol: TACC1
  hgvsc: ENST00000520611.1:c.-92A>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428949
  ensembl transcript: ENST00000521050
  gene symbol: TACC1
  hgvsc: ENST00000521050.1:c.317A>T
  hgvsp: ENSP00000428949.1:p.Glu106Val
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430959
  ensembl transcript: ENST00000520973
  gene symbol: TACC1
  hgvsc: ENST00000520973.1:c.988+22A>T
  variant of: http://identifiers.org/hgnc/11522
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Glu532Val
num of homozygotes: 0
population: Other
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
population: Latino
reference allele: A
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/8-38684837-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38684837
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 38684837
    reference: chr 8
allele count: 2
allele frequency: 1.647799363949445e-5
allele num: 121374
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000522955
  gene symbol: TACC1
  hgvsc: ENST00000522955.1:n.1520A>C
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000321703
  ensembl transcript: ENST00000317827
  gene symbol: TACC1
  hgvsc: ENST00000317827.4:c.1604A>C
  hgvsp: ENSP00000321703.4:p.Glu535Ala
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428450
  ensembl transcript: ENST00000520615
  gene symbol: TACC1
  hgvsc: ENST00000520615.1:c.1019A>C
  hgvsp: ENSP00000428450.1:p.Glu340Ala
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430355
  ensembl transcript: ENST00000522904
  gene symbol: TACC1
  hgvsc: ENST00000522904.1:c.1489+31A>C
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000473342
  ensembl transcript: ENST00000520340
  gene symbol: TACC1
  hgvsc: ENST00000520340.1:c.1465+31A>C
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000276520
  ensembl transcript: ENST00000276520
  gene symbol: TACC1
  hgvsc: ENST00000276520.8:c.374A>C
  hgvsp: ENSP00000276520.8:p.Glu125Ala
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000327818
  ensembl transcript: ENST00000348567
  gene symbol: TACC1
  hgvsc: ENST00000348567.4:c.290A>C
  hgvsp: ENSP00000327818.5:p.Glu97Ala
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428949
  ensembl transcript: ENST00000521050
  gene symbol: TACC1
  hgvsc: ENST00000521050.1:c.326A>C
  hgvsp: ENSP00000428949.1:p.Glu109Ala
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428687
  ensembl transcript: ENST00000519416
  gene symbol: TACC1
  hgvsc: ENST00000519416.1:c.1016A>C
  hgvsp: ENSP00000428687.1:p.Glu339Ala
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428466
  ensembl transcript: ENST00000521642
  gene symbol: TACC1
  hgvsc: ENST00000521642.1:c.290A>C
  hgvsp: ENSP00000428466.1:p.Glu97Ala
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000522752
  gene symbol: TACC1
  hgvsc: ENST00000522752.1:n.293+31A>C
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430959
  ensembl transcript: ENST00000520973
  gene symbol: TACC1
  hgvsc: ENST00000520973.1:c.988+31A>C
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430306
  ensembl transcript: ENST00000518809
  gene symbol: TACC1
  hgvsc: ENST00000518809.1:c.553A>C
  hgvsp: ENSP00000430306.1:p.Glu185Ala
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000523239
  gene symbol: TACC1
  hgvsc: ENST00000523239.1:n.246A>C
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000369263
  ensembl transcript: ENST00000379931
  gene symbol: TACC1
  hgvsc: ENST00000379931.3:c.1640A>C
  hgvsp: ENSP00000369263.3:p.Glu547Ala
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428253
  ensembl transcript: ENST00000521866
  gene symbol: TACC1
  hgvsc: ENST00000521866.1:c.933+31A>C
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000429418
  ensembl transcript: ENST00000520611
  gene symbol: TACC1
  hgvsc: ENST00000520611.1:c.-83A>C
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000393647
  ensembl transcript: ENST00000443286
  gene symbol: TACC1
  hgvsc: ENST00000443286.2:c.1621+31A>C
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428706
  ensembl transcript: ENST00000518415
  gene symbol: TACC1
  hgvsc: ENST00000518415.1:c.1438+31A>C
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000332794
  ensembl transcript: ENST00000330691
  gene symbol: TACC1
  hgvsc: ENST00000330691.6:c.326A>C
  hgvsp: ENSP00000332794.6:p.Glu109Ala
  variant of: http://identifiers.org/hgnc/11522
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Glu535Ala
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum

8-38684838-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38684838
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 38684838
    reference: chr 8
allele count: 1
allele frequency: 8.239132584121543e-6
allele num: 121372
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428949
  ensembl transcript: ENST00000521050
  gene symbol: TACC1
  hgvsc: ENST00000521050.1:c.327A>G
  hgvsp: ENST00000521050.1:c.327A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000321703
  ensembl transcript: ENST00000317827
  gene symbol: TACC1
  hgvsc: ENST00000317827.4:c.1605A>G
  hgvsp: ENST00000317827.4:c.1605A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428450
  ensembl transcript: ENST00000520615
  gene symbol: TACC1
  hgvsc: ENST00000520615.1:c.1020A>G
  hgvsp: ENST00000520615.1:c.1020A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000522955
  gene symbol: TACC1
  hgvsc: ENST00000522955.1:n.1521A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428253
  ensembl transcript: ENST00000521866
  gene symbol: TACC1
  hgvsc: ENST00000521866.1:c.933+32A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430959
  ensembl transcript: ENST00000520973
  gene symbol: TACC1
  hgvsc: ENST00000520973.1:c.988+32A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000327818
  ensembl transcript: ENST00000348567
  gene symbol: TACC1
  hgvsc: ENST00000348567.4:c.291A>G
  hgvsp: ENST00000348567.4:c.291A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000523239
  gene symbol: TACC1
  hgvsc: ENST00000523239.1:n.247A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428466
  ensembl transcript: ENST00000521642
  gene symbol: TACC1
  hgvsc: ENST00000521642.1:c.291A>G
  hgvsp: ENST00000521642.1:c.291A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000429418
  ensembl transcript: ENST00000520611
  gene symbol: TACC1
  hgvsc: ENST00000520611.1:c.-82A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430355
  ensembl transcript: ENST00000522904
  gene symbol: TACC1
  hgvsc: ENST00000522904.1:c.1489+32A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428687
  ensembl transcript: ENST00000519416
  gene symbol: TACC1
  hgvsc: ENST00000519416.1:c.1017A>G
  hgvsp: ENST00000519416.1:c.1017A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000276520
  ensembl transcript: ENST00000276520
  gene symbol: TACC1
  hgvsc: ENST00000276520.8:c.375A>G
  hgvsp: ENST00000276520.8:c.375A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000393647
  ensembl transcript: ENST00000443286
  gene symbol: TACC1
  hgvsc: ENST00000443286.2:c.1621+32A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000369263
  ensembl transcript: ENST00000379931
  gene symbol: TACC1
  hgvsc: ENST00000379931.3:c.1641A>G
  hgvsp: ENST00000379931.3:c.1641A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000332794
  ensembl transcript: ENST00000330691
  gene symbol: TACC1
  hgvsc: ENST00000330691.6:c.327A>G
  hgvsp: ENST00000330691.6:c.327A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430306
  ensembl transcript: ENST00000518809
  gene symbol: TACC1
  hgvsc: ENST00000518809.1:c.554A>G
  hgvsp: ENST00000518809.1:c.554A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000473342
  ensembl transcript: ENST00000520340
  gene symbol: TACC1
  hgvsc: ENST00000520340.1:c.1465+32A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428706
  ensembl transcript: ENST00000518415
  gene symbol: TACC1
  hgvsc: ENST00000518415.1:c.1438+32A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000522752
  gene symbol: TACC1
  hgvsc: ENST00000522752.1:n.293+32A>G
  variant of: http://identifiers.org/hgnc/11522
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Glu535Glu
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
population: Other
reference allele: A
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: ReadPosRankSum

8-38684846-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38684846
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 38684846
    reference: chr 8
allele count: 22
allele frequency: 1.81260916850674e-4
allele num: 121372
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428687
  ensembl transcript: ENST00000519416
  gene symbol: TACC1
  hgvsc: ENST00000519416.1:c.1025A>G
  hgvsp: ENSP00000428687.1:p.Asn342Ser
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000276520
  ensembl transcript: ENST00000276520
  gene symbol: TACC1
  hgvsc: ENST00000276520.8:c.383A>G
  hgvsp: ENSP00000276520.8:p.Asn128Ser
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430355
  ensembl transcript: ENST00000522904
  gene symbol: TACC1
  hgvsc: ENST00000522904.1:c.1489+40A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000429418
  ensembl transcript: ENST00000520611
  gene symbol: TACC1
  hgvsc: ENST00000520611.1:c.-74A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428450
  ensembl transcript: ENST00000520615
  gene symbol: TACC1
  hgvsc: ENST00000520615.1:c.1028A>G
  hgvsp: ENSP00000428450.1:p.Asn343Ser
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000393647
  ensembl transcript: ENST00000443286
  gene symbol: TACC1
  hgvsc: ENST00000443286.2:c.1621+40A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428706
  ensembl transcript: ENST00000518415
  gene symbol: TACC1
  hgvsc: ENST00000518415.1:c.1438+40A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430959
  ensembl transcript: ENST00000520973
  gene symbol: TACC1
  hgvsc: ENST00000520973.1:c.988+40A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428949
  ensembl transcript: ENST00000521050
  gene symbol: TACC1
  hgvsc: ENST00000521050.1:c.335A>G
  hgvsp: ENSP00000428949.1:p.Asn112Ser
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000321703
  ensembl transcript: ENST00000317827
  gene symbol: TACC1
  hgvsc: ENST00000317827.4:c.1613A>G
  hgvsp: ENSP00000321703.4:p.Asn538Ser
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000473342
  ensembl transcript: ENST00000520340
  gene symbol: TACC1
  hgvsc: ENST00000520340.1:c.1465+40A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428466
  ensembl transcript: ENST00000521642
  gene symbol: TACC1
  hgvsc: ENST00000521642.1:c.299A>G
  hgvsp: ENSP00000428466.1:p.Asn100Ser
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000327818
  ensembl transcript: ENST00000348567
  gene symbol: TACC1
  hgvsc: ENST00000348567.4:c.299A>G
  hgvsp: ENSP00000327818.5:p.Asn100Ser
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000332794
  ensembl transcript: ENST00000330691
  gene symbol: TACC1
  hgvsc: ENST00000330691.6:c.335A>G
  hgvsp: ENSP00000332794.6:p.Asn112Ser
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000523239
  gene symbol: TACC1
  hgvsc: ENST00000523239.1:n.255A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000369263
  ensembl transcript: ENST00000379931
  gene symbol: TACC1
  hgvsc: ENST00000379931.3:c.1649A>G
  hgvsp: ENSP00000369263.3:p.Asn550Ser
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428253
  ensembl transcript: ENST00000521866
  gene symbol: TACC1
  hgvsc: ENST00000521866.1:c.933+40A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430306
  ensembl transcript: ENST00000518809
  gene symbol: TACC1
  hgvsc: ENST00000518809.1:c.562A>G
  hgvsp: ENSP00000430306.1:p.Asn188Ser
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000522955
  gene symbol: TACC1
  hgvsc: ENST00000522955.1:n.1529A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000522752
  gene symbol: TACC1
  hgvsc: ENST00000522752.1:n.293+40A>G
  variant of: http://identifiers.org/hgnc/11522
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Asn538Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: Other
population: South Asian
population: European (Finnish)
reference allele: A
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum

8-38684848-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38684848
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 38684848
    reference: chr 8
allele count: 3
allele frequency: 2.471699045924168e-5
allele num: 121374
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428450
  ensembl transcript: ENST00000520615
  gene symbol: TACC1
  hgvsc: ENST00000520615.1:c.1030G>A
  hgvsp: ENSP00000428450.1:p.Val344Ile
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430355
  ensembl transcript: ENST00000522904
  gene symbol: TACC1
  hgvsc: ENST00000522904.1:c.1489+42G>A
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000327818
  ensembl transcript: ENST00000348567
  gene symbol: TACC1
  hgvsc: ENST00000348567.4:c.301G>A
  hgvsp: ENSP00000327818.5:p.Val101Ile
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428253
  ensembl transcript: ENST00000521866
  gene symbol: TACC1
  hgvsc: ENST00000521866.1:c.933+42G>A
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000393647
  ensembl transcript: ENST00000443286
  gene symbol: TACC1
  hgvsc: ENST00000443286.2:c.1621+42G>A
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428949
  ensembl transcript: ENST00000521050
  gene symbol: TACC1
  hgvsc: ENST00000521050.1:c.337G>A
  hgvsp: ENSP00000428949.1:p.Val113Ile
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428706
  ensembl transcript: ENST00000518415
  gene symbol: TACC1
  hgvsc: ENST00000518415.1:c.1438+42G>A
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000429418
  ensembl transcript: ENST00000520611
  gene symbol: TACC1
  hgvsc: ENST00000520611.1:c.-72G>A
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000523239
  gene symbol: TACC1
  hgvsc: ENST00000523239.1:n.257G>A
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000369263
  ensembl transcript: ENST00000379931
  gene symbol: TACC1
  hgvsc: ENST00000379931.3:c.1651G>A
  hgvsp: ENSP00000369263.3:p.Val551Ile
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000522955
  gene symbol: TACC1
  hgvsc: ENST00000522955.1:n.1531G>A
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430959
  ensembl transcript: ENST00000520973
  gene symbol: TACC1
  hgvsc: ENST00000520973.1:c.988+42G>A
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000321703
  ensembl transcript: ENST00000317827
  gene symbol: TACC1
  hgvsc: ENST00000317827.4:c.1615G>A
  hgvsp: ENSP00000321703.4:p.Val539Ile
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000276520
  ensembl transcript: ENST00000276520
  gene symbol: TACC1
  hgvsc: ENST00000276520.8:c.385G>A
  hgvsp: ENSP00000276520.8:p.Val129Ile
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430306
  ensembl transcript: ENST00000518809
  gene symbol: TACC1
  hgvsc: ENST00000518809.1:c.564G>A
  hgvsp: ENSP00000430306.1:p.Val189Ile
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428466
  ensembl transcript: ENST00000521642
  gene symbol: TACC1
  hgvsc: ENST00000521642.1:c.301G>A
  hgvsp: ENSP00000428466.1:p.Val101Ile
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000522752
  gene symbol: TACC1
  hgvsc: ENST00000522752.1:n.293+42G>A
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000332794
  ensembl transcript: ENST00000330691
  gene symbol: TACC1
  hgvsc: ENST00000330691.6:c.337G>A
  hgvsp: ENSP00000332794.6:p.Val113Ile
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000473342
  ensembl transcript: ENST00000520340
  gene symbol: TACC1
  hgvsc: ENST00000520340.1:c.1465+42G>A
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428687
  ensembl transcript: ENST00000519416
  gene symbol: TACC1
  hgvsc: ENST00000519416.1:c.1027G>A
  hgvsp: ENSP00000428687.1:p.Val343Ile
  variant of: http://identifiers.org/hgnc/11522
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Val539Ile
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: MQ
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

