7-140051025-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 140051025
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 140051025
    reference: chr 7
allele count: 2
allele frequency: 1.748435150540266e-5
allele num: 114388
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl transcript: ENST00000460560
  gene symbol: SLC37A3
  hgvsc: ENST00000460560.1:n.1417+48G>A
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000419285
  ensembl transcript: ENST00000485734
  gene symbol: SLC37A3
  hgvsc: ENST00000485734.1:c.218+48G>A
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000417447
  ensembl transcript: ENST00000492027
  gene symbol: SLC37A3
  hgvsc: ENST00000492027.1:c.85+48G>A
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000412208
  ensembl transcript: ENST00000429996
  gene symbol: SLC37A3
  hgvsc: ENST00000429996.2:c.*783+48G>A
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000417365
  ensembl transcript: ENST00000477571
  gene symbol: SLC37A3
  hgvsc: ENST00000477571.1:c.*122+48G>A
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000321498
  ensembl transcript: ENST00000326232
  gene symbol: SLC37A3
  hgvsc: ENST00000326232.9:c.882+48G>A
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000343358
  ensembl transcript: ENST00000340308
  gene symbol: SLC37A3
  hgvsc: ENST00000340308.3:c.882+48G>A
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl transcript: ENST00000487319
  gene symbol: SLC37A3
  hgvsc: ENST00000487319.1:n.133+48G>A
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000397481
  ensembl transcript: ENST00000447932
  gene symbol: SLC37A3
  hgvsc: ENST00000447932.2:c.882+48G>A
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000420771
  ensembl transcript: ENST00000485861
  gene symbol: SLC37A3
  hgvsc: ENST00000485861.1:c.393-2458G>A
  variant of: http://identifiers.org/hgnc/20651
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1455
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2251
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5806
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11369
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1050
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7386
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 618
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2789
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7966
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13095
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4003
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 731
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 332
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2902
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3408
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
population: Latino
population: African
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ

7-140051026-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 140051026
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 140051026
    reference: chr 7
allele count: 1
allele frequency: 8.727526618956187e-6
allele num: 114580
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000343358
  ensembl transcript: ENST00000340308
  gene symbol: SLC37A3
  hgvsc: ENST00000340308.3:c.882+47C>G
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000321498
  ensembl transcript: ENST00000326232
  gene symbol: SLC37A3
  hgvsc: ENST00000326232.9:c.882+47C>G
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000417365
  ensembl transcript: ENST00000477571
  gene symbol: SLC37A3
  hgvsc: ENST00000477571.1:c.*122+47C>G
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000419285
  ensembl transcript: ENST00000485734
  gene symbol: SLC37A3
  hgvsc: ENST00000485734.1:c.218+47C>G
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000397481
  ensembl transcript: ENST00000447932
  gene symbol: SLC37A3
  hgvsc: ENST00000447932.2:c.882+47C>G
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000412208
  ensembl transcript: ENST00000429996
  gene symbol: SLC37A3
  hgvsc: ENST00000429996.2:c.*783+47C>G
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl transcript: ENST00000460560
  gene symbol: SLC37A3
  hgvsc: ENST00000460560.1:n.1417+47C>G
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000417447
  ensembl transcript: ENST00000492027
  gene symbol: SLC37A3
  hgvsc: ENST00000492027.1:c.85+47C>G
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl transcript: ENST00000487319
  gene symbol: SLC37A3
  hgvsc: ENST00000487319.1:n.133+47C>G
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000420771
  ensembl transcript: ENST00000485861
  gene symbol: SLC37A3
  hgvsc: ENST00000485861.1:c.393-2459C>G
  variant of: http://identifiers.org/hgnc/20651
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 731
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6874
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 618
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11495
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2251
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2776
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1050
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13951
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7533
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5762
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4030
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1457
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1488
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3003
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 374
  bin: 5.75e1
  variant carriers: 0
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: G
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: QD

7-140051026-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 140051026
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 140051026
    reference: chr 7
allele count: 2
allele frequency: 1.745505323791237e-5
allele num: 114580
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000417447
  ensembl transcript: ENST00000492027
  gene symbol: SLC37A3
  hgvsc: ENST00000492027.1:c.85+47C>A
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl transcript: ENST00000487319
  gene symbol: SLC37A3
  hgvsc: ENST00000487319.1:n.133+47C>A
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000419285
  ensembl transcript: ENST00000485734
  gene symbol: SLC37A3
  hgvsc: ENST00000485734.1:c.218+47C>A
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000321498
  ensembl transcript: ENST00000326232
  gene symbol: SLC37A3
  hgvsc: ENST00000326232.9:c.882+47C>A
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl transcript: ENST00000460560
  gene symbol: SLC37A3
  hgvsc: ENST00000460560.1:n.1417+47C>A
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000343358
  ensembl transcript: ENST00000340308
  gene symbol: SLC37A3
  hgvsc: ENST00000340308.3:c.882+47C>A
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000397481
  ensembl transcript: ENST00000447932
  gene symbol: SLC37A3
  hgvsc: ENST00000447932.2:c.882+47C>A
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000417365
  ensembl transcript: ENST00000477571
  gene symbol: SLC37A3
  hgvsc: ENST00000477571.1:c.*122+47C>A
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000420771
  ensembl transcript: ENST00000485861
  gene symbol: SLC37A3
  hgvsc: ENST00000485861.1:c.393-2459C>A
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000412208
  ensembl transcript: ENST00000429996
  gene symbol: SLC37A3
  hgvsc: ENST00000429996.2:c.*783+47C>A
  variant of: http://identifiers.org/hgnc/20651
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1457
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6874
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2251
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11495
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 731
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2776
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13951
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 618
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5762
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7533
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4030
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1050
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2602
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1733
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 158
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: ReadPosRankSum

7-140051037-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 140051037
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 140051037
    reference: chr 7
allele count: 21
allele frequency: 1.821809664266505e-4
allele num: 115270
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000417365
  ensembl transcript: ENST00000477571
  gene symbol: SLC37A3
  hgvsc: ENST00000477571.1:c.*122+36G>A
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl transcript: ENST00000487319
  gene symbol: SLC37A3
  hgvsc: ENST00000487319.1:n.133+36G>A
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl transcript: ENST00000460560
  gene symbol: SLC37A3
  hgvsc: ENST00000460560.1:n.1417+36G>A
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000420771
  ensembl transcript: ENST00000485861
  gene symbol: SLC37A3
  hgvsc: ENST00000485861.1:c.393-2470G>A
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000412208
  ensembl transcript: ENST00000429996
  gene symbol: SLC37A3
  hgvsc: ENST00000429996.2:c.*783+36G>A
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000321498
  ensembl transcript: ENST00000326232
  gene symbol: SLC37A3
  hgvsc: ENST00000326232.9:c.882+36G>A
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000419285
  ensembl transcript: ENST00000485734
  gene symbol: SLC37A3
  hgvsc: ENST00000485734.1:c.218+36G>A
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000343358
  ensembl transcript: ENST00000340308
  gene symbol: SLC37A3
  hgvsc: ENST00000340308.3:c.882+36G>A
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000417447
  ensembl transcript: ENST00000492027
  gene symbol: SLC37A3
  hgvsc: ENST00000492027.1:c.85+36G>A
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000397481
  ensembl transcript: ENST00000447932
  gene symbol: SLC37A3
  hgvsc: ENST00000447932.2:c.882+36G>A
  variant of: http://identifiers.org/hgnc/20651
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2130
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18572
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4443
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8196
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2696
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12415
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1052
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2264
  bin: 4.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 734
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1460
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 4101
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1979
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 683
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1710
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff

7-140051048-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 140051048
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 140051048
    reference: chr 7
allele count: 1
allele frequency: 8.581481163648846e-6
allele num: 116530
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000397481
  ensembl transcript: ENST00000447932
  gene symbol: SLC37A3
  hgvsc: ENST00000447932.2:c.882+25C>T
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000419285
  ensembl transcript: ENST00000485734
  gene symbol: SLC37A3
  hgvsc: ENST00000485734.1:c.218+25C>T
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl transcript: ENST00000460560
  gene symbol: SLC37A3
  hgvsc: ENST00000460560.1:n.1417+25C>T
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000417365
  ensembl transcript: ENST00000477571
  gene symbol: SLC37A3
  hgvsc: ENST00000477571.1:c.*122+25C>T
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000417447
  ensembl transcript: ENST00000492027
  gene symbol: SLC37A3
  hgvsc: ENST00000492027.1:c.85+25C>T
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000321498
  ensembl transcript: ENST00000326232
  gene symbol: SLC37A3
  hgvsc: ENST00000326232.9:c.882+25C>T
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl transcript: ENST00000487319
  gene symbol: SLC37A3
  hgvsc: ENST00000487319.1:n.133+25C>T
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000412208
  ensembl transcript: ENST00000429996
  gene symbol: SLC37A3
  hgvsc: ENST00000429996.2:c.*783+25C>T
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000343358
  ensembl transcript: ENST00000340308
  gene symbol: SLC37A3
  hgvsc: ENST00000340308.3:c.882+25C>T
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000420771
  ensembl transcript: ENST00000485861
  gene symbol: SLC37A3
  hgvsc: ENST00000485861.1:c.393-2481C>T
  variant of: http://identifiers.org/hgnc/20651
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1056
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4199
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2292
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2280
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 936
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8962
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 621
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20217
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13355
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2645
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1474
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 737
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 807
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1751
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 867
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
population: Latino
reference allele: G
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD

7-140051048-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 140051048
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 140051048
    reference: chr 7
allele count: 1
allele frequency: 8.581481163648846e-6
allele num: 116530
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000419285
  ensembl transcript: ENST00000485734
  gene symbol: SLC37A3
  hgvsc: ENST00000485734.1:c.218+25C>G
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000412208
  ensembl transcript: ENST00000429996
  gene symbol: SLC37A3
  hgvsc: ENST00000429996.2:c.*783+25C>G
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000397481
  ensembl transcript: ENST00000447932
  gene symbol: SLC37A3
  hgvsc: ENST00000447932.2:c.882+25C>G
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000417447
  ensembl transcript: ENST00000492027
  gene symbol: SLC37A3
  hgvsc: ENST00000492027.1:c.85+25C>G
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl transcript: ENST00000460560
  gene symbol: SLC37A3
  hgvsc: ENST00000460560.1:n.1417+25C>G
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000343358
  ensembl transcript: ENST00000340308
  gene symbol: SLC37A3
  hgvsc: ENST00000340308.3:c.882+25C>G
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl transcript: ENST00000487319
  gene symbol: SLC37A3
  hgvsc: ENST00000487319.1:n.133+25C>G
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000417365
  ensembl transcript: ENST00000477571
  gene symbol: SLC37A3
  hgvsc: ENST00000477571.1:c.*122+25C>G
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000420771
  ensembl transcript: ENST00000485861
  gene symbol: SLC37A3
  hgvsc: ENST00000485861.1:c.393-2481C>G
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000321498
  ensembl transcript: ENST00000326232
  gene symbol: SLC37A3
  hgvsc: ENST00000326232.9:c.882+25C>G
  variant of: http://identifiers.org/hgnc/20651
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1474
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2280
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1056
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 936
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4199
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13355
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 621
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2645
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 737
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2292
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8962
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20217
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2309
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 253
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 276
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff

7-140051050-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 140051050
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 140051050
    reference: chr 7
allele count: 2
allele frequency: 1.713561122725248e-5
allele num: 116716
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000343358
  ensembl transcript: ENST00000340308
  gene symbol: SLC37A3
  hgvsc: ENST00000340308.3:c.882+23C>T
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000321498
  ensembl transcript: ENST00000326232
  gene symbol: SLC37A3
  hgvsc: ENST00000326232.9:c.882+23C>T
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000419285
  ensembl transcript: ENST00000485734
  gene symbol: SLC37A3
  hgvsc: ENST00000485734.1:c.218+23C>T
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl transcript: ENST00000460560
  gene symbol: SLC37A3
  hgvsc: ENST00000460560.1:n.1417+23C>T
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000412208
  ensembl transcript: ENST00000429996
  gene symbol: SLC37A3
  hgvsc: ENST00000429996.2:c.*783+23C>T
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000417447
  ensembl transcript: ENST00000492027
  gene symbol: SLC37A3
  hgvsc: ENST00000492027.1:c.85+23C>T
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000397481
  ensembl transcript: ENST00000447932
  gene symbol: SLC37A3
  hgvsc: ENST00000447932.2:c.882+23C>T
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000417365
  ensembl transcript: ENST00000477571
  gene symbol: SLC37A3
  hgvsc: ENST00000477571.1:c.*122+23C>T
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl transcript: ENST00000487319
  gene symbol: SLC37A3
  hgvsc: ENST00000487319.1:n.133+23C>T
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000420771
  ensembl transcript: ENST00000485861
  gene symbol: SLC37A3
  hgvsc: ENST00000485861.1:c.393-2483C>T
  variant of: http://identifiers.org/hgnc/20651
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1475
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20413
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9019
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 621
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13501
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 739
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2413
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2204
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1059
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4227
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2299
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2397
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP

7-140051059-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 140051059
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 140051059
    reference: chr 7
allele count: 2
allele frequency: 1.700304354479452e-5
allele num: 117626
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000420771
  ensembl transcript: ENST00000485861
  gene symbol: SLC37A3
  hgvsc: ENST00000485861.1:c.393-2492A>G
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000343358
  ensembl transcript: ENST00000340308
  gene symbol: SLC37A3
  hgvsc: ENST00000340308.3:c.882+14A>G
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000417447
  ensembl transcript: ENST00000492027
  gene symbol: SLC37A3
  hgvsc: ENST00000492027.1:c.85+14A>G
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000419285
  ensembl transcript: ENST00000485734
  gene symbol: SLC37A3
  hgvsc: ENST00000485734.1:c.218+14A>G
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000417365
  ensembl transcript: ENST00000477571
  gene symbol: SLC37A3
  hgvsc: ENST00000477571.1:c.*122+14A>G
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000321498
  ensembl transcript: ENST00000326232
  gene symbol: SLC37A3
  hgvsc: ENST00000326232.9:c.882+14A>G
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl transcript: ENST00000487319
  gene symbol: SLC37A3
  hgvsc: ENST00000487319.1:n.133+14A>G
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl transcript: ENST00000460560
  gene symbol: SLC37A3
  hgvsc: ENST00000460560.1:n.1417+14A>G
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000397481
  ensembl transcript: ENST00000447932
  gene symbol: SLC37A3
  hgvsc: ENST00000447932.2:c.882+14A>G
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000412208
  ensembl transcript: ENST00000429996
  gene symbol: SLC37A3
  hgvsc: ENST00000429996.2:c.*783+14A>G
  variant of: http://identifiers.org/hgnc/20651
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9339
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 741
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13833
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1607
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 623
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21254
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1056
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1810
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4265
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1489
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2304
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 409
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3709
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 570
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: T
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ

7-140051063-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 140051063
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 140051063
    reference: chr 7
allele count: 51767
allele frequency: 4.327042027483366e-1
allele num: 119636
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000321498
  ensembl transcript: ENST00000326232
  gene symbol: SLC37A3
  hgvsc: ENST00000326232.9:c.882+10G>A
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000397481
  ensembl transcript: ENST00000447932
  gene symbol: SLC37A3
  hgvsc: ENST00000447932.2:c.882+10G>A
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl transcript: ENST00000460560
  gene symbol: SLC37A3
  hgvsc: ENST00000460560.1:n.1417+10G>A
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000419285
  ensembl transcript: ENST00000485734
  gene symbol: SLC37A3
  hgvsc: ENST00000485734.1:c.218+10G>A
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000417447
  ensembl transcript: ENST00000492027
  gene symbol: SLC37A3
  hgvsc: ENST00000492027.1:c.85+10G>A
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000343358
  ensembl transcript: ENST00000340308
  gene symbol: SLC37A3
  hgvsc: ENST00000340308.3:c.882+10G>A
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000412208
  ensembl transcript: ENST00000429996
  gene symbol: SLC37A3
  hgvsc: ENST00000429996.2:c.*783+10G>A
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000417365
  ensembl transcript: ENST00000477571
  gene symbol: SLC37A3
  hgvsc: ENST00000477571.1:c.*122+10G>A
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000420771
  ensembl transcript: ENST00000485861
  gene symbol: SLC37A3
  hgvsc: ENST00000485861.1:c.393-2496G>A
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl transcript: ENST00000487319
  gene symbol: SLC37A3
  hgvsc: ENST00000487319.1:n.133+10G>A
  variant of: http://identifiers.org/hgnc/20651
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6933
  bin: 2.75e1
  variant carriers: 2262
genotype depth: GenotypeDepth
  all individuals: 4545
  bin: 5.25e1
  variant carriers: 4128
genotype depth: GenotypeDepth
  all individuals: 5869
  bin: 4.75e1
  variant carriers: 5256
genotype depth: GenotypeDepth
  all individuals: 952
  bin: 1.25e1
  variant carriers: 530
genotype depth: GenotypeDepth
  all individuals: 773
  bin: 7.75e1
  variant carriers: 707
genotype depth: GenotypeDepth
  all individuals: 647
  bin: 7.5e0
  variant carriers: 78
genotype depth: GenotypeDepth
  all individuals: 7888
  bin: 2.25e1
  variant carriers: 1766
genotype depth: GenotypeDepth
  all individuals: 1447
  bin: 1.75e1
  variant carriers: 1280
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1040
  bin: 7.25e1
  variant carriers: 945
genotype depth: GenotypeDepth
  all individuals: 6825
  bin: 3.25e1
  variant carriers: 3525
genotype depth: GenotypeDepth
  all individuals: 6434
  bin: 4.25e1
  variant carriers: 5468
genotype depth: GenotypeDepth
  all individuals: 6523
  bin: 3.75e1
  variant carriers: 4848
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 8.75e1
  variant carriers: 457
genotype depth: GenotypeDepth
  all individuals: 3182
  bin: 5.75e1
  variant carriers: 2897
genotype depth: GenotypeDepth
  all individuals: 635
  bin: 8.25e1
  variant carriers: 580
genotype depth: GenotypeDepth
  all individuals: 1457
  bin: 6.75e1
  variant carriers: 1331
genotype depth: GenotypeDepth
  all individuals: 2456
  bin: 9.75e1
  variant carriers: 2335
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 9.25e1
  variant carriers: 400
genotype depth: GenotypeDepth
  all individuals: 2163
  bin: 6.25e1
  variant carriers: 1951
genotype quality: GenotypeQuality
  all individuals: 1475
  bin: 7.25e1
  variant carriers: 219
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 2.5e0
  variant carriers: 26
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 1.75e1
  variant carriers: 31
num of homozygotes: 11189
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
population: South Asian
reference allele: C
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: VQSLOD

7-140051064-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 140051064
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 140051064
    reference: chr 7
allele count: 1102
allele frequency: 9.168358348031548e-3
allele num: 120196
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000321498
  ensembl transcript: ENST00000326232
  gene symbol: SLC37A3
  hgvsc: ENST00000326232.9:c.882+9C>T
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000419285
  ensembl transcript: ENST00000485734
  gene symbol: SLC37A3
  hgvsc: ENST00000485734.1:c.218+9C>T
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000412208
  ensembl transcript: ENST00000429996
  gene symbol: SLC37A3
  hgvsc: ENST00000429996.2:c.*783+9C>T
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000417447
  ensembl transcript: ENST00000492027
  gene symbol: SLC37A3
  hgvsc: ENST00000492027.1:c.85+9C>T
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl transcript: ENST00000487319
  gene symbol: SLC37A3
  hgvsc: ENST00000487319.1:n.133+9C>T
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000397481
  ensembl transcript: ENST00000447932
  gene symbol: SLC37A3
  hgvsc: ENST00000447932.2:c.882+9C>T
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000420771
  ensembl transcript: ENST00000485861
  gene symbol: SLC37A3
  hgvsc: ENST00000485861.1:c.393-2497C>T
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000417365
  ensembl transcript: ENST00000477571
  gene symbol: SLC37A3
  hgvsc: ENST00000477571.1:c.*122+9C>T
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000343358
  ensembl transcript: ENST00000340308
  gene symbol: SLC37A3
  hgvsc: ENST00000340308.3:c.882+9C>T
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl transcript: ENST00000460560
  gene symbol: SLC37A3
  hgvsc: ENST00000460560.1:n.1417+9C>T
  variant of: http://identifiers.org/hgnc/20651
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1103
  bin: 7.25e1
  variant carriers: 28
genotype depth: GenotypeDepth
  all individuals: 558
  bin: 7.5e0
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 9.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1427
  bin: 1.75e1
  variant carriers: 95
genotype depth: GenotypeDepth
  all individuals: 7767
  bin: 2.25e1
  variant carriers: 110
genotype depth: GenotypeDepth
  all individuals: 5830
  bin: 4.75e1
  variant carriers: 95
genotype depth: GenotypeDepth
  all individuals: 6599
  bin: 3.25e1
  variant carriers: 89
genotype depth: GenotypeDepth
  all individuals: 852
  bin: 1.25e1
  variant carriers: 35
genotype depth: GenotypeDepth
  all individuals: 657
  bin: 8.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 2235
  bin: 6.25e1
  variant carriers: 42
genotype depth: GenotypeDepth
  all individuals: 776
  bin: 7.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 6945
  bin: 2.75e1
  variant carriers: 110
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 8.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 2596
  bin: 9.75e1
  variant carriers: 42
genotype depth: GenotypeDepth
  all individuals: 6428
  bin: 3.75e1
  variant carriers: 97
genotype depth: GenotypeDepth
  all individuals: 3372
  bin: 5.75e1
  variant carriers: 62
genotype depth: GenotypeDepth
  all individuals: 6315
  bin: 4.25e1
  variant carriers: 103
genotype depth: GenotypeDepth
  all individuals: 1586
  bin: 6.75e1
  variant carriers: 34
genotype depth: GenotypeDepth
  all individuals: 4686
  bin: 5.25e1
  variant carriers: 92
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 343
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 539
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 30
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
reference allele: G
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD

7-140051064-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 140051064
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 140051064
    reference: chr 7
allele count: 2
allele frequency: 1.663948883490299e-5
allele num: 120196
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000397481
  ensembl transcript: ENST00000447932
  gene symbol: SLC37A3
  hgvsc: ENST00000447932.2:c.882+9C>G
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000321498
  ensembl transcript: ENST00000326232
  gene symbol: SLC37A3
  hgvsc: ENST00000326232.9:c.882+9C>G
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000412208
  ensembl transcript: ENST00000429996
  gene symbol: SLC37A3
  hgvsc: ENST00000429996.2:c.*783+9C>G
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl transcript: ENST00000460560
  gene symbol: SLC37A3
  hgvsc: ENST00000460560.1:n.1417+9C>G
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000343358
  ensembl transcript: ENST00000340308
  gene symbol: SLC37A3
  hgvsc: ENST00000340308.3:c.882+9C>G
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000419285
  ensembl transcript: ENST00000485734
  gene symbol: SLC37A3
  hgvsc: ENST00000485734.1:c.218+9C>G
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000417447
  ensembl transcript: ENST00000492027
  gene symbol: SLC37A3
  hgvsc: ENST00000492027.1:c.85+9C>G
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000417365
  ensembl transcript: ENST00000477571
  gene symbol: SLC37A3
  hgvsc: ENST00000477571.1:c.*122+9C>G
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl transcript: ENST00000487319
  gene symbol: SLC37A3
  hgvsc: ENST00000487319.1:n.133+9C>G
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000420771
  ensembl transcript: ENST00000485861
  gene symbol: SLC37A3
  hgvsc: ENST00000485861.1:c.393-2497C>G
  variant of: http://identifiers.org/hgnc/20651
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6428
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1103
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4686
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2596
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 776
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 558
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7767
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1427
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6315
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5830
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1586
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6945
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 852
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2235
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 657
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3372
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6599
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 435
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 364
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: South Asian
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP

7-140051073-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 140051073
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 140051073
    reference: chr 7
allele count: 1
allele frequency: 8.29228651508367e-6
allele num: 120594
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000417447
  ensembl transcript: ENST00000492027
  gene symbol: SLC37A3
  hgvsc: ENST00000492027.1:c.85G>A
  hgvsp: ENST00000492027.1:c.85G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000419285
  ensembl transcript: ENST00000485734
  gene symbol: SLC37A3
  hgvsc: ENST00000485734.1:c.218G>A
  hgvsp: ENST00000485734.1:c.218G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000343358
  ensembl transcript: ENST00000340308
  gene symbol: SLC37A3
  hgvsc: ENST00000340308.3:c.882G>A
  hgvsp: ENST00000340308.3:c.882G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000417365
  ensembl transcript: ENST00000477571
  gene symbol: SLC37A3
  hgvsc: ENST00000477571.1:c.*122G>A
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000412208
  ensembl transcript: ENST00000429996
  gene symbol: SLC37A3
  hgvsc: ENST00000429996.2:c.*783G>A
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000321498
  ensembl transcript: ENST00000326232
  gene symbol: SLC37A3
  hgvsc: ENST00000326232.9:c.882G>A
  hgvsp: ENST00000326232.9:c.882G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000157800
  ensembl transcript: ENST00000460560
  gene symbol: SLC37A3
  hgvsc: ENST00000460560.1:n.1417G>A
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000157800
  ensembl transcript: ENST00000487319
  gene symbol: SLC37A3
  hgvsc: ENST00000487319.1:n.133G>A
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000397481
  ensembl transcript: ENST00000447932
  gene symbol: SLC37A3
  hgvsc: ENST00000447932.2:c.882G>A
  hgvsp: ENST00000447932.2:c.882G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000420771
  ensembl transcript: ENST00000485861
  gene symbol: SLC37A3
  hgvsc: ENST00000485861.1:c.393-2506G>A
  variant of: http://identifiers.org/hgnc/20651
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7183
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 795
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4672
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6322
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3354
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2216
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6457
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5804
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 771
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8479
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1093
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1570
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 653
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2578
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6744
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.882G>A
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum

7-140051074-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 140051074
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 140051074
    reference: chr 7
allele count: 143
allele frequency: 1.185069778234495e-3
allele num: 120668
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000157800
  ensembl transcript: ENST00000460560
  gene symbol: SLC37A3
  hgvsc: ENST00000460560.1:n.1416C>T
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000419285
  ensembl transcript: ENST00000485734
  gene symbol: SLC37A3
  hgvsc: ENST00000485734.1:c.217C>T
  hgvsp: ENSP00000419285.1:p.Pro73Leu
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000417365
  ensembl transcript: ENST00000477571
  gene symbol: SLC37A3
  hgvsc: ENST00000477571.1:c.*121C>T
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000417447
  ensembl transcript: ENST00000492027
  gene symbol: SLC37A3
  hgvsc: ENST00000492027.1:c.84C>T
  hgvsp: ENSP00000417447.1:p.Pro29Leu
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000157800
  ensembl transcript: ENST00000487319
  gene symbol: SLC37A3
  hgvsc: ENST00000487319.1:n.132C>T
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000343358
  ensembl transcript: ENST00000340308
  gene symbol: SLC37A3
  hgvsc: ENST00000340308.3:c.881C>T
  hgvsp: ENSP00000343358.3:p.Pro294Leu
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000397481
  ensembl transcript: ENST00000447932
  gene symbol: SLC37A3
  hgvsc: ENST00000447932.2:c.881C>T
  hgvsp: ENSP00000397481.2:p.Pro294Leu
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000321498
  ensembl transcript: ENST00000326232
  gene symbol: SLC37A3
  hgvsc: ENST00000326232.9:c.881C>T
  hgvsp: ENSP00000321498.9:p.Pro294Leu
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000420771
  ensembl transcript: ENST00000485861
  gene symbol: SLC37A3
  hgvsc: ENST00000485861.1:c.393-2507C>T
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000412208
  ensembl transcript: ENST00000429996
  gene symbol: SLC37A3
  hgvsc: ENST00000429996.2:c.*782C>T
  variant of: http://identifiers.org/hgnc/20651
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2214
  bin: 6.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6763
  bin: 3.25e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 2579
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7196
  bin: 2.75e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8616
  bin: 2.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 6322
  bin: 4.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 682
  bin: 1.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 1574
  bin: 6.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 3364
  bin: 5.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5803
  bin: 4.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 6452
  bin: 3.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 653
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4671
  bin: 5.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 773
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1095
  bin: 7.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
hgvs: p.Pro294Leu
num of homozygotes: 3
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: QD

7-140051075-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 140051075
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 140051075
    reference: chr 7
allele count: 9
allele frequency: 7.454774368829103e-5
allele num: 120728
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000420771
  ensembl transcript: ENST00000485861
  gene symbol: SLC37A3
  hgvsc: ENST00000485861.1:c.393-2508C>T
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000412208
  ensembl transcript: ENST00000429996
  gene symbol: SLC37A3
  hgvsc: ENST00000429996.2:c.*781C>T
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000157800
  ensembl transcript: ENST00000487319
  gene symbol: SLC37A3
  hgvsc: ENST00000487319.1:n.131C>T
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000321498
  ensembl transcript: ENST00000326232
  gene symbol: SLC37A3
  hgvsc: ENST00000326232.9:c.880C>T
  hgvsp: ENSP00000321498.9:p.Pro294Ser
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000157800
  ensembl transcript: ENST00000460560
  gene symbol: SLC37A3
  hgvsc: ENST00000460560.1:n.1415C>T
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000417447
  ensembl transcript: ENST00000492027
  gene symbol: SLC37A3
  hgvsc: ENST00000492027.1:c.83C>T
  hgvsp: ENSP00000417447.1:p.Pro29Ser
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000397481
  ensembl transcript: ENST00000447932
  gene symbol: SLC37A3
  hgvsc: ENST00000447932.2:c.880C>T
  hgvsp: ENSP00000397481.2:p.Pro294Ser
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000419285
  ensembl transcript: ENST00000485734
  gene symbol: SLC37A3
  hgvsc: ENST00000485734.1:c.216C>T
  hgvsp: ENSP00000419285.1:p.Pro73Ser
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000417365
  ensembl transcript: ENST00000477571
  gene symbol: SLC37A3
  hgvsc: ENST00000477571.1:c.*120C>T
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000343358
  ensembl transcript: ENST00000340308
  gene symbol: SLC37A3
  hgvsc: ENST00000340308.3:c.880C>T
  hgvsp: ENSP00000343358.3:p.Pro294Ser
  variant of: http://identifiers.org/hgnc/20651
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6763
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5800
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4673
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6318
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6458
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7218
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1096
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2212
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 621
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8695
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3363
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 618
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1578
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 773
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 654
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2579
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Pro294Ser
num of homozygotes: 0
population: African
population: Other
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: ReadPosRankSum

7-140051078-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 140051078
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 140051078
    reference: chr 7
allele count: 1
allele frequency: 8.275953389830508e-6
allele num: 120832
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000420771
  ensembl transcript: ENST00000485861
  gene symbol: SLC37A3
  hgvsc: ENST00000485861.1:c.393-2511A>G
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000417365
  ensembl transcript: ENST00000477571
  gene symbol: SLC37A3
  hgvsc: ENST00000477571.1:c.*117A>G
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000343358
  ensembl transcript: ENST00000340308
  gene symbol: SLC37A3
  hgvsc: ENST00000340308.3:c.877A>G
  hgvsp: ENSP00000343358.3:p.Ile293Val
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000412208
  ensembl transcript: ENST00000429996
  gene symbol: SLC37A3
  hgvsc: ENST00000429996.2:c.*778A>G
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000419285
  ensembl transcript: ENST00000485734
  gene symbol: SLC37A3
  hgvsc: ENST00000485734.1:c.213A>G
  hgvsp: ENSP00000419285.1:p.Ile72Val
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000321498
  ensembl transcript: ENST00000326232
  gene symbol: SLC37A3
  hgvsc: ENST00000326232.9:c.877A>G
  hgvsp: ENSP00000321498.9:p.Ile293Val
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000417447
  ensembl transcript: ENST00000492027
  gene symbol: SLC37A3
  hgvsc: ENST00000492027.1:c.80A>G
  hgvsp: ENSP00000417447.1:p.Ile28Val
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157800
  ensembl transcript: ENST00000460560
  gene symbol: SLC37A3
  hgvsc: ENST00000460560.1:n.1412A>G
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000397481
  ensembl transcript: ENST00000447932
  gene symbol: SLC37A3
  hgvsc: ENST00000447932.2:c.877A>G
  hgvsp: ENSP00000397481.2:p.Ile293Val
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157800
  ensembl transcript: ENST00000487319
  gene symbol: SLC37A3
  hgvsc: ENST00000487319.1:n.128A>G
  variant of: http://identifiers.org/hgnc/20651
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7264
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 654
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6316
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8905
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4672
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6457
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5800
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6788
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2579
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3365
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 773
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1096
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1578
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2212
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 329
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Ile293Val
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
reference allele: T
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: DP

7-140051079-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 140051079
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 140051079
    reference: chr 7
allele count: 4
allele frequency: 3.309943068979214e-5
allele num: 120848
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000397481
  ensembl transcript: ENST00000447932
  gene symbol: SLC37A3
  hgvsc: ENST00000447932.2:c.876C>G
  hgvsp: ENST00000447932.2:c.876C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000420771
  ensembl transcript: ENST00000485861
  gene symbol: SLC37A3
  hgvsc: ENST00000485861.1:c.393-2512C>G
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157800
  ensembl transcript: ENST00000487319
  gene symbol: SLC37A3
  hgvsc: ENST00000487319.1:n.127C>G
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000412208
  ensembl transcript: ENST00000429996
  gene symbol: SLC37A3
  hgvsc: ENST00000429996.2:c.*777C>G
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157800
  ensembl transcript: ENST00000460560
  gene symbol: SLC37A3
  hgvsc: ENST00000460560.1:n.1411C>G
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000417447
  ensembl transcript: ENST00000492027
  gene symbol: SLC37A3
  hgvsc: ENST00000492027.1:c.79C>G
  hgvsp: ENST00000492027.1:c.79C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000419285
  ensembl transcript: ENST00000485734
  gene symbol: SLC37A3
  hgvsc: ENST00000485734.1:c.212C>G
  hgvsp: ENST00000485734.1:c.212C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000321498
  ensembl transcript: ENST00000326232
  gene symbol: SLC37A3
  hgvsc: ENST00000326232.9:c.876C>G
  hgvsp: ENST00000326232.9:c.876C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000343358
  ensembl transcript: ENST00000340308
  gene symbol: SLC37A3
  hgvsc: ENST00000340308.3:c.876C>G
  hgvsp: ENST00000340308.3:c.876C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000417365
  ensembl transcript: ENST00000477571
  gene symbol: SLC37A3
  hgvsc: ENST00000477571.1:c.*116C>G
  variant of: http://identifiers.org/hgnc/20651
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7273
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2579
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3365
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 654
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1097
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6317
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1578
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2213
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4671
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8975
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6457
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5800
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 773
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6793
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 321
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Val292Val
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Other
population: European (Finnish)
population: African
population: East Asian
population: Latino
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ

7-140051085-AG-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 140051085
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 140051084
    reference: chr 7
allele count: 1
allele frequency: 8.264189613566494e-6
allele num: 121004
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000417447
  ensembl transcript: ENST00000492027
  gene symbol: SLC37A3
  hgvsc: ENST00000492027.1:c.72delC
  hgvsp: ENSP00000417447.1:p.Pro25LeufsTer7
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157800
  ensembl transcript: ENST00000460560
  gene symbol: SLC37A3
  hgvsc: ENST00000460560.1:n.1404delC
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000343358
  ensembl transcript: ENST00000340308
  gene symbol: SLC37A3
  hgvsc: ENST00000340308.3:c.869delC
  hgvsp: ENSP00000343358.3:p.Pro290LeufsTer13
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000397481
  ensembl transcript: ENST00000447932
  gene symbol: SLC37A3
  hgvsc: ENST00000447932.2:c.869delC
  hgvsp: ENSP00000397481.2:p.Pro290LeufsTer13
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000419285
  ensembl transcript: ENST00000485734
  gene symbol: SLC37A3
  hgvsc: ENST00000485734.1:c.205delC
  hgvsp: ENSP00000419285.1:p.Pro69LeufsTer13
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000321498
  ensembl transcript: ENST00000326232
  gene symbol: SLC37A3
  hgvsc: ENST00000326232.9:c.869delC
  hgvsp: ENSP00000321498.9:p.Pro290LeufsTer13
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157800
  ensembl transcript: ENST00000487319
  gene symbol: SLC37A3
  hgvsc: ENST00000487319.1:n.120delC
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000417365
  ensembl transcript: ENST00000477571
  gene symbol: SLC37A3
  hgvsc: ENST00000477571.1:c.*109delC
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000412208
  ensembl transcript: ENST00000429996
  gene symbol: SLC37A3
  hgvsc: ENST00000429996.2:c.*770delC
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000420771
  ensembl transcript: ENST00000485861
  gene symbol: SLC37A3
  hgvsc: ENST00000485861.1:c.393-2519delC
  variant of: http://identifiers.org/hgnc/20651
canonical: true
consequence: frameshift
filter: VQSRTrancheINDEL96.00to97.00
genotype depth: GenotypeDepth
  all individuals: 4671
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2214
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1579
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7432
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6315
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6846
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2579
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5801
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6456
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 773
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 654
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9191
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3370
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1098
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 172
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Pro290LeufsTer13
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Other
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: AG
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum

7-140051091-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 140051091
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 140051091
    reference: chr 7
allele count: 52028
allele frequency: 4.294227372521831e-1
allele num: 121158
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000321498
  ensembl transcript: ENST00000326232
  gene symbol: SLC37A3
  hgvsc: ENST00000326232.9:c.864C>T
  hgvsp: ENST00000326232.9:c.864C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000343358
  ensembl transcript: ENST00000340308
  gene symbol: SLC37A3
  hgvsc: ENST00000340308.3:c.864C>T
  hgvsp: ENST00000340308.3:c.864C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000417447
  ensembl transcript: ENST00000492027
  gene symbol: SLC37A3
  hgvsc: ENST00000492027.1:c.67C>T
  hgvsp: ENST00000492027.1:c.67C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000397481
  ensembl transcript: ENST00000447932
  gene symbol: SLC37A3
  hgvsc: ENST00000447932.2:c.864C>T
  hgvsp: ENST00000447932.2:c.864C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157800
  ensembl transcript: ENST00000460560
  gene symbol: SLC37A3
  hgvsc: ENST00000460560.1:n.1399C>T
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000419285
  ensembl transcript: ENST00000485734
  gene symbol: SLC37A3
  hgvsc: ENST00000485734.1:c.200C>T
  hgvsp: ENST00000485734.1:c.200C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157800
  ensembl transcript: ENST00000487319
  gene symbol: SLC37A3
  hgvsc: ENST00000487319.1:n.115C>T
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000412208
  ensembl transcript: ENST00000429996
  gene symbol: SLC37A3
  hgvsc: ENST00000429996.2:c.*765C>T
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000417365
  ensembl transcript: ENST00000477571
  gene symbol: SLC37A3
  hgvsc: ENST00000477571.1:c.*104C>T
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000420771
  ensembl transcript: ENST00000485861
  gene symbol: SLC37A3
  hgvsc: ENST00000485861.1:c.393-2524C>T
  variant of: http://identifiers.org/hgnc/20651
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4074
  bin: 5.75e1
  variant carriers: 3765
genotype depth: GenotypeDepth
  all individuals: 3031
  bin: 4.75e1
  variant carriers: 2392
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 1.25e1
  variant carriers: 48
genotype depth: GenotypeDepth
  all individuals: 4241
  bin: 6.25e1
  variant carriers: 4032
genotype depth: GenotypeDepth
  all individuals: 5861
  bin: 2.75e1
  variant carriers: 867
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2954
  bin: 7.75e1
  variant carriers: 2885
genotype depth: GenotypeDepth
  all individuals: 4589
  bin: 3.25e1
  variant carriers: 1203
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 1.75e1
  variant carriers: 181
genotype depth: GenotypeDepth
  all individuals: 4048
  bin: 6.75e1
  variant carriers: 3909
genotype depth: GenotypeDepth
  all individuals: 3133
  bin: 3.75e1
  variant carriers: 1424
genotype depth: GenotypeDepth
  all individuals: 6400
  bin: 9.75e1
  variant carriers: 6267
genotype depth: GenotypeDepth
  all individuals: 1247
  bin: 9.25e1
  variant carriers: 1214
genotype depth: GenotypeDepth
  all individuals: 7071
  bin: 2.25e1
  variant carriers: 530
genotype depth: GenotypeDepth
  all individuals: 1682
  bin: 8.75e1
  variant carriers: 1648
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 7.5e0
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 2789
  bin: 4.25e1
  variant carriers: 1801
genotype depth: GenotypeDepth
  all individuals: 2166
  bin: 8.25e1
  variant carriers: 2111
genotype depth: GenotypeDepth
  all individuals: 3533
  bin: 7.25e1
  variant carriers: 3422
genotype depth: GenotypeDepth
  all individuals: 3503
  bin: 5.25e1
  variant carriers: 3061
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 5.25e1
  variant carriers: 32
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.25e1
  variant carriers: 8
hgvs: p.Cys288Cys
num of homozygotes: 11283
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: MQ

7-140051096-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 140051096
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 140051096
    reference: chr 7
allele count: 7
allele frequency: 5.771958178040173e-5
allele num: 121276
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000321498
  ensembl transcript: ENST00000326232
  gene symbol: SLC37A3
  hgvsc: ENST00000326232.9:c.859T>C
  hgvsp: ENSP00000321498.9:p.Cys287Arg
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000417447
  ensembl transcript: ENST00000492027
  gene symbol: SLC37A3
  hgvsc: ENST00000492027.1:c.62T>C
  hgvsp: ENSP00000417447.1:p.Cys22Arg
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000412208
  ensembl transcript: ENST00000429996
  gene symbol: SLC37A3
  hgvsc: ENST00000429996.2:c.*760T>C
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000417365
  ensembl transcript: ENST00000477571
  gene symbol: SLC37A3
  hgvsc: ENST00000477571.1:c.*99T>C
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000419285
  ensembl transcript: ENST00000485734
  gene symbol: SLC37A3
  hgvsc: ENST00000485734.1:c.195T>C
  hgvsp: ENSP00000419285.1:p.Cys66Arg
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000343358
  ensembl transcript: ENST00000340308
  gene symbol: SLC37A3
  hgvsc: ENST00000340308.3:c.859T>C
  hgvsp: ENSP00000343358.3:p.Cys287Arg
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000397481
  ensembl transcript: ENST00000447932
  gene symbol: SLC37A3
  hgvsc: ENST00000447932.2:c.859T>C
  hgvsp: ENSP00000397481.2:p.Cys287Arg
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157800
  ensembl transcript: ENST00000487319
  gene symbol: SLC37A3
  hgvsc: ENST00000487319.1:n.110T>C
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157800
  ensembl transcript: ENST00000460560
  gene symbol: SLC37A3
  hgvsc: ENST00000460560.1:n.1394T>C
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000420771
  ensembl transcript: ENST00000485861
  gene symbol: SLC37A3
  hgvsc: ENST00000485861.1:c.393-2529T>C
  variant of: http://identifiers.org/hgnc/20651
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1375
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 896
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12222
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2031
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6338
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4658
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10427
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3291
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 966
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8448
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7826
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 635
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Cys287Arg
num of homozygotes: 0
population: East Asian
population: Latino
population: Other
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum

7-140051099-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 140051099
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 140051099
    reference: chr 7
allele count: 6
allele frequency: 4.94641384995878e-5
allele num: 121300
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000417365
  ensembl transcript: ENST00000477571
  gene symbol: SLC37A3
  hgvsc: ENST00000477571.1:c.*96G>C
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000321498
  ensembl transcript: ENST00000326232
  gene symbol: SLC37A3
  hgvsc: ENST00000326232.9:c.856G>C
  hgvsp: ENSP00000321498.9:p.Ala286Pro
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000343358
  ensembl transcript: ENST00000340308
  gene symbol: SLC37A3
  hgvsc: ENST00000340308.3:c.856G>C
  hgvsp: ENSP00000343358.3:p.Ala286Pro
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157800
  ensembl transcript: ENST00000460560
  gene symbol: SLC37A3
  hgvsc: ENST00000460560.1:n.1391G>C
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157800
  ensembl transcript: ENST00000487319
  gene symbol: SLC37A3
  hgvsc: ENST00000487319.1:n.107G>C
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000417447
  ensembl transcript: ENST00000492027
  gene symbol: SLC37A3
  hgvsc: ENST00000492027.1:c.59G>C
  hgvsp: ENSP00000417447.1:p.Ala21Pro
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000419285
  ensembl transcript: ENST00000485734
  gene symbol: SLC37A3
  hgvsc: ENST00000485734.1:c.192G>C
  hgvsp: ENSP00000419285.1:p.Ala65Pro
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000397481
  ensembl transcript: ENST00000447932
  gene symbol: SLC37A3
  hgvsc: ENST00000447932.2:c.856G>C
  hgvsp: ENSP00000397481.2:p.Ala286Pro
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000412208
  ensembl transcript: ENST00000429996
  gene symbol: SLC37A3
  hgvsc: ENST00000429996.2:c.*757G>C
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000420771
  ensembl transcript: ENST00000485861
  gene symbol: SLC37A3
  hgvsc: ENST00000485861.1:c.393-2532G>C
  variant of: http://identifiers.org/hgnc/20651
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7827
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12230
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2029
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4659
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6347
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 895
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10450
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1373
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 965
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 635
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8463
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3290
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Ala286Pro
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
population: Latino
reference allele: C
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: MQRankSum

7-140051102-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 140051102
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 140051102
    reference: chr 7
allele count: 1
allele frequency: 8.242935804015958e-6
allele num: 121316
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000397481
  ensembl transcript: ENST00000447932
  gene symbol: SLC37A3
  hgvsc: ENST00000447932.2:c.853C>G
  hgvsp: ENSP00000397481.2:p.Gln285Glu
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000343358
  ensembl transcript: ENST00000340308
  gene symbol: SLC37A3
  hgvsc: ENST00000340308.3:c.853C>G
  hgvsp: ENSP00000343358.3:p.Gln285Glu
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000420771
  ensembl transcript: ENST00000485861
  gene symbol: SLC37A3
  hgvsc: ENST00000485861.1:c.393-2535C>G
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157800
  ensembl transcript: ENST00000487319
  gene symbol: SLC37A3
  hgvsc: ENST00000487319.1:n.104C>G
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000417447
  ensembl transcript: ENST00000492027
  gene symbol: SLC37A3
  hgvsc: ENST00000492027.1:c.56C>G
  hgvsp: ENSP00000417447.1:p.Gln20Glu
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157800
  ensembl transcript: ENST00000460560
  gene symbol: SLC37A3
  hgvsc: ENST00000460560.1:n.1388C>G
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000412208
  ensembl transcript: ENST00000429996
  gene symbol: SLC37A3
  hgvsc: ENST00000429996.2:c.*754C>G
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000419285
  ensembl transcript: ENST00000485734
  gene symbol: SLC37A3
  hgvsc: ENST00000485734.1:c.189C>G
  hgvsp: ENSP00000419285.1:p.Gln64Glu
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000321498
  ensembl transcript: ENST00000326232
  gene symbol: SLC37A3
  hgvsc: ENST00000326232.9:c.853C>G
  hgvsp: ENSP00000321498.9:p.Gln285Glu
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000417365
  ensembl transcript: ENST00000477571
  gene symbol: SLC37A3
  hgvsc: ENST00000477571.1:c.*93C>G
  variant of: http://identifiers.org/hgnc/20651
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2028
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 894
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6341
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7825
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4657
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12291
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10432
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 965
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1374
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8471
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3287
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17718
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Gln285Glu
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
population: European (Finnish)
population: Latino
population: African
reference allele: G
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: DP

7-140051115-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 140051115
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 140051115
    reference: chr 7
allele count: 13
allele frequency: 1.071228451827681e-4
allele num: 121356
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000321498
  ensembl transcript: ENST00000326232
  gene symbol: SLC37A3
  hgvsc: ENST00000326232.9:c.840G>A
  hgvsp: ENST00000326232.9:c.840G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000343358
  ensembl transcript: ENST00000340308
  gene symbol: SLC37A3
  hgvsc: ENST00000340308.3:c.840G>A
  hgvsp: ENST00000340308.3:c.840G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000417447
  ensembl transcript: ENST00000492027
  gene symbol: SLC37A3
  hgvsc: ENST00000492027.1:c.43G>A
  hgvsp: ENST00000492027.1:c.43G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157800
  ensembl transcript: ENST00000460560
  gene symbol: SLC37A3
  hgvsc: ENST00000460560.1:n.1375G>A
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000417365
  ensembl transcript: ENST00000477571
  gene symbol: SLC37A3
  hgvsc: ENST00000477571.1:c.*80G>A
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000397481
  ensembl transcript: ENST00000447932
  gene symbol: SLC37A3
  hgvsc: ENST00000447932.2:c.840G>A
  hgvsp: ENST00000447932.2:c.840G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000412208
  ensembl transcript: ENST00000429996
  gene symbol: SLC37A3
  hgvsc: ENST00000429996.2:c.*741G>A
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000419285
  ensembl transcript: ENST00000485734
  gene symbol: SLC37A3
  hgvsc: ENST00000485734.1:c.176G>A
  hgvsp: ENST00000485734.1:c.176G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157800
  ensembl transcript: ENST00000487319
  gene symbol: SLC37A3
  hgvsc: ENST00000487319.1:n.91G>A
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000420771
  ensembl transcript: ENST00000485861
  gene symbol: SLC37A3
  hgvsc: ENST00000485861.1:c.393-2548G>A
  variant of: http://identifiers.org/hgnc/20651
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1370
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4658
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 894
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6344
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7820
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8479
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3287
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2033
  bin: 5.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 12355
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 965
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 10448
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Ala280Ala
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD

7-140051116-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 140051116
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 140051116
    reference: chr 7
allele count: 1201
allele frequency: 9.896176664469347e-3
allele num: 121360
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000321498
  ensembl transcript: ENST00000326232
  gene symbol: SLC37A3
  hgvsc: ENST00000326232.9:c.839C>T
  hgvsp: ENSP00000321498.9:p.Ala280Val
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000397481
  ensembl transcript: ENST00000447932
  gene symbol: SLC37A3
  hgvsc: ENST00000447932.2:c.839C>T
  hgvsp: ENSP00000397481.2:p.Ala280Val
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000343358
  ensembl transcript: ENST00000340308
  gene symbol: SLC37A3
  hgvsc: ENST00000340308.3:c.839C>T
  hgvsp: ENSP00000343358.3:p.Ala280Val
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000417365
  ensembl transcript: ENST00000477571
  gene symbol: SLC37A3
  hgvsc: ENST00000477571.1:c.*79C>T
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000417447
  ensembl transcript: ENST00000492027
  gene symbol: SLC37A3
  hgvsc: ENST00000492027.1:c.42C>T
  hgvsp: ENSP00000417447.1:p.Ala15Val
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000419285
  ensembl transcript: ENST00000485734
  gene symbol: SLC37A3
  hgvsc: ENST00000485734.1:c.175C>T
  hgvsp: ENSP00000419285.1:p.Ala59Val
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000420771
  ensembl transcript: ENST00000485861
  gene symbol: SLC37A3
  hgvsc: ENST00000485861.1:c.393-2549C>T
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000412208
  ensembl transcript: ENST00000429996
  gene symbol: SLC37A3
  hgvsc: ENST00000429996.2:c.*740C>T
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157800
  ensembl transcript: ENST00000460560
  gene symbol: SLC37A3
  hgvsc: ENST00000460560.1:n.1374C>T
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157800
  ensembl transcript: ENST00000487319
  gene symbol: SLC37A3
  hgvsc: ENST00000487319.1:n.90C>T
  variant of: http://identifiers.org/hgnc/20651
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1392
  bin: 9.75e1
  variant carriers: 559
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 910
  bin: 6.75e1
  variant carriers: 62
genotype depth: GenotypeDepth
  all individuals: 8321
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1363
  bin: 6.25e1
  variant carriers: 44
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 9.25e1
  variant carriers: 68
genotype depth: GenotypeDepth
  all individuals: 6299
  bin: 4.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 8.75e1
  variant carriers: 74
genotype depth: GenotypeDepth
  all individuals: 7768
  bin: 3.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10303
  bin: 3.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 12208
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3253
  bin: 5.25e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2020
  bin: 5.75e1
  variant carriers: 41
genotype depth: GenotypeDepth
  all individuals: 653
  bin: 7.25e1
  variant carriers: 69
genotype depth: GenotypeDepth
  all individuals: 4620
  bin: 4.75e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 7.75e1
  variant carriers: 79
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 8.25e1
  variant carriers: 73
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4124
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Ala280Val
num of homozygotes: 58
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
population: European (Finnish)
reference allele: G
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum

http://identifiers.org/exac.variant/7-140051122-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 140051122
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 140051122
    reference: chr 7
allele count: 1
allele frequency: 8.238996819747227e-6
allele num: 121374
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157800
  ensembl transcript: ENST00000460560
  gene symbol: SLC37A3
  hgvsc: ENST00000460560.1:n.1368T>G
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157800
  ensembl transcript: ENST00000487319
  gene symbol: SLC37A3
  hgvsc: ENST00000487319.1:n.84T>G
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000343358
  ensembl transcript: ENST00000340308
  gene symbol: SLC37A3
  hgvsc: ENST00000340308.3:c.833T>G
  hgvsp: ENSP00000343358.3:p.Val278Gly
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000417447
  ensembl transcript: ENST00000492027
  gene symbol: SLC37A3
  hgvsc: ENST00000492027.1:c.36T>G
  hgvsp: ENSP00000417447.1:p.Val13Gly
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000321498
  ensembl transcript: ENST00000326232
  gene symbol: SLC37A3
  hgvsc: ENST00000326232.9:c.833T>G
  hgvsp: ENSP00000321498.9:p.Val278Gly
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000419285
  ensembl transcript: ENST00000485734
  gene symbol: SLC37A3
  hgvsc: ENST00000485734.1:c.169T>G
  hgvsp: ENSP00000419285.1:p.Val57Gly
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000417365
  ensembl transcript: ENST00000477571
  gene symbol: SLC37A3
  hgvsc: ENST00000477571.1:c.*73T>G
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000420771
  ensembl transcript: ENST00000485861
  gene symbol: SLC37A3
  hgvsc: ENST00000485861.1:c.393-2555T>G
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000412208
  ensembl transcript: ENST00000429996
  gene symbol: SLC37A3
  hgvsc: ENST00000429996.2:c.*734T>G
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000397481
  ensembl transcript: ENST00000447932
  gene symbol: SLC37A3
  hgvsc: ENST00000447932.2:c.833T>G
  hgvsp: ENSP00000397481.2:p.Val278Gly
  variant of: http://identifiers.org/hgnc/20651
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8355
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10484
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7920
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12361
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3306
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 888
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1372
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6447
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2032
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 869
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4727
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Val278Gly
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum

http://identifiers.org/exac.variant/7-140051132-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 140051132
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 140051132
    reference: chr 7
allele count: 1
allele frequency: 8.238453806989504e-6
allele num: 121382
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000343358
  ensembl transcript: ENST00000340308
  gene symbol: SLC37A3
  hgvsc: ENST00000340308.3:c.823G>T
  hgvsp: ENSP00000343358.3:p.Val275Phe
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000417447
  ensembl transcript: ENST00000492027
  gene symbol: SLC37A3
  hgvsc: ENST00000492027.1:c.26G>T
  hgvsp: ENSP00000417447.1:p.Val10Phe
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000321498
  ensembl transcript: ENST00000326232
  gene symbol: SLC37A3
  hgvsc: ENST00000326232.9:c.823G>T
  hgvsp: ENSP00000321498.9:p.Val275Phe
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000397481
  ensembl transcript: ENST00000447932
  gene symbol: SLC37A3
  hgvsc: ENST00000447932.2:c.823G>T
  hgvsp: ENSP00000397481.2:p.Val275Phe
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000412208
  ensembl transcript: ENST00000429996
  gene symbol: SLC37A3
  hgvsc: ENST00000429996.2:c.*724G>T
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000419285
  ensembl transcript: ENST00000485734
  gene symbol: SLC37A3
  hgvsc: ENST00000485734.1:c.159G>T
  hgvsp: ENSP00000419285.1:p.Val54Phe
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000420771
  ensembl transcript: ENST00000485861
  gene symbol: SLC37A3
  hgvsc: ENST00000485861.1:c.393-2565G>T
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157800
  ensembl transcript: ENST00000487319
  gene symbol: SLC37A3
  hgvsc: ENST00000487319.1:n.74G>T
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000417365
  ensembl transcript: ENST00000477571
  gene symbol: SLC37A3
  hgvsc: ENST00000477571.1:c.*63G>T
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157800
  ensembl transcript: ENST00000460560
  gene symbol: SLC37A3
  hgvsc: ENST00000460560.1:n.1358G>T
  variant of: http://identifiers.org/hgnc/20651
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10485
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2032
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 887
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3306
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12381
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4727
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7918
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1371
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 869
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8355
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6445
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3305
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Val275Phe
num of homozygotes: 0
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
population: African
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD

7-140051148-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 140051148
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 140051148
    reference: chr 7
allele count: 1
allele frequency: 8.237775141689733e-6
allele num: 121392
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000321498
  ensembl transcript: ENST00000326232
  gene symbol: SLC37A3
  hgvsc: ENST00000326232.9:c.807C>T
  hgvsp: ENST00000326232.9:c.807C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000419285
  ensembl transcript: ENST00000485734
  gene symbol: SLC37A3
  hgvsc: ENST00000485734.1:c.143C>T
  hgvsp: ENST00000485734.1:c.143C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000420771
  ensembl transcript: ENST00000485861
  gene symbol: SLC37A3
  hgvsc: ENST00000485861.1:c.393-2581C>T
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000343358
  ensembl transcript: ENST00000340308
  gene symbol: SLC37A3
  hgvsc: ENST00000340308.3:c.807C>T
  hgvsp: ENST00000340308.3:c.807C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000397481
  ensembl transcript: ENST00000447932
  gene symbol: SLC37A3
  hgvsc: ENST00000447932.2:c.807C>T
  hgvsp: ENST00000447932.2:c.807C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157800
  ensembl transcript: ENST00000487319
  gene symbol: SLC37A3
  hgvsc: ENST00000487319.1:n.58C>T
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157800
  ensembl transcript: ENST00000460560
  gene symbol: SLC37A3
  hgvsc: ENST00000460560.1:n.1342C>T
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000417365
  ensembl transcript: ENST00000477571
  gene symbol: SLC37A3
  hgvsc: ENST00000477571.1:c.*47C>T
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000417447
  ensembl transcript: ENST00000492027
  gene symbol: SLC37A3
  hgvsc: ENST00000492027.1:c.10C>T
  hgvsp: ENST00000492027.1:c.10C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000412208
  ensembl transcript: ENST00000429996
  gene symbol: SLC37A3
  hgvsc: ENST00000429996.2:c.*708C>T
  variant of: http://identifiers.org/hgnc/20651
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10483
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 870
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8369
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6444
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7917
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12388
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1371
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3306
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2032
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4727
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 887
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3171
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ile269Ile
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: G
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: ClippingRankSum

7-140051160-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 140051160
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 140051160
    reference: chr 7
allele count: 4
allele frequency: 3.295055768818887e-5
allele num: 121394
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000343358
  ensembl transcript: ENST00000340308
  gene symbol: SLC37A3
  hgvsc: ENST00000340308.3:c.795G>A
  hgvsp: ENST00000340308.3:c.795G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000417365
  ensembl transcript: ENST00000477571
  gene symbol: SLC37A3
  hgvsc: ENST00000477571.1:c.*35G>A
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157800
  ensembl transcript: ENST00000460560
  gene symbol: SLC37A3
  hgvsc: ENST00000460560.1:n.1330G>A
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157800
  ensembl transcript: ENST00000487319
  gene symbol: SLC37A3
  hgvsc: ENST00000487319.1:n.46G>A
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000419285
  ensembl transcript: ENST00000485734
  gene symbol: SLC37A3
  hgvsc: ENST00000485734.1:c.131G>A
  hgvsp: ENST00000485734.1:c.131G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000321498
  ensembl transcript: ENST00000326232
  gene symbol: SLC37A3
  hgvsc: ENST00000326232.9:c.795G>A
  hgvsp: ENST00000326232.9:c.795G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000412208
  ensembl transcript: ENST00000429996
  gene symbol: SLC37A3
  hgvsc: ENST00000429996.2:c.*696G>A
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000420771
  ensembl transcript: ENST00000485861
  gene symbol: SLC37A3
  hgvsc: ENST00000485861.1:c.393-2593G>A
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000397481
  ensembl transcript: ENST00000447932
  gene symbol: SLC37A3
  hgvsc: ENST00000447932.2:c.795G>A
  hgvsp: ENST00000447932.2:c.795G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20651
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6445
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7918
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1371
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4727
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 871
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 886
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2032
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12387
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3305
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8368
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10485
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18039
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Pro265Pro
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum

7-140051161-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 140051161
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 140051161
    reference: chr 7
allele count: 1
allele frequency: 8.237775141689733e-6
allele num: 121392
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157800
  ensembl transcript: ENST00000460560
  gene symbol: SLC37A3
  hgvsc: ENST00000460560.1:n.1329C>T
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000419285
  ensembl transcript: ENST00000485734
  gene symbol: SLC37A3
  hgvsc: ENST00000485734.1:c.130C>T
  hgvsp: ENSP00000419285.1:p.Pro44Leu
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000412208
  ensembl transcript: ENST00000429996
  gene symbol: SLC37A3
  hgvsc: ENST00000429996.2:c.*695C>T
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000397481
  ensembl transcript: ENST00000447932
  gene symbol: SLC37A3
  hgvsc: ENST00000447932.2:c.794C>T
  hgvsp: ENSP00000397481.2:p.Pro265Leu
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000321498
  ensembl transcript: ENST00000326232
  gene symbol: SLC37A3
  hgvsc: ENST00000326232.9:c.794C>T
  hgvsp: ENSP00000321498.9:p.Pro265Leu
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000343358
  ensembl transcript: ENST00000340308
  gene symbol: SLC37A3
  hgvsc: ENST00000340308.3:c.794C>T
  hgvsp: ENSP00000343358.3:p.Pro265Leu
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000419701
  ensembl transcript: ENST00000484416
  gene symbol: SLC37A3
  hgvsc: ENST00000484416.1:c.*160C>T
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000420771
  ensembl transcript: ENST00000485861
  gene symbol: SLC37A3
  hgvsc: ENST00000485861.1:c.393-2594C>T
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000417365
  ensembl transcript: ENST00000477571
  gene symbol: SLC37A3
  hgvsc: ENST00000477571.1:c.*34C>T
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157800
  ensembl transcript: ENST00000487319
  gene symbol: SLC37A3
  hgvsc: ENST00000487319.1:n.45C>T
  variant of: http://identifiers.org/hgnc/20651
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6445
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10485
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7917
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12388
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8371
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3306
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2032
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 870
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1371
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4727
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 886
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17973
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Pro265Leu
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
population: European (Finnish)
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD

7-140051171-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 140051171
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 140051171
    reference: chr 7
allele count: 1
allele frequency: 8.237910865804433e-6
allele num: 121390
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000412208
  ensembl transcript: ENST00000429996
  gene symbol: SLC37A3
  hgvsc: ENST00000429996.2:c.*685G>A
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000343358
  ensembl transcript: ENST00000340308
  gene symbol: SLC37A3
  hgvsc: ENST00000340308.3:c.784G>A
  hgvsp: ENSP00000343358.3:p.Glu262Lys
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000417365
  ensembl transcript: ENST00000477571
  gene symbol: SLC37A3
  hgvsc: ENST00000477571.1:c.*24G>A
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000420771
  ensembl transcript: ENST00000485861
  gene symbol: SLC37A3
  hgvsc: ENST00000485861.1:c.393-2604G>A
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000321498
  ensembl transcript: ENST00000326232
  gene symbol: SLC37A3
  hgvsc: ENST00000326232.9:c.784G>A
  hgvsp: ENSP00000321498.9:p.Glu262Lys
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000419285
  ensembl transcript: ENST00000485734
  gene symbol: SLC37A3
  hgvsc: ENST00000485734.1:c.120G>A
  hgvsp: ENSP00000419285.1:p.Glu41Lys
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157800
  ensembl transcript: ENST00000487319
  gene symbol: SLC37A3
  hgvsc: ENST00000487319.1:n.35G>A
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000419701
  ensembl transcript: ENST00000484416
  gene symbol: SLC37A3
  hgvsc: ENST00000484416.1:c.*150G>A
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000397481
  ensembl transcript: ENST00000447932
  gene symbol: SLC37A3
  hgvsc: ENST00000447932.2:c.784G>A
  hgvsp: ENSP00000397481.2:p.Glu262Lys
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157800
  ensembl transcript: ENST00000460560
  gene symbol: SLC37A3
  hgvsc: ENST00000460560.1:n.1319G>A
  variant of: http://identifiers.org/hgnc/20651
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7917
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 869
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10484
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2032
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8372
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 886
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3307
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12387
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1371
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6445
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4727
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Glu262Lys
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Latino
population: Other
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ

7-140051172-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 140051172
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 140051172
    reference: chr 7
allele count: 4
allele frequency: 3.295164346321773e-5
allele num: 121390
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000412208
  ensembl transcript: ENST00000429996
  gene symbol: SLC37A3
  hgvsc: ENST00000429996.2:c.*684C>T
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157800
  ensembl transcript: ENST00000487319
  gene symbol: SLC37A3
  hgvsc: ENST00000487319.1:n.34C>T
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000419285
  ensembl transcript: ENST00000485734
  gene symbol: SLC37A3
  hgvsc: ENST00000485734.1:c.119C>T
  hgvsp: ENST00000485734.1:c.119C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000417365
  ensembl transcript: ENST00000477571
  gene symbol: SLC37A3
  hgvsc: ENST00000477571.1:c.*23C>T
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000420771
  ensembl transcript: ENST00000485861
  gene symbol: SLC37A3
  hgvsc: ENST00000485861.1:c.393-2605C>T
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000321498
  ensembl transcript: ENST00000326232
  gene symbol: SLC37A3
  hgvsc: ENST00000326232.9:c.783C>T
  hgvsp: ENST00000326232.9:c.783C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000343358
  ensembl transcript: ENST00000340308
  gene symbol: SLC37A3
  hgvsc: ENST00000340308.3:c.783C>T
  hgvsp: ENST00000340308.3:c.783C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000397481
  ensembl transcript: ENST00000447932
  gene symbol: SLC37A3
  hgvsc: ENST00000447932.2:c.783C>T
  hgvsp: ENST00000447932.2:c.783C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000419701
  ensembl transcript: ENST00000484416
  gene symbol: SLC37A3
  hgvsc: ENST00000484416.1:c.*149C>T
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157800
  ensembl transcript: ENST00000460560
  gene symbol: SLC37A3
  hgvsc: ENST00000460560.1:n.1318C>T
  variant of: http://identifiers.org/hgnc/20651
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1371
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12386
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8372
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 887
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10485
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4728
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6445
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7917
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2032
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3306
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 868
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Asp261Asp
num of homozygotes: 0
population: Latino
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum

7-140051177-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 140051177
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 140051177
    reference: chr 7
allele count: 1
allele frequency: 8.238182327451271e-6
allele num: 121386
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000321498
  ensembl transcript: ENST00000326232
  gene symbol: SLC37A3
  hgvsc: ENST00000326232.9:c.778G>A
  hgvsp: ENSP00000321498.9:p.Glu260Lys
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000397481
  ensembl transcript: ENST00000447932
  gene symbol: SLC37A3
  hgvsc: ENST00000447932.2:c.778G>A
  hgvsp: ENSP00000397481.2:p.Glu260Lys
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157800
  ensembl transcript: ENST00000487319
  gene symbol: SLC37A3
  hgvsc: ENST00000487319.1:n.29G>A
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000420771
  ensembl transcript: ENST00000485861
  gene symbol: SLC37A3
  hgvsc: ENST00000485861.1:c.393-2610G>A
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157800
  ensembl transcript: ENST00000460560
  gene symbol: SLC37A3
  hgvsc: ENST00000460560.1:n.1313G>A
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000412208
  ensembl transcript: ENST00000429996
  gene symbol: SLC37A3
  hgvsc: ENST00000429996.2:c.*679G>A
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000417365
  ensembl transcript: ENST00000477571
  gene symbol: SLC37A3
  hgvsc: ENST00000477571.1:c.*18G>A
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000419285
  ensembl transcript: ENST00000485734
  gene symbol: SLC37A3
  hgvsc: ENST00000485734.1:c.114G>A
  hgvsp: ENSP00000419285.1:p.Glu39Lys
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000343358
  ensembl transcript: ENST00000340308
  gene symbol: SLC37A3
  hgvsc: ENST00000340308.3:c.778G>A
  hgvsp: ENSP00000343358.3:p.Glu260Lys
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000419701
  ensembl transcript: ENST00000484416
  gene symbol: SLC37A3
  hgvsc: ENST00000484416.1:c.*144G>A
  variant of: http://identifiers.org/hgnc/20651
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7917
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4729
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6446
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1371
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8367
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 886
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3306
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12386
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 865
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2033
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10484
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7018
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18036
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Glu260Lys
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQ

7-140051181-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 140051181
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 140051181
    reference: chr 7
allele count: 2
allele frequency: 1.647609318878308e-5
allele num: 121388
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000397481
  ensembl transcript: ENST00000447932
  gene symbol: SLC37A3
  hgvsc: ENST00000447932.2:c.774A>G
  hgvsp: ENST00000447932.2:c.774A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157800
  ensembl transcript: ENST00000460560
  gene symbol: SLC37A3
  hgvsc: ENST00000460560.1:n.1309A>G
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000419285
  ensembl transcript: ENST00000485734
  gene symbol: SLC37A3
  hgvsc: ENST00000485734.1:c.110A>G
  hgvsp: ENST00000485734.1:c.110A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000417365
  ensembl transcript: ENST00000477571
  gene symbol: SLC37A3
  hgvsc: ENST00000477571.1:c.*14A>G
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000343358
  ensembl transcript: ENST00000340308
  gene symbol: SLC37A3
  hgvsc: ENST00000340308.3:c.774A>G
  hgvsp: ENST00000340308.3:c.774A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000412208
  ensembl transcript: ENST00000429996
  gene symbol: SLC37A3
  hgvsc: ENST00000429996.2:c.*675A>G
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157800
  ensembl transcript: ENST00000487319
  gene symbol: SLC37A3
  hgvsc: ENST00000487319.1:n.25A>G
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000419701
  ensembl transcript: ENST00000484416
  gene symbol: SLC37A3
  hgvsc: ENST00000484416.1:c.*140A>G
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000321498
  ensembl transcript: ENST00000326232
  gene symbol: SLC37A3
  hgvsc: ENST00000326232.9:c.774A>G
  hgvsp: ENST00000326232.9:c.774A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000420771
  ensembl transcript: ENST00000485861
  gene symbol: SLC37A3
  hgvsc: ENST00000485861.1:c.393-2614A>G
  variant of: http://identifiers.org/hgnc/20651
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 886
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1371
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4729
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8361
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7918
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6446
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2033
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10484
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 866
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3306
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12386
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18028
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Glu258Glu
num of homozygotes: 0
population: Other
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
population: European (Finnish)
reference allele: T
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum

7-140051184-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 140051184
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 140051184
    reference: chr 7
allele count: 1
allele frequency: 8.238046594391538e-6
allele num: 121388
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157800
  ensembl transcript: ENST00000460560
  gene symbol: SLC37A3
  hgvsc: ENST00000460560.1:n.1306T>A
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000321498
  ensembl transcript: ENST00000326232
  gene symbol: SLC37A3
  hgvsc: ENST00000326232.9:c.771T>A
  hgvsp: ENST00000326232.9:c.771T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000419285
  ensembl transcript: ENST00000485734
  gene symbol: SLC37A3
  hgvsc: ENST00000485734.1:c.107T>A
  hgvsp: ENST00000485734.1:c.107T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000397481
  ensembl transcript: ENST00000447932
  gene symbol: SLC37A3
  hgvsc: ENST00000447932.2:c.771T>A
  hgvsp: ENST00000447932.2:c.771T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000343358
  ensembl transcript: ENST00000340308
  gene symbol: SLC37A3
  hgvsc: ENST00000340308.3:c.771T>A
  hgvsp: ENST00000340308.3:c.771T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000417365
  ensembl transcript: ENST00000477571
  gene symbol: SLC37A3
  hgvsc: ENST00000477571.1:c.*11T>A
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157800
  ensembl transcript: ENST00000487319
  gene symbol: SLC37A3
  hgvsc: ENST00000487319.1:n.22T>A
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000412208
  ensembl transcript: ENST00000429996
  gene symbol: SLC37A3
  hgvsc: ENST00000429996.2:c.*672T>A
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000419701
  ensembl transcript: ENST00000484416
  gene symbol: SLC37A3
  hgvsc: ENST00000484416.1:c.*137T>A
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000420771
  ensembl transcript: ENST00000485861
  gene symbol: SLC37A3
  hgvsc: ENST00000485861.1:c.393-2617T>A
  variant of: http://identifiers.org/hgnc/20651
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3307
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7918
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4729
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 864
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12388
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10487
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 886
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8355
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6445
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2033
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1371
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2198
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Gly257Gly
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD

http://identifiers.org/exac.variant/7-140051189-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 140051189
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 140051189
    reference: chr 7
allele count: 1
allele frequency: 8.238589553468446e-6
allele num: 121380
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000397481
  ensembl transcript: ENST00000447932
  gene symbol: SLC37A3
  hgvsc: ENST00000447932.2:c.766G>T
  hgvsp: ENSP00000397481.2:p.Gly256Cys
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000419701
  ensembl transcript: ENST00000484416
  gene symbol: SLC37A3
  hgvsc: ENST00000484416.1:c.*132G>T
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000412208
  ensembl transcript: ENST00000429996
  gene symbol: SLC37A3
  hgvsc: ENST00000429996.2:c.*667G>T
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000417365
  ensembl transcript: ENST00000477571
  gene symbol: SLC37A3
  hgvsc: ENST00000477571.1:c.*6G>T
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000321498
  ensembl transcript: ENST00000326232
  gene symbol: SLC37A3
  hgvsc: ENST00000326232.9:c.766G>T
  hgvsp: ENSP00000321498.9:p.Gly256Cys
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157800
  ensembl transcript: ENST00000487319
  gene symbol: SLC37A3
  hgvsc: ENST00000487319.1:n.17G>T
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157800
  ensembl transcript: ENST00000460560
  gene symbol: SLC37A3
  hgvsc: ENST00000460560.1:n.1301G>T
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000343358
  ensembl transcript: ENST00000340308
  gene symbol: SLC37A3
  hgvsc: ENST00000340308.3:c.766G>T
  hgvsp: ENSP00000343358.3:p.Gly256Cys
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000419285
  ensembl transcript: ENST00000485734
  gene symbol: SLC37A3
  hgvsc: ENST00000485734.1:c.102G>T
  hgvsp: ENSP00000419285.1:p.Gly35Cys
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000420771
  ensembl transcript: ENST00000485861
  gene symbol: SLC37A3
  hgvsc: ENST00000485861.1:c.393-2622G>T
  variant of: http://identifiers.org/hgnc/20651
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6445
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7919
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1371
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 886
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3307
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4729
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8346
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12392
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10485
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2032
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 865
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4776
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7015
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Gly256Cys
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: MQ