8-38684853-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38684853
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 38684853
    reference: chr 8
allele count: 44028
allele frequency: 3.629558794433819e-1
allele num: 121304
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428687
  ensembl transcript: ENST00000519416
  gene symbol: TACC1
  hgvsc: ENST00000519416.1:c.1032T>C
  hgvsp: ENST00000519416.1:c.1032T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430306
  ensembl transcript: ENST00000518809
  gene symbol: TACC1
  hgvsc: ENST00000518809.1:c.569T>C
  hgvsp: ENST00000518809.1:c.569T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428253
  ensembl transcript: ENST00000521866
  gene symbol: TACC1
  hgvsc: ENST00000521866.1:c.933+47T>C
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000522955
  gene symbol: TACC1
  hgvsc: ENST00000522955.1:n.1536T>C
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000473342
  ensembl transcript: ENST00000520340
  gene symbol: TACC1
  hgvsc: ENST00000520340.1:c.1465+47T>C
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428450
  ensembl transcript: ENST00000520615
  gene symbol: TACC1
  hgvsc: ENST00000520615.1:c.1035T>C
  hgvsp: ENST00000520615.1:c.1035T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000369263
  ensembl transcript: ENST00000379931
  gene symbol: TACC1
  hgvsc: ENST00000379931.3:c.1656T>C
  hgvsp: ENST00000379931.3:c.1656T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000332794
  ensembl transcript: ENST00000330691
  gene symbol: TACC1
  hgvsc: ENST00000330691.6:c.342T>C
  hgvsp: ENST00000330691.6:c.342T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000523239
  gene symbol: TACC1
  hgvsc: ENST00000523239.1:n.262T>C
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428466
  ensembl transcript: ENST00000521642
  gene symbol: TACC1
  hgvsc: ENST00000521642.1:c.306T>C
  hgvsp: ENST00000521642.1:c.306T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428949
  ensembl transcript: ENST00000521050
  gene symbol: TACC1
  hgvsc: ENST00000521050.1:c.342T>C
  hgvsp: ENST00000521050.1:c.342T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000321703
  ensembl transcript: ENST00000317827
  gene symbol: TACC1
  hgvsc: ENST00000317827.4:c.1620T>C
  hgvsp: ENST00000317827.4:c.1620T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000327818
  ensembl transcript: ENST00000348567
  gene symbol: TACC1
  hgvsc: ENST00000348567.4:c.306T>C
  hgvsp: ENST00000348567.4:c.306T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430959
  ensembl transcript: ENST00000520973
  gene symbol: TACC1
  hgvsc: ENST00000520973.1:c.988+47T>C
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000393647
  ensembl transcript: ENST00000443286
  gene symbol: TACC1
  hgvsc: ENST00000443286.2:c.1621+47T>C
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000522752
  gene symbol: TACC1
  hgvsc: ENST00000522752.1:n.293+47T>C
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000429418
  ensembl transcript: ENST00000520611
  gene symbol: TACC1
  hgvsc: ENST00000520611.1:c.-67T>C
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000276520
  ensembl transcript: ENST00000276520
  gene symbol: TACC1
  hgvsc: ENST00000276520.8:c.390T>C
  hgvsp: ENST00000276520.8:c.390T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430355
  ensembl transcript: ENST00000522904
  gene symbol: TACC1
  hgvsc: ENST00000522904.1:c.1489+47T>C
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428706
  ensembl transcript: ENST00000518415
  gene symbol: TACC1
  hgvsc: ENST00000518415.1:c.1438+47T>C
  variant of: http://identifiers.org/hgnc/11522
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Pro540Pro
num of homozygotes: 8358
population: South Asian
population: European (Non-Finnish)
population: Latino
population: African
population: Other
population: European (Finnish)
population: East Asian
reference allele: T
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS

8-38684862-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38684862
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 38684862
    reference: chr 8
allele count: 21
allele frequency: 1.731045056629903e-4
allele num: 121314
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000393647
  ensembl transcript: ENST00000443286
  gene symbol: TACC1
  hgvsc: ENST00000443286.2:c.1621+56C>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000321703
  ensembl transcript: ENST00000317827
  gene symbol: TACC1
  hgvsc: ENST00000317827.4:c.1629C>T
  hgvsp: ENST00000317827.4:c.1629C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430306
  ensembl transcript: ENST00000518809
  gene symbol: TACC1
  hgvsc: ENST00000518809.1:c.578C>T
  hgvsp: ENST00000518809.1:c.578C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428450
  ensembl transcript: ENST00000520615
  gene symbol: TACC1
  hgvsc: ENST00000520615.1:c.1044C>T
  hgvsp: ENST00000520615.1:c.1044C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000369263
  ensembl transcript: ENST00000379931
  gene symbol: TACC1
  hgvsc: ENST00000379931.3:c.1665C>T
  hgvsp: ENST00000379931.3:c.1665C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000332794
  ensembl transcript: ENST00000330691
  gene symbol: TACC1
  hgvsc: ENST00000330691.6:c.351C>T
  hgvsp: ENST00000330691.6:c.351C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000473342
  ensembl transcript: ENST00000520340
  gene symbol: TACC1
  hgvsc: ENST00000520340.1:c.1465+56C>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000276520
  ensembl transcript: ENST00000276520
  gene symbol: TACC1
  hgvsc: ENST00000276520.8:c.399C>T
  hgvsp: ENST00000276520.8:c.399C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428706
  ensembl transcript: ENST00000518415
  gene symbol: TACC1
  hgvsc: ENST00000518415.1:c.1438+56C>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430355
  ensembl transcript: ENST00000522904
  gene symbol: TACC1
  hgvsc: ENST00000522904.1:c.1489+56C>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000327818
  ensembl transcript: ENST00000348567
  gene symbol: TACC1
  hgvsc: ENST00000348567.4:c.315C>T
  hgvsp: ENST00000348567.4:c.315C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428466
  ensembl transcript: ENST00000521642
  gene symbol: TACC1
  hgvsc: ENST00000521642.1:c.315C>T
  hgvsp: ENST00000521642.1:c.315C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430959
  ensembl transcript: ENST00000520973
  gene symbol: TACC1
  hgvsc: ENST00000520973.1:c.988+56C>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428949
  ensembl transcript: ENST00000521050
  gene symbol: TACC1
  hgvsc: ENST00000521050.1:c.351C>T
  hgvsp: ENST00000521050.1:c.351C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428253
  ensembl transcript: ENST00000521866
  gene symbol: TACC1
  hgvsc: ENST00000521866.1:c.933+56C>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000522752
  gene symbol: TACC1
  hgvsc: ENST00000522752.1:n.293+56C>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000429418
  ensembl transcript: ENST00000520611
  gene symbol: TACC1
  hgvsc: ENST00000520611.1:c.-58C>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000522955
  gene symbol: TACC1
  hgvsc: ENST00000522955.1:n.1545C>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428687
  ensembl transcript: ENST00000519416
  gene symbol: TACC1
  hgvsc: ENST00000519416.1:c.1041C>T
  hgvsp: ENST00000519416.1:c.1041C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000523239
  gene symbol: TACC1
  hgvsc: ENST00000523239.1:n.271C>T
  variant of: http://identifiers.org/hgnc/11522
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Thr543Thr
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Other
population: African
population: European (Finnish)
population: Latino
population: East Asian
reference allele: C
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum

8-38684868-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38684868
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 38684868
    reference: chr 8
allele count: 2
allele frequency: 1.648967746190884e-5
allele num: 121288
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000393647
  ensembl transcript: ENST00000443286
  gene symbol: TACC1
  hgvsc: ENST00000443286.2:c.1621+62T>C
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000473342
  ensembl transcript: ENST00000520340
  gene symbol: TACC1
  hgvsc: ENST00000520340.1:c.1465+62T>C
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428949
  ensembl transcript: ENST00000521050
  gene symbol: TACC1
  hgvsc: ENST00000521050.1:c.357T>C
  hgvsp: ENST00000521050.1:c.357T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000327818
  ensembl transcript: ENST00000348567
  gene symbol: TACC1
  hgvsc: ENST00000348567.4:c.321T>C
  hgvsp: ENST00000348567.4:c.321T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430306
  ensembl transcript: ENST00000518809
  gene symbol: TACC1
  hgvsc: ENST00000518809.1:c.584T>C
  hgvsp: ENST00000518809.1:c.584T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428450
  ensembl transcript: ENST00000520615
  gene symbol: TACC1
  hgvsc: ENST00000520615.1:c.1050T>C
  hgvsp: ENST00000520615.1:c.1050T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000369263
  ensembl transcript: ENST00000379931
  gene symbol: TACC1
  hgvsc: ENST00000379931.3:c.1671T>C
  hgvsp: ENST00000379931.3:c.1671T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000522752
  gene symbol: TACC1
  hgvsc: ENST00000522752.1:n.293+62T>C
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000522955
  gene symbol: TACC1
  hgvsc: ENST00000522955.1:n.1551T>C
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000276520
  ensembl transcript: ENST00000276520
  gene symbol: TACC1
  hgvsc: ENST00000276520.8:c.405T>C
  hgvsp: ENST00000276520.8:c.405T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000332794
  ensembl transcript: ENST00000330691
  gene symbol: TACC1
  hgvsc: ENST00000330691.6:c.357T>C
  hgvsp: ENST00000330691.6:c.357T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000523239
  gene symbol: TACC1
  hgvsc: ENST00000523239.1:n.277T>C
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430355
  ensembl transcript: ENST00000522904
  gene symbol: TACC1
  hgvsc: ENST00000522904.1:c.1489+62T>C
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430959
  ensembl transcript: ENST00000520973
  gene symbol: TACC1
  hgvsc: ENST00000520973.1:c.988+62T>C
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000321703
  ensembl transcript: ENST00000317827
  gene symbol: TACC1
  hgvsc: ENST00000317827.4:c.1635T>C
  hgvsp: ENST00000317827.4:c.1635T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428687
  ensembl transcript: ENST00000519416
  gene symbol: TACC1
  hgvsc: ENST00000519416.1:c.1047T>C
  hgvsp: ENST00000519416.1:c.1047T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000429418
  ensembl transcript: ENST00000520611
  gene symbol: TACC1
  hgvsc: ENST00000520611.1:c.-52T>C
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428466
  ensembl transcript: ENST00000521642
  gene symbol: TACC1
  hgvsc: ENST00000521642.1:c.321T>C
  hgvsp: ENST00000521642.1:c.321T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428253
  ensembl transcript: ENST00000521866
  gene symbol: TACC1
  hgvsc: ENST00000521866.1:c.933+62T>C
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428706
  ensembl transcript: ENST00000518415
  gene symbol: TACC1
  hgvsc: ENST00000518415.1:c.1438+62T>C
  variant of: http://identifiers.org/hgnc/11522
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Asn545Asn
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: East Asian
population: Latino
population: African
population: South Asian
reference allele: T
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: ReadPosRankSum

8-38684870-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38684870
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 38684870
    reference: chr 8
allele count: 1
allele frequency: 8.244974687927709e-6
allele num: 121286
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430306
  ensembl transcript: ENST00000518809
  gene symbol: TACC1
  hgvsc: ENST00000518809.1:c.586A>G
  hgvsp: ENSP00000430306.1:p.His196Arg
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428949
  ensembl transcript: ENST00000521050
  gene symbol: TACC1
  hgvsc: ENST00000521050.1:c.359A>G
  hgvsp: ENSP00000428949.1:p.His120Arg
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428466
  ensembl transcript: ENST00000521642
  gene symbol: TACC1
  hgvsc: ENST00000521642.1:c.323A>G
  hgvsp: ENSP00000428466.1:p.His108Arg
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428687
  ensembl transcript: ENST00000519416
  gene symbol: TACC1
  hgvsc: ENST00000519416.1:c.1049A>G
  hgvsp: ENSP00000428687.1:p.His350Arg
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000332794
  ensembl transcript: ENST00000330691
  gene symbol: TACC1
  hgvsc: ENST00000330691.6:c.359A>G
  hgvsp: ENSP00000332794.6:p.His120Arg
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000369263
  ensembl transcript: ENST00000379931
  gene symbol: TACC1
  hgvsc: ENST00000379931.3:c.1673A>G
  hgvsp: ENSP00000369263.3:p.His558Arg
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428706
  ensembl transcript: ENST00000518415
  gene symbol: TACC1
  hgvsc: ENST00000518415.1:c.1438+64A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000327818
  ensembl transcript: ENST00000348567
  gene symbol: TACC1
  hgvsc: ENST00000348567.4:c.323A>G
  hgvsp: ENSP00000327818.5:p.His108Arg
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000429418
  ensembl transcript: ENST00000520611
  gene symbol: TACC1
  hgvsc: ENST00000520611.1:c.-50A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000393647
  ensembl transcript: ENST00000443286
  gene symbol: TACC1
  hgvsc: ENST00000443286.2:c.1621+64A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000276520
  ensembl transcript: ENST00000276520
  gene symbol: TACC1
  hgvsc: ENST00000276520.8:c.407A>G
  hgvsp: ENSP00000276520.8:p.His136Arg
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430959
  ensembl transcript: ENST00000520973
  gene symbol: TACC1
  hgvsc: ENST00000520973.1:c.988+64A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428450
  ensembl transcript: ENST00000520615
  gene symbol: TACC1
  hgvsc: ENST00000520615.1:c.1052A>G
  hgvsp: ENSP00000428450.1:p.His351Arg
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428253
  ensembl transcript: ENST00000521866
  gene symbol: TACC1
  hgvsc: ENST00000521866.1:c.933+64A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000522752
  gene symbol: TACC1
  hgvsc: ENST00000522752.1:n.293+64A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430355
  ensembl transcript: ENST00000522904
  gene symbol: TACC1
  hgvsc: ENST00000522904.1:c.1489+64A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000522955
  gene symbol: TACC1
  hgvsc: ENST00000522955.1:n.1553A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000321703
  ensembl transcript: ENST00000317827
  gene symbol: TACC1
  hgvsc: ENST00000317827.4:c.1637A>G
  hgvsp: ENSP00000321703.4:p.His546Arg
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000523239
  gene symbol: TACC1
  hgvsc: ENST00000523239.1:n.279A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000473342
  ensembl transcript: ENST00000520340
  gene symbol: TACC1
  hgvsc: ENST00000520340.1:c.1465+64A>G
  variant of: http://identifiers.org/hgnc/11522
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.His546Arg
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
population: Other
population: South Asian
population: East Asian
reference allele: A
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

8-38684872-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38684872
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 38684872
    reference: chr 8
allele count: 1
allele frequency: 8.244974687927709e-6
allele num: 121286
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000369263
  ensembl transcript: ENST00000379931
  gene symbol: TACC1
  hgvsc: ENST00000379931.3:c.1675G>A
  hgvsp: ENSP00000369263.3:p.Ala559Thr
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000332794
  ensembl transcript: ENST00000330691
  gene symbol: TACC1
  hgvsc: ENST00000330691.6:c.361G>A
  hgvsp: ENSP00000332794.6:p.Ala121Thr
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430959
  ensembl transcript: ENST00000520973
  gene symbol: TACC1
  hgvsc: ENST00000520973.1:c.988+66G>A
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428687
  ensembl transcript: ENST00000519416
  gene symbol: TACC1
  hgvsc: ENST00000519416.1:c.1051G>A
  hgvsp: ENSP00000428687.1:p.Ala351Thr
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000321703
  ensembl transcript: ENST00000317827
  gene symbol: TACC1
  hgvsc: ENST00000317827.4:c.1639G>A
  hgvsp: ENSP00000321703.4:p.Ala547Thr
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428706
  ensembl transcript: ENST00000518415
  gene symbol: TACC1
  hgvsc: ENST00000518415.1:c.1438+66G>A
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000393647
  ensembl transcript: ENST00000443286
  gene symbol: TACC1
  hgvsc: ENST00000443286.2:c.1621+66G>A
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000327818
  ensembl transcript: ENST00000348567
  gene symbol: TACC1
  hgvsc: ENST00000348567.4:c.325G>A
  hgvsp: ENSP00000327818.5:p.Ala109Thr
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428949
  ensembl transcript: ENST00000521050
  gene symbol: TACC1
  hgvsc: ENST00000521050.1:c.361G>A
  hgvsp: ENSP00000428949.1:p.Ala121Thr
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428253
  ensembl transcript: ENST00000521866
  gene symbol: TACC1
  hgvsc: ENST00000521866.1:c.933+66G>A
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430355
  ensembl transcript: ENST00000522904
  gene symbol: TACC1
  hgvsc: ENST00000522904.1:c.1489+66G>A
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430306
  ensembl transcript: ENST00000518809
  gene symbol: TACC1
  hgvsc: ENST00000518809.1:c.588G>A
  hgvsp: ENSP00000430306.1:p.Ala197Thr
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428466
  ensembl transcript: ENST00000521642
  gene symbol: TACC1
  hgvsc: ENST00000521642.1:c.325G>A
  hgvsp: ENSP00000428466.1:p.Ala109Thr
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428450
  ensembl transcript: ENST00000520615
  gene symbol: TACC1
  hgvsc: ENST00000520615.1:c.1054G>A
  hgvsp: ENSP00000428450.1:p.Ala352Thr
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000276520
  ensembl transcript: ENST00000276520
  gene symbol: TACC1
  hgvsc: ENST00000276520.8:c.409G>A
  hgvsp: ENSP00000276520.8:p.Ala137Thr
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000522955
  gene symbol: TACC1
  hgvsc: ENST00000522955.1:n.1555G>A
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000429418
  ensembl transcript: ENST00000520611
  gene symbol: TACC1
  hgvsc: ENST00000520611.1:c.-48G>A
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000473342
  ensembl transcript: ENST00000520340
  gene symbol: TACC1
  hgvsc: ENST00000520340.1:c.1465+66G>A
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000522752
  gene symbol: TACC1
  hgvsc: ENST00000522752.1:n.293+66G>A
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000523239
  gene symbol: TACC1
  hgvsc: ENST00000523239.1:n.281G>A
  variant of: http://identifiers.org/hgnc/11522
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Ala547Thr
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum

8-38684873-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38684873
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 38684873
    reference: chr 8
allele count: 12
allele frequency: 9.894622272794736e-5
allele num: 121278
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428687
  ensembl transcript: ENST00000519416
  gene symbol: TACC1
  hgvsc: ENST00000519416.1:c.1052C>T
  hgvsp: ENSP00000428687.1:p.Ala351Val
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000369263
  ensembl transcript: ENST00000379931
  gene symbol: TACC1
  hgvsc: ENST00000379931.3:c.1676C>T
  hgvsp: ENSP00000369263.3:p.Ala559Val
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000429418
  ensembl transcript: ENST00000520611
  gene symbol: TACC1
  hgvsc: ENST00000520611.1:c.-47C>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000276520
  ensembl transcript: ENST00000276520
  gene symbol: TACC1
  hgvsc: ENST00000276520.8:c.410C>T
  hgvsp: ENSP00000276520.8:p.Ala137Val
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430306
  ensembl transcript: ENST00000518809
  gene symbol: TACC1
  hgvsc: ENST00000518809.1:c.589C>T
  hgvsp: ENSP00000430306.1:p.Ala197Val
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000393647
  ensembl transcript: ENST00000443286
  gene symbol: TACC1
  hgvsc: ENST00000443286.2:c.1621+67C>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428253
  ensembl transcript: ENST00000521866
  gene symbol: TACC1
  hgvsc: ENST00000521866.1:c.933+67C>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000522955
  gene symbol: TACC1
  hgvsc: ENST00000522955.1:n.1556C>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428949
  ensembl transcript: ENST00000521050
  gene symbol: TACC1
  hgvsc: ENST00000521050.1:c.362C>T
  hgvsp: ENSP00000428949.1:p.Ala121Val
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000327818
  ensembl transcript: ENST00000348567
  gene symbol: TACC1
  hgvsc: ENST00000348567.4:c.326C>T
  hgvsp: ENSP00000327818.5:p.Ala109Val
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000332794
  ensembl transcript: ENST00000330691
  gene symbol: TACC1
  hgvsc: ENST00000330691.6:c.362C>T
  hgvsp: ENSP00000332794.6:p.Ala121Val
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428450
  ensembl transcript: ENST00000520615
  gene symbol: TACC1
  hgvsc: ENST00000520615.1:c.1055C>T
  hgvsp: ENSP00000428450.1:p.Ala352Val
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430355
  ensembl transcript: ENST00000522904
  gene symbol: TACC1
  hgvsc: ENST00000522904.1:c.1489+67C>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428706
  ensembl transcript: ENST00000518415
  gene symbol: TACC1
  hgvsc: ENST00000518415.1:c.1438+67C>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000523239
  gene symbol: TACC1
  hgvsc: ENST00000523239.1:n.282C>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000473342
  ensembl transcript: ENST00000520340
  gene symbol: TACC1
  hgvsc: ENST00000520340.1:c.1465+67C>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000321703
  ensembl transcript: ENST00000317827
  gene symbol: TACC1
  hgvsc: ENST00000317827.4:c.1640C>T
  hgvsp: ENSP00000321703.4:p.Ala547Val
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000522752
  gene symbol: TACC1
  hgvsc: ENST00000522752.1:n.293+67C>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430959
  ensembl transcript: ENST00000520973
  gene symbol: TACC1
  hgvsc: ENST00000520973.1:c.988+67C>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428466
  ensembl transcript: ENST00000521642
  gene symbol: TACC1
  hgvsc: ENST00000521642.1:c.326C>T
  hgvsp: ENSP00000428466.1:p.Ala109Val
  variant of: http://identifiers.org/hgnc/11522
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Ala547Val
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum

8-38684874-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38684874
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 38684874
    reference: chr 8
allele count: 3
allele frequency: 2.473818751546137e-5
allele num: 121270
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430306
  ensembl transcript: ENST00000518809
  gene symbol: TACC1
  hgvsc: ENST00000518809.1:c.590G>A
  hgvsp: ENST00000518809.1:c.590G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000327818
  ensembl transcript: ENST00000348567
  gene symbol: TACC1
  hgvsc: ENST00000348567.4:c.327G>A
  hgvsp: ENST00000348567.4:c.327G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000429418
  ensembl transcript: ENST00000520611
  gene symbol: TACC1
  hgvsc: ENST00000520611.1:c.-46G>A
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000321703
  ensembl transcript: ENST00000317827
  gene symbol: TACC1
  hgvsc: ENST00000317827.4:c.1641G>A
  hgvsp: ENST00000317827.4:c.1641G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000332794
  ensembl transcript: ENST00000330691
  gene symbol: TACC1
  hgvsc: ENST00000330691.6:c.363G>A
  hgvsp: ENST00000330691.6:c.363G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000522955
  gene symbol: TACC1
  hgvsc: ENST00000522955.1:n.1557G>A
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428687
  ensembl transcript: ENST00000519416
  gene symbol: TACC1
  hgvsc: ENST00000519416.1:c.1053G>A
  hgvsp: ENST00000519416.1:c.1053G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430959
  ensembl transcript: ENST00000520973
  gene symbol: TACC1
  hgvsc: ENST00000520973.1:c.988+68G>A
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428949
  ensembl transcript: ENST00000521050
  gene symbol: TACC1
  hgvsc: ENST00000521050.1:c.363G>A
  hgvsp: ENST00000521050.1:c.363G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428706
  ensembl transcript: ENST00000518415
  gene symbol: TACC1
  hgvsc: ENST00000518415.1:c.1438+68G>A
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430355
  ensembl transcript: ENST00000522904
  gene symbol: TACC1
  hgvsc: ENST00000522904.1:c.1489+68G>A
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000276520
  ensembl transcript: ENST00000276520
  gene symbol: TACC1
  hgvsc: ENST00000276520.8:c.411G>A
  hgvsp: ENST00000276520.8:c.411G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428253
  ensembl transcript: ENST00000521866
  gene symbol: TACC1
  hgvsc: ENST00000521866.1:c.933+68G>A
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000369263
  ensembl transcript: ENST00000379931
  gene symbol: TACC1
  hgvsc: ENST00000379931.3:c.1677G>A
  hgvsp: ENST00000379931.3:c.1677G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428450
  ensembl transcript: ENST00000520615
  gene symbol: TACC1
  hgvsc: ENST00000520615.1:c.1056G>A
  hgvsp: ENST00000520615.1:c.1056G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000393647
  ensembl transcript: ENST00000443286
  gene symbol: TACC1
  hgvsc: ENST00000443286.2:c.1621+68G>A
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000523239
  gene symbol: TACC1
  hgvsc: ENST00000523239.1:n.283G>A
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000473342
  ensembl transcript: ENST00000520340
  gene symbol: TACC1
  hgvsc: ENST00000520340.1:c.1465+68G>A
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000522752
  gene symbol: TACC1
  hgvsc: ENST00000522752.1:n.293+68G>A
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428466
  ensembl transcript: ENST00000521642
  gene symbol: TACC1
  hgvsc: ENST00000521642.1:c.327G>A
  hgvsp: ENST00000521642.1:c.327G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/11522
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Ala547Ala
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: Other
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: DP

8-38684880-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38684880
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 38684880
    reference: chr 8
allele count: 38
allele frequency: 3.134847959873946e-4
allele num: 121218
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000429418
  ensembl transcript: ENST00000520611
  gene symbol: TACC1
  hgvsc: ENST00000520611.1:c.-40A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430306
  ensembl transcript: ENST00000518809
  gene symbol: TACC1
  hgvsc: ENST00000518809.1:c.596A>G
  hgvsp: ENST00000518809.1:c.596A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000327818
  ensembl transcript: ENST00000348567
  gene symbol: TACC1
  hgvsc: ENST00000348567.4:c.333A>G
  hgvsp: ENST00000348567.4:c.333A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428687
  ensembl transcript: ENST00000519416
  gene symbol: TACC1
  hgvsc: ENST00000519416.1:c.1059A>G
  hgvsp: ENST00000519416.1:c.1059A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000473342
  ensembl transcript: ENST00000520340
  gene symbol: TACC1
  hgvsc: ENST00000520340.1:c.1465+74A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000523239
  gene symbol: TACC1
  hgvsc: ENST00000523239.1:n.289A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428466
  ensembl transcript: ENST00000521642
  gene symbol: TACC1
  hgvsc: ENST00000521642.1:c.333A>G
  hgvsp: ENST00000521642.1:c.333A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428450
  ensembl transcript: ENST00000520615
  gene symbol: TACC1
  hgvsc: ENST00000520615.1:c.1062A>G
  hgvsp: ENST00000520615.1:c.1062A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000369263
  ensembl transcript: ENST00000379931
  gene symbol: TACC1
  hgvsc: ENST00000379931.3:c.1683A>G
  hgvsp: ENST00000379931.3:c.1683A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000393647
  ensembl transcript: ENST00000443286
  gene symbol: TACC1
  hgvsc: ENST00000443286.2:c.1621+74A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428253
  ensembl transcript: ENST00000521866
  gene symbol: TACC1
  hgvsc: ENST00000521866.1:c.933+74A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000522955
  gene symbol: TACC1
  hgvsc: ENST00000522955.1:n.1563A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428949
  ensembl transcript: ENST00000521050
  gene symbol: TACC1
  hgvsc: ENST00000521050.1:c.369A>G
  hgvsp: ENST00000521050.1:c.369A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430959
  ensembl transcript: ENST00000520973
  gene symbol: TACC1
  hgvsc: ENST00000520973.1:c.988+74A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000332794
  ensembl transcript: ENST00000330691
  gene symbol: TACC1
  hgvsc: ENST00000330691.6:c.369A>G
  hgvsp: ENST00000330691.6:c.369A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428706
  ensembl transcript: ENST00000518415
  gene symbol: TACC1
  hgvsc: ENST00000518415.1:c.1438+74A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000321703
  ensembl transcript: ENST00000317827
  gene symbol: TACC1
  hgvsc: ENST00000317827.4:c.1647A>G
  hgvsp: ENST00000317827.4:c.1647A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000276520
  ensembl transcript: ENST00000276520
  gene symbol: TACC1
  hgvsc: ENST00000276520.8:c.417A>G
  hgvsp: ENST00000276520.8:c.417A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000522752
  gene symbol: TACC1
  hgvsc: ENST00000522752.1:n.293+74A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430355
  ensembl transcript: ENST00000522904
  gene symbol: TACC1
  hgvsc: ENST00000522904.1:c.1489+74A>G
  variant of: http://identifiers.org/hgnc/11522
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Ser549Ser
num of homozygotes: 1
population: Other
population: South Asian
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: DP