7-140051194-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 140051194
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 140051194
    reference: chr 7
allele count: 3
allele frequency: 2.471576866040534e-5
allele num: 121380
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000420771
  ensembl transcript: ENST00000485861
  gene symbol: SLC37A3
  hgvsc: ENST00000485861.1:c.393-2627T>A
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000321498
  ensembl transcript: ENST00000326232
  gene symbol: SLC37A3
  hgvsc: ENST00000326232.9:c.761T>A
  hgvsp: ENSP00000321498.9:p.Ile254Asn
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157800
  ensembl transcript: ENST00000487319
  gene symbol: SLC37A3
  hgvsc: ENST00000487319.1:n.12T>A
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000343358
  ensembl transcript: ENST00000340308
  gene symbol: SLC37A3
  hgvsc: ENST00000340308.3:c.761T>A
  hgvsp: ENSP00000343358.3:p.Ile254Asn
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000417365
  ensembl transcript: ENST00000477571
  gene symbol: SLC37A3
  hgvsc: ENST00000477571.1:c.*1T>A
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000412208
  ensembl transcript: ENST00000429996
  gene symbol: SLC37A3
  hgvsc: ENST00000429996.2:c.*662T>A
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000419701
  ensembl transcript: ENST00000484416
  gene symbol: SLC37A3
  hgvsc: ENST00000484416.1:c.*127T>A
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000419285
  ensembl transcript: ENST00000485734
  gene symbol: SLC37A3
  hgvsc: ENST00000485734.1:c.97T>A
  hgvsp: ENSP00000419285.1:p.Ile33Asn
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000397481
  ensembl transcript: ENST00000447932
  gene symbol: SLC37A3
  hgvsc: ENST00000447932.2:c.761T>A
  hgvsp: ENSP00000397481.2:p.Ile254Asn
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157800
  ensembl transcript: ENST00000460560
  gene symbol: SLC37A3
  hgvsc: ENST00000460560.1:n.1296T>A
  variant of: http://identifiers.org/hgnc/20651
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1371
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2032
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10485
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8345
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6445
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3307
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 886
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12387
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4729
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 866
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7918
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4200
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2198
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Ile254Asn
num of homozygotes: 1
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ

7-140051205-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 140051205
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 140051205
    reference: chr 7
allele count: 1
allele frequency: 8.241441263248117e-6
allele num: 121338
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000397481
  ensembl transcript: ENST00000447932
  gene symbol: SLC37A3
  hgvsc: ENST00000447932.2:c.750C>T
  hgvsp: ENST00000447932.2:c.750C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000419701
  ensembl transcript: ENST00000484416
  gene symbol: SLC37A3
  hgvsc: ENST00000484416.1:c.*116C>T
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157800
  ensembl transcript: ENST00000460560
  gene symbol: SLC37A3
  hgvsc: ENST00000460560.1:n.1285C>T
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000417365
  ensembl transcript: ENST00000477571
  gene symbol: SLC37A3
  hgvsc: ENST00000477571.1:c.665C>T
  hgvsp: ENSP00000417365.1:p.Thr222Ile
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000419285
  ensembl transcript: ENST00000485734
  gene symbol: SLC37A3
  hgvsc: ENST00000485734.1:c.86C>T
  hgvsp: ENST00000485734.1:c.86C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000343358
  ensembl transcript: ENST00000340308
  gene symbol: SLC37A3
  hgvsc: ENST00000340308.3:c.750C>T
  hgvsp: ENST00000340308.3:c.750C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000420771
  ensembl transcript: ENST00000485861
  gene symbol: SLC37A3
  hgvsc: ENST00000485861.1:c.393-2638C>T
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000412208
  ensembl transcript: ENST00000429996
  gene symbol: SLC37A3
  hgvsc: ENST00000429996.2:c.*651C>T
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000321498
  ensembl transcript: ENST00000326232
  gene symbol: SLC37A3
  hgvsc: ENST00000326232.9:c.750C>T
  hgvsp: ENST00000326232.9:c.750C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157800
  ensembl transcript: ENST00000487319
  gene symbol: SLC37A3
  hgvsc: ENST00000487319.1:n.1C>T
  variant of: http://identifiers.org/hgnc/20651
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 886
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3307
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1371
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12383
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8305
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10484
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 865
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4729
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6445
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7920
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2032
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17969
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Thr222Ile
num of homozygotes: 0
population: East Asian
population: Other
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: DP

7-140051206-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 140051206
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 140051206
    reference: chr 7
allele count: 1
allele frequency: 8.241441263248117e-6
allele num: 121338
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000419701
  ensembl transcript: ENST00000484416
  gene symbol: SLC37A3
  hgvsc: ENST00000484416.1:c.*115A>G
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000417365
  ensembl transcript: ENST00000477571
  gene symbol: SLC37A3
  hgvsc: ENST00000477571.1:c.664A>G
  hgvsp: ENSP00000417365.1:p.Thr222Ala
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000343358
  ensembl transcript: ENST00000340308
  gene symbol: SLC37A3
  hgvsc: ENST00000340308.3:c.749A>G
  hgvsp: ENSP00000343358.3:p.His250Arg
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000420771
  ensembl transcript: ENST00000485861
  gene symbol: SLC37A3
  hgvsc: ENST00000485861.1:c.393-2639A>G
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000412208
  ensembl transcript: ENST00000429996
  gene symbol: SLC37A3
  hgvsc: ENST00000429996.2:c.*650A>G
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157800
  ensembl transcript: ENST00000460560
  gene symbol: SLC37A3
  hgvsc: ENST00000460560.1:n.1284A>G
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000321498
  ensembl transcript: ENST00000326232
  gene symbol: SLC37A3
  hgvsc: ENST00000326232.9:c.749A>G
  hgvsp: ENSP00000321498.9:p.His250Arg
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000419285
  ensembl transcript: ENST00000485734
  gene symbol: SLC37A3
  hgvsc: ENST00000485734.1:c.85A>G
  hgvsp: ENSP00000419285.1:p.His29Arg
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000397481
  ensembl transcript: ENST00000447932
  gene symbol: SLC37A3
  hgvsc: ENST00000447932.2:c.749A>G
  hgvsp: ENSP00000397481.2:p.His250Arg
  variant of: http://identifiers.org/hgnc/20651
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6445
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1371
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3307
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 886
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7921
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4729
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8305
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10483
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 865
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12381
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2032
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.His250Arg
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
population: Other
reference allele: T
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum

7-140051213-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 140051213
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 140051213
    reference: chr 7
allele count: 1
allele frequency: 8.246198502490351e-6
allele num: 121268
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000412208
  ensembl transcript: ENST00000429996
  gene symbol: SLC37A3
  hgvsc: ENST00000429996.2:c.*643G>A
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157800
  ensembl transcript: ENST00000460560
  gene symbol: SLC37A3
  hgvsc: ENST00000460560.1:n.1277G>A
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000419701
  ensembl transcript: ENST00000484416
  gene symbol: SLC37A3
  hgvsc: ENST00000484416.1:c.*108G>A
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000397481
  ensembl transcript: ENST00000447932
  gene symbol: SLC37A3
  hgvsc: ENST00000447932.2:c.742G>A
  hgvsp: ENSP00000397481.2:p.Asp248Asn
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000417365
  ensembl transcript: ENST00000477571
  gene symbol: SLC37A3
  hgvsc: ENST00000477571.1:c.657G>A
  hgvsp: ENST00000477571.1:c.657G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000420771
  ensembl transcript: ENST00000485861
  gene symbol: SLC37A3
  hgvsc: ENST00000485861.1:c.393-2646G>A
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000321498
  ensembl transcript: ENST00000326232
  gene symbol: SLC37A3
  hgvsc: ENST00000326232.9:c.742G>A
  hgvsp: ENSP00000321498.9:p.Asp248Asn
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000343358
  ensembl transcript: ENST00000340308
  gene symbol: SLC37A3
  hgvsc: ENST00000340308.3:c.742G>A
  hgvsp: ENSP00000343358.3:p.Asp248Asn
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000419285
  ensembl transcript: ENST00000485734
  gene symbol: SLC37A3
  hgvsc: ENST00000485734.1:c.78G>A
  hgvsp: ENSP00000419285.1:p.Asp27Asn
  variant of: http://identifiers.org/hgnc/20651
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 886
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10482
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7921
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6446
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4729
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8247
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1371
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12355
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2032
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3307
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 865
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 119
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6999
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Asp248Asn
num of homozygotes: 0
population: Other
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: C
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP

7-140051217-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 140051217
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 140051217
    reference: chr 7
allele count: 1
allele frequency: 8.251505899826718e-6
allele num: 121190
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000420771
  ensembl transcript: ENST00000485861
  gene symbol: SLC37A3
  hgvsc: ENST00000485861.1:c.393-2650A>G
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000417365
  ensembl transcript: ENST00000477571
  gene symbol: SLC37A3
  hgvsc: ENST00000477571.1:c.653A>G
  hgvsp: ENSP00000417365.1:p.Lys218Arg
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000343358
  ensembl transcript: ENST00000340308
  gene symbol: SLC37A3
  hgvsc: ENST00000340308.3:c.738A>G
  hgvsp: ENST00000340308.3:c.738A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000412208
  ensembl transcript: ENST00000429996
  gene symbol: SLC37A3
  hgvsc: ENST00000429996.2:c.*639A>G
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000419701
  ensembl transcript: ENST00000484416
  gene symbol: SLC37A3
  hgvsc: ENST00000484416.1:c.*104A>G
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000321498
  ensembl transcript: ENST00000326232
  gene symbol: SLC37A3
  hgvsc: ENST00000326232.9:c.738A>G
  hgvsp: ENST00000326232.9:c.738A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157800
  ensembl transcript: ENST00000460560
  gene symbol: SLC37A3
  hgvsc: ENST00000460560.1:n.1273A>G
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000419285
  ensembl transcript: ENST00000485734
  gene symbol: SLC37A3
  hgvsc: ENST00000485734.1:c.74A>G
  hgvsp: ENST00000485734.1:c.74A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000397481
  ensembl transcript: ENST00000447932
  gene symbol: SLC37A3
  hgvsc: ENST00000447932.2:c.738A>G
  hgvsp: ENST00000447932.2:c.738A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20651
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12317
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1371
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4730
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6446
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10479
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7919
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 886
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 864
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3307
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8183
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2032
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 185
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2197
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Lys218Arg
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
population: African
population: European (Finnish)
reference allele: T
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: MQ

7-140051220-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 140051220
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 140051220
    reference: chr 7
allele count: 1
allele frequency: 8.252459232851389e-6
allele num: 121176
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000343358
  ensembl transcript: ENST00000340308
  gene symbol: SLC37A3
  hgvsc: ENST00000340308.3:c.735T>A
  hgvsp: ENSP00000343358.3:p.Phe245Leu
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000412208
  ensembl transcript: ENST00000429996
  gene symbol: SLC37A3
  hgvsc: ENST00000429996.2:c.*636T>A
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000419285
  ensembl transcript: ENST00000485734
  gene symbol: SLC37A3
  hgvsc: ENST00000485734.1:c.71T>A
  hgvsp: ENSP00000419285.1:p.Phe24Leu
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000420771
  ensembl transcript: ENST00000485861
  gene symbol: SLC37A3
  hgvsc: ENST00000485861.1:c.393-2653T>A
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000419701
  ensembl transcript: ENST00000484416
  gene symbol: SLC37A3
  hgvsc: ENST00000484416.1:c.*101T>A
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000417365
  ensembl transcript: ENST00000477571
  gene symbol: SLC37A3
  hgvsc: ENST00000477571.1:c.650T>A
  hgvsp: ENSP00000417365.1:p.Leu217Ter
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000321498
  ensembl transcript: ENST00000326232
  gene symbol: SLC37A3
  hgvsc: ENST00000326232.9:c.735T>A
  hgvsp: ENSP00000321498.9:p.Phe245Leu
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157800
  ensembl transcript: ENST00000460560
  gene symbol: SLC37A3
  hgvsc: ENST00000460560.1:n.1270T>A
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000397481
  ensembl transcript: ENST00000447932
  gene symbol: SLC37A3
  hgvsc: ENST00000447932.2:c.735T>A
  hgvsp: ENSP00000397481.2:p.Phe245Leu
  variant of: http://identifiers.org/hgnc/20651
canonical: false
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8183
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2032
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10466
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12319
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7913
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 886
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4730
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6443
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 864
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3307
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1371
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3306
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3161
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Leu217Ter
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: A
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum

7-140051239-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 140051239
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 140051239
    reference: chr 7
allele count: 1
allele frequency: 8.299443937256203e-6
allele num: 120490
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000397481
  ensembl transcript: ENST00000447932
  gene symbol: SLC37A3
  hgvsc: ENST00000447932.2:c.716T>C
  hgvsp: ENSP00000397481.2:p.Ile239Thr
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000412208
  ensembl transcript: ENST00000429996
  gene symbol: SLC37A3
  hgvsc: ENST00000429996.2:c.*617T>C
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000321498
  ensembl transcript: ENST00000326232
  gene symbol: SLC37A3
  hgvsc: ENST00000326232.9:c.716T>C
  hgvsp: ENSP00000321498.9:p.Ile239Thr
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000420771
  ensembl transcript: ENST00000485861
  gene symbol: SLC37A3
  hgvsc: ENST00000485861.1:c.393-2672T>C
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000343358
  ensembl transcript: ENST00000340308
  gene symbol: SLC37A3
  hgvsc: ENST00000340308.3:c.716T>C
  hgvsp: ENSP00000343358.3:p.Ile239Thr
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157800
  ensembl transcript: ENST00000460560
  gene symbol: SLC37A3
  hgvsc: ENST00000460560.1:n.1251T>C
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000417365
  ensembl transcript: ENST00000477571
  gene symbol: SLC37A3
  hgvsc: ENST00000477571.1:c.631T>C
  hgvsp: ENST00000477571.1:c.631T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000419285
  ensembl transcript: ENST00000485734
  gene symbol: SLC37A3
  hgvsc: ENST00000485734.1:c.52T>C
  hgvsp: ENSP00000419285.1:p.Ile18Thr
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000419701
  ensembl transcript: ENST00000484416
  gene symbol: SLC37A3
  hgvsc: ENST00000484416.1:c.*82T>C
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000418585
  ensembl transcript: ENST00000490760
  gene symbol: SLC37A3
  hgvsc: ENST00000490760.1:c.*265T>C
  variant of: http://identifiers.org/hgnc/20651
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10251
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6434
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7760
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 886
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 864
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7871
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11726
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1372
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 812
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4730
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3307
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2031
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6799
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 202
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Ile239Thr
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: FS
site quality: BaseQRankSum

7-140051240-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 140051240
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 140051240
    reference: chr 7
allele count: 1
allele frequency: 8.302200083022e-6
allele num: 120450
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000343358
  ensembl transcript: ENST00000340308
  gene symbol: SLC37A3
  hgvsc: ENST00000340308.3:c.715A>T
  hgvsp: ENSP00000343358.3:p.Ile239Phe
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000418585
  ensembl transcript: ENST00000490760
  gene symbol: SLC37A3
  hgvsc: ENST00000490760.1:c.*264A>T
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000419285
  ensembl transcript: ENST00000485734
  gene symbol: SLC37A3
  hgvsc: ENST00000485734.1:c.51A>T
  hgvsp: ENSP00000419285.1:p.Ile18Phe
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000412208
  ensembl transcript: ENST00000429996
  gene symbol: SLC37A3
  hgvsc: ENST00000429996.2:c.*616A>T
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000419701
  ensembl transcript: ENST00000484416
  gene symbol: SLC37A3
  hgvsc: ENST00000484416.1:c.*81A>T
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157800
  ensembl transcript: ENST00000460560
  gene symbol: SLC37A3
  hgvsc: ENST00000460560.1:n.1250A>T
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000397481
  ensembl transcript: ENST00000447932
  gene symbol: SLC37A3
  hgvsc: ENST00000447932.2:c.715A>T
  hgvsp: ENSP00000397481.2:p.Ile239Phe
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000417365
  ensembl transcript: ENST00000477571
  gene symbol: SLC37A3
  hgvsc: ENST00000477571.1:c.630A>T
  hgvsp: ENST00000477571.1:c.630A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000321498
  ensembl transcript: ENST00000326232
  gene symbol: SLC37A3
  hgvsc: ENST00000326232.9:c.715A>T
  hgvsp: ENSP00000321498.9:p.Ile239Phe
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000420771
  ensembl transcript: ENST00000485861
  gene symbol: SLC37A3
  hgvsc: ENST00000485861.1:c.393-2673A>T
  variant of: http://identifiers.org/hgnc/20651
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4728
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2031
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10227
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11668
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7733
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 873
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3307
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7869
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 886
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 864
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1371
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6433
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 218
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Ile239Phe
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD

7-140051244-CGA-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 140051244
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 140051242
    reference: chr 7
allele count: 1
allele frequency: 8.311861025683651e-6
allele num: 120310
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157800
  ensembl transcript: ENST00000460560
  gene symbol: SLC37A3
  hgvsc: ENST00000460560.1:n.1244_1245delTC
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000418585
  ensembl transcript: ENST00000490760
  gene symbol: SLC37A3
  hgvsc: ENST00000490760.1:c.*258_*259delTC
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000419285
  ensembl transcript: ENST00000485734
  gene symbol: SLC37A3
  hgvsc: ENST00000485734.1:c.45_46delTC
  hgvsp: ENSP00000419285.1:p.Ser16GlyfsTer3
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000412208
  ensembl transcript: ENST00000429996
  gene symbol: SLC37A3
  hgvsc: ENST00000429996.2:c.*610_*611delTC
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000343358
  ensembl transcript: ENST00000340308
  gene symbol: SLC37A3
  hgvsc: ENST00000340308.3:c.709_710delTC
  hgvsp: ENSP00000343358.3:p.Ser237GlyfsTer3
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000397481
  ensembl transcript: ENST00000447932
  gene symbol: SLC37A3
  hgvsc: ENST00000447932.2:c.709_710delTC
  hgvsp: ENSP00000397481.2:p.Ser237GlyfsTer3
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000420771
  ensembl transcript: ENST00000485861
  gene symbol: SLC37A3
  hgvsc: ENST00000485861.1:c.393-2679_393-2678delTC
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000417365
  ensembl transcript: ENST00000477571
  gene symbol: SLC37A3
  hgvsc: ENST00000477571.1:c.624_625delTC
  hgvsp: ENSP00000417365.1:p.Arg209GlyfsTer242
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000419701
  ensembl transcript: ENST00000484416
  gene symbol: SLC37A3
  hgvsc: ENST00000484416.1:c.*75_*76delTC
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000321498
  ensembl transcript: ENST00000326232
  gene symbol: SLC37A3
  hgvsc: ENST00000326232.9:c.709_710delTC
  hgvsp: ENSP00000321498.9:p.Ser237GlyfsTer3
  variant of: http://identifiers.org/hgnc/20651
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1045
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10127
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7832
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7726
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2031
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11527
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 886
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6417
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 611
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3308
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4723
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1370
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 864
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Ser237GlyfsTer3
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
population: Other
reference allele: CGA
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS

7-140051245-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 140051245
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 140051245
    reference: chr 7
allele count: 4
allele frequency: 3.326126725428239e-5
allele num: 120260
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000321498
  ensembl transcript: ENST00000326232
  gene symbol: SLC37A3
  hgvsc: ENST00000326232.9:c.710C>T
  hgvsp: ENSP00000321498.9:p.Ser237Leu
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000419285
  ensembl transcript: ENST00000485734
  gene symbol: SLC37A3
  hgvsc: ENST00000485734.1:c.46C>T
  hgvsp: ENSP00000419285.1:p.Ser16Leu
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000418585
  ensembl transcript: ENST00000490760
  gene symbol: SLC37A3
  hgvsc: ENST00000490760.1:c.*259C>T
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000417365
  ensembl transcript: ENST00000477571
  gene symbol: SLC37A3
  hgvsc: ENST00000477571.1:c.625C>T
  hgvsp: ENSP00000417365.1:p.Arg209Trp
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000419701
  ensembl transcript: ENST00000484416
  gene symbol: SLC37A3
  hgvsc: ENST00000484416.1:c.*76C>T
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000343358
  ensembl transcript: ENST00000340308
  gene symbol: SLC37A3
  hgvsc: ENST00000340308.3:c.710C>T
  hgvsp: ENSP00000343358.3:p.Ser237Leu
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000420771
  ensembl transcript: ENST00000485861
  gene symbol: SLC37A3
  hgvsc: ENST00000485861.1:c.393-2678C>T
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000397481
  ensembl transcript: ENST00000447932
  gene symbol: SLC37A3
  hgvsc: ENST00000447932.2:c.710C>T
  hgvsp: ENSP00000397481.2:p.Ser237Leu
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000412208
  ensembl transcript: ENST00000429996
  gene symbol: SLC37A3
  hgvsc: ENST00000429996.2:c.*611C>T
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157800
  ensembl transcript: ENST00000460560
  gene symbol: SLC37A3
  hgvsc: ENST00000460560.1:n.1245C>T
  variant of: http://identifiers.org/hgnc/20651
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1114
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 886
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10083
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6408
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7715
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1370
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7824
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4721
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2031
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3308
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 864
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11461
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Ser237Leu
num of homozygotes: 0
population: East Asian
population: Other
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD

http://identifiers.org/exac.variant/7-140051252-C-CAA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 140051252
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 140051254
    reference: chr 7
allele count: 6
allele frequency: 5.00575662011313e-5
allele num: 119862
alternate allele: CAA
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000418585
  ensembl transcript: ENST00000490760
  gene symbol: SLC37A3
  hgvsc: ENST00000490760.1:c.*253-2_*253-1insTT
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000397481
  ensembl transcript: ENST00000447932
  gene symbol: SLC37A3
  hgvsc: ENST00000447932.2:c.704-2_704-1insTT
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000343358
  ensembl transcript: ENST00000340308
  gene symbol: SLC37A3
  hgvsc: ENST00000340308.3:c.704-2_704-1insTT
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157800
  ensembl transcript: ENST00000460560
  gene symbol: SLC37A3
  hgvsc: ENST00000460560.1:n.1237_1238insTT
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000417365
  ensembl transcript: ENST00000477571
  gene symbol: SLC37A3
  hgvsc: ENST00000477571.1:c.619-2_619-1insTT
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: true
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000321498
  ensembl transcript: ENST00000326232
  gene symbol: SLC37A3
  hgvsc: ENST00000326232.9:c.704-2_704-1insTT
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000419701
  ensembl transcript: ENST00000484416
  gene symbol: SLC37A3
  hgvsc: ENST00000484416.1:c.*70-2_*70-1insTT
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000420771
  ensembl transcript: ENST00000485861
  gene symbol: SLC37A3
  hgvsc: ENST00000485861.1:c.393-2686_393-2685insTT
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000419285
  ensembl transcript: ENST00000485734
  gene symbol: SLC37A3
  hgvsc: ENST00000485734.1:c.40-2_40-1insTT
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000412208
  ensembl transcript: ENST00000429996
  gene symbol: SLC37A3
  hgvsc: ENST00000429996.2:c.*603_*604insTT
  variant of: http://identifiers.org/hgnc/20651
canonical: true
consequence: splice acceptor
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 7750
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9881
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4712
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6379
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1459
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2029
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 863
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3304
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 743
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11104
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 886
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1370
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7604
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3072
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3298
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 196
  bin: 3.75e1
  variant carriers: 0
hgvs: c.704-2_704-1insTT
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
reference allele: C
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum

7-140051252-C-CAATTTCTTCTGGTGACACCAGGAGTCCAAAGAAGATAACGA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 140051252
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 140051293
    reference: chr 7
allele count: 1
allele frequency: 8.342927700188551e-6
allele num: 119862
alternate allele: CAATTTCTTCTGGTGACACCAGGAGTCCAAAGAAGATAACGA
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157800
  ensembl transcript: ENST00000460560
  gene symbol: SLC37A3
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000417365
  ensembl transcript: ENST00000477571
  gene symbol: SLC37A3
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000397481
  ensembl transcript: ENST00000447932
  gene symbol: SLC37A3
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: true
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000321498
  ensembl transcript: ENST00000326232
  gene symbol: SLC37A3
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000343358
  ensembl transcript: ENST00000340308
  gene symbol: SLC37A3
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000412208
  ensembl transcript: ENST00000429996
  gene symbol: SLC37A3
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000418585
  ensembl transcript: ENST00000490760
  gene symbol: SLC37A3
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000419285
  ensembl transcript: ENST00000485734
  gene symbol: SLC37A3
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000420771
  ensembl transcript: ENST00000485861
  gene symbol: SLC37A3
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000419701
  ensembl transcript: ENST00000484416
  gene symbol: SLC37A3
  variant of: http://identifiers.org/hgnc/20651
canonical: true
consequence: splice acceptor
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 886
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 743
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 863
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1370
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1459
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2029
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7750
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3304
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11104
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7604
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6379
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9881
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4712
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6491
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 403
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3072
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
reference allele: C
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: MQ

7-140051253-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 140051253
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 140051253
    reference: chr 7
allele count: 1
allele frequency: 8.358548287333457e-6
allele num: 119638
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000419701
  ensembl transcript: ENST00000484416
  gene symbol: SLC37A3
  hgvsc: ENST00000484416.1:c.*70-2A>T
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: true
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000321498
  ensembl transcript: ENST00000326232
  gene symbol: SLC37A3
  hgvsc: ENST00000326232.9:c.704-2A>T
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000417365
  ensembl transcript: ENST00000477571
  gene symbol: SLC37A3
  hgvsc: ENST00000477571.1:c.619-2A>T
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157800
  ensembl transcript: ENST00000460560
  gene symbol: SLC37A3
  hgvsc: ENST00000460560.1:n.1237A>T
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000397481
  ensembl transcript: ENST00000447932
  gene symbol: SLC37A3
  hgvsc: ENST00000447932.2:c.704-2A>T
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000418585
  ensembl transcript: ENST00000490760
  gene symbol: SLC37A3
  hgvsc: ENST00000490760.1:c.*253-2A>T
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000412208
  ensembl transcript: ENST00000429996
  gene symbol: SLC37A3
  hgvsc: ENST00000429996.2:c.*603A>T
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000343358
  ensembl transcript: ENST00000340308
  gene symbol: SLC37A3
  hgvsc: ENST00000340308.3:c.704-2A>T
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000419285
  ensembl transcript: ENST00000485734
  gene symbol: SLC37A3
  hgvsc: ENST00000485734.1:c.40-2A>T
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000420771
  ensembl transcript: ENST00000485861
  gene symbol: SLC37A3
  hgvsc: ENST00000485861.1:c.393-2686A>T
  variant of: http://identifiers.org/hgnc/20651
canonical: true
consequence: splice acceptor
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 806
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7707
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6358
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 751
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3300
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 887
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1372
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2032
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1597
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7527
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9847
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4703
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 866
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11022
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4147
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6435
  bin: 6.75e1
  variant carriers: 0
hgvs: c.704-2A>T
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
reference allele: T
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum

7-140051253-T-TTTCTTCTGGTGACACCAGGAGTCC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 140051253
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 140051277
    reference: chr 7
allele count: 6
allele frequency: 5.015128972400073e-5
allele num: 119638
alternate allele: TTTCTTCTGGTGACACCAGGAGTCC
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000419285
  ensembl transcript: ENST00000485734
  gene symbol: SLC37A3
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000343358
  ensembl transcript: ENST00000340308
  gene symbol: SLC37A3
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000420771
  ensembl transcript: ENST00000485861
  gene symbol: SLC37A3
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000417365
  ensembl transcript: ENST00000477571
  gene symbol: SLC37A3
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000397481
  ensembl transcript: ENST00000447932
  gene symbol: SLC37A3
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000412208
  ensembl transcript: ENST00000429996
  gene symbol: SLC37A3
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000321498
  ensembl transcript: ENST00000326232
  gene symbol: SLC37A3
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000418585
  ensembl transcript: ENST00000490760
  gene symbol: SLC37A3
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157800
  ensembl transcript: ENST00000460560
  gene symbol: SLC37A3
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000419701
  ensembl transcript: ENST00000484416
  gene symbol: SLC37A3
  variant of: http://identifiers.org/hgnc/20651
canonical: true
consequence: splice region
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 806
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3300
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 887
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1597
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11022
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2032
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7527
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 751
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7707
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9847
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1372
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 866
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4703
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6358
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6435
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3047
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: T
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: DP

7-140051254-A-ATTTCTTCTGGTGACACCAGGAGTCC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 140051254
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 140051279
    reference: chr 7
allele count: 1
allele frequency: 8.353800143685363e-6
allele num: 119706
alternate allele: ATTTCTTCTGGTGACACCAGGAGTCC
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000419285
  ensembl transcript: ENST00000485734
  gene symbol: SLC37A3
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157800
  ensembl transcript: ENST00000460560
  gene symbol: SLC37A3
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000321498
  ensembl transcript: ENST00000326232
  gene symbol: SLC37A3
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000412208
  ensembl transcript: ENST00000429996
  gene symbol: SLC37A3
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000417365
  ensembl transcript: ENST00000477571
  gene symbol: SLC37A3
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000343358
  ensembl transcript: ENST00000340308
  gene symbol: SLC37A3
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000418585
  ensembl transcript: ENST00000490760
  gene symbol: SLC37A3
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000397481
  ensembl transcript: ENST00000447932
  gene symbol: SLC37A3
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000420771
  ensembl transcript: ENST00000485861
  gene symbol: SLC37A3
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000419701
  ensembl transcript: ENST00000484416
  gene symbol: SLC37A3
  variant of: http://identifiers.org/hgnc/20651
canonical: true
consequence: splice region
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 6342
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 781
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2027
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7492
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 843
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9829
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1694
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3303
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4687
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 871
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 886
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1369
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 608
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7687
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10957
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 503
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4150
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3294
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15042
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: A
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: QD

7-140051256-A-AGAAG
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 140051256
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 140051260
    reference: chr 7
allele count: 6
allele frequency: 5.028579091168139e-5
allele num: 119318
alternate allele: AGAAG
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000412208
  ensembl transcript: ENST00000429996
  gene symbol: SLC37A3
  hgvsc: ENST00000429996.2:c.*599_*600insCTTC
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000417365
  ensembl transcript: ENST00000477571
  gene symbol: SLC37A3
  hgvsc: ENST00000477571.1:c.619-6_619-5insCTTC
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000397481
  ensembl transcript: ENST00000447932
  gene symbol: SLC37A3
  hgvsc: ENST00000447932.2:c.704-6_704-5insCTTC
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000418585
  ensembl transcript: ENST00000490760
  gene symbol: SLC37A3
  hgvsc: ENST00000490760.1:c.*253-6_*253-5insCTTC
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000343358
  ensembl transcript: ENST00000340308
  gene symbol: SLC37A3
  hgvsc: ENST00000340308.3:c.704-6_704-5insCTTC
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000321498
  ensembl transcript: ENST00000326232
  gene symbol: SLC37A3
  hgvsc: ENST00000326232.9:c.704-6_704-5insCTTC
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000419285
  ensembl transcript: ENST00000485734
  gene symbol: SLC37A3
  hgvsc: ENST00000485734.1:c.40-6_40-5insCTTC
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157800
  ensembl transcript: ENST00000460560
  gene symbol: SLC37A3
  hgvsc: ENST00000460560.1:n.1233_1234insCTTC
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000419701
  ensembl transcript: ENST00000484416
  gene symbol: SLC37A3
  hgvsc: ENST00000484416.1:c.*70-6_*70-5insCTTC
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000420771
  ensembl transcript: ENST00000485861
  gene symbol: SLC37A3
  hgvsc: ENST00000485861.1:c.393-2690_393-2689insCTTC
  variant of: http://identifiers.org/hgnc/20651
canonical: true
consequence: splice region
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1345
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6270
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2008
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1960
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 902
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4590
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7656
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10862
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 972
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 871
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9873
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7393
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 867
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3194
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4121
  bin: 8.25e1
  variant carriers: 0
hgvs: c.704-6_704-5insCTTC
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum

7-140051257-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 140051257
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 140051257
    reference: chr 7
allele count: 1
allele frequency: 8.383635144198524e-6
allele num: 119280
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000419285
  ensembl transcript: ENST00000485734
  gene symbol: SLC37A3
  hgvsc: ENST00000485734.1:c.40-6T>C
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000343358
  ensembl transcript: ENST00000340308
  gene symbol: SLC37A3
  hgvsc: ENST00000340308.3:c.704-6T>C
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157800
  ensembl transcript: ENST00000460560
  gene symbol: SLC37A3
  hgvsc: ENST00000460560.1:n.1233T>C
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000419701
  ensembl transcript: ENST00000484416
  gene symbol: SLC37A3
  hgvsc: ENST00000484416.1:c.*70-6T>C
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000321498
  ensembl transcript: ENST00000326232
  gene symbol: SLC37A3
  hgvsc: ENST00000326232.9:c.704-6T>C
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000397481
  ensembl transcript: ENST00000447932
  gene symbol: SLC37A3
  hgvsc: ENST00000447932.2:c.704-6T>C
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000417365
  ensembl transcript: ENST00000477571
  gene symbol: SLC37A3
  hgvsc: ENST00000477571.1:c.619-6T>C
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000412208
  ensembl transcript: ENST00000429996
  gene symbol: SLC37A3
  hgvsc: ENST00000429996.2:c.*599T>C
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000418585
  ensembl transcript: ENST00000490760
  gene symbol: SLC37A3
  hgvsc: ENST00000490760.1:c.*253-6T>C
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000420771
  ensembl transcript: ENST00000485861
  gene symbol: SLC37A3
  hgvsc: ENST00000485861.1:c.393-2690T>C
  variant of: http://identifiers.org/hgnc/20651
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 971
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7658
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6268
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 872
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 910
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3193
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1344
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4589
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7393
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10860
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2005
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 867
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9872
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1961
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6139
  bin: 6.75e1
  variant carriers: 0
hgvs: c.704-6T>C
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Other
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum

7-140051258-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 140051258
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 140051258
    reference: chr 7
allele count: 2
allele frequency: 1.679543164259321e-5
allele num: 119080
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000419285
  ensembl transcript: ENST00000485734
  gene symbol: SLC37A3
  hgvsc: ENST00000485734.1:c.40-7A>T
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000321498
  ensembl transcript: ENST00000326232
  gene symbol: SLC37A3
  hgvsc: ENST00000326232.9:c.704-7A>T
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000419701
  ensembl transcript: ENST00000484416
  gene symbol: SLC37A3
  hgvsc: ENST00000484416.1:c.*70-7A>T
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000417365
  ensembl transcript: ENST00000477571
  gene symbol: SLC37A3
  hgvsc: ENST00000477571.1:c.619-7A>T
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000412208
  ensembl transcript: ENST00000429996
  gene symbol: SLC37A3
  hgvsc: ENST00000429996.2:c.*598A>T
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000343358
  ensembl transcript: ENST00000340308
  gene symbol: SLC37A3
  hgvsc: ENST00000340308.3:c.704-7A>T
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000397481
  ensembl transcript: ENST00000447932
  gene symbol: SLC37A3
  hgvsc: ENST00000447932.2:c.704-7A>T
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157800
  ensembl transcript: ENST00000460560
  gene symbol: SLC37A3
  hgvsc: ENST00000460560.1:n.1232A>T
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000418585
  ensembl transcript: ENST00000490760
  gene symbol: SLC37A3
  hgvsc: ENST00000490760.1:c.*253-7A>T
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000420771
  ensembl transcript: ENST00000485861
  gene symbol: SLC37A3
  hgvsc: ENST00000485861.1:c.393-2691A>T
  variant of: http://identifiers.org/hgnc/20651
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4546
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9921
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6248
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 976
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7673
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3146
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 872
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 936
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1334
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7378
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1916
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 868
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2069
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10891
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4116
  bin: 8.25e1
  variant carriers: 0
hgvs: c.704-7A>T
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: Other
reference allele: T
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD

7-140051261-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 140051261
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 140051261
    reference: chr 7
allele count: 1
allele frequency: 8.551978927923921e-6
allele num: 116932
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000412208
  ensembl transcript: ENST00000429996
  gene symbol: SLC37A3
  hgvsc: ENST00000429996.2:c.*595G>C
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000418585
  ensembl transcript: ENST00000490760
  gene symbol: SLC37A3
  hgvsc: ENST00000490760.1:c.*253-10G>C
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000419701
  ensembl transcript: ENST00000484416
  gene symbol: SLC37A3
  hgvsc: ENST00000484416.1:c.*70-10G>C
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000343358
  ensembl transcript: ENST00000340308
  gene symbol: SLC37A3
  hgvsc: ENST00000340308.3:c.704-10G>C
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000420771
  ensembl transcript: ENST00000485861
  gene symbol: SLC37A3
  hgvsc: ENST00000485861.1:c.393-2694G>C
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000417365
  ensembl transcript: ENST00000477571
  gene symbol: SLC37A3
  hgvsc: ENST00000477571.1:c.619-10G>C
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157800
  ensembl transcript: ENST00000460560
  gene symbol: SLC37A3
  hgvsc: ENST00000460560.1:n.1229G>C
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000419285
  ensembl transcript: ENST00000485734
  gene symbol: SLC37A3
  hgvsc: ENST00000485734.1:c.40-10G>C
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000321498
  ensembl transcript: ENST00000326232
  gene symbol: SLC37A3
  hgvsc: ENST00000326232.9:c.704-10G>C
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000397481
  ensembl transcript: ENST00000447932
  gene symbol: SLC37A3
  hgvsc: ENST00000447932.2:c.704-10G>C
  variant of: http://identifiers.org/hgnc/20651
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10764
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 720
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 531
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7900
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7210
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6372
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1726
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1170
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4472
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2510
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1052
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2946
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1153
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 848
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10047
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2986
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 878
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1183
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP

http://identifiers.org/exac.variant/7-140051264-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 140051264
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 140051264
    reference: chr 7
allele count: 2
allele frequency: 1.69284940411701e-5
allele num: 118144
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000418585
  ensembl transcript: ENST00000490760
  gene symbol: SLC37A3
  hgvsc: ENST00000490760.1:c.*253-13G>T
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000420771
  ensembl transcript: ENST00000485861
  gene symbol: SLC37A3
  hgvsc: ENST00000485861.1:c.393-2697G>T
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000397481
  ensembl transcript: ENST00000447932
  gene symbol: SLC37A3
  hgvsc: ENST00000447932.2:c.704-13G>T
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000343358
  ensembl transcript: ENST00000340308
  gene symbol: SLC37A3
  hgvsc: ENST00000340308.3:c.704-13G>T
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000321498
  ensembl transcript: ENST00000326232
  gene symbol: SLC37A3
  hgvsc: ENST00000326232.9:c.704-13G>T
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000419285
  ensembl transcript: ENST00000485734
  gene symbol: SLC37A3
  hgvsc: ENST00000485734.1:c.40-13G>T
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000412208
  ensembl transcript: ENST00000429996
  gene symbol: SLC37A3
  hgvsc: ENST00000429996.2:c.*592G>T
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157800
  ensembl transcript: ENST00000460560
  gene symbol: SLC37A3
  hgvsc: ENST00000460560.1:n.1226G>T
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000419701
  ensembl transcript: ENST00000484416
  gene symbol: SLC37A3
  hgvsc: ENST00000484416.1:c.*70-13G>T
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000417365
  ensembl transcript: ENST00000477571
  gene symbol: SLC37A3
  hgvsc: ENST00000477571.1:c.619-13G>T
  variant of: http://identifiers.org/hgnc/20651
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6356
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1167
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2572
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 717
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7242
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1726
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4495
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9992
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7904
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1079
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1141
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2988
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 846
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10676
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17917
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 727
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3330
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
reference allele: C
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum

7-140051264-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 140051264
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 140051264
    reference: chr 7
allele count: 1
allele frequency: 8.464247020585048e-6
allele num: 118144
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000418585
  ensembl transcript: ENST00000490760
  gene symbol: SLC37A3
  hgvsc: ENST00000490760.1:c.*253-13G>A
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157800
  ensembl transcript: ENST00000460560
  gene symbol: SLC37A3
  hgvsc: ENST00000460560.1:n.1226G>A
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000417365
  ensembl transcript: ENST00000477571
  gene symbol: SLC37A3
  hgvsc: ENST00000477571.1:c.619-13G>A
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000343358
  ensembl transcript: ENST00000340308
  gene symbol: SLC37A3
  hgvsc: ENST00000340308.3:c.704-13G>A
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000412208
  ensembl transcript: ENST00000429996
  gene symbol: SLC37A3
  hgvsc: ENST00000429996.2:c.*592G>A
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000321498
  ensembl transcript: ENST00000326232
  gene symbol: SLC37A3
  hgvsc: ENST00000326232.9:c.704-13G>A
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000397481
  ensembl transcript: ENST00000447932
  gene symbol: SLC37A3
  hgvsc: ENST00000447932.2:c.704-13G>A
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000420771
  ensembl transcript: ENST00000485861
  gene symbol: SLC37A3
  hgvsc: ENST00000485861.1:c.393-2697G>A
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000419701
  ensembl transcript: ENST00000484416
  gene symbol: SLC37A3
  hgvsc: ENST00000484416.1:c.*70-13G>A
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000419285
  ensembl transcript: ENST00000485734
  gene symbol: SLC37A3
  hgvsc: ENST00000485734.1:c.40-13G>A
  variant of: http://identifiers.org/hgnc/20651
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4495
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7242
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1079
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1167
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7904
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1726
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2988
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2572
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10676
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9992
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 717
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6356
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1141
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 846
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 179
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 148
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 311
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Other
population: African
population: South Asian
population: European (Finnish)
population: Latino
reference allele: C
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: MQRankSum

7-140051265-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 140051265
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 140051265
    reference: chr 7
allele count: 4
allele frequency: 3.439794988218702e-5
allele num: 116286
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000397481
  ensembl transcript: ENST00000447932
  gene symbol: SLC37A3
  hgvsc: ENST00000447932.2:c.704-14C>T
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000343358
  ensembl transcript: ENST00000340308
  gene symbol: SLC37A3
  hgvsc: ENST00000340308.3:c.704-14C>T
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000419701
  ensembl transcript: ENST00000484416
  gene symbol: SLC37A3
  hgvsc: ENST00000484416.1:c.*70-14C>T
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000417365
  ensembl transcript: ENST00000477571
  gene symbol: SLC37A3
  hgvsc: ENST00000477571.1:c.619-14C>T
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000321498
  ensembl transcript: ENST00000326232
  gene symbol: SLC37A3
  hgvsc: ENST00000326232.9:c.704-14C>T
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157800
  ensembl transcript: ENST00000460560
  gene symbol: SLC37A3
  hgvsc: ENST00000460560.1:n.1225C>T
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000418585
  ensembl transcript: ENST00000490760
  gene symbol: SLC37A3
  hgvsc: ENST00000490760.1:c.*253-14C>T
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000412208
  ensembl transcript: ENST00000429996
  gene symbol: SLC37A3
  hgvsc: ENST00000429996.2:c.*591C>T
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000420771
  ensembl transcript: ENST00000485861
  gene symbol: SLC37A3
  hgvsc: ENST00000485861.1:c.393-2698C>T
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000419285
  ensembl transcript: ENST00000485734
  gene symbol: SLC37A3
  hgvsc: ENST00000485734.1:c.40-14C>T
  variant of: http://identifiers.org/hgnc/20651
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7194
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7914
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1194
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2705
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2932
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4462
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1129
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1119
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 846
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9915
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6351
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1684
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10565
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 609
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4427
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 218
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
population: East Asian
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/7-140051266-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 140051266
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 140051266
    reference: chr 7
allele count: 981
allele frequency: 8.784497734477139e-3
allele num: 111674
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157800
  ensembl transcript: ENST00000460560
  gene symbol: SLC37A3
  hgvsc: ENST00000460560.1:n.1224T>G
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000418585
  ensembl transcript: ENST00000490760
  gene symbol: SLC37A3
  hgvsc: ENST00000490760.1:c.*253-15T>G
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000321498
  ensembl transcript: ENST00000326232
  gene symbol: SLC37A3
  hgvsc: ENST00000326232.9:c.704-15T>G
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000420771
  ensembl transcript: ENST00000485861
  gene symbol: SLC37A3
  hgvsc: ENST00000485861.1:c.393-2699T>G
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000417365
  ensembl transcript: ENST00000477571
  gene symbol: SLC37A3
  hgvsc: ENST00000477571.1:c.619-15T>G
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000397481
  ensembl transcript: ENST00000447932
  gene symbol: SLC37A3
  hgvsc: ENST00000447932.2:c.704-15T>G
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000412208
  ensembl transcript: ENST00000429996
  gene symbol: SLC37A3
  hgvsc: ENST00000429996.2:c.*590T>G
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000419701
  ensembl transcript: ENST00000484416
  gene symbol: SLC37A3
  hgvsc: ENST00000484416.1:c.*70-15T>G
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000419285
  ensembl transcript: ENST00000485734
  gene symbol: SLC37A3
  hgvsc: ENST00000485734.1:c.40-15T>G
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000343358
  ensembl transcript: ENST00000340308
  gene symbol: SLC37A3
  hgvsc: ENST00000340308.3:c.704-15T>G
  variant of: http://identifiers.org/hgnc/20651
canonical: false
consequence: 3' UTR
filter: VQSRTrancheSNP99.90to99.95
genotype depth: GenotypeDepth
  all individuals: 6392
  bin: 4.25e1
  variant carriers: 132
genotype depth: GenotypeDepth
  all individuals: 2668
  bin: 1.25e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 1133
  bin: 1.75e1
  variant carriers: 48
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 8.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 4557
  bin: 4.75e1
  variant carriers: 129
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 7.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 7913
  bin: 3.75e1
  variant carriers: 132
genotype depth: GenotypeDepth
  all individuals: 1112
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 857
  bin: 9.75e1
  variant carriers: 33
genotype depth: GenotypeDepth
  all individuals: 1121
  bin: 6.25e1
  variant carriers: 34
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 7.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 8.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 9798
  bin: 3.25e1
  variant carriers: 96
genotype depth: GenotypeDepth
  all individuals: 10499
  bin: 2.75e1
  variant carriers: 80
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 6.75e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 2973
  bin: 5.25e1
  variant carriers: 87
genotype depth: GenotypeDepth
  all individuals: 1733
  bin: 5.75e1
  variant carriers: 73
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 9.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 7095
  bin: 2.25e1
  variant carriers: 64
genotype quality: GenotypeQuality
  all individuals: 3987
  bin: 8.25e1
  variant carriers: 17
genotype quality: GenotypeQuality
  all individuals: 141
  bin: 5.25e1
  variant carriers: 17
genotype quality: GenotypeQuality
  all individuals: 12072
  bin: 6.25e1
  variant carriers: 15
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
reference allele: A
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum

7-140051268-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 140051268
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 140051268
    reference: chr 7
allele count: 2
allele frequency: 1.680474566017443e-5
allele num: 119014
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000417365
  ensembl transcript: ENST00000477571
  gene symbol: SLC37A3
  hgvsc: ENST00000477571.1:c.619-17T>C
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000419285
  ensembl transcript: ENST00000485734
  gene symbol: SLC37A3
  hgvsc: ENST00000485734.1:c.40-17T>C
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000412208
  ensembl transcript: ENST00000429996
  gene symbol: SLC37A3
  hgvsc: ENST00000429996.2:c.*588T>C
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000397481
  ensembl transcript: ENST00000447932
  gene symbol: SLC37A3
  hgvsc: ENST00000447932.2:c.704-17T>C
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000321498
  ensembl transcript: ENST00000326232
  gene symbol: SLC37A3
  hgvsc: ENST00000326232.9:c.704-17T>C
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000418585
  ensembl transcript: ENST00000490760
  gene symbol: SLC37A3
  hgvsc: ENST00000490760.1:c.*253-17T>C
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000419701
  ensembl transcript: ENST00000484416
  gene symbol: SLC37A3
  hgvsc: ENST00000484416.1:c.*70-17T>C
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000343358
  ensembl transcript: ENST00000340308
  gene symbol: SLC37A3
  hgvsc: ENST00000340308.3:c.704-17T>C
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000420771
  ensembl transcript: ENST00000485861
  gene symbol: SLC37A3
  hgvsc: ENST00000485861.1:c.393-2701T>C
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157800
  ensembl transcript: ENST00000460560
  gene symbol: SLC37A3
  hgvsc: ENST00000460560.1:n.1222T>C
  variant of: http://identifiers.org/hgnc/20651
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 919
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2970
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7612
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10347
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2515
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1827
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1295
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6776
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9611
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 830
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6155
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 625
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1065
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1527
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4390
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20936
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 124
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 590
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
population: Other
reference allele: A
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD

http://identifiers.org/exac.variant/7-140051270-C-CCA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 140051270
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 140051272
    reference: chr 7
allele count: 1
allele frequency: 8.412126922171002e-6
allele num: 118876
alternate allele: CCA
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000419285
  ensembl transcript: ENST00000485734
  gene symbol: SLC37A3
  hgvsc: ENST00000485734.1:c.40-21_40-20dupTG
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000419701
  ensembl transcript: ENST00000484416
  gene symbol: SLC37A3
  hgvsc: ENST00000484416.1:c.*70-21_*70-20dupTG
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000418585
  ensembl transcript: ENST00000490760
  gene symbol: SLC37A3
  hgvsc: ENST00000490760.1:c.*253-21_*253-20dupTG
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157800
  ensembl transcript: ENST00000460560
  gene symbol: SLC37A3
  hgvsc: ENST00000460560.1:n.1218_1219dupTG
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000321498
  ensembl transcript: ENST00000326232
  gene symbol: SLC37A3
  hgvsc: ENST00000326232.9:c.704-21_704-20dupTG
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000417365
  ensembl transcript: ENST00000477571
  gene symbol: SLC37A3
  hgvsc: ENST00000477571.1:c.619-21_619-20dupTG
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000397481
  ensembl transcript: ENST00000447932
  gene symbol: SLC37A3
  hgvsc: ENST00000447932.2:c.704-21_704-20dupTG
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000412208
  ensembl transcript: ENST00000429996
  gene symbol: SLC37A3
  hgvsc: ENST00000429996.2:c.*584_*585dupTG
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000420771
  ensembl transcript: ENST00000485861
  gene symbol: SLC37A3
  hgvsc: ENST00000485861.1:c.393-2705_393-2704dupTG
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000343358
  ensembl transcript: ENST00000340308
  gene symbol: SLC37A3
  hgvsc: ENST00000340308.3:c.704-21_704-20dupTG
  variant of: http://identifiers.org/hgnc/20651
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6685
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2971
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 921
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7605
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1093
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9589
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 885
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6151
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4386
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1527
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2638
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 625
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1827
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 753
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10265
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1294
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 117
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 131
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
population: European (Finnish)
population: African
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP

7-140051294-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 140051294
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 140051294
    reference: chr 7
allele count: 1
allele frequency: 8.514261387824607e-6
allele num: 117450
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000397481
  ensembl transcript: ENST00000447932
  gene symbol: SLC37A3
  hgvsc: ENST00000447932.2:c.704-43G>A
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157800
  ensembl transcript: ENST00000460560
  gene symbol: SLC37A3
  hgvsc: ENST00000460560.1:n.1196G>A
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000419701
  ensembl transcript: ENST00000484416
  gene symbol: SLC37A3
  hgvsc: ENST00000484416.1:c.*70-43G>A
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000343358
  ensembl transcript: ENST00000340308
  gene symbol: SLC37A3
  hgvsc: ENST00000340308.3:c.704-43G>A
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000412208
  ensembl transcript: ENST00000429996
  gene symbol: SLC37A3
  hgvsc: ENST00000429996.2:c.*562G>A
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000420771
  ensembl transcript: ENST00000485861
  gene symbol: SLC37A3
  hgvsc: ENST00000485861.1:c.393-2727G>A
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000321498
  ensembl transcript: ENST00000326232
  gene symbol: SLC37A3
  hgvsc: ENST00000326232.9:c.704-43G>A
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000418585
  ensembl transcript: ENST00000490760
  gene symbol: SLC37A3
  hgvsc: ENST00000490760.1:c.*253-43G>A
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000417365
  ensembl transcript: ENST00000477571
  gene symbol: SLC37A3
  hgvsc: ENST00000477571.1:c.619-43G>A
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000419285
  ensembl transcript: ENST00000485734
  gene symbol: SLC37A3
  hgvsc: ENST00000485734.1:c.40-43G>A
  variant of: http://identifiers.org/hgnc/20651
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2969
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1292
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8729
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6105
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3041
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6194
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1827
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7520
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1526
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2626
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 920
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4382
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 752
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8972
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1616
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 577
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 622
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5123
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2536
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 951
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
population: African
reference allele: C
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum

7-140051295-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 140051295
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 140051295
    reference: chr 7
allele count: 19
allele frequency: 1.618122977346278e-4
allele num: 117420
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000419701
  ensembl transcript: ENST00000484416
  gene symbol: SLC37A3
  hgvsc: ENST00000484416.1:c.*70-44C>T
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000419285
  ensembl transcript: ENST00000485734
  gene symbol: SLC37A3
  hgvsc: ENST00000485734.1:c.40-44C>T
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000412208
  ensembl transcript: ENST00000429996
  gene symbol: SLC37A3
  hgvsc: ENST00000429996.2:c.*561C>T
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000321498
  ensembl transcript: ENST00000326232
  gene symbol: SLC37A3
  hgvsc: ENST00000326232.9:c.704-44C>T
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000343358
  ensembl transcript: ENST00000340308
  gene symbol: SLC37A3
  hgvsc: ENST00000340308.3:c.704-44C>T
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000397481
  ensembl transcript: ENST00000447932
  gene symbol: SLC37A3
  hgvsc: ENST00000447932.2:c.704-44C>T
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000417365
  ensembl transcript: ENST00000477571
  gene symbol: SLC37A3
  hgvsc: ENST00000477571.1:c.619-44C>T
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157800
  ensembl transcript: ENST00000460560
  gene symbol: SLC37A3
  hgvsc: ENST00000460560.1:n.1195C>T
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000418585
  ensembl transcript: ENST00000490760
  gene symbol: SLC37A3
  hgvsc: ENST00000490760.1:c.*253-44C>T
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000420771
  ensembl transcript: ENST00000485861
  gene symbol: SLC37A3
  hgvsc: ENST00000485861.1:c.393-2728C>T
  variant of: http://identifiers.org/hgnc/20651
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7509
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6106
  bin: 4.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 2598
  bin: 1.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 6343
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 577
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8913
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1826
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4378
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8650
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 752
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 622
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1526
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1652
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3036
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1293
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 919
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2970
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 861
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2487
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9119
  bin: 6.25e1
  variant carriers: 1
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum

7-140051709-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 140051709
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 140051709
    reference: chr 7
allele count: 103
allele frequency: 6.82661717921527e-3
allele num: 15088
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000419701
  ensembl transcript: ENST00000484416
  gene symbol: SLC37A3
  hgvsc: ENST00000484416.1:c.*69+153C>T
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000417365
  ensembl transcript: ENST00000477571
  gene symbol: SLC37A3
  hgvsc: ENST00000477571.1:c.619-458C>T
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000412208
  ensembl transcript: ENST00000429996
  gene symbol: SLC37A3
  hgvsc: ENST00000429996.2:c.*147C>T
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000418585
  ensembl transcript: ENST00000490760
  gene symbol: SLC37A3
  hgvsc: ENST00000490760.1:c.*252+153C>T
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157800
  ensembl transcript: ENST00000464865
  gene symbol: SLC37A3
  hgvsc: ENST00000464865.1:n.839C>T
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157800
  ensembl transcript: ENST00000460560
  gene symbol: SLC37A3
  hgvsc: ENST00000460560.1:n.781C>T
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157800
  ensembl transcript: ENST00000473707
  gene symbol: SLC37A3
  hgvsc: ENST00000473707.1:n.566C>T
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000419285
  ensembl transcript: ENST00000485734
  gene symbol: SLC37A3
  hgvsc: ENST00000485734.1:c.39+153C>T
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000420771
  ensembl transcript: ENST00000485861
  gene symbol: SLC37A3
  hgvsc: ENST00000485861.1:c.393-3142C>T
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000417449
  ensembl transcript: ENST00000464834
  gene symbol: SLC37A3
  hgvsc: ENST00000464834.1:c.*130C>T
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000321498
  ensembl transcript: ENST00000326232
  gene symbol: SLC37A3
  hgvsc: ENST00000326232.9:c.703+153C>T
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000343358
  ensembl transcript: ENST00000340308
  gene symbol: SLC37A3
  hgvsc: ENST00000340308.3:c.703+153C>T
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000397481
  ensembl transcript: ENST00000447932
  gene symbol: SLC37A3
  hgvsc: ENST00000447932.2:c.703+153C>T
  variant of: http://identifiers.org/hgnc/20651
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2658
  bin: 7.5e0
  variant carriers: 31
genotype depth: GenotypeDepth
  all individuals: 867
  bin: 3.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 808
  bin: 3.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 2.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1086
  bin: 1.25e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 24888
  bin: 2.5e0
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 926
  bin: 2.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 1.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 6.25e1
  variant carriers: 7
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: East Asian
reference allele: G
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum

7-140051717-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 140051717
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 140051717
    reference: chr 7
allele count: 1
allele frequency: 6.591957811470006e-5
allele num: 15170
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000419285
  ensembl transcript: ENST00000485734
  gene symbol: SLC37A3
  hgvsc: ENST00000485734.1:c.39+145A>G
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000321498
  ensembl transcript: ENST00000326232
  gene symbol: SLC37A3
  hgvsc: ENST00000326232.9:c.703+145A>G
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000343358
  ensembl transcript: ENST00000340308
  gene symbol: SLC37A3
  hgvsc: ENST00000340308.3:c.703+145A>G
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157800
  ensembl transcript: ENST00000460560
  gene symbol: SLC37A3
  hgvsc: ENST00000460560.1:n.773A>G
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000418585
  ensembl transcript: ENST00000490760
  gene symbol: SLC37A3
  hgvsc: ENST00000490760.1:c.*252+145A>G
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000412208
  ensembl transcript: ENST00000429996
  gene symbol: SLC37A3
  hgvsc: ENST00000429996.2:c.*139A>G
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157800
  ensembl transcript: ENST00000473707
  gene symbol: SLC37A3
  hgvsc: ENST00000473707.1:n.558A>G
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000397481
  ensembl transcript: ENST00000447932
  gene symbol: SLC37A3
  hgvsc: ENST00000447932.2:c.703+145A>G
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000417449
  ensembl transcript: ENST00000464834
  gene symbol: SLC37A3
  hgvsc: ENST00000464834.1:c.*122A>G
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157800
  ensembl transcript: ENST00000464865
  gene symbol: SLC37A3
  hgvsc: ENST00000464865.1:n.831A>G
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000420771
  ensembl transcript: ENST00000485861
  gene symbol: SLC37A3
  hgvsc: ENST00000485861.1:c.393-3150A>G
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000417365
  ensembl transcript: ENST00000477571
  gene symbol: SLC37A3
  hgvsc: ENST00000477571.1:c.619-466A>G
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000419701
  ensembl transcript: ENST00000484416
  gene symbol: SLC37A3
  hgvsc: ENST00000484416.1:c.*69+145A>G
  variant of: http://identifiers.org/hgnc/20651
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 936
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 733
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 637
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1099
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 880
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24955
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2680
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: Other
reference allele: T
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum

7-140051722-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 140051722
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 140051722
    reference: chr 7
allele count: 782
allele frequency: 5.116461659251505e-2
allele num: 15284
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000417449
  ensembl transcript: ENST00000464834
  gene symbol: SLC37A3
  hgvsc: ENST00000464834.1:c.*117G>A
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000412208
  ensembl transcript: ENST00000429996
  gene symbol: SLC37A3
  hgvsc: ENST00000429996.2:c.*134G>A
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000417365
  ensembl transcript: ENST00000477571
  gene symbol: SLC37A3
  hgvsc: ENST00000477571.1:c.619-471G>A
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157800
  ensembl transcript: ENST00000473707
  gene symbol: SLC37A3
  hgvsc: ENST00000473707.1:n.553G>A
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157800
  ensembl transcript: ENST00000464865
  gene symbol: SLC37A3
  hgvsc: ENST00000464865.1:n.826G>A
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157800
  ensembl transcript: ENST00000460560
  gene symbol: SLC37A3
  hgvsc: ENST00000460560.1:n.768G>A
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000419701
  ensembl transcript: ENST00000484416
  gene symbol: SLC37A3
  hgvsc: ENST00000484416.1:c.*69+140G>A
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000343358
  ensembl transcript: ENST00000340308
  gene symbol: SLC37A3
  hgvsc: ENST00000340308.3:c.703+140G>A
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000321498
  ensembl transcript: ENST00000326232
  gene symbol: SLC37A3
  hgvsc: ENST00000326232.9:c.703+140G>A
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000397481
  ensembl transcript: ENST00000447932
  gene symbol: SLC37A3
  hgvsc: ENST00000447932.2:c.703+140G>A
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000418585
  ensembl transcript: ENST00000490760
  gene symbol: SLC37A3
  hgvsc: ENST00000490760.1:c.*252+140G>A
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000420771
  ensembl transcript: ENST00000485861
  gene symbol: SLC37A3
  hgvsc: ENST00000485861.1:c.393-3155G>A
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000419285
  ensembl transcript: ENST00000485734
  gene symbol: SLC37A3
  hgvsc: ENST00000485734.1:c.39+140G>A
  variant of: http://identifiers.org/hgnc/20651
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 1.75e1
  variant carriers: 64
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 5.75e1
  variant carriers: 56
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 2.25e1
  variant carriers: 34
genotype depth: GenotypeDepth
  all individuals: 1153
  bin: 1.25e1
  variant carriers: 101
genotype depth: GenotypeDepth
  all individuals: 727
  bin: 4.75e1
  variant carriers: 62
genotype depth: GenotypeDepth
  all individuals: 955
  bin: 2.75e1
  variant carriers: 29
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.25e1
  variant carriers: 43
genotype depth: GenotypeDepth
  all individuals: 24803
  bin: 2.5e0
  variant carriers: 168
genotype depth: GenotypeDepth
  all individuals: 2767
  bin: 7.5e0
  variant carriers: 211
genotype depth: GenotypeDepth
  all individuals: 793
  bin: 4.25e1
  variant carriers: 58
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 6.25e1
  variant carriers: 59
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 5.25e1
  variant carriers: 69
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 7.75e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 867
  bin: 3.25e1
  variant carriers: 28
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.75e1
  variant carriers: 10
genotype quality: GenotypeQuality
num of homozygotes: 33
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
population: Other
reference allele: C
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP

7-140051723-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 140051723
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 140051723
    reference: chr 7
allele count: 4
allele frequency: 2.591009198082653e-4
allele num: 15438
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157800
  ensembl transcript: ENST00000473707
  gene symbol: SLC37A3
  hgvsc: ENST00000473707.1:n.552C>T
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000397481
  ensembl transcript: ENST00000447932
  gene symbol: SLC37A3
  hgvsc: ENST00000447932.2:c.703+139C>T
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000417449
  ensembl transcript: ENST00000464834
  gene symbol: SLC37A3
  hgvsc: ENST00000464834.1:c.*116C>T
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000417365
  ensembl transcript: ENST00000477571
  gene symbol: SLC37A3
  hgvsc: ENST00000477571.1:c.619-472C>T
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000343358
  ensembl transcript: ENST00000340308
  gene symbol: SLC37A3
  hgvsc: ENST00000340308.3:c.703+139C>T
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157800
  ensembl transcript: ENST00000464865
  gene symbol: SLC37A3
  hgvsc: ENST00000464865.1:n.825C>T
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000419285
  ensembl transcript: ENST00000485734
  gene symbol: SLC37A3
  hgvsc: ENST00000485734.1:c.39+139C>T
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000420771
  ensembl transcript: ENST00000485861
  gene symbol: SLC37A3
  hgvsc: ENST00000485861.1:c.393-3156C>T
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157800
  ensembl transcript: ENST00000460560
  gene symbol: SLC37A3
  hgvsc: ENST00000460560.1:n.767C>T
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000412208
  ensembl transcript: ENST00000429996
  gene symbol: SLC37A3
  hgvsc: ENST00000429996.2:c.*133C>T
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000321498
  ensembl transcript: ENST00000326232
  gene symbol: SLC37A3
  hgvsc: ENST00000326232.9:c.703+139C>T
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000419701
  ensembl transcript: ENST00000484416
  gene symbol: SLC37A3
  hgvsc: ENST00000484416.1:c.*69+139C>T
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000418585
  ensembl transcript: ENST00000490760
  gene symbol: SLC37A3
  hgvsc: ENST00000490760.1:c.*252+139C>T
  variant of: http://identifiers.org/hgnc/20651
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25534
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 784
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 788
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2763
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1146
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1078
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: Latino
population: East Asian
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQ

7-140051724-GC-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 140051724
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 140051723
    reference: chr 7
allele count: 1
allele frequency: 6.466632177961717e-5
allele num: 15464
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157800
  ensembl transcript: ENST00000460560
  gene symbol: SLC37A3
  hgvsc: ENST00000460560.1:n.765delG
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000321498
  ensembl transcript: ENST00000326232
  gene symbol: SLC37A3
  hgvsc: ENST00000326232.9:c.703+137delG
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000417449
  ensembl transcript: ENST00000464834
  gene symbol: SLC37A3
  hgvsc: ENST00000464834.1:c.*114delG
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000343358
  ensembl transcript: ENST00000340308
  gene symbol: SLC37A3
  hgvsc: ENST00000340308.3:c.703+137delG
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000412208
  ensembl transcript: ENST00000429996
  gene symbol: SLC37A3
  hgvsc: ENST00000429996.2:c.*131delG
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157800
  ensembl transcript: ENST00000464865
  gene symbol: SLC37A3
  hgvsc: ENST00000464865.1:n.823delG
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000420771
  ensembl transcript: ENST00000485861
  gene symbol: SLC37A3
  hgvsc: ENST00000485861.1:c.393-3158delG
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000419285
  ensembl transcript: ENST00000485734
  gene symbol: SLC37A3
  hgvsc: ENST00000485734.1:c.39+137delG
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000397481
  ensembl transcript: ENST00000447932
  gene symbol: SLC37A3
  hgvsc: ENST00000447932.2:c.703+137delG
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157800
  ensembl transcript: ENST00000473707
  gene symbol: SLC37A3
  hgvsc: ENST00000473707.1:n.550delG
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000419701
  ensembl transcript: ENST00000484416
  gene symbol: SLC37A3
  hgvsc: ENST00000484416.1:c.*69+137delG
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000417365
  ensembl transcript: ENST00000477571
  gene symbol: SLC37A3
  hgvsc: ENST00000477571.1:c.619-474delG
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000418585
  ensembl transcript: ENST00000490760
  gene symbol: SLC37A3
  hgvsc: ENST00000490760.1:c.*252+137delG
  variant of: http://identifiers.org/hgnc/20651
canonical: false
consequence: 3' UTR
filter: VQSRTrancheINDEL95.00to96.00
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 916
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 784
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1146
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1079
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25677
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2788
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: GC
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum

7-140051751-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 140051751
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 140051751
    reference: chr 7
allele count: 0
allele frequency: 0.0e0
allele num: 16566
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000420771
  ensembl transcript: ENST00000485861
  gene symbol: SLC37A3
  hgvsc: ENST00000485861.1:c.393-3184T>C
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000397481
  ensembl transcript: ENST00000447932
  gene symbol: SLC37A3
  hgvsc: ENST00000447932.2:c.703+111T>C
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000419285
  ensembl transcript: ENST00000485734
  gene symbol: SLC37A3
  hgvsc: ENST00000485734.1:c.39+111T>C
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157800
  ensembl transcript: ENST00000460560
  gene symbol: SLC37A3
  hgvsc: ENST00000460560.1:n.739T>C
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000343358
  ensembl transcript: ENST00000340308
  gene symbol: SLC37A3
  hgvsc: ENST00000340308.3:c.703+111T>C
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000412208
  ensembl transcript: ENST00000429996
  gene symbol: SLC37A3
  hgvsc: ENST00000429996.2:c.*105T>C
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000418585
  ensembl transcript: ENST00000490760
  gene symbol: SLC37A3
  hgvsc: ENST00000490760.1:c.*252+111T>C
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000419701
  ensembl transcript: ENST00000484416
  gene symbol: SLC37A3
  hgvsc: ENST00000484416.1:c.*69+111T>C
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157800
  ensembl transcript: ENST00000464865
  gene symbol: SLC37A3
  hgvsc: ENST00000464865.1:n.797T>C
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157800
  ensembl transcript: ENST00000473707
  gene symbol: SLC37A3
  hgvsc: ENST00000473707.1:n.524T>C
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000417449
  ensembl transcript: ENST00000464834
  gene symbol: SLC37A3
  hgvsc: ENST00000464834.1:c.*88T>C
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000321498
  ensembl transcript: ENST00000326232
  gene symbol: SLC37A3
  hgvsc: ENST00000326232.9:c.703+111T>C
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000417365
  ensembl transcript: ENST00000477571
  gene symbol: SLC37A3
  hgvsc: ENST00000477571.1:c.619-500T>C
  variant of: http://identifiers.org/hgnc/20651
canonical: false
consequence: 3' UTR
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 31895
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 877
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 788
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1513
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4977
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1244
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
population: African
reference allele: A
site quality: DP
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD

7-140051769-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 140051769
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 140051769
    reference: chr 7
allele count: 0
allele frequency: 0.0e0
allele num: 18384
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000420771
  ensembl transcript: ENST00000485861
  gene symbol: SLC37A3
  hgvsc: ENST00000485861.1:c.393-3202G>A
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000419285
  ensembl transcript: ENST00000485734
  gene symbol: SLC37A3
  hgvsc: ENST00000485734.1:c.39+93G>A
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000157800
  ensembl transcript: ENST00000473707
  gene symbol: SLC37A3
  hgvsc: ENST00000473707.1:n.506G>A
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000321498
  ensembl transcript: ENST00000326232
  gene symbol: SLC37A3
  hgvsc: ENST00000326232.9:c.703+93G>A
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000397481
  ensembl transcript: ENST00000447932
  gene symbol: SLC37A3
  hgvsc: ENST00000447932.2:c.703+93G>A
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000343358
  ensembl transcript: ENST00000340308
  gene symbol: SLC37A3
  hgvsc: ENST00000340308.3:c.703+93G>A
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000412208
  ensembl transcript: ENST00000429996
  gene symbol: SLC37A3
  hgvsc: ENST00000429996.2:c.*87G>A
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000417449
  ensembl transcript: ENST00000464834
  gene symbol: SLC37A3
  hgvsc: ENST00000464834.1:c.*70G>A
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000157800
  ensembl transcript: ENST00000464865
  gene symbol: SLC37A3
  hgvsc: ENST00000464865.1:n.779G>A
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000418585
  ensembl transcript: ENST00000490760
  gene symbol: SLC37A3
  hgvsc: ENST00000490760.1:c.*252+93G>A
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000417365
  ensembl transcript: ENST00000477571
  gene symbol: SLC37A3
  hgvsc: ENST00000477571.1:c.619-518G>A
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000157800
  ensembl transcript: ENST00000460560
  gene symbol: SLC37A3
  hgvsc: ENST00000460560.1:n.721G>A
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000419701
  ensembl transcript: ENST00000484416
  gene symbol: SLC37A3
  hgvsc: ENST00000484416.1:c.*69+93G>A
  variant of: http://identifiers.org/hgnc/20651
canonical: false
consequence: splice region
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2270
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9909
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1479
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 818
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1005
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 789
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 809
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33389
  bin: 2.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: n.721G>A
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
population: European (Finnish)
population: African
population: Latino
reference allele: C
site quality: FS
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD

7-140051782-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 140051782
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 140051782
    reference: chr 7
allele count: 0
allele frequency: 0.0e0
allele num: 20808
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl transcript: ENST00000464865
  gene symbol: SLC37A3
  hgvsc: ENST00000464865.1:n.779-13T>A
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000397481
  ensembl transcript: ENST00000447932
  gene symbol: SLC37A3
  hgvsc: ENST00000447932.2:c.703+80T>A
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000343358
  ensembl transcript: ENST00000340308
  gene symbol: SLC37A3
  hgvsc: ENST00000340308.3:c.703+80T>A
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000417449
  ensembl transcript: ENST00000464834
  gene symbol: SLC37A3
  hgvsc: ENST00000464834.1:c.*70-13T>A
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000412208
  ensembl transcript: ENST00000429996
  gene symbol: SLC37A3
  hgvsc: ENST00000429996.2:c.*87-13T>A
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000420771
  ensembl transcript: ENST00000485861
  gene symbol: SLC37A3
  hgvsc: ENST00000485861.1:c.393-3215T>A
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl transcript: ENST00000460560
  gene symbol: SLC37A3
  hgvsc: ENST00000460560.1:n.721-13T>A
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000419285
  ensembl transcript: ENST00000485734
  gene symbol: SLC37A3
  hgvsc: ENST00000485734.1:c.39+80T>A
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000418585
  ensembl transcript: ENST00000490760
  gene symbol: SLC37A3
  hgvsc: ENST00000490760.1:c.*252+80T>A
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl transcript: ENST00000473707
  gene symbol: SLC37A3
  hgvsc: ENST00000473707.1:n.506-13T>A
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000417365
  ensembl transcript: ENST00000477571
  gene symbol: SLC37A3
  hgvsc: ENST00000477571.1:c.619-531T>A
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000419701
  ensembl transcript: ENST00000484416
  gene symbol: SLC37A3
  hgvsc: ENST00000484416.1:c.*69+80T>A
  variant of: http://identifiers.org/hgnc/20651
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157800
  ensembl protein: ENSP00000321498
  ensembl transcript: ENST00000326232
  gene symbol: SLC37A3
  hgvsc: ENST00000326232.9:c.703+80T>A
  variant of: http://identifiers.org/hgnc/20651
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 1674
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3069
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
reference allele: A