http://identifiers.org/exac.variant/8-38684921-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38684921
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 38684921
    reference: chr 8
allele count: 1
allele frequency: 8.688852202624033e-6
allele num: 115090
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428687
  ensembl transcript: ENST00000519416
  gene symbol: TACC1
  hgvsc: ENST00000519416.1:c.1072+28A>C
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428450
  ensembl transcript: ENST00000520615
  gene symbol: TACC1
  hgvsc: ENST00000520615.1:c.1075+28A>C
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430306
  ensembl transcript: ENST00000518809
  gene symbol: TACC1
  hgvsc: ENST00000518809.1:c.609+28A>C
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000332794
  ensembl transcript: ENST00000330691
  gene symbol: TACC1
  hgvsc: ENST00000330691.6:c.382+28A>C
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430959
  ensembl transcript: ENST00000520973
  gene symbol: TACC1
  hgvsc: ENST00000520973.1:c.988+115A>C
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000522955
  gene symbol: TACC1
  hgvsc: ENST00000522955.1:n.1604A>C
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000369263
  ensembl transcript: ENST00000379931
  gene symbol: TACC1
  hgvsc: ENST00000379931.3:c.1696+28A>C
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428949
  ensembl transcript: ENST00000521050
  gene symbol: TACC1
  hgvsc: ENST00000521050.1:c.382+28A>C
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000473342
  ensembl transcript: ENST00000520340
  gene symbol: TACC1
  hgvsc: ENST00000520340.1:c.1465+115A>C
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000393647
  ensembl transcript: ENST00000443286
  gene symbol: TACC1
  hgvsc: ENST00000443286.2:c.1621+115A>C
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000327818
  ensembl transcript: ENST00000348567
  gene symbol: TACC1
  hgvsc: ENST00000348567.4:c.346+28A>C
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000321703
  ensembl transcript: ENST00000317827
  gene symbol: TACC1
  hgvsc: ENST00000317827.4:c.1660+28A>C
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428466
  ensembl transcript: ENST00000521642
  gene symbol: TACC1
  hgvsc: ENST00000521642.1:c.346+28A>C
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000522752
  gene symbol: TACC1
  hgvsc: ENST00000522752.1:n.293+115A>C
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000523239
  gene symbol: TACC1
  hgvsc: ENST00000523239.1:n.302+28A>C
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428253
  ensembl transcript: ENST00000521866
  gene symbol: TACC1
  hgvsc: ENST00000521866.1:c.933+115A>C
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428706
  ensembl transcript: ENST00000518415
  gene symbol: TACC1
  hgvsc: ENST00000518415.1:c.1438+115A>C
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000276520
  ensembl transcript: ENST00000276520
  gene symbol: TACC1
  hgvsc: ENST00000276520.8:c.430+28A>C
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000429418
  ensembl transcript: ENST00000520611
  gene symbol: TACC1
  hgvsc: ENST00000520611.1:c.-27+28A>C
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430355
  ensembl transcript: ENST00000522904
  gene symbol: TACC1
  hgvsc: ENST00000522904.1:c.1489+115A>C
  variant of: http://identifiers.org/hgnc/11522
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: African
population: Latino
reference allele: A
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP

8-38684926-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38684926
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 38684926
    reference: chr 8
allele count: 10
allele frequency: 8.918697156719346e-5
allele num: 112124
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428466
  ensembl transcript: ENST00000521642
  gene symbol: TACC1
  hgvsc: ENST00000521642.1:c.346+33C>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430306
  ensembl transcript: ENST00000518809
  gene symbol: TACC1
  hgvsc: ENST00000518809.1:c.609+33C>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428253
  ensembl transcript: ENST00000521866
  gene symbol: TACC1
  hgvsc: ENST00000521866.1:c.933+120C>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000321703
  ensembl transcript: ENST00000317827
  gene symbol: TACC1
  hgvsc: ENST00000317827.4:c.1660+33C>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428706
  ensembl transcript: ENST00000518415
  gene symbol: TACC1
  hgvsc: ENST00000518415.1:c.1438+120C>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428687
  ensembl transcript: ENST00000519416
  gene symbol: TACC1
  hgvsc: ENST00000519416.1:c.1072+33C>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000276520
  ensembl transcript: ENST00000276520
  gene symbol: TACC1
  hgvsc: ENST00000276520.8:c.430+33C>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430959
  ensembl transcript: ENST00000520973
  gene symbol: TACC1
  hgvsc: ENST00000520973.1:c.988+120C>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430355
  ensembl transcript: ENST00000522904
  gene symbol: TACC1
  hgvsc: ENST00000522904.1:c.1489+120C>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000332794
  ensembl transcript: ENST00000330691
  gene symbol: TACC1
  hgvsc: ENST00000330691.6:c.382+33C>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000369263
  ensembl transcript: ENST00000379931
  gene symbol: TACC1
  hgvsc: ENST00000379931.3:c.1696+33C>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000393647
  ensembl transcript: ENST00000443286
  gene symbol: TACC1
  hgvsc: ENST00000443286.2:c.1621+120C>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000327818
  ensembl transcript: ENST00000348567
  gene symbol: TACC1
  hgvsc: ENST00000348567.4:c.346+33C>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000429418
  ensembl transcript: ENST00000520611
  gene symbol: TACC1
  hgvsc: ENST00000520611.1:c.-27+33C>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428949
  ensembl transcript: ENST00000521050
  gene symbol: TACC1
  hgvsc: ENST00000521050.1:c.382+33C>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000473342
  ensembl transcript: ENST00000520340
  gene symbol: TACC1
  hgvsc: ENST00000520340.1:c.1465+120C>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000522955
  gene symbol: TACC1
  hgvsc: ENST00000522955.1:n.1609C>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000523239
  gene symbol: TACC1
  hgvsc: ENST00000523239.1:n.302+33C>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000522752
  gene symbol: TACC1
  hgvsc: ENST00000522752.1:n.293+120C>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428450
  ensembl transcript: ENST00000520615
  gene symbol: TACC1
  hgvsc: ENST00000520615.1:c.1075+33C>T
  variant of: http://identifiers.org/hgnc/11522
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD

8-38684929-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38684929
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 38684929
    reference: chr 8
allele count: 1
allele frequency: 9.115437905636987e-6
allele num: 109704
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430306
  ensembl transcript: ENST00000518809
  gene symbol: TACC1
  hgvsc: ENST00000518809.1:c.609+36A>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430355
  ensembl transcript: ENST00000522904
  gene symbol: TACC1
  hgvsc: ENST00000522904.1:c.1489+123A>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428949
  ensembl transcript: ENST00000521050
  gene symbol: TACC1
  hgvsc: ENST00000521050.1:c.382+36A>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430959
  ensembl transcript: ENST00000520973
  gene symbol: TACC1
  hgvsc: ENST00000520973.1:c.988+123A>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000369263
  ensembl transcript: ENST00000379931
  gene symbol: TACC1
  hgvsc: ENST00000379931.3:c.1696+36A>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428466
  ensembl transcript: ENST00000521642
  gene symbol: TACC1
  hgvsc: ENST00000521642.1:c.346+36A>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000522752
  gene symbol: TACC1
  hgvsc: ENST00000522752.1:n.293+123A>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428687
  ensembl transcript: ENST00000519416
  gene symbol: TACC1
  hgvsc: ENST00000519416.1:c.1072+36A>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000393647
  ensembl transcript: ENST00000443286
  gene symbol: TACC1
  hgvsc: ENST00000443286.2:c.1621+123A>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000522955
  gene symbol: TACC1
  hgvsc: ENST00000522955.1:n.1612A>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000473342
  ensembl transcript: ENST00000520340
  gene symbol: TACC1
  hgvsc: ENST00000520340.1:c.1465+123A>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000327818
  ensembl transcript: ENST00000348567
  gene symbol: TACC1
  hgvsc: ENST00000348567.4:c.346+36A>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428450
  ensembl transcript: ENST00000520615
  gene symbol: TACC1
  hgvsc: ENST00000520615.1:c.1075+36A>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000321703
  ensembl transcript: ENST00000317827
  gene symbol: TACC1
  hgvsc: ENST00000317827.4:c.1660+36A>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000429418
  ensembl transcript: ENST00000520611
  gene symbol: TACC1
  hgvsc: ENST00000520611.1:c.-27+36A>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000523239
  gene symbol: TACC1
  hgvsc: ENST00000523239.1:n.302+36A>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000332794
  ensembl transcript: ENST00000330691
  gene symbol: TACC1
  hgvsc: ENST00000330691.6:c.382+36A>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000276520
  ensembl transcript: ENST00000276520
  gene symbol: TACC1
  hgvsc: ENST00000276520.8:c.430+36A>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428706
  ensembl transcript: ENST00000518415
  gene symbol: TACC1
  hgvsc: ENST00000518415.1:c.1438+123A>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428253
  ensembl transcript: ENST00000521866
  gene symbol: TACC1
  hgvsc: ENST00000521866.1:c.933+123A>T
  variant of: http://identifiers.org/hgnc/11522
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5677
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
population: European (Finnish)
population: East Asian
reference allele: A
site quality: MQ
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD

8-38684940-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38684940
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 38684940
    reference: chr 8
allele count: 1
allele frequency: 9.987016878058524e-6
allele num: 100130
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000393647
  ensembl transcript: ENST00000443286
  gene symbol: TACC1
  hgvsc: ENST00000443286.2:c.1621+134T>A
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000321703
  ensembl transcript: ENST00000317827
  gene symbol: TACC1
  hgvsc: ENST00000317827.4:c.1660+47T>A
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428253
  ensembl transcript: ENST00000521866
  gene symbol: TACC1
  hgvsc: ENST00000521866.1:c.933+134T>A
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000522955
  gene symbol: TACC1
  hgvsc: ENST00000522955.1:n.1623T>A
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430355
  ensembl transcript: ENST00000522904
  gene symbol: TACC1
  hgvsc: ENST00000522904.1:c.1489+134T>A
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428706
  ensembl transcript: ENST00000518415
  gene symbol: TACC1
  hgvsc: ENST00000518415.1:c.1438+134T>A
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430959
  ensembl transcript: ENST00000520973
  gene symbol: TACC1
  hgvsc: ENST00000520973.1:c.988+134T>A
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428466
  ensembl transcript: ENST00000521642
  gene symbol: TACC1
  hgvsc: ENST00000521642.1:c.346+47T>A
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000522752
  gene symbol: TACC1
  hgvsc: ENST00000522752.1:n.293+134T>A
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000276520
  ensembl transcript: ENST00000276520
  gene symbol: TACC1
  hgvsc: ENST00000276520.8:c.430+47T>A
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000327818
  ensembl transcript: ENST00000348567
  gene symbol: TACC1
  hgvsc: ENST00000348567.4:c.346+47T>A
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428687
  ensembl transcript: ENST00000519416
  gene symbol: TACC1
  hgvsc: ENST00000519416.1:c.1072+47T>A
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000369263
  ensembl transcript: ENST00000379931
  gene symbol: TACC1
  hgvsc: ENST00000379931.3:c.1696+47T>A
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430306
  ensembl transcript: ENST00000518809
  gene symbol: TACC1
  hgvsc: ENST00000518809.1:c.609+47T>A
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428450
  ensembl transcript: ENST00000520615
  gene symbol: TACC1
  hgvsc: ENST00000520615.1:c.1075+47T>A
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000332794
  ensembl transcript: ENST00000330691
  gene symbol: TACC1
  hgvsc: ENST00000330691.6:c.382+47T>A
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000473342
  ensembl transcript: ENST00000520340
  gene symbol: TACC1
  hgvsc: ENST00000520340.1:c.1465+134T>A
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000429418
  ensembl transcript: ENST00000520611
  gene symbol: TACC1
  hgvsc: ENST00000520611.1:c.-27+47T>A
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428949
  ensembl transcript: ENST00000521050
  gene symbol: TACC1
  hgvsc: ENST00000521050.1:c.382+47T>A
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000523239
  gene symbol: TACC1
  hgvsc: ENST00000523239.1:n.302+47T>A
  variant of: http://identifiers.org/hgnc/11522
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
reference allele: T
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum

8-38684967-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38684967
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 38684967
    reference: chr 8
allele count: 0
allele frequency: 0.0e0
allele num: 73026
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430355
  ensembl transcript: ENST00000522904
  gene symbol: TACC1
  hgvsc: ENST00000522904.1:c.1489+161A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000522752
  gene symbol: TACC1
  hgvsc: ENST00000522752.1:n.293+161A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000321703
  ensembl transcript: ENST00000317827
  gene symbol: TACC1
  hgvsc: ENST00000317827.4:c.1660+74A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000393647
  ensembl transcript: ENST00000443286
  gene symbol: TACC1
  hgvsc: ENST00000443286.2:c.1621+161A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430959
  ensembl transcript: ENST00000520973
  gene symbol: TACC1
  hgvsc: ENST00000520973.1:c.988+161A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000523239
  gene symbol: TACC1
  hgvsc: ENST00000523239.1:n.302+74A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428706
  ensembl transcript: ENST00000518415
  gene symbol: TACC1
  hgvsc: ENST00000518415.1:c.1438+161A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000327818
  ensembl transcript: ENST00000348567
  gene symbol: TACC1
  hgvsc: ENST00000348567.4:c.346+74A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000369263
  ensembl transcript: ENST00000379931
  gene symbol: TACC1
  hgvsc: ENST00000379931.3:c.1696+74A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428466
  ensembl transcript: ENST00000521642
  gene symbol: TACC1
  hgvsc: ENST00000521642.1:c.346+74A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430306
  ensembl transcript: ENST00000518809
  gene symbol: TACC1
  hgvsc: ENST00000518809.1:c.609+74A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428450
  ensembl transcript: ENST00000520615
  gene symbol: TACC1
  hgvsc: ENST00000520615.1:c.1075+74A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428687
  ensembl transcript: ENST00000519416
  gene symbol: TACC1
  hgvsc: ENST00000519416.1:c.1072+74A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000276520
  ensembl transcript: ENST00000276520
  gene symbol: TACC1
  hgvsc: ENST00000276520.8:c.430+74A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428949
  ensembl transcript: ENST00000521050
  gene symbol: TACC1
  hgvsc: ENST00000521050.1:c.382+74A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000522955
  gene symbol: TACC1
  hgvsc: ENST00000522955.1:n.1650A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000473342
  ensembl transcript: ENST00000520340
  gene symbol: TACC1
  hgvsc: ENST00000520340.1:c.1465+161A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000429418
  ensembl transcript: ENST00000520611
  gene symbol: TACC1
  hgvsc: ENST00000520611.1:c.-27+74A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000332794
  ensembl transcript: ENST00000330691
  gene symbol: TACC1
  hgvsc: ENST00000330691.6:c.382+74A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428253
  ensembl transcript: ENST00000521866
  gene symbol: TACC1
  hgvsc: ENST00000521866.1:c.933+161A>G
  variant of: http://identifiers.org/hgnc/11522
canonical: false
consequence: non coding transcript exon
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
population: Other
population: East Asian
population: African
reference allele: A
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum

8-38684971-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38684971
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 38684971
    reference: chr 8
allele count: 1
allele frequency: 1.466017709493931e-5
allele num: 68212
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430306
  ensembl transcript: ENST00000518809
  gene symbol: TACC1
  hgvsc: ENST00000518809.1:c.609+78T>C
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428450
  ensembl transcript: ENST00000520615
  gene symbol: TACC1
  hgvsc: ENST00000520615.1:c.1075+78T>C
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000327818
  ensembl transcript: ENST00000348567
  gene symbol: TACC1
  hgvsc: ENST00000348567.4:c.346+78T>C
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430355
  ensembl transcript: ENST00000522904
  gene symbol: TACC1
  hgvsc: ENST00000522904.1:c.1489+165T>C
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000321703
  ensembl transcript: ENST00000317827
  gene symbol: TACC1
  hgvsc: ENST00000317827.4:c.1660+78T>C
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000369263
  ensembl transcript: ENST00000379931
  gene symbol: TACC1
  hgvsc: ENST00000379931.3:c.1696+78T>C
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000522955
  gene symbol: TACC1
  hgvsc: ENST00000522955.1:n.1654T>C
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428706
  ensembl transcript: ENST00000518415
  gene symbol: TACC1
  hgvsc: ENST00000518415.1:c.1438+165T>C
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000332794
  ensembl transcript: ENST00000330691
  gene symbol: TACC1
  hgvsc: ENST00000330691.6:c.382+78T>C
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428687
  ensembl transcript: ENST00000519416
  gene symbol: TACC1
  hgvsc: ENST00000519416.1:c.1072+78T>C
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430959
  ensembl transcript: ENST00000520973
  gene symbol: TACC1
  hgvsc: ENST00000520973.1:c.988+165T>C
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000522752
  gene symbol: TACC1
  hgvsc: ENST00000522752.1:n.293+165T>C
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000393647
  ensembl transcript: ENST00000443286
  gene symbol: TACC1
  hgvsc: ENST00000443286.2:c.1621+165T>C
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428466
  ensembl transcript: ENST00000521642
  gene symbol: TACC1
  hgvsc: ENST00000521642.1:c.346+78T>C
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000523239
  gene symbol: TACC1
  hgvsc: ENST00000523239.1:n.302+78T>C
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428253
  ensembl transcript: ENST00000521866
  gene symbol: TACC1
  hgvsc: ENST00000521866.1:c.933+165T>C
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000473342
  ensembl transcript: ENST00000520340
  gene symbol: TACC1
  hgvsc: ENST00000520340.1:c.1465+165T>C
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428949
  ensembl transcript: ENST00000521050
  gene symbol: TACC1
  hgvsc: ENST00000521050.1:c.382+78T>C
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000276520
  ensembl transcript: ENST00000276520
  gene symbol: TACC1
  hgvsc: ENST00000276520.8:c.430+78T>C
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000429418
  ensembl transcript: ENST00000520611
  gene symbol: TACC1
  hgvsc: ENST00000520611.1:c.-27+78T>C
  variant of: http://identifiers.org/hgnc/11522
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1714
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: Other
population: South Asian
population: African
reference allele: T
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: MQ

8-38684985-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38684985
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 38684985
    reference: chr 8
allele count: 2
allele frequency: 3.495403544339194e-5
allele num: 57218
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000369263
  ensembl transcript: ENST00000379931
  gene symbol: TACC1
  hgvsc: ENST00000379931.3:c.1696+92G>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428687
  ensembl transcript: ENST00000519416
  gene symbol: TACC1
  hgvsc: ENST00000519416.1:c.1072+92G>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428450
  ensembl transcript: ENST00000520615
  gene symbol: TACC1
  hgvsc: ENST00000520615.1:c.1075+92G>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000321703
  ensembl transcript: ENST00000317827
  gene symbol: TACC1
  hgvsc: ENST00000317827.4:c.1660+92G>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000522752
  gene symbol: TACC1
  hgvsc: ENST00000522752.1:n.293+179G>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430355
  ensembl transcript: ENST00000522904
  gene symbol: TACC1
  hgvsc: ENST00000522904.1:c.1489+179G>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430306
  ensembl transcript: ENST00000518809
  gene symbol: TACC1
  hgvsc: ENST00000518809.1:c.609+92G>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000393647
  ensembl transcript: ENST00000443286
  gene symbol: TACC1
  hgvsc: ENST00000443286.2:c.1621+179G>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430959
  ensembl transcript: ENST00000520973
  gene symbol: TACC1
  hgvsc: ENST00000520973.1:c.988+179G>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000276520
  ensembl transcript: ENST00000276520
  gene symbol: TACC1
  hgvsc: ENST00000276520.8:c.430+92G>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000523239
  gene symbol: TACC1
  hgvsc: ENST00000523239.1:n.302+92G>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428253
  ensembl transcript: ENST00000521866
  gene symbol: TACC1
  hgvsc: ENST00000521866.1:c.933+179G>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000332794
  ensembl transcript: ENST00000330691
  gene symbol: TACC1
  hgvsc: ENST00000330691.6:c.382+92G>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000327818
  ensembl transcript: ENST00000348567
  gene symbol: TACC1
  hgvsc: ENST00000348567.4:c.346+92G>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428466
  ensembl transcript: ENST00000521642
  gene symbol: TACC1
  hgvsc: ENST00000521642.1:c.346+92G>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000522955
  gene symbol: TACC1
  hgvsc: ENST00000522955.1:n.1668G>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000473342
  ensembl transcript: ENST00000520340
  gene symbol: TACC1
  hgvsc: ENST00000520340.1:c.1465+179G>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428706
  ensembl transcript: ENST00000518415
  gene symbol: TACC1
  hgvsc: ENST00000518415.1:c.1438+179G>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000429418
  ensembl transcript: ENST00000520611
  gene symbol: TACC1
  hgvsc: ENST00000520611.1:c.-27+92G>T
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428949
  ensembl transcript: ENST00000521050
  gene symbol: TACC1
  hgvsc: ENST00000521050.1:c.382+92G>T
  variant of: http://identifiers.org/hgnc/11522
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
population: South Asian
population: European (Finnish)
reference allele: G
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ

8-38684987-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38684987
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 38684987
    reference: chr 8
allele count: 2
allele frequency: 3.568497305784534e-5
allele num: 56046
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428450
  ensembl transcript: ENST00000520615
  gene symbol: TACC1
  hgvsc: ENST00000520615.1:c.1075+94A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000327818
  ensembl transcript: ENST00000348567
  gene symbol: TACC1
  hgvsc: ENST00000348567.4:c.346+94A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428687
  ensembl transcript: ENST00000519416
  gene symbol: TACC1
  hgvsc: ENST00000519416.1:c.1072+94A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430306
  ensembl transcript: ENST00000518809
  gene symbol: TACC1
  hgvsc: ENST00000518809.1:c.609+94A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000321703
  ensembl transcript: ENST00000317827
  gene symbol: TACC1
  hgvsc: ENST00000317827.4:c.1660+94A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430355
  ensembl transcript: ENST00000522904
  gene symbol: TACC1
  hgvsc: ENST00000522904.1:c.1489+181A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000430959
  ensembl transcript: ENST00000520973
  gene symbol: TACC1
  hgvsc: ENST00000520973.1:c.988+181A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428706
  ensembl transcript: ENST00000518415
  gene symbol: TACC1
  hgvsc: ENST00000518415.1:c.1438+181A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000523239
  gene symbol: TACC1
  hgvsc: ENST00000523239.1:n.302+94A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000393647
  ensembl transcript: ENST00000443286
  gene symbol: TACC1
  hgvsc: ENST00000443286.2:c.1621+181A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428466
  ensembl transcript: ENST00000521642
  gene symbol: TACC1
  hgvsc: ENST00000521642.1:c.346+94A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428949
  ensembl transcript: ENST00000521050
  gene symbol: TACC1
  hgvsc: ENST00000521050.1:c.382+94A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000522955
  gene symbol: TACC1
  hgvsc: ENST00000522955.1:n.1670A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000429418
  ensembl transcript: ENST00000520611
  gene symbol: TACC1
  hgvsc: ENST00000520611.1:c.-27+94A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000369263
  ensembl transcript: ENST00000379931
  gene symbol: TACC1
  hgvsc: ENST00000379931.3:c.1696+94A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000473342
  ensembl transcript: ENST00000520340
  gene symbol: TACC1
  hgvsc: ENST00000520340.1:c.1465+181A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000428253
  ensembl transcript: ENST00000521866
  gene symbol: TACC1
  hgvsc: ENST00000521866.1:c.933+181A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000276520
  ensembl transcript: ENST00000276520
  gene symbol: TACC1
  hgvsc: ENST00000276520.8:c.430+94A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl protein: ENSP00000332794
  ensembl transcript: ENST00000330691
  gene symbol: TACC1
  hgvsc: ENST00000330691.6:c.382+94A>G
  variant of: http://identifiers.org/hgnc/11522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000147526
  ensembl transcript: ENST00000522752
  gene symbol: TACC1
  hgvsc: ENST00000522752.1:n.293+181A>G
  variant of: http://identifiers.org/hgnc/11522
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: A

GenotypeDepth
all individuals: 6145
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9656
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 533
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7271
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8971
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4586
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 74
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 874
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 21
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 682
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8412
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 388
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1799
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1235
bin: 7.25e1
variant carriers: 1

GenotypeDepth
all individuals: 56
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1804
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2694
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1323
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4181
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3060
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4322
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3501
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2011
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4335
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2500
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4025
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36765
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 30
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 5.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8652
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11544
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498621268433042e-5
allele num: 66728
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.39e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.92e0

FS
type: SiteQuality
SIO_000300: 2.427e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-3

VQSLOD
type: SiteQuality
SIO_000300: -4.13e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.15e-1

QD
type: SiteQuality
SIO_000300: 1.346e1

MQ
type: SiteQuality
SIO_000300: 5.908e1

DP
type: SiteQuality
SIO_000300: 2.906268e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.377e0

GenotypeDepth
all individuals: 682
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1800
bin: 9.75e1
variant carriers: 2

GenotypeDepth
all individuals: 2694
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1804
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8967
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8411
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1316
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7272
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4180
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 22
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 66
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 81
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 388
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1234
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9657
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 874
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 533
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6146
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4578
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3052
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36763
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 16
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4322
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4329
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4025
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2009
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2499
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3501
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 3.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
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MQ
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GenotypeQuality
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GenotypeQuality
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Other
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African
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European (Finnish)
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European (Non-Finnish)
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East Asian
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DP
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FS
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MQ
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East Asian
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African
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European (Non-Finnish)
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allele frequency: 1.540452276788465e-5
allele num: 64916
num of homozygotes: 0

South Asian
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East Asian
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African
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European (Finnish)
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Latino
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Other
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VQSLOD
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BaseQRankSum
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ReadPosRankSum
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MQ
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ClippingRankSum
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FS
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MQRankSum
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DP
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InbreedingCoeff
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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allele num: 6560
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African
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Other
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East Asian
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South Asian
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Latino
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European (Non-Finnish)
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ClippingRankSum
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MQRankSum
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QD
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InbreedingCoeff
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DP
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VQSLOD
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MQ
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FS
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ReadPosRankSum
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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num of homozygotes: 0

Other
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num of homozygotes: 0

South Asian
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East Asian
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allele frequency: 1.161710037174721e-4
allele num: 8608
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European (Finnish)
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allele frequency: 0.0e0
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European (Non-Finnish)
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InbreedingCoeff
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MQ
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VQSLOD
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ClippingRankSum
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ReadPosRankSum
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FS
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QD
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MQRankSum
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DP
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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Latino
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European (Non-Finnish)
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African
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Other
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European (Finnish)
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South Asian
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MQ
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InbreedingCoeff
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VQSLOD
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ReadPosRankSum
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BaseQRankSum
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FS
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MQRankSum
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QD
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ClippingRankSum
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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African
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Latino
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East Asian
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European (Finnish)
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Other
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South Asian
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DP
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BaseQRankSum
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MQ
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VQSLOD
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ReadPosRankSum
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MQRankSum
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FS
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ClippingRankSum
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InbreedingCoeff
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QD
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11488
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14442
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8634
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65888
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 888
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.691800736576855e-5
allele num: 10318
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6594
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -2.314e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.203e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.68e-1

MQ
type: SiteQuality
SIO_000300: 5.956e1

QD
type: SiteQuality
SIO_000300: 1.569e1

MQRankSum
type: SiteQuality
SIO_000300: -5.26e-1

DP
type: SiteQuality
SIO_000300: 1.821702e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.22e0

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: splice_region_variant
consequence: intron_variant
ensembl gene: ENSG00000147526
ensembl transcript: ENST00000522752
gene symbol: TACC1
hgvsc: ENST00000522752.1:n.173-5C>T
variant of: http://identifiers.org/hgnc/11522

Annotation
canonical: false
consequence: splice_region_variant
consequence: intron_variant
ensembl gene: ENSG00000147526
ensembl protein: ENSP00000276520
ensembl transcript: ENST00000276520
gene symbol: TACC1
hgvsc: ENST00000276520.8:c.223-5C>T
variant of: http://identifiers.org/hgnc/11522

GenotypeDepth
all individuals: 11
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 185
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 956
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 81
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 18353
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 171
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 114
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 654
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 204
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1522
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 317
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 18209
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4554
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 573
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 508
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1053
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 9838
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 347
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 425
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2631
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1097
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 94
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 89
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2298
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3012
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1578
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 263
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2540
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 237
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7010
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 103
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 148
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27365
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11101
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3614
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 4.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10348
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15066
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.511898642315019e-5
allele num: 66142
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11504
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8642
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6598
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 890
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.371e0

MQRankSum
type: SiteQuality
SIO_000300: 3.06e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.7e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.55e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.6e-1

MQ
type: SiteQuality
SIO_000300: 5.916e1

DP
type: SiteQuality
SIO_000300: 1.83324e6

QD
type: SiteQuality
SIO_000300: 1.531e1

FS
type: SiteQuality
SIO_000300: 3.437e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.7e-3

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
consequence: splice_region_variant
ensembl gene: ENSG00000147526
ensembl transcript: ENST00000522752
gene symbol: TACC1
hgvsc: ENST00000522752.1:n.173G>A
variant of: http://identifiers.org/hgnc/11522

Annotation
canonical: false
consequence: missense_variant
consequence: splice_region_variant
ensembl gene: ENSG00000147526
ensembl protein: ENSP00000332794
ensembl transcript: ENST00000330691
gene symbol: TACC1
hgvsc: ENST00000330691.6:c.175G>A
hgvsp: ENSP00000332794.6:p.Asp59Asn
variant of: http://identifiers.org/hgnc/11522