GenotypeQuality
all individuals: 2713
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3344
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 206
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 542
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3116
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9343
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 11435
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 497
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6324
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2579
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2612
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 319
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2040
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1494
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1807
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1501
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4187
bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.110903717529942e-5
allele num: 64290
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6508
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8334
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12920
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11278
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10220
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 838
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.22e-1

QD
type: SiteQuality
SIO_000300: 9.859999999999999e0

BaseQRankSum
type: SiteQuality
SIO_000300: -8.3e-1

FS
type: SiteQuality
SIO_000300: 1.79e0

MQRankSum
type: SiteQuality
SIO_000300: 8.129999999999999e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.98e-1

DP
type: SiteQuality
SIO_000300: 1.661929e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.74e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.4e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 158
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 12892
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6427
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 281
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2878
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1733
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4194
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2602
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 310
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1703
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 417
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3122
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9342
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2858
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1517
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2060
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3342
bin: 8.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6500
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 832
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10240
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8332
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13062
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11292
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.554678026180778e-5
allele num: 64322
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.1e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.64e-1

FS
type: SiteQuality
SIO_000300: 1.165e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.22e0

DP
type: SiteQuality
SIO_000300: 1.669884e6

MQRankSum
type: SiteQuality
SIO_000300: 4.44e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.3e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 6.51e-1

QD
type: SiteQuality
SIO_000300: 7.43e0

GenotypeQuality
all individuals: 3003
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1517
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 281
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2858
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 12892
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2878
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1703
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4194
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 310
bin: 1.25e1
variant carriers: 1

GenotypeQuality
all individuals: 417
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1488
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9342
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 374
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2060
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3342
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3122
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6427
bin: 6.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13062
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6500
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11292
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.109356052361556e-5
allele num: 64322
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10240
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8332
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 832
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.22e0

DP
type: SiteQuality
SIO_000300: 1.669884e6

VQSLOD
type: SiteQuality
SIO_000300: 6.51e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.1e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.3e-3

MQRankSum
type: SiteQuality
SIO_000300: 4.44e-1

FS
type: SiteQuality
SIO_000300: 1.165e0

QD
type: SiteQuality
SIO_000300: 7.43e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.64e-1

GenotypeQuality
all individuals: 2177
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4616
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1217
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 198
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 137
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 413
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 137
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 303
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 97
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2910
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3387
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18209
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1645
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9423
bin: 9.75e1
variant carriers: 21

GenotypeQuality
all individuals: 3673
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7043
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 746
bin: 4.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11352
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6524
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10276
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.176470588235294e-3
allele num: 850
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13236
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 8
allele frequency: 1.237930180737806e-4
allele num: 64624
num of homozygotes: 0

East Asian
type: Population
allele count: 12
allele frequency: 1.42721217887726e-3
allele num: 8408
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.721293e6

VQSLOD
type: SiteQuality
SIO_000300: 3.03e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.04e-1

FS
type: SiteQuality
SIO_000300: 1.049e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -8.699999999999999e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -2.9e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -3.039e0

QD
type: SiteQuality
SIO_000300: 1.277e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

GenotypeQuality
all individuals: 7517
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20275
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 253
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3582
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3985
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 341
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 314
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5018
bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2470
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2309
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 2.5e0
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GenotypeQuality
all individuals: 93
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1193
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9509
bin: 9.75e1
variant carriers: 1

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 860
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6544
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.535862386730149e-5
allele num: 65110
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13764
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10324
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8502
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11426
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.3e-3

DP
type: SiteQuality
SIO_000300: 1.768239e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.65e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 6.885e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.73e-1

MQRankSum
type: SiteQuality
SIO_000300: -4.9e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -2.854e0

VQSLOD
type: SiteQuality
SIO_000300: 7.98e-1

QD
type: SiteQuality
SIO_000300: 1.339e1

GenotypeQuality
all individuals: 93
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1751
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3985
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5018
bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 9509
bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20275
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1193
bin: 3.25e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 9.686168151879117e-5
allele num: 10324
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 860
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8502
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6544
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11426
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13764
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65110
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 6.885e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.73e-1

DP
type: SiteQuality
SIO_000300: 1.768239e6

VQSLOD
type: SiteQuality
SIO_000300: 7.98e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.65e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.854e0

MQRankSum
type: SiteQuality
SIO_000300: -4.9e-2

QD
type: SiteQuality
SIO_000300: 1.339e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.3e-3

GenotypeQuality
all individuals: 711
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3611
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 266
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 122
bin: 5.75e1
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GenotypeQuality
all individuals: 1768
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 796
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variant carriers: 0

GenotypeQuality
all individuals: 224
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 20709
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GenotypeQuality
all individuals: 1076
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9525
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 292
bin: 4.75e1
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GenotypeQuality
all individuals: 7570
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4023
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2334
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11434
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 862
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13856
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 1.934984520123839e-4
allele num: 10336
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65160
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8518
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6550
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -4.09e-1

FS
type: SiteQuality
SIO_000300: 1.4642e1

MQ
type: SiteQuality
SIO_000300: 5.954e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.299999999999999e-3

QD
type: SiteQuality
SIO_000300: 3.068e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.53e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.73e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.57e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.356e0

DP
type: SiteQuality
SIO_000300: 1.774609e6

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

GenotypeQuality
all individuals: 2408
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4170
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5255
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variant carriers: 0

GenotypeQuality
all individuals: 9597
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 7751
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variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 7.5e0
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GenotypeQuality
all individuals: 212
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 168
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 722
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 200
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1942
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1828
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 146
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21505
bin: 6.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14282
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 874
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6570
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10364
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11486
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65464
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.329373398555789e-4
allele num: 8586
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.463e1

FS
type: SiteQuality
SIO_000300: 2.96e0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.28e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.39e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.3e-3

DP
type: SiteQuality
SIO_000300: 1.796619e6

BaseQRankSum
type: SiteQuality
SIO_000300: 4.87e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.62e0

VQSLOD
type: SiteQuality
SIO_000300: 8.76e-1

MQ
type: SiteQuality
SIO_000300: 5.975e1

GenotypeQuality
all individuals: 40344
bin: 9.75e1
variant carriers: 37686

GenotypeQuality
all individuals: 346
bin: 5.25e1
variant carriers: 217

GenotypeQuality
all individuals: 1671
bin: 8.25e1
variant carriers: 360

GenotypeQuality
all individuals: 273
bin: 3.25e1
variant carriers: 60

GenotypeQuality
all individuals: 52
bin: 7.5e0
variant carriers: 19

GenotypeQuality
all individuals: 49
bin: 1.25e1
variant carriers: 24

GenotypeQuality
all individuals: 2004
bin: 7.75e1
variant carriers: 309

GenotypeQuality
all individuals: 179
bin: 4.25e1
variant carriers: 92

GenotypeQuality
all individuals: 270
bin: 4.75e1
variant carriers: 159

GenotypeQuality
all individuals: 7480
bin: 6.25e1
variant carriers: 267

GenotypeQuality
all individuals: 2933
bin: 6.75e1
variant carriers: 273

GenotypeQuality
all individuals: 1153
bin: 9.25e1
variant carriers: 401

GenotypeQuality
all individuals: 830
bin: 8.75e1
variant carriers: 233

GenotypeQuality
all individuals: 212
bin: 2.75e1
variant carriers: 40

GenotypeQuality
all individuals: 671
bin: 2.25e1
variant carriers: 52

GenotypeQuality
all individuals: 261
bin: 3.75e1
variant carriers: 115

GenotypeQuality
all individuals: 322
bin: 5.75e1
variant carriers: 162

European (Finnish)
type: Population
allele count: 2929
allele frequency: 4.450015192950471e-1
allele num: 6582
num of homozygotes: 661

Other
type: Population
allele count: 396
allele frequency: 4.439461883408072e-1
allele num: 892
num of homozygotes: 91

European (Non-Finnish)
type: Population
allele count: 30245
allele frequency: 4.578413563427187e-1
allele num: 66060
num of homozygotes: 6885

African
type: Population
allele count: 3294
allele frequency: 3.174021969550973e-1
allele num: 10378
num of homozygotes: 506

Latino
type: Population
allele count: 4716
allele frequency: 4.103010266225857e-1
allele num: 11494
num of homozygotes: 959

East Asian
type: Population
allele count: 3794
allele frequency: 4.411627906976744e-1
allele num: 8600
num of homozygotes: 838

South Asian
type: Population
allele count: 6393
allele frequency: 4.09021113243762e-1
allele num: 15630
num of homozygotes: 1249

MQ
type: SiteQuality
SIO_000300: 5.968e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.06e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.754e0

MQRankSum
type: SiteQuality
SIO_000300: 5.5e-2

FS
type: SiteQuality
SIO_000300: 1.644e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.07e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.43e-1

DP
type: SiteQuality
SIO_000300: 2.629231e6

QD
type: SiteQuality
SIO_000300: 1.863e1

VQSLOD
type: SiteQuality
SIO_000300: 3.56e0

GenotypeQuality
all individuals: 1926
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 435
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 231
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 34113
bin: 9.75e1
variant carriers: 1055

GenotypeQuality
all individuals: 364
bin: 3.25e1
variant carriers: 2

GenotypeQuality
all individuals: 221
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 1.25e1
variant carriers: 1

GenotypeQuality
all individuals: 615
bin: 5.25e1
variant carriers: 4

GenotypeQuality
all individuals: 22
bin: 7.5e0
variant carriers: 1

GenotypeQuality
all individuals: 1447
bin: 8.75e1
variant carriers: 3

GenotypeQuality
all individuals: 8256
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 2460
bin: 9.25e1
variant carriers: 2

GenotypeQuality
all individuals: 2581
bin: 8.25e1
variant carriers: 2

GenotypeQuality
all individuals: 620
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3663
bin: 6.75e1
variant carriers: 5

GenotypeQuality
all individuals: 2810
bin: 7.75e1
variant carriers: 1

Latino
type: Population
allele count: 11
allele frequency: 9.520512376666089e-4
allele num: 11554
num of homozygotes: 0

Other
type: Population
allele count: 7
allele frequency: 7.79510022271715e-3
allele num: 898
num of homozygotes: 0

East Asian
type: Population
allele count: 147
allele frequency: 1.699814986123959e-2
allele num: 8648
num of homozygotes: 2

European (Non-Finnish)
type: Population
allele count: 14
allele frequency: 2.112187320841254e-4
allele num: 66282
num of homozygotes: 0

African
type: Population
allele count: 114
allele frequency: 1.096997690531178e-2
allele num: 10392
num of homozygotes: 1

South Asian
type: Population
allele count: 809
allele frequency: 5.115720247881624e-2
allele num: 15814
num of homozygotes: 27

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

QD
type: SiteQuality
SIO_000300: 1.469e1

MQRankSum
type: SiteQuality
SIO_000300: 1.85e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.96e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.667631e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.12e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.4e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 2.04e0

VQSLOD
type: SiteQuality
SIO_000300: 6.13e0

GenotypeQuality
all individuals: 1926
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 343
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 539
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2460
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2581
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8256
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 221
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 620
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34113
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 3663
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1447
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 615
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2810
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 231
bin: 4.25e1
variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10392
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15814
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 898
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: 2
allele frequency: 3.017410458344649e-5
allele num: 66282
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.469e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.4e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 2.04e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.96e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.85e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.13e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.12e-1

DP
type: SiteQuality
SIO_000300: 2.667631e6

GenotypeQuality
all individuals: 393
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 14
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 128
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 211
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 167
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1988
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 226
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 310
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 340
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3818
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 432
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9569
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2652
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2892
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33500
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1489
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2540
bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16064
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66406
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10400
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: 11560
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.108647450110865e-3
allele num: 902
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.32e-1

MQ
type: SiteQuality
SIO_000300: 5.936e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.423e0

QD
type: SiteQuality
SIO_000300: 1.014e1

MQRankSum
type: SiteQuality
SIO_000300: -2.66e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.3e-2

FS
type: SiteQuality
SIO_000300: 1.0355e1

DP
type: SiteQuality
SIO_000300: 2.671598e6

VQSLOD
type: SiteQuality
SIO_000300: -1.216e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.3e-2

GenotypeQuality
all individuals: 1491
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 401
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3829
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2895
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 276
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2533
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 7
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 347
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 158
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 9816
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 182
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 285
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2651
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1986
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33586
bin: 9.75e1
variant carriers: 138

GenotypeQuality
all individuals: 169
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 65
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: 11560
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10400
num of homozygotes: 0

South Asian
type: Population
allele count: 133
allele frequency: 8.252668155869943e-3
allele num: 16116
num of homozygotes: 3

Other
type: Population
allele count: 1
allele frequency: 1.108647450110865e-3
allele num: 902
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 9
allele frequency: 1.354891157077048e-4
allele num: 66426
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.674006e6

VQSLOD
type: SiteQuality
SIO_000300: -7.748e-1

FS
type: SiteQuality
SIO_000300: 4.1e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.93e0

MQRankSum
type: SiteQuality
SIO_000300: 2.6e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -9.3e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.2e-2

MQ
type: SiteQuality
SIO_000300: 5.919e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.55e-1

QD
type: SiteQuality
SIO_000300: 1.414e1

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

GenotypeQuality
all individuals: 146
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2664
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 274
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 339
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3850
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 131
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2540
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2912
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2000
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1496
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 167
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 9942
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 377
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 252
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33531
bin: 9.75e1
variant carriers: 9

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10402
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11562
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 9
allele frequency: 1.35423876734178e-4
allele num: 66458
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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16140
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 1.11e0

QD
type: SiteQuality
SIO_000300: 1.283e1

VQSLOD
type: SiteQuality
SIO_000300: 3.52e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.687e0

MQRankSum
type: SiteQuality
SIO_000300: -3.88e-1

DP
type: SiteQuality
SIO_000300: 2.675047e6

MQ
type: SiteQuality
SIO_000300: 5.873e1

FS
type: SiteQuality
SIO_000300: 1.38e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.06e-1

GenotypeQuality
all individuals: 124
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 131
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 285
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 242
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 117
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2928
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 175
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 91
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2666
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2545
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1999
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1504
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10135
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3880
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33536
bin: 9.75e1
variant carriers: 1

African
type: Population
allele count: 1
allele frequency: 9.613535858488752e-5
allele num: 10402
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66500
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: 6612
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11564
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16200
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 2.18e0

QD
type: SiteQuality
SIO_000300: 1.377e1

VQSLOD
type: SiteQuality
SIO_000300: -2.281e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.56e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -2.2e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 2.68e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.17e-1

DP
type: SiteQuality
SIO_000300: 2.677611e6

GenotypeQuality
all individuals: 2000
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2546
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2665
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 160
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 267
bin: 3.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 121
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 232
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3883
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1505
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2928
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10223
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33538
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 112
bin: 4.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.015218502812114e-5
allele num: 66498
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16216
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10400
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: 11564
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.17e-2

QD
type: SiteQuality
SIO_000300: 1.476e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.09e-1

DP
type: SiteQuality
SIO_000300: 2.678418e6

MQRankSum
type: SiteQuality
SIO_000300: 3.21e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.41e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.921e0

VQSLOD
type: SiteQuality
SIO_000300: 5.33e0

MQ
type: SiteQuality
SIO_000300: 5.913e1

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

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

GenotypeQuality
all individuals: 6
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2696
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 163
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33550
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 10584
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 66
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variant carriers: 0

GenotypeQuality
all individuals: 2020
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variant carriers: 0

GenotypeQuality
all individuals: 86
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variant carriers: 0

GenotypeQuality
all individuals: 2554
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2957
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1516
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3926
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 226
bin: 2.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11568
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: 1
allele frequency: 1.502448991856726e-5
allele num: 66558
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16300
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.464e1

FS
type: SiteQuality
SIO_000300: 1.035e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 8.7e-1

MQ
type: SiteQuality
SIO_000300: 5.956e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.76e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.544e0

MQRankSum
type: SiteQuality
SIO_000300: 1.02e-1

DP
type: SiteQuality
SIO_000300: 2.683685e6

ClippingRankSum
type: SiteQuality
SIO_000300: -4.34e-1

GenotypeQuality
all individuals: 1868
bin: 7.75e1
variant carriers: 118

GenotypeQuality
all individuals: 71
bin: 5.75e1
variant carriers: 37

GenotypeQuality
all individuals: 52
bin: 3.75e1
variant carriers: 14

GenotypeQuality
all individuals: 925
bin: 9.25e1
variant carriers: 146

GenotypeQuality
all individuals: 13
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 4.25e1
variant carriers: 12

GenotypeQuality
all individuals: 46
bin: 4.75e1
variant carriers: 22

GenotypeQuality
all individuals: 10
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variant carriers: 4

GenotypeQuality
all individuals: 94
bin: 2.25e1
variant carriers: 9

GenotypeQuality
all individuals: 1347
bin: 7.25e1
variant carriers: 58

GenotypeQuality
all individuals: 27
bin: 2.75e1
variant carriers: 8

GenotypeQuality
all individuals: 8264
bin: 6.25e1
variant carriers: 58

GenotypeQuality
all individuals: 2897
bin: 6.75e1
variant carriers: 87

GenotypeQuality
all individuals: 42747
bin: 9.75e1
variant carriers: 39919

GenotypeQuality
all individuals: 46
bin: 3.25e1
variant carriers: 18

GenotypeQuality
all individuals: 711
bin: 8.75e1
variant carriers: 90

GenotypeQuality
all individuals: 10
bin: 1.75e1
variant carriers: 4

GenotypeQuality
all individuals: 1473
bin: 8.25e1
variant carriers: 133

Other
type: Population
allele count: 394
allele frequency: 4.358407079646018e-1
allele num: 904
num of homozygotes: 90

African
type: Population
allele count: 3301
allele frequency: 3.17281814686659e-1
allele num: 10404
num of homozygotes: 509

European (Finnish)
type: Population
allele count: 2944
allele frequency: 4.453857791225416e-1
allele num: 6610
num of homozygotes: 670

European (Non-Finnish)
type: Population
allele count: 30373
allele frequency: 4.559004533037135e-1
allele num: 66622
num of homozygotes: 6932

East Asian
type: Population
allele count: 3806
allele frequency: 4.408153810516562e-1
allele num: 8634
num of homozygotes: 845

Latino
type: Population
allele count: 4745
allele frequency: 4.103961252378481e-1
allele num: 11562
num of homozygotes: 972

South Asian
type: Population
allele count: 6465
allele frequency: 3.936792108147607e-1
allele num: 16422
num of homozygotes: 1265

FS
type: SiteQuality
SIO_000300: 6.13e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.18e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -2.422e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.12e-1

MQRankSum
type: SiteQuality
SIO_000300: 8.500000000000001e-2

VQSLOD
type: SiteQuality
SIO_000300: 4.11e0

QD
type: SiteQuality
SIO_000300: 1.897e1

DP
type: SiteQuality
SIO_000300: 3.555929e6

ClippingRankSum
type: SiteQuality
SIO_000300: 3.0e-2

MQ
type: SiteQuality
SIO_000300: 5.966e1

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

GenotypeQuality
all individuals: 19
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 3.25e1
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GenotypeQuality
all individuals: 18164
bin: 9.75e1
variant carriers: 7

GenotypeQuality
all individuals: 2190
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variant carriers: 0

GenotypeQuality
all individuals: 3
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GenotypeQuality
all individuals: 7005
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GenotypeQuality
all individuals: 42
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variant carriers: 0

GenotypeQuality
all individuals: 52
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variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3280
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 33
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3196
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4797
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17547
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4198
bin: 8.25e1
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: 11574
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: 10406
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16464
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 7
allele frequency: 1.050136517747307e-4
allele num: 66658
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.1e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -1.628e0

QD
type: SiteQuality
SIO_000300: 1.349e1

MQ
type: SiteQuality
SIO_000300: 5.952e1

VQSLOD
type: SiteQuality
SIO_000300: 2.73e0

MQRankSum
type: SiteQuality
SIO_000300: 4.18e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.334191e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.2e-2

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

GenotypeQuality
all individuals: 4785
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18157
bin: 9.75e1
variant carriers: 6

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 49
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variant carriers: 0

GenotypeQuality
all individuals: 3189
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
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GenotypeQuality
all individuals: 3281
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variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 28
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variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4188
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2190
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6974
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17601
bin: 6.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 1.921968095329617e-4
allele num: 10406
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66660
num of homozygotes: 0

East Asian
type: Population
allele count: 4
allele frequency: 4.622140050843541e-4
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: 16484
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11574
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.7e-3

QD
type: SiteQuality
SIO_000300: 1.687e1

FS
type: SiteQuality
SIO_000300: 3.002e0

MQ
type: SiteQuality
SIO_000300: 5.934e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.7e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.685e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.72e-1

DP
type: SiteQuality
SIO_000300: 2.334749e6

VQSLOD
type: SiteQuality
SIO_000300: 8.39e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.4e-2

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: 1

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: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499835018148004e-5
allele num: 66674
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16492
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11572
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.955e1

MQRankSum
type: SiteQuality
SIO_000300: 1.85e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.58e-1

BaseQRankSum
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SIO_000300: -2.362e0

VQSLOD
type: SiteQuality
SIO_000300: -2.893e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.15e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.7e-3

QD
type: SiteQuality
SIO_000300: 2.818e1

FS
type: SiteQuality
SIO_000300: 4.705e0

DP
type: SiteQuality
SIO_000300: 2.334727e6

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: 13

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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variant carriers: 0

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

African
type: Population
allele count: 1
allele frequency: 9.609840476648087e-5
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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 12
allele frequency: 1.799208348326736e-4
allele num: 66696
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -2.091e0

DP
type: SiteQuality
SIO_000300: 2.33616e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.42e-1

FS
type: SiteQuality
SIO_000300: 6.4e-1

QD
type: SiteQuality
SIO_000300: 1.405e1

MQRankSum
type: SiteQuality
SIO_000300: -1.39e-1

MQ
type: SiteQuality
SIO_000300: 5.976e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.28e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.88e0

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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1143

GenotypeQuality
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GenotypeQuality
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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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variant carriers: 0

GenotypeQuality
all individuals: 6
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GenotypeQuality
all individuals: 17731
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variant carriers: 0

GenotypeQuality
all individuals: 5
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variant carriers: 0

Latino
type: Population
allele count: 75
allele frequency: 6.478921907394609e-3
allele num: 11576
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 1.817520901490367e-4
allele num: 16506
num of homozygotes: 0

African
type: Population
allele count: 1097
allele frequency: 1.054199500288295e-1
allele num: 10406
num of homozygotes: 57

European (Non-Finnish)
type: Population
allele count: 15
allele frequency: 2.248942996791508e-4
allele num: 66698
num of homozygotes: 0

Other
type: Population
allele count: 9
allele frequency: 9.933774834437087e-3
allele num: 906
num of homozygotes: 1

East Asian
type: Population
allele count: 2
allele frequency: 2.31107002542177e-4
allele num: 8654
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.971e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.19e-2

VQSLOD
type: SiteQuality
SIO_000300: 6.28e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.7e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.69e-1

DP
type: SiteQuality
SIO_000300: 2.396143e6

QD
type: SiteQuality
SIO_000300: 1.49e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 2.64e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.34e0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 9
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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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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 17982
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variant carriers: 1

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: 16510
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: 6614
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
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: 1.499160470136723e-5
allele num: 66704
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.39e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.41e-1

QD
type: SiteQuality
SIO_000300: 1.788e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 1.028e0

MQRankSum
type: SiteQuality
SIO_000300: 2.11e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.4e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 1.49e-1

DP
type: SiteQuality
SIO_000300: 2.324538e6

BaseQRankSum
type: SiteQuality
SIO_000300: 3.97e0

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
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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: 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: 11578
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: 1.498980693128672e-5
allele num: 66712
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16510
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: 6614
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.85e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 2.324575e6

BaseQRankSum
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FS
type: SiteQuality
SIO_000300: 3.183e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.54e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 1.53e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.37e-1

QD
type: SiteQuality
SIO_000300: 1.091e1

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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variant carriers: 0

GenotypeQuality
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variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.498800959232614e-5
allele num: 66720
num of homozygotes: 0

South Asian
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Other
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QD
type: SiteQuality
SIO_000300: 1.596e1

DP
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ReadPosRankSum
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BaseQRankSum
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VQSLOD
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MQRankSum
type: SiteQuality
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InbreedingCoeff
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FS
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MQ
type: SiteQuality
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ClippingRankSum
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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
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.727414061150458e-4
allele num: 11578
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

South Asian
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allele count: 1
allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66724
num of homozygotes: 0