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
consequence: splice_region_variant
ensembl gene: ENSG00000147526
ensembl transcript: ENST00000523239
gene symbol: TACC1
hgvsc: ENST00000523239.1:n.95G>A
variant of: http://identifiers.org/hgnc/11522

GenotypeDepth
all individuals: 1522
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 18559
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 81
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2633
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 204
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 157
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 425
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 18411
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 10
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 419
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 767
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 956
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9896
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 317
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 655
bin: 5.75e1
variant carriers: 1

GenotypeDepth
all individuals: 4554
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 508
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 114
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 347
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 171
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 97
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2585
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3042
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 797
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 173
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 195
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7109
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27740
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1586
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3666
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2306
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11105
bin: 9.75e1
variant carriers: 1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10360
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11518
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.508568670045861e-5
allele num: 66288
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15504
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8648
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 892
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6600
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 6.95e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.98e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.29e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.840725e6

FS
type: SiteQuality
SIO_000300: 5.894e0

QD
type: SiteQuality
SIO_000300: 1.448e1

MQRankSum
type: SiteQuality
SIO_000300: -2.11e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.84e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.39e-2

Annotation
canonical: false
consequence: missense_variant
consequence: splice_region_variant
ensembl gene: ENSG00000147526
ensembl protein: ENSP00000276520
ensembl transcript: ENST00000276520
gene symbol: TACC1
hgvsc: ENST00000276520.8:c.225T>G
hgvsp: ENSP00000276520.8:p.Asp75Glu
variant of: http://identifiers.org/hgnc/11522

Annotation
canonical: false
consequence: missense_variant
consequence: splice_region_variant
ensembl gene: ENSG00000147526
ensembl protein: ENSP00000428687
ensembl transcript: ENST00000519416
gene symbol: TACC1
hgvsc: ENST00000519416.1:c.867T>G
hgvsp: ENSP00000428687.1:p.Asp289Glu
variant of: http://identifiers.org/hgnc/11522

Annotation
canonical: false
consequence: missense_variant
consequence: splice_region_variant
ensembl gene: ENSG00000147526
ensembl protein: ENSP00000327818
ensembl transcript: ENST00000348567
gene symbol: TACC1
hgvsc: ENST00000348567.4:c.141T>G
hgvsp: ENSP00000327818.5:p.Asp47Glu
variant of: http://identifiers.org/hgnc/11522

GenotypeDepth
all individuals: 508
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 426
bin: 6.75e1
variant carriers: 1

GenotypeDepth
all individuals: 650
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 18703
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4559
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 365
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 18439
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 655
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 955
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1522
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 171
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2634
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 204
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 81
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9908
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 139
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 348
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 317
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 114
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 682
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27915
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11107
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 170
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 143
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2596
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3042
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3669
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7131
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 80
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2305
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1588
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.014408874419726e-5
allele num: 66348
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8648
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 896
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10370
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15662
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11522
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6600
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.22e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.06e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.18e0

FS
type: SiteQuality
SIO_000300: 6.31e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.7e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.03e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.08e0

DP
type: SiteQuality
SIO_000300: 1.843519e6

QD
type: SiteQuality
SIO_000300: 1.288e1

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000147526
ensembl protein: ENSP00000393647
ensembl transcript: ENST00000443286
gene symbol: TACC1
hgvsc: ENST00000443286.2:c.1510G>A
hgvsp: ENSP00000393647.2:p.Ala504Thr
variant of: http://identifiers.org/hgnc/11522

GenotypeDepth
all individuals: 114
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 18639
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 957
bin: 5.25e1
variant carriers: 2

GenotypeDepth
all individuals: 508
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 215
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 18898
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2633
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 386
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 4564
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 426
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 655
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 9957
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 172
bin: 8.25e1
variant carriers: 1

GenotypeDepth
all individuals: 349
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 101
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 81
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 204
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1523
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 317
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3060
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 404
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2316
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7207
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 109
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3710
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11115
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 64
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1592
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 28180
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2628
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 7.5e0
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11544
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 898
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6606
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.504619180885318e-5
allele num: 66462
num of homozygotes: 0

African
type: Population
allele count: 3
allele frequency: 2.891844997108155e-4
allele num: 10374
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8648
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16068
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.82e-1

MQRankSum
type: SiteQuality
SIO_000300: -5.92e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.29e0

FS
type: SiteQuality
SIO_000300: 5.483e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.743e0

QD
type: SiteQuality
SIO_000300: 1.063e1

MQ
type: SiteQuality
SIO_000300: 5.974e1

DP
type: SiteQuality
SIO_000300: 1.850831e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.51e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.06e-1

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000147526
ensembl transcript: ENST00000522955
gene symbol: TACC1
hgvsc: ENST00000522955.1:n.1379C>T
variant of: http://identifiers.org/hgnc/11522

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000147526
ensembl protein: ENSP00000276520
ensembl transcript: ENST00000276520
gene symbol: TACC1
hgvsc: ENST00000276520.8:c.233C>T
hgvsp: ENSP00000276520.8:p.Ala78Val
variant of: http://identifiers.org/hgnc/11522

GenotypeDepth
all individuals: 115
bin: 8.75e1
variant carriers: 1

GenotypeDepth
all individuals: 656
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 172
bin: 8.25e1
variant carriers: 1

GenotypeDepth
all individuals: 360
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 81
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4569
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 9984
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 200
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 18704
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2633
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 18840
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 205
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 104
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 955
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 318
bin: 7.25e1
variant carriers: 1

GenotypeDepth
all individuals: 1522
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 508
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 426
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 348
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2317
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7204
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 97
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 378
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3060
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1594
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2625
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 107
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11115
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 28111
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3704
bin: 7.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16094
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8648
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 2.598752598752599e-4
allele num: 11544
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10378
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 902
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6608
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66466
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.02e-1

QD
type: SiteQuality
SIO_000300: 1.042e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.42e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.935e0

MQRankSum
type: SiteQuality
SIO_000300: -7.92e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.86e-1

FS
type: SiteQuality
SIO_000300: 5.22e-1

DP
type: SiteQuality
SIO_000300: 1.852158e6

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000147526
ensembl protein: ENSP00000428466
ensembl transcript: ENST00000521642
gene symbol: TACC1
hgvsc: ENST00000521642.1:c.151G>A
hgvsp: ENSP00000428466.1:p.Val51Met
variant of: http://identifiers.org/hgnc/11522

Annotation
canonical: false
consequence: 5_prime_UTR_variant
ensembl gene: ENSG00000147526
ensembl protein: ENSP00000429418
ensembl transcript: ENST00000520611
gene symbol: TACC1
hgvsc: ENST00000520611.1:c.-222G>A
variant of: http://identifiers.org/hgnc/11522

GenotypeDepth
all individuals: 317
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 171
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 656
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 205
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 182
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 10010
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 18711
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2633
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 303
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 18902
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 83
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 955
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 426
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 81
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 508
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4574
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 114
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1521
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 349
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 8
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2635
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 76
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7251
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11115
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3076
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 329
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3726
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1601
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2329
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28282
bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.503759398496241e-5
allele num: 66500
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10384
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16180
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6610
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11542
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.6e-3

FS
type: SiteQuality
SIO_000300: 6.74e-1

QD
type: SiteQuality
SIO_000300: 1.282e1

MQ
type: SiteQuality
SIO_000300: 5.972e1

DP
type: SiteQuality
SIO_000300: 1.853562e6

BaseQRankSum
type: SiteQuality
SIO_000300: -4.733e0

VQSLOD
type: SiteQuality
SIO_000300: 8.9e-2

MQRankSum
type: SiteQuality
SIO_000300: -1.362e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.8e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.75e-1

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000147526
ensembl protein: ENSP00000428706
ensembl transcript: ENST00000518415
gene symbol: TACC1
hgvsc: ENST00000518415.1:c.1332G>T
hgvsp: ENST00000518415.1:c.1332G>T(p.%3D)
variant of: http://identifiers.org/hgnc/11522

GenotypeDepth
all individuals: 260
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 205
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1521
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4577
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2634
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 159
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 316
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 18764
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 508
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 18908
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 350
bin: 9.75e1
variant carriers: 2

GenotypeDepth
all individuals: 657
bin: 5.75e1
variant carriers: 1

GenotypeDepth
all individuals: 955
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 72
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 427
bin: 6.75e1
variant carriers: 1

GenotypeDepth
all individuals: 171
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 114
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 81
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 10022
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3726
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3083
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2641
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7262
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 282
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2330
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11117
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 41
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28274
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1602
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 79
bin: 2.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10382
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.509650652396128e-5
allele num: 66524
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6610
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.662508662508663e-5
allele num: 11544
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16240
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 3.69e-1

FS
type: SiteQuality
SIO_000300: 5.7e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.339e0

MQRankSum
type: SiteQuality
SIO_000300: -3.81e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.9e-1

QD
type: SiteQuality
SIO_000300: 1.281e1

DP
type: SiteQuality
SIO_000300: 1.855234e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.6e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.07e0

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000147526
ensembl protein: ENSP00000332794
ensembl transcript: ENST00000330691
gene symbol: TACC1
hgvsc: ENST00000330691.6:c.199A>G
hgvsp: ENSP00000332794.6:p.Ile67Val
variant of: http://identifiers.org/hgnc/11522

GenotypeDepth
all individuals: 114
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 316
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 82
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 10094
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 205
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 958
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 106
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 657
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 426
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2636
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1524
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 509
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 40
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 350
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 171
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 82
bin: 9.25e1
variant carriers: 1

GenotypeDepth
all individuals: 18907
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 18937
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4589
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1617
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7304
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 123
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 28430
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11128
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2345
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3767
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3121
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2650
bin: 7.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16432
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66634
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.15606936416185e-4
allele num: 8650
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10394
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6610
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11548
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.860443e6

QD
type: SiteQuality
SIO_000300: 1.627e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.05e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.01e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.38e0

MQ
type: SiteQuality
SIO_000300: 5.945e1

FS
type: SiteQuality
SIO_000300: 1.86e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.18e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.02e-1

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000147526
ensembl protein: ENSP00000327818
ensembl transcript: ENST00000348567
gene symbol: TACC1
hgvsc: ENST00000348567.4:c.166T>C
hgvsp: ENSP00000327818.5:p.Ser56Pro
variant of: http://identifiers.org/hgnc/11522

Annotation
canonical: false
consequence: 5_prime_UTR_variant
ensembl gene: ENSG00000147526
ensembl protein: ENSP00000429418
ensembl transcript: ENST00000520611
gene symbol: TACC1
hgvsc: ENST00000520611.1:c.-207T>C
variant of: http://identifiers.org/hgnc/11522

GenotypeDepth
all individuals: 18919
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 657
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 18962
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 509
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 68
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 427
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1524
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 10104
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4589
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 958
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 316
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 81
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 205
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 2638
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 26
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 171
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 114
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 85
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 351
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 33
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3123
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7314
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2651
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11128
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 28507
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3772
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 101
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1617
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2345
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11550
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500375093773443e-5
allele num: 66650
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10398
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16458
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8652
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.861306e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

MQRankSum
type: SiteQuality
SIO_000300: 9.81e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.67e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.11e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.31e-1

FS
type: SiteQuality
SIO_000300: 1.615e0

QD
type: SiteQuality
SIO_000300: 1.4e1

MQ
type: SiteQuality
SIO_000300: 5.967e1

VQSLOD
type: SiteQuality
SIO_000300: 4.38e-1

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000147526
ensembl protein: ENSP00000428253
ensembl transcript: ENST00000521866
gene symbol: TACC1
hgvsc: ENST00000521866.1:c.853A>G
hgvsp: ENSP00000428253.1:p.Asn285Ser
variant of: http://identifiers.org/hgnc/11522

GenotypeDepth
all individuals: 34
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 657
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 15
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2641
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 18931
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 81
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 316
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 114
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4600
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 172
bin: 8.25e1
variant carriers: 1

GenotypeDepth
all individuals: 1525
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 509
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 35
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 18981
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 350
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 205
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 427
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 10155
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 958
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1628
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11130
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 8
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3781
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7338
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2660
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3150
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28553
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2355
bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11552
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499205421126803e-5
allele num: 66702
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16502
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -7.27e-1

FS
type: SiteQuality
SIO_000300: 1.784e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.14e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.19e0

MQ
type: SiteQuality
SIO_000300: 5.932e1

VQSLOD
type: SiteQuality
SIO_000300: 4.88e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-3

DP
type: SiteQuality
SIO_000300: 1.863569e6

QD
type: SiteQuality
SIO_000300: 1.417e1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.64e-1

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000147526
ensembl transcript: ENST00000523239
gene symbol: TACC1
hgvsc: ENST00000523239.1:n.138G>C
variant of: http://identifiers.org/hgnc/11522

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000147526
ensembl protein: ENSP00000430355
ensembl transcript: ENST00000522904
gene symbol: TACC1
hgvsc: ENST00000522904.1:c.1412G>C
hgvsp: ENSP00000430355.1:p.Arg471Thr
variant of: http://identifiers.org/hgnc/11522

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 509
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 657
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4604
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 15
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 31
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 10166
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2643
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 205
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 351
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 18922
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 316
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 81
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1525
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 31
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 171
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 115
bin: 8.75e1
variant carriers: 1

GenotypeDepth
all individuals: 958
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 427
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 18979
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2355
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2661
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1629
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28544
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7339
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3784
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11132
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 7
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3153
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11554
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.998231043684226e-5
allele num: 66706
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16502
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

QD
type: SiteQuality
SIO_000300: 1.084e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.537e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.08e0

FS
type: SiteQuality
SIO_000300: 5.27e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 1.26e0

DP
type: SiteQuality
SIO_000300: 1.863965e6

VQSLOD
type: SiteQuality
SIO_000300: 3.59e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.83e-1

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000147526
ensembl transcript: ENST00000517336
gene symbol: TACC1
hgvsc: ENST00000517336.1:n.217G>A
variant of: http://identifiers.org/hgnc/11522

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000147526
ensembl protein: ENSP00000473342
ensembl transcript: ENST00000520340
gene symbol: TACC1
hgvsc: ENST00000520340.1:c.1389G>A
hgvsp: ENST00000520340.1:c.1389G>A(p.%3D)
variant of: http://identifiers.org/hgnc/11522

GenotypeDepth
all individuals: 28
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 10167
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 81
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 427
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 15
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 18980
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 511
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 30
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 4599
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 657
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 350
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 205
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 958
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2645
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 18923
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 317
bin: 7.25e1
variant carriers: 1

GenotypeDepth
all individuals: 115
bin: 8.75e1
variant carriers: 1

GenotypeDepth
all individuals: 1527
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 171
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3784
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11133
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28537
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2357
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7342
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1629
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2661
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3154
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 4.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11554
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.49907057624273e-5
allele num: 66708
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16502
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.101321585903084e-3
allele num: 908
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.95e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.25e0

FS
type: SiteQuality
SIO_000300: 3.702e0

MQRankSum
type: SiteQuality
SIO_000300: 1.72e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -9.58e-2

DP
type: SiteQuality
SIO_000300: 1.864095e6

BaseQRankSum
type: SiteQuality
SIO_000300: 4.44e-1

QD
type: SiteQuality
SIO_000300: 1.003e1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.099999999999999e-2

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000147526
ensembl protein: ENSP00000428687
ensembl transcript: ENST00000519416
gene symbol: TACC1
hgvsc: ENST00000519416.1:c.910G>T
hgvsp: ENSP00000428687.1:p.Asp304Tyr
variant of: http://identifiers.org/hgnc/11522

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000147526
ensembl transcript: ENST00000522752
gene symbol: TACC1
hgvsc: ENST00000522752.1:n.218G>T
variant of: http://identifiers.org/hgnc/11522

GenotypeDepth
all individuals: 2646
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 205
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 959
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 427
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 10167
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 28
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 316
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 114
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 15
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 657
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 18926
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1527
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 18980
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 171
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 512
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4596
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 81
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 28
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 351
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 28549
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2663
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1629
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7343
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11134
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2357
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3784
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3155
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 4.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498980693128672e-5
allele num: 66712
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11554
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16504
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.984e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

FS
type: SiteQuality
SIO_000300: 2.918e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.649e0

VQSLOD
type: SiteQuality
SIO_000300: 7.97e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.16e-1

DP
type: SiteQuality
SIO_000300: 1.864147e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.75e-1

MQRankSum
type: SiteQuality
SIO_000300: 9.91e-1

QD
type: SiteQuality
SIO_000300: 1.232e1

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000147526
ensembl protein: ENSP00000430355
ensembl transcript: ENST00000522904
gene symbol: TACC1
hgvsc: ENST00000522904.1:c.1415A>G
hgvsp: ENSP00000430355.1:p.Asp472Gly
variant of: http://identifiers.org/hgnc/11522

Annotation
canonical: false
consequence: 5_prime_UTR_variant
ensembl gene: ENSG00000147526
ensembl protein: ENSP00000429418
ensembl transcript: ENST00000520611
gene symbol: TACC1
hgvsc: ENST00000520611.1:c.-188A>G
variant of: http://identifiers.org/hgnc/11522

GenotypeDepth
all individuals: 512
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 657
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 26
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 14
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 18931
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 205
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 427
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 27
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 172
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 18978
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 82
bin: 9.25e1
variant carriers: 1

GenotypeDepth
all individuals: 10169
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2647
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 114
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 316
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 350
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4595
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1525
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 959
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1629
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11135
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 14
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3154
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7345
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2357
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2661
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28552
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3783
bin: 7.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66714
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16504
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.655011251514626e-5
allele num: 11554
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.86419e6

VQSLOD
type: SiteQuality
SIO_000300: 9.63e-1

QD
type: SiteQuality
SIO_000300: 1.386e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.69e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -7.43e-1

FS
type: SiteQuality
SIO_000300: 2.754e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.82e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.42e-1

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000147526
ensembl transcript: ENST00000522752
gene symbol: TACC1
hgvsc: ENST00000522752.1:n.223C>G
variant of: http://identifiers.org/hgnc/11522

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000147526
ensembl protein: ENSP00000428466
ensembl transcript: ENST00000521642
gene symbol: TACC1
hgvsc: ENST00000521642.1:c.189C>G
hgvsp: ENST00000521642.1:c.189C>G(p.%3D)
variant of: http://identifiers.org/hgnc/11522

GenotypeDepth
all individuals: 81
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 657
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1527
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 962
bin: 5.25e1
variant carriers: 1

GenotypeDepth
all individuals: 173
bin: 8.25e1
variant carriers: 1

GenotypeDepth
all individuals: 2651
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 4599
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 16
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 316
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 512
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 427
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 26
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 10170
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 350
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 114
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 23
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 205
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 18974
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 18923
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1628
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7345
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11137
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 2
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3780
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3156
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2660
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2356
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28544
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 5.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11558
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.21153380179307e-4
allele num: 16508
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66714
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -2.9e-2

MQRankSum
type: SiteQuality
SIO_000300: 5.07e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 9.76e-1

QD
type: SiteQuality
SIO_000300: 1.415e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.139e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.83e-1

FS
type: SiteQuality
SIO_000300: 2.199e0

DP
type: SiteQuality
SIO_000300: 1.864507e6

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000147526
ensembl protein: ENSP00000428253
ensembl transcript: ENST00000521866
gene symbol: TACC1
hgvsc: ENST00000521866.1:c.868C>G
hgvsp: ENSP00000428253.1:p.Ala290Gly
variant of: http://identifiers.org/hgnc/11522

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000147526
ensembl transcript: ENST00000522752
gene symbol: TACC1
hgvsc: ENST00000522752.1:n.228C>G
variant of: http://identifiers.org/hgnc/11522

GenotypeDepth
all individuals: 351
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 316
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 16
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 961
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 18
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 24
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 10171
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 81
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 18985
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 172
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2649
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 114
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 18918
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 658
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 427
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 512
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4601
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1527
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 204
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11139
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 14
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3781
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3156
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2663
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28546
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1631
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7351
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2358
bin: 9.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498756032493031e-5
allele num: 66722
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11558
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 6.906e0

MQ
type: SiteQuality
SIO_000300: 5.976e1

VQSLOD
type: SiteQuality
SIO_000300: 8.2e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.58e0

MQRankSum
type: SiteQuality
SIO_000300: 1.98e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -1.362e0

DP
type: SiteQuality
SIO_000300: 1.864728e6

BaseQRankSum
type: SiteQuality
SIO_000300: -4.182e0

QD
type: SiteQuality
SIO_000300: 1.642e1

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000147526
ensembl transcript: ENST00000523239
gene symbol: TACC1
hgvsc: ENST00000523239.1:n.170G>A
variant of: http://identifiers.org/hgnc/11522

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000147526
ensembl protein: ENSP00000327818
ensembl transcript: ENST00000348567
gene symbol: TACC1
hgvsc: ENST00000348567.4:c.214G>A
hgvsp: ENSP00000327818.5:p.Ala72Thr
variant of: http://identifiers.org/hgnc/11522

GenotypeDepth
all individuals: 9
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 512
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 204
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 114
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 10174
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 19002
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 18
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2651
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 172
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 18908
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 960
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1528
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 81
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 15
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 351
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 658
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4605
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 316
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 427
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3784
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1632
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28548
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7351
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2661
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3161
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11140
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2357
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 4.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11558
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498531439189594e-5
allele num: 66732
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

QD
type: SiteQuality
SIO_000300: 1.337e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.39e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.16e-1

FS
type: SiteQuality
SIO_000300: 2.705e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.21e0

MQRankSum
type: SiteQuality
SIO_000300: 1.01e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.428e0

DP
type: SiteQuality
SIO_000300: 1.865125e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000147526
ensembl transcript: ENST00000522752
gene symbol: TACC1
hgvsc: ENST00000522752.1:n.252C>T
variant of: http://identifiers.org/hgnc/11522

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000147526
ensembl transcript: ENST00000522955
gene symbol: TACC1
hgvsc: ENST00000522955.1:n.1448C>T
variant of: http://identifiers.org/hgnc/11522

GenotypeDepth
all individuals: 1528
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 513
bin: 6.25e1
variant carriers: 2

GenotypeDepth
all individuals: 19
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 430
bin: 6.75e1
variant carriers: 3

GenotypeDepth
all individuals: 10174
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 173
bin: 8.25e1
variant carriers: 2

GenotypeDepth
all individuals: 316
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 18
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4604
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 206
bin: 7.75e1
variant carriers: 2

GenotypeDepth
all individuals: 18896
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 82
bin: 9.25e1
variant carriers: 1

GenotypeDepth
all individuals: 114
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 660
bin: 5.75e1
variant carriers: 2

GenotypeDepth
all individuals: 18998
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 961
bin: 5.25e1
variant carriers: 1

GenotypeDepth
all individuals: 357
bin: 9.75e1
variant carriers: 6

GenotypeDepth
all individuals: 2647
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 11155
bin: 9.75e1
variant carriers: 19

GenotypeQuality
all individuals: 2
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 7346
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3160
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3784
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1631
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28544
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2659
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2356
bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.650519031141868e-5
allele num: 11560
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.101321585903084e-3
allele num: 908
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

South Asian
type: Population
allele count: 7
allele frequency: 4.239341085271318e-4
allele num: 16512
num of homozygotes: 1

European (Non-Finnish)
type: Population
allele count: 11
allele frequency: 1.648483395276346e-4
allele num: 66728
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.9e-1

QD
type: SiteQuality
SIO_000300: 1.504e1

MQ
type: SiteQuality
SIO_000300: 5.961e1

FS
type: SiteQuality
SIO_000300: 1.748e0

VQSLOD
type: SiteQuality
SIO_000300: 2.64e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.26e-1

DP
type: SiteQuality
SIO_000300: 1.866191e6

BaseQRankSum
type: SiteQuality
SIO_000300: -3.437e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.99e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.59e-2

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000147526
ensembl protein: ENSP00000428466
ensembl transcript: ENST00000521642
gene symbol: TACC1
hgvsc: ENST00000521642.1:c.221C>T
hgvsp: ENSP00000428466.1:p.Thr74Met
variant of: http://identifiers.org/hgnc/11522

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000147526
ensembl transcript: ENST00000523239
gene symbol: TACC1
hgvsc: ENST00000523239.1:n.177C>T
variant of: http://identifiers.org/hgnc/11522

GenotypeDepth
all individuals: 18891
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 19
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 204
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 658
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2650
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4604
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 19
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 514
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 173
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 9
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 354
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 963
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 115
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1531
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 431
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 81
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 316
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 10176
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 18997
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 7348
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2356
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3784
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3160
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2659
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28540
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11155
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1630
bin: 8.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11558
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498576352465158e-5
allele num: 66730
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 3.79e-1

FS
type: SiteQuality
SIO_000300: 7.559e0

QD
type: SiteQuality
SIO_000300: 1.335e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.37e0

MQ
type: SiteQuality
SIO_000300: 5.958e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 2.28e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.03e-1

DP
type: SiteQuality
SIO_000300: 1.866043e6

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000147526
ensembl transcript: ENST00000522752
gene symbol: TACC1
hgvsc: ENST00000522752.1:n.256G>A
variant of: http://identifiers.org/hgnc/11522

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000147526
ensembl transcript: ENST00000517336
gene symbol: TACC1
hgvsc: ENST00000517336.1:n.256G>A
variant of: http://identifiers.org/hgnc/11522

GenotypeDepth
all individuals: 18
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 20
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 81
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 10178
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 204
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 515
bin: 6.25e1
variant carriers: 1

GenotypeDepth
all individuals: 963
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2649
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 18890
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4604
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 316
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 18995
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 658
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 115
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 355
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 431
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 173
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1531
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1631
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 28536
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3784
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11157
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 4
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2658
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2356
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7349
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3159
bin: 8.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.997332374186974e-5
allele num: 66726
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11556
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.27e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.71e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.81e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 1.42e0

DP
type: SiteQuality
SIO_000300: 1.866134e6

BaseQRankSum
type: SiteQuality
SIO_000300: -4.16e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.28e-1

QD
type: SiteQuality
SIO_000300: 1.423e1

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000147526
ensembl protein: ENSP00000428466
ensembl transcript: ENST00000521642
gene symbol: TACC1
hgvsc: ENST00000521642.1:c.250G>A
hgvsp: ENSP00000428466.1:p.Glu84Lys
variant of: http://identifiers.org/hgnc/11522

GenotypeDepth
all individuals: 4608
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 356
bin: 9.75e1
variant carriers: 2

GenotypeDepth
all individuals: 657
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 204
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 514
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 19010
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 10
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 317
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 432
bin: 6.75e1
variant carriers: 1

GenotypeDepth
all individuals: 116
bin: 8.75e1
variant carriers: 1

GenotypeDepth
all individuals: 10183
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2651
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 26
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 20
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1533
bin: 4.75e1
variant carriers: 2

GenotypeDepth
all individuals: 18850
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 964
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 173
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 81
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3783
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3166
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2658
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28521
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2356
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7344
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1630
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11160
bin: 9.75e1
variant carriers: 6

GenotypeQuality
all individuals: 20
bin: 2.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11560
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 8.991188635137565e-5
allele num: 66732
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6610
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.284e1

DP
type: SiteQuality
SIO_000300: 1.866566e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.9e-2

MQRankSum
type: SiteQuality
SIO_000300: 7.31e-1

MQ
type: SiteQuality
SIO_000300: 5.981e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.54e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.39e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.83e-1

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000147526
ensembl transcript: ENST00000522752
gene symbol: TACC1
hgvsc: ENST00000522752.1:n.289G>A
variant of: http://identifiers.org/hgnc/11522

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000147526
ensembl protein: ENSP00000430355
ensembl transcript: ENST00000522904
gene symbol: TACC1
hgvsc: ENST00000522904.1:c.1485G>A
hgvsp: ENST00000522904.1:c.1485G>A(p.%3D)
variant of: http://identifiers.org/hgnc/11522

GenotypeDepth
all individuals: 10
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 4608
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 19
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 431
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 963
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 658
bin: 5.75e1
variant carriers: 1

GenotypeDepth
all individuals: 18854
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 317
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 10186
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 206
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 514
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 19010
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2650
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 25
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 115
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1531
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 81
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 354
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 173
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3167
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2658
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28529
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3783
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7349
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11159
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2356
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1630
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 4.25e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6610
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11560
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66732
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.866379e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.218e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.25e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

FS
type: SiteQuality
SIO_000300: 3.658e0

MQ
type: SiteQuality
SIO_000300: 5.961e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.255e0

QD
type: SiteQuality
SIO_000300: 1.639e1

VQSLOD
type: SiteQuality
SIO_000300: -1.42e0

MQRankSum
type: SiteQuality
SIO_000300: -1.681e0

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000147526
ensembl transcript: ENST00000517336
gene symbol: TACC1
hgvsc: ENST00000517336.1:n.292A>T
variant of: http://identifiers.org/hgnc/11522

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
consequence: splice_region_variant
ensembl gene: ENSG00000147526
ensembl transcript: ENST00000522752
gene symbol: TACC1
hgvsc: ENST00000522752.1:n.292A>T
variant of: http://identifiers.org/hgnc/11522