Other
type: Population
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QD
type: SiteQuality
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InbreedingCoeff
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FS
type: SiteQuality
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DP
type: SiteQuality
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MQRankSum
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VQSLOD
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MQ
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ReadPosRankSum
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ClippingRankSum
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BaseQRankSum
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SIO_000300: -1.112e0

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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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 2198
bin: 8.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498756032493031e-5
allele num: 66722
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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.26e-1

VQSLOD
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SIO_000300: 1.72e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 2.324635e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 4.93e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.32e0

FS
type: SiteQuality
SIO_000300: 1.945e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.56e0

QD
type: SiteQuality
SIO_000300: 1.308e1

GenotypeQuality
all individuals: 1
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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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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66720
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.155535012710885e-4
allele num: 8654
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: 11578
num of homozygotes: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6614
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VQSLOD
type: SiteQuality
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DP
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ReadPosRankSum
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SIO_000300: 1.65e0

QD
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SIO_000300: 1.226e1

BaseQRankSum
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SIO_000300: 1.83e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
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SIO_000300: 5.82e-1

FS
type: SiteQuality
SIO_000300: 7.749e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.512e0

MQ
type: SiteQuality
SIO_000300: 5.8e1

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
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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: 0

Latino
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allele count: 4
allele frequency: 3.454828122300915e-4
allele num: 11578
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: 10404
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66720
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: 1.23e0

VQSLOD
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SIO_000300: -1.083e0

QD
type: SiteQuality
SIO_000300: 7.19e0

MQ
type: SiteQuality
SIO_000300: 5.978e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.52e-1

FS
type: SiteQuality
SIO_000300: 1.894e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.33e-1

DP
type: SiteQuality
SIO_000300: 2.324714e6

MQRankSum
type: SiteQuality
SIO_000300: -3.6e-1

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
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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: 0

GenotypeQuality
all individuals: 17972
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GenotypeQuality
all individuals: 2
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variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
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: 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 (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66716
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.131e0

FS
type: SiteQuality
SIO_000300: 6.04e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 2.324289e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.13e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.25e-1

MQRankSum
type: SiteQuality
SIO_000300: -5.24e-1

QD
type: SiteQuality
SIO_000300: 1.263e1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.52e-1

MQ
type: SiteQuality
SIO_000300: 5.944e1

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
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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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bin: 7.25e1
variant carriers: 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: 8654
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66718
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.727414061150458e-4
allele num: 11578
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.962e1

QD
type: SiteQuality
SIO_000300: 1.282e1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.05e-1

VQSLOD
type: SiteQuality
SIO_000300: -6.552e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.94e0

DP
type: SiteQuality
SIO_000300: 2.324375e6

FS
type: SiteQuality
SIO_000300: 7.94e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.76e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
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SIO_000300: 2.17e0

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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bin: 7.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66718
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
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MQRankSum
type: SiteQuality
SIO_000300: -1.611e0

MQ
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SIO_000300: 5.975e1

QD
type: SiteQuality
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DP
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InbreedingCoeff
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SIO_000300: 0.0e0

ClippingRankSum
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BaseQRankSum
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SIO_000300: 2.91e0

ReadPosRankSum
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SIO_000300: 2.53e0

FS
type: SiteQuality
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VQSLOD
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SIO_000300: -2.048e0

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
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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: 0

GenotypeQuality
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variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
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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)
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allele count: 1
allele frequency: 1.49902563333833e-5
allele num: 66710
num of homozygotes: 0

FS
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SIO_000300: 0.0e0

QD
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ClippingRankSum
type: SiteQuality
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MQRankSum
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ReadPosRankSum
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BaseQRankSum
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VQSLOD
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DP
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.945e1

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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variant carriers: 0

Latino
type: Population
allele count: 3
allele frequency: 2.591121091725686e-4
allele num: 11578
num of homozygotes: 1

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

African
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allele frequency: 0.0e0
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Other
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South Asian
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
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FS
type: SiteQuality
SIO_000300: 1.3343e1

ReadPosRankSum
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DP
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InbreedingCoeff
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MQRankSum
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VQSLOD
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QD
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BaseQRankSum
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ClippingRankSum
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MQ
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SIO_000300: 5.973e1

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
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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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allele frequency: 0.0e0
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num of homozygotes: 0

Other
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Latino
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allele frequency: 8.637070305752289e-5
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num of homozygotes: 0

African
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European (Non-Finnish)
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European (Finnish)
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allele frequency: 0.0e0
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South Asian
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FS
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InbreedingCoeff
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ReadPosRankSum
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VQSLOD
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MQRankSum
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QD
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BaseQRankSum
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MQ
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ClippingRankSum
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DP
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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

European (Non-Finnish)
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allele frequency: 1.499700059988002e-5
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num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

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

European (Non-Finnish)
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allele frequency: 0.0e0
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South Asian
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East Asian
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Other
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African
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

VQSLOD
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InbreedingCoeff
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FS
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ClippingRankSum
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MQRankSum
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BaseQRankSum
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DP
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QD
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ReadPosRankSum
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MQ
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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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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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European (Finnish)
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East Asian
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South Asian
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African
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European (Non-Finnish)
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num of homozygotes: 0

QD
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MQ
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InbreedingCoeff
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VQSLOD
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DP
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ClippingRankSum
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BaseQRankSum
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MQRankSum
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FS
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ReadPosRankSum
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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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European (Non-Finnish)
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Other
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East Asian
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Latino
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South Asian
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European (Finnish)
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ClippingRankSum
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DP
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InbreedingCoeff
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VQSLOD
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ReadPosRankSum
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MQRankSum
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MQ
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QD
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FS
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BaseQRankSum
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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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Latino
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South Asian
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East Asian
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Other
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European (Finnish)
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European (Non-Finnish)
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DP
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FS
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VQSLOD
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MQ
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InbreedingCoeff
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ReadPosRankSum
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BaseQRankSum
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MQRankSum
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ClippingRankSum
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QD
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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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allele num: 66348
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African
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European (Finnish)
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East Asian
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Latino
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South Asian
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Other
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DP
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QD
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MQRankSum
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InbreedingCoeff
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MQ
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ReadPosRankSum
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ClippingRankSum
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VQSLOD
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BaseQRankSum
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FS
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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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bin: 4.75e1
variant carriers: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 898
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: 4
allele frequency: 3.849114703618168e-4
allele num: 10392
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15828
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66324
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.28e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.14e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.91e-1

DP
type: SiteQuality
SIO_000300: 2.291747e6

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.01e0

MQ
type: SiteQuality
SIO_000300: 5.948e1

QD
type: SiteQuality
SIO_000300: 1.433e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.9e-3

VQSLOD
type: SiteQuality
SIO_000300: 2.64e0

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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bin: 2.25e1
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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: 0

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

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.514233797698365e-4
allele num: 6604
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 5
allele frequency: 7.553326484983986e-5
allele num: 66196
num of homozygotes: 0

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

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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allele count: 0
allele frequency: 0.0e0
allele num: 8646
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.01e0

DP
type: SiteQuality
SIO_000300: 2.278323e6

ClippingRankSum
type: SiteQuality
SIO_000300: -5.94e-1

MQ
type: SiteQuality
SIO_000300: 5.683e1

QD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: 9.389999999999999e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.17e0

VQSLOD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 1.5e-3

MQRankSum
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SIO_000300: -4.198e0

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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bin: 2.25e1
variant carriers: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8646
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6604
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: 1.510665296996797e-5
allele num: 66196
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15614
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.37e0

BaseQRankSum
type: SiteQuality
SIO_000300: 9.389999999999999e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.17e0

MQRankSum
type: SiteQuality
SIO_000300: -4.198e0

InbreedingCoeff
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SIO_000300: 1.5e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -5.94e-1

VQSLOD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 2.278323e6

FS
type: SiteQuality
SIO_000300: 1.01e0

MQ
type: SiteQuality
SIO_000300: 5.683e1

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
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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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bin: 9.75e1
variant carriers: 1

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10342
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.512172992590352e-5
allele num: 66130
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6538
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8646
num of homozygotes: 0

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: -6.43e-1

VQSLOD
type: SiteQuality
SIO_000300: -5.901999999999999e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.274304e6

MQ
type: SiteQuality
SIO_000300: 5.684e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.57e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.4e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.07e0

QD
type: SiteQuality
SIO_000300: 5.0e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.079e0

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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variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10342
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.529519730804527e-4
allele num: 6538
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8646
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.560864962951762e-5
allele num: 66130
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 882
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15552
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.57e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.4e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.07e0

MQ
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: -3.079e0

QD
type: SiteQuality
SIO_000300: 5.0e-1

VQSLOD
type: SiteQuality
SIO_000300: -5.901999999999999e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.43e-1

DP
type: SiteQuality
SIO_000300: 2.274304e6

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 count: 0
allele frequency: 0.0e0
allele num: 10344
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.511578692786746e-5
allele num: 66156
num of homozygotes: 0

Latino
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num of homozygotes: 0

South Asian
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BaseQRankSum
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FS
type: SiteQuality
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MQRankSum
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MQ
type: SiteQuality
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VQSLOD
type: SiteQuality
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ClippingRankSum
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InbreedingCoeff
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ReadPosRankSum
type: SiteQuality
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DP
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 4.1e-1

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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allele count: 0
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allele num: 8640
num of homozygotes: 0

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

European (Finnish)
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allele count: 1
allele frequency: 1.520218911523259e-4
allele num: 6578
num of homozygotes: 0

European (Non-Finnish)
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allele count: 5
allele frequency: 7.581501137225171e-5
allele num: 65950
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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DP
type: SiteQuality
SIO_000300: 2.253317e6

BaseQRankSum
type: SiteQuality
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QD
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MQRankSum
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InbreedingCoeff
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FS
type: SiteQuality
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ClippingRankSum
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VQSLOD
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MQ
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ReadPosRankSum
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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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allele count: 0
allele frequency: 0.0e0
allele num: 8638
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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Other
type: Population
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Latino
type: Population
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allele frequency: 0.0e0
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African
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allele frequency: 9.703085581214826e-5
allele num: 10306
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European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 65934
num of homozygotes: 0

South Asian
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QD
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VQSLOD
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InbreedingCoeff
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MQRankSum
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MQ
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DP
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BaseQRankSum
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FS
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ReadPosRankSum
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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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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bin: 2.5e0
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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: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15376
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.036744609778318e-5
allele num: 65860
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8638
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10256
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11528
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6540
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 882
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.247567e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.628e0

FS
type: SiteQuality
SIO_000300: 8.577999999999999e0

QD
type: SiteQuality
SIO_000300: 4.71e0

MQ
type: SiteQuality
SIO_000300: 5.875e1

MQRankSum
type: SiteQuality
SIO_000300: -3.46e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.09e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.5e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -1.004e0

VQSLOD
type: SiteQuality
SIO_000300: -2.582e0

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
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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: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6198
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9872
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15240
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8582
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 858
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11464
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.545165178157545e-5
allele num: 64718
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.874e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.032e0

QD
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SIO_000300: 8.75e0

MQRankSum
type: SiteQuality
SIO_000300: 1.06e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.03e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.44e0

VQSLOD
type: SiteQuality
SIO_000300: -1.318e0

DP
type: SiteQuality
SIO_000300: 2.208033e6

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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variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 872
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.529145513487063e-5
allele num: 65396
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10110
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8614
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.537042729787888e-4
allele num: 6506
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15148
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11498
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.678e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.404e0

DP
type: SiteQuality
SIO_000300: 2.20631e6

MQRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 1.287e0

MQ
type: SiteQuality
SIO_000300: 5.945e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.5e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.62e0

VQSLOD
type: SiteQuality
SIO_000300: 1.58e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -9.24e-1

GenotypeQuality
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bin: 2.25e1
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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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
all individuals: 12687
bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65396
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8614
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 872
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.891196834817012e-5
allele num: 10110
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15148
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6506
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11498
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.58e-1

MQ
type: SiteQuality
SIO_000300: 5.945e1

BaseQRankSum
type: SiteQuality
SIO_000300: -9.24e-1

FS
type: SiteQuality
SIO_000300: 1.287e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.404e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.5e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.62e0

DP
type: SiteQuality
SIO_000300: 2.20631e6

QD
type: SiteQuality
SIO_000300: 1.678e1

MQRankSum
type: SiteQuality
SIO_000300: 3.75e-1

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
all individuals: 3274
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variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11464
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.665920119447555e-5
allele num: 64296
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6076
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.012145748987854e-4
allele num: 9880
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 836
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8592
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15142
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 5.17e0

DP
type: SiteQuality
SIO_000300: 2.197229e6

MQRankSum
type: SiteQuality
SIO_000300: 1.75e-1

QD
type: SiteQuality
SIO_000300: 1.344e1

MQ
type: SiteQuality
SIO_000300: 5.967e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.04e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.5e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -2.619e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.24e-1

GenotypeQuality
all individuals: 725
bin: 3.25e1
variant carriers: 10

GenotypeQuality
all individuals: 5336
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GenotypeQuality
all individuals: 92
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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
all individuals: 4354
bin: 7.75e1
variant carriers: 25

European (Non-Finnish)
type: Population
allele count: 569
allele frequency: 9.270422626999902e-3
allele num: 61378
num of homozygotes: 0

Latino
type: Population
allele count: 14
allele frequency: 1.232394366197183e-3
allele num: 11360
num of homozygotes: 0

African
type: Population
allele count: 147
allele frequency: 1.636971046770601e-2
allele num: 8980
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 209
allele frequency: 3.749551489056333e-2
allele num: 5574
num of homozygotes: 0

East Asian
type: Population
allele count: 22
allele frequency: 2.599858189553297e-3
allele num: 8462
num of homozygotes: 0

Other
type: Population
allele count: 16
allele frequency: 2.010050251256281e-2
allele num: 796
num of homozygotes: 0

South Asian
type: Population
allele count: 4
allele frequency: 2.644802962179318e-4
allele num: 15124
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 3.49e0

BaseQRankSum
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SIO_000300: -3.492e0

MQ
type: SiteQuality
SIO_000300: 5.903e1

FS
type: SiteQuality
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VQSLOD
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ReadPosRankSum
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MQRankSum
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SIO_000300: -8.500000000000001e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.57e-2

DP
type: SiteQuality
SIO_000300: 2.207636e6

ClippingRankSum
type: SiteQuality
SIO_000300: 2.07e0

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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variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.034717164360282e-5
allele num: 65904
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10350
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8630
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11546
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 882
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.81e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 7.66e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -4.28e-1

DP
type: SiteQuality
SIO_000300: 2.338238e6

FS
type: SiteQuality
SIO_000300: 6.711e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.16e0

VQSLOD
type: SiteQuality
SIO_000300: 5.15e-1

QD
type: SiteQuality
SIO_000300: 1.46e1

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
all individuals: 4128
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variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.678242286630158e-5
allele num: 14974
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65884
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 882
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8630
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: 10348
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

MQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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FS
type: SiteQuality
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QD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: -6.27e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.86e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.109e0

MQ
type: SiteQuality
SIO_000300: 6.072e1

DP
type: SiteQuality
SIO_000300: 2.335183e6

GenotypeQuality
all individuals: 123
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 278
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1101
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2667
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 343
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3349
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 336
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 20909
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 9340
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1363
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 316
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 785
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 511
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4066
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4361
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2175
bin: 8.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8580
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11524
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 870
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65472
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.10126402499645e-5
allele num: 14082
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10316
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 8.81e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -1.226e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -1.791e0

DP
type: SiteQuality
SIO_000300: 2.295483e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.01e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.01e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.66e0

GenotypeQuality
all individuals: 2653
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 545
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4064
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 279
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1380
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 123
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 411
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4347
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 342
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1146
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2178
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3345
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 387
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5104
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20916
bin: 9.75e1
variant carriers: 18

GenotypeQuality
all individuals: 962
bin: 2.75e1
variant carriers: 0

Latino
type: Population
allele count: 2
allele frequency: 1.736714136853074e-4
allele num: 11516
num of homozygotes: 0

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

South Asian
type: Population
allele count: 17
allele frequency: 1.209103840682788e-3
allele num: 14060
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 872
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8580
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10318
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65468
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.05e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.1e-3

QD
type: SiteQuality
SIO_000300: 1.338e1

MQRankSum
type: SiteQuality
SIO_000300: 9.8e-2

DP
type: SiteQuality
SIO_000300: 2.293751e6

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.76e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.54e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.152e0

GenotypeDepth
all individuals: 504
bin: 5.25e1
variant carriers: 3

GenotypeDepth
all individuals: 817
bin: 4.25e1
variant carriers: 16

GenotypeDepth
all individuals: 732
bin: 4.75e1
variant carriers: 11

GenotypeDepth
all individuals: 2
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 73
bin: 5.75e1
variant carriers: 3

GenotypeQuality
all individuals: 116
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1096
bin: 1.25e1
variant carriers: 2

GenotypeQuality
all individuals: 3243
bin: 9.75e1
variant carriers: 104

GenotypeQuality
all individuals: 1037
bin: 1.75e1
variant carriers: 4

GenotypeQuality
all individuals: 1257
bin: 2.25e1
variant carriers: 7

GenotypeQuality
all individuals: 276
bin: 3.75e1
variant carriers: 2

GenotypeQuality
all individuals: 888
bin: 6.25e1
variant carriers: 3

GenotypeQuality
all individuals: 137
bin: 5.25e1
variant carriers: 3

GenotypeQuality
all individuals: 13617
bin: 7.5e0
variant carriers: 12

GenotypeQuality
all individuals: 434
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 239
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 317
bin: 9.25e1
variant carriers: 2

GenotypeQuality
all individuals: 274
bin: 7.75e1
variant carriers: 2

GenotypeQuality
all individuals: 195
bin: 8.75e1
variant carriers: 2

GenotypeQuality
all individuals: 389
bin: 2.75e1
variant carriers: 2

GenotypeQuality
all individuals: 10700
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 146
bin: 4.75e1
variant carriers: 3

GenotypeQuality
all individuals: 305
bin: 8.25e1
variant carriers: 2

GenotypeQuality
all individuals: 400
bin: 6.75e1
variant carriers: 4

South Asian
type: Population
allele count: 55
allele frequency: 7.082152974504249e-3
allele num: 7766
num of homozygotes: 0

Latino
type: Population
allele count: 5
allele frequency: 2.016129032258064e-2
allele num: 248
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.01010101010101e-3
allele num: 990
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 42
allele frequency: 7.622504537205082e-3
allele num: 5510
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 164
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 400
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 3.25707e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.62e-2

VQSLOD
type: SiteQuality
SIO_000300: 4.63e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 2.38e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.398e1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.22e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.38e-1

GenotypeDepth
all individuals: 206
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 817
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 354
bin: 5.75e1
variant carriers: 1

GenotypeDepth
all individuals: 810
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16009
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 426
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1652
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 281
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8398
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 267
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1048
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 105
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 124
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 720
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1068
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 202
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 311
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 251
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3183
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 405
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 321
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 406
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5578
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.287664177182591e-4
allele num: 7766
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 244
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 392
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1014
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 166
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.18e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -9.350000000000001e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.15e-2

FS
type: SiteQuality
SIO_000300: 3.175e0

VQSLOD
type: SiteQuality
SIO_000300: -3.3e-2

QD
type: SiteQuality
SIO_000300: 1.441e1

DP
type: SiteQuality
SIO_000300: 3.30009e5

ClippingRankSum
type: SiteQuality
SIO_000300: 1.17e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.53e-1

GenotypeDepth
all individuals: 768
bin: 3.75e1
variant carriers: 34

GenotypeDepth
all individuals: 141
bin: 6.75e1
variant carriers: 55

GenotypeDepth
all individuals: 15
bin: 8.75e1
variant carriers: 9

GenotypeDepth
all individuals: 21
bin: 8.25e1
variant carriers: 12

GenotypeQuality
all individuals: 238
bin: 3.75e1
variant carriers: 5

GenotypeQuality
all individuals: 940
bin: 1.25e1
variant carriers: 33

GenotypeQuality
all individuals: 319
bin: 9.25e1
variant carriers: 18

GenotypeQuality
all individuals: 7817
bin: 2.5e0
variant carriers: 2

GenotypeQuality
all individuals: 16608
bin: 7.5e0
variant carriers: 74

GenotypeQuality
all individuals: 413
bin: 3.25e1
variant carriers: 18

GenotypeQuality
all individuals: 1710
bin: 2.25e1
variant carriers: 31

GenotypeQuality
all individuals: 1074
bin: 6.25e1
variant carriers: 23

GenotypeQuality
all individuals: 294
bin: 8.25e1
variant carriers: 14

GenotypeQuality
all individuals: 429
bin: 2.75e1
variant carriers: 54

GenotypeQuality
all individuals: 40
bin: 5.75e1
variant carriers: 19

GenotypeQuality
all individuals: 49
bin: 5.25e1
variant carriers: 11

GenotypeQuality
all individuals: 397
bin: 6.75e1
variant carriers: 15

GenotypeQuality
all individuals: 84
bin: 4.75e1
variant carriers: 4

GenotypeQuality
all individuals: 556
bin: 1.75e1
variant carriers: 21

GenotypeQuality
all individuals: 273
bin: 7.75e1
variant carriers: 6

GenotypeQuality
all individuals: 3534
bin: 9.75e1
variant carriers: 748

GenotypeQuality
all individuals: 103
bin: 4.25e1
variant carriers: 7

GenotypeQuality
all individuals: 239
bin: 7.25e1
variant carriers: 6

GenotypeQuality
all individuals: 206
bin: 8.75e1
variant carriers: 22

East Asian
type: Population
allele count: 9
allele frequency: 2.261306532663317e-2
allele num: 398
num of homozygotes: 0

Latino
type: Population
allele count: 6
allele frequency: 2.479338842975207e-2
allele num: 242
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 267
allele frequency: 4.707334273624824e-2
allele num: 5672
num of homozygotes: 10

African
type: Population
allele count: 18
allele frequency: 1.750972762645914e-2
allele num: 1028
num of homozygotes: 1

European (Finnish)
type: Population
allele count: 2
allele frequency: 1.428571428571428e-1
allele num: 14
num of homozygotes: 0

South Asian
type: Population
allele count: 475
allele frequency: 6.117980422462648e-2
allele num: 7764
num of homozygotes: 22

Other
type: Population
allele count: 5
allele frequency: 3.012048192771084e-2
allele num: 166
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.06e-1

QD
type: SiteQuality
SIO_000300: 1.472e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.7e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.53e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.62e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 6.02e0

BaseQRankSum
type: SiteQuality
SIO_000300: -8.89e-1

DP
type: SiteQuality
SIO_000300: 3.41591e5

GenotypeDepth
all individuals: 113
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 350
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 914
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 707
bin: 4.75e1
variant carriers: 2

GenotypeQuality
all individuals: 600
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 257
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1934
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 105
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 440
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 428
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 91
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1287
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 268
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6681
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3058
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 986
bin: 1.25e1
variant carriers: 1

GenotypeQuality
all individuals: 299
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 196
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 305
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 315
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18313
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 438
bin: 6.75e1
variant carriers: 0

South Asian
type: Population
allele count: 4
allele frequency: 5.15331100231899e-4
allele num: 7762
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1060
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5782
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 170
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 248
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 404
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.752e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.770000000000001e-2

FS
type: SiteQuality
SIO_000300: 6.64e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 9.22e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.4e-2

DP
type: SiteQuality
SIO_000300: 3.35026e5

MQRankSum
type: SiteQuality
SIO_000300: 1.45e0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.500000000000001e-2

QD
type: SiteQuality
SIO_000300: 1.268e1

MQ
type: SiteQuality
SIO_000300: 5.959e1

GenotypeDepth
all individuals: 3
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 787
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 53
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 28
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6496
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 18656
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 438
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 297
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 102
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 264
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 259
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2022
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 437
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 315
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 86
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 550
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 961
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 435
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 307
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3059
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 195
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1301
bin: 6.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 248
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1072
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7760
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 2.450980392156863e-3
allele num: 408
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 168
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5796
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 3.3607e5

QD
type: SiteQuality
SIO_000300: 1.335e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.75e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.749e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 1.05e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.031e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 8.25e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.749e0

GenotypeDepth
all individuals: 53
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 962
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 113
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 349
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 326
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2719
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 284
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 536
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2062
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 319
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4248
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 336
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 538
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28843
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 685
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 204
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3060
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 136
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 334
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6544
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 176
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7764
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 264
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 40
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 452
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1326
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 3.83832e5

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -1.98e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.11e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.43e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.98e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.98e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 9.22e-1

QD
type: SiteQuality
SIO_000300: 1.48e1

GenotypeDepth
all individuals: 28
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 200
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 350
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8683
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 698
bin: 1.25e1
variant carriers: 1

GenotypeQuality
all individuals: 878
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1434
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 31746
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3065
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 125
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 367
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 325
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2890
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 335
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 313
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 647
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 300
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 350
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 207
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7652
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 182
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 536
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7794
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 144
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1784
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 292
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 4.45283e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 2.15e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.67e-2

QD
type: SiteQuality
SIO_000300: 1.767e1