GenotypeDepth
all individuals: 514
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 19004
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2650
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 29
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 10187
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 10
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 317
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 431
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4608
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 354
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 19
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 174
bin: 8.25e1
variant carriers: 1

GenotypeDepth
all individuals: 18854
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 206
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 964
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1531
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 115
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 81
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 657
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28523
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1631
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2356
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11159
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 11
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2659
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3784
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3166
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7348
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 4.25e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 9.609840476648087e-5
allele num: 10406
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11556
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66732
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 1.01e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.41e0

DP
type: SiteQuality
SIO_000300: 1.866399e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.409e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.737e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.362e1

VQSLOD
type: SiteQuality
SIO_000300: -2.444e-1

FS
type: SiteQuality
SIO_000300: 4.096e0

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000147526
ensembl transcript: ENST00000523239
gene symbol: TACC1
hgvsc: ENST00000523239.1:n.215G>C
variant of: http://identifiers.org/hgnc/11522

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000147526
ensembl transcript: ENST00000522955
gene symbol: TACC1
hgvsc: ENST00000522955.1:n.1489G>C
variant of: http://identifiers.org/hgnc/11522

GenotypeDepth
all individuals: 355
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 316
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 17
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 431
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 206
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1531
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 964
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 10185
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 18855
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 115
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 29
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 173
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4610
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 81
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 11
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 657
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 19005
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2650
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 514
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2658
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2356
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3166
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1631
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28528
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 7344
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3785
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11158
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 11
bin: 2.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11558
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498531439189594e-5
allele num: 66732
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

QD
type: SiteQuality
SIO_000300: 1.036e1

MQRankSum
type: SiteQuality
SIO_000300: 1.63e0

DP
type: SiteQuality
SIO_000300: 1.866407e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.78e-1

MQ
type: SiteQuality
SIO_000300: 5.934e1

VQSLOD
type: SiteQuality
SIO_000300: -3.406e0

BaseQRankSum
type: SiteQuality
SIO_000300: -6.321e0

FS
type: SiteQuality
SIO_000300: 1.0913e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.987e0

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000147526
ensembl transcript: ENST00000523239
gene symbol: TACC1
hgvsc: ENST00000523239.1:n.218G>A
variant of: http://identifiers.org/hgnc/11522

GenotypeDepth
all individuals: 174
bin: 8.25e1
variant carriers: 1

GenotypeDepth
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 18
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 19007
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 116
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 18850
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4609
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 31
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 514
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2651
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 11
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 316
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 657
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1531
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 964
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 10184
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 206
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 431
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 81
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 354
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1631
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7343
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28520
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3785
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2660
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3164
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2358
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11159
bin: 9.75e1
variant carriers: 1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.211240310077519e-4
allele num: 16512
num of homozygotes: 1

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11554
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66730
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 3.49e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.075e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 2.912e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.866424e6

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000147526
ensembl transcript: ENST00000522955
gene symbol: TACC1
hgvsc: ENST00000522955.1:n.1497A>G
variant of: http://identifiers.org/hgnc/11522

GenotypeDepth
all individuals: 316
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 514
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 32
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 431
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 18838
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 81
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 657
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 964
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 10183
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4610
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1535
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 354
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 19
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 11
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 116
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 206
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 174
bin: 8.25e1
variant carriers: 1

GenotypeDepth
all individuals: 2653
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 19011
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28522
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3167
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2357
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7343
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11161
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1632
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3786
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2660
bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498576352465158e-5
allele num: 66730
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8652
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11556
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 4.426e0

MQRankSum
type: SiteQuality
SIO_000300: 1.35e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.56e-1

QD
type: SiteQuality
SIO_000300: 1.217e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.225e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.24e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -1.612e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.866587e6

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 19009
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 12
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 4612
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 316
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 10179
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 18
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 207
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 35
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 18824
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2655
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1539
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 431
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 82
bin: 9.25e1
variant carriers: 1

GenotypeDepth
all individuals: 659
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 117
bin: 8.75e1
variant carriers: 1

GenotypeDepth
all individuals: 355
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 514
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 969
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 173
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11167
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 7
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1631
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2361
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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European (Non-Finnish)
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South Asian
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African
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InbreedingCoeff
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MQRankSum
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DP
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QD
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ReadPosRankSum
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BaseQRankSum
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FS
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VQSLOD
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MQ
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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European (Non-Finnish)
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African
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South Asian
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European (Finnish)
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Latino
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FS
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DP
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MQRankSum
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VQSLOD
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BaseQRankSum
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MQ
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QD
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ClippingRankSum
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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Latino
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East Asian
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Other
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European (Non-Finnish)
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South Asian
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QD
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VQSLOD
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MQRankSum
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FS
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DP
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MQ
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BaseQRankSum
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ReadPosRankSum
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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East Asian
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European (Non-Finnish)
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European (Finnish)
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Latino
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South Asian
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BaseQRankSum
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FS
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InbreedingCoeff
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VQSLOD
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MQRankSum
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ClippingRankSum
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MQ
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DP
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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African
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MQ
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MQRankSum
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FS
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VQSLOD
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QD
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InbreedingCoeff
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ClippingRankSum
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ReadPosRankSum
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 3

South Asian
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allele count: 1
allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

East Asian
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allele count: 1
allele frequency: 1.155535012710885e-4
allele num: 8654
num of homozygotes: 0

African
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allele count: 1
allele frequency: 9.609840476648087e-5
allele num: 10406
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11556
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66726
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

MQ
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SIO_000300: 6.0e1

FS
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QD
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BaseQRankSum
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InbreedingCoeff
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SIO_000300: 4.0e-4

DP
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SIO_000300: 1.868939e6

ClippingRankSum
type: SiteQuality
SIO_000300: 5.9e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.14e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.9e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.58e0

GenotypeDepth
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variant carriers: 1393

GenotypeDepth
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variant carriers: 47

GenotypeDepth
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variant carriers: 1950

GenotypeDepth
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variant carriers: 2882

GenotypeDepth
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variant carriers: 1855

GenotypeDepth
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variant carriers: 10

GenotypeDepth
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variant carriers: 3094

GenotypeDepth
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GenotypeDepth
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variant carriers: 123

GenotypeDepth
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variant carriers: 9424

GenotypeDepth
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variant carriers: 17

GenotypeDepth
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variant carriers: 2730

GenotypeDepth
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variant carriers: 3092

GenotypeDepth
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GenotypeDepth
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variant carriers: 271

GenotypeDepth
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variant carriers: 2306

GenotypeDepth
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variant carriers: 944

GenotypeDepth
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variant carriers: 2756

GenotypeDepth
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variant carriers: 2251

GenotypeDepth
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variant carriers: 530

GenotypeQuality
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variant carriers: 7

GenotypeQuality
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variant carriers: 3

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 13

GenotypeQuality
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variant carriers: 35475

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 12

GenotypeQuality
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variant carriers: 14

GenotypeQuality
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variant carriers: 4

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 19

GenotypeQuality
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variant carriers: 3

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 3

GenotypeQuality
all individuals: 97
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variant carriers: 23

GenotypeQuality
all individuals: 127
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variant carriers: 55

South Asian
type: Population
allele count: 4780
allele frequency: 2.895215021199273e-1
allele num: 16510
num of homozygotes: 746

European (Non-Finnish)
type: Population
allele count: 27194
allele frequency: 4.076816982489806e-1
allele num: 66704
num of homozygotes: 5557

Latino
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allele count: 2881
allele frequency: 2.496533795493934e-1
allele num: 11540
num of homozygotes: 385

African
type: Population
allele count: 3952
allele frequency: 3.798539023452518e-1
allele num: 10404
num of homozygotes: 754

Other
type: Population
allele count: 327
allele frequency: 3.609271523178808e-1
allele num: 906
num of homozygotes: 59

European (Finnish)
type: Population
allele count: 2645
allele frequency: 4.00272397094431e-1
allele num: 6608
num of homozygotes: 553

East Asian
type: Population
allele count: 2249
allele frequency: 2.605421686746988e-1
allele num: 8632
num of homozygotes: 304

QD
type: SiteQuality
SIO_000300: 1.742e1

BaseQRankSum
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SIO_000300: -2.035e0

DP
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SIO_000300: 3.861507e6

ClippingRankSum
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SIO_000300: -2.27e-1

MQRankSum
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SIO_000300: 2.5e-2

MQ
type: SiteQuality
SIO_000300: 5.943e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.65e-2

VQSLOD
type: SiteQuality
SIO_000300: 2.69e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.23e-1

FS
type: SiteQuality
SIO_000300: 5.49e-1

GenotypeDepth
all individuals: 11916
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variant carriers: 3

GenotypeDepth
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variant carriers: 0

GenotypeDepth
all individuals: 11
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
all individuals: 518
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variant carriers: 1

GenotypeDepth
all individuals: 31137
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variant carriers: 2

GenotypeDepth
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variant carriers: 2

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 1

GenotypeDepth
all individuals: 50
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variant carriers: 4

GenotypeDepth
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variant carriers: 1

GenotypeDepth
all individuals: 1683
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variant carriers: 2

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
all individuals: 258
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variant carriers: 1

GenotypeDepth
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variant carriers: 2

GenotypeDepth
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variant carriers: 2

GenotypeDepth
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variant carriers: 0

GenotypeQuality
all individuals: 12
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variant carriers: 0

GenotypeQuality
all individuals: 3
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variant carriers: 0

GenotypeQuality
all individuals: 207
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variant carriers: 0

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
all individuals: 9
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 21

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 528
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variant carriers: 0

GenotypeQuality
all individuals: 214
bin: 8.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 15
allele frequency: 2.248808131690204e-4
allele num: 66702
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10402
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6600
num of homozygotes: 0

Latino
type: Population
allele count: 6
allele frequency: 5.201109570041609e-4
allele num: 11536
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.359e1

BaseQRankSum
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SIO_000300: -2.614e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.671155e6

MQ
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SIO_000300: 5.924e1

VQSLOD
type: SiteQuality
SIO_000300: 2.34e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.9e-2

MQRankSum
type: SiteQuality
SIO_000300: 3.12e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.06e-1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 1

GenotypeDepth
all individuals: 33
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
all individuals: 11
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variant carriers: 0

GenotypeDepth
all individuals: 27
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
all individuals: 60
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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variant carriers: 1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 1703
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variant carriers: 0

GenotypeQuality
all individuals: 16
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 7
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GenotypeQuality
all individuals: 1002
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variant carriers: 2

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6600
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.999040307101727e-5
allele num: 66688
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8652
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

MQRankSum
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SIO_000300: 1.48e0

FS
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SIO_000300: 3.646e0

ClippingRankSum
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BaseQRankSum
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DP
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SIO_000300: 1.669532e6

InbreedingCoeff
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SIO_000300: -1.0e-4

VQSLOD
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QD
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SIO_000300: 1.35e1

MQ
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SIO_000300: 5.922e1

ReadPosRankSum
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SIO_000300: -1.6e-1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
all individuals: 3
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1000
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GenotypeQuality
all individuals: 8
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variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6600
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499520153550864e-5
allele num: 66688
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11532
num of homozygotes: 0

Other
type: Population
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South Asian
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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num of homozygotes: 0

MQRankSum
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SIO_000300: -5.1e-2

DP
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BaseQRankSum
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FS
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QD
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VQSLOD
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MQ
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ReadPosRankSum
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SIO_000300: 1.32e0

InbreedingCoeff
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SIO_000300: -1.0e-4

ClippingRankSum
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
all individuals: 1528
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 11
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variant carriers: 0

GenotypeQuality
all individuals: 6
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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Latino
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European (Non-Finnish)
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African
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South Asian
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European (Finnish)
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VQSLOD
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ClippingRankSum
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QD
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FS
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ReadPosRankSum
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InbreedingCoeff
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DP
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MQRankSum
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MQ
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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South Asian
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East Asian
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European (Finnish)
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Latino
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European (Non-Finnish)
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Other
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DP
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VQSLOD
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QD
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ReadPosRankSum
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ClippingRankSum
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MQ
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FS
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MQRankSum
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InbreedingCoeff
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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African
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Other
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Latino
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European (Non-Finnish)
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allele frequency: 4.498965237995261e-5
allele num: 66682
num of homozygotes: 0

South Asian
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MQRankSum
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SIO_000300: 8.71e-1

BaseQRankSum
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ClippingRankSum
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FS
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ReadPosRankSum
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MQ
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InbreedingCoeff
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VQSLOD
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QD
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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South Asian
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East Asian
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Latino
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African
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European (Non-Finnish)
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European (Finnish)
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FS
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MQRankSum
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ClippingRankSum
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BaseQRankSum
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VQSLOD
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ReadPosRankSum
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MQ
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InbreedingCoeff
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QD
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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South Asian
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European (Non-Finnish)
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Other
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European (Finnish)
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African
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Latino
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MQ
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InbreedingCoeff
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QD
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FS
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MQRankSum
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VQSLOD
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ReadPosRankSum
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ClippingRankSum
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BaseQRankSum
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DP
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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East Asian
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South Asian
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MQRankSum
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DP
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FS
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QD
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African
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South Asian
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European (Finnish)
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East Asian
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FS
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DP
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MQRankSum
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VQSLOD
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ClippingRankSum
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InbreedingCoeff
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ReadPosRankSum
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QD
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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Latino
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European (Non-Finnish)
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East Asian
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African
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ClippingRankSum
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FS
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QD
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MQ
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VQSLOD
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ReadPosRankSum
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MQRankSum
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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Latino
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South Asian
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East Asian
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MQ
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DP
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East Asian
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GenotypeQuality
all individuals: 5287
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 216
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4265
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2499
bin: 3.75e1
variant carriers: 0

African
type: Population
allele count: 2
allele frequency: 3.492839678658749e-4
allele num: 5726
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 31660
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4634
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4178
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 410
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7036
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3574
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.491e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.71e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.06e-2

DP
type: SiteQuality
SIO_000300: 6.37347e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.58e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.33e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.23e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.231e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
all individuals: 125
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7762
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1062
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 263
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 12
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 197
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 499
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 24068
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 19648
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 31
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4971
bin: 1.75e1
variant carriers: 2

GenotypeDepth
all individuals: 384
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 54
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 960
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 17
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 66
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 38
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 9
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 25
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 728
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9383
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 135
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22464
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 868
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 836
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5003
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 156
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1201
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 217
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 709
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5311
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2529
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4850
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 191
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4918
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 139
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 180
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 367
bin: 6.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4050
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5654
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.227472243738704e-5
allele num: 30984
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4570
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.456876456876457e-4
allele num: 6864
num of homozygotes: 0