7-95614110-AAAAT-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95614110
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 95614106
    reference: chr 7
allele count: 2
allele frequency: 1.716001716001716e-5
allele num: 116550
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000438377
  ensembl transcript: ENST00000537881
  gene symbol: DYNC1I1
  hgvsc: ENST00000537881.1:c.521-5_521-2delTAAA
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000320130
  ensembl transcript: ENST00000324972
  gene symbol: DYNC1I1
  hgvsc: ENST00000324972.6:c.632-5_632-2delTAAA
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000392337
  ensembl transcript: ENST00000447467
  gene symbol: DYNC1I1
  hgvsc: ENST00000447467.2:c.581-5_581-2delTAAA
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000398118
  ensembl transcript: ENST00000437599
  gene symbol: DYNC1I1
  hgvsc: ENST00000437599.1:c.572-5_572-2delTAAA
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000352348
  ensembl transcript: ENST00000359388
  gene symbol: DYNC1I1
  hgvsc: ENST00000359388.4:c.521-5_521-2delTAAA
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000412444
  ensembl transcript: ENST00000457059
  gene symbol: DYNC1I1
  hgvsc: ENST00000457059.1:c.581-5_581-2delTAAA
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl transcript: ENST00000519371
  gene symbol: DYNC1I1
  hgvsc: ENST00000519371.1:n.239-5_239-2delTAAA
  variant of: http://identifiers.org/hgnc/2963
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1509
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9588
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1551
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 830
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5239
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 869
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2845
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12551
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 787
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21855
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4137
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 278
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 176
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21796
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 330
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 410
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 126
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 197
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: AAAAT
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum

7-95614113-AT-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95614113
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 95614112
    reference: chr 7
allele count: 1
allele frequency: 8.54978540038645e-6
allele num: 116962
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000392337
  ensembl transcript: ENST00000447467
  gene symbol: DYNC1I1
  hgvsc: ENST00000447467.2:c.581-13delT
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000352348
  ensembl transcript: ENST00000359388
  gene symbol: DYNC1I1
  hgvsc: ENST00000359388.4:c.521-13delT
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000320130
  ensembl transcript: ENST00000324972
  gene symbol: DYNC1I1
  hgvsc: ENST00000324972.6:c.632-13delT
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000398118
  ensembl transcript: ENST00000437599
  gene symbol: DYNC1I1
  hgvsc: ENST00000437599.1:c.572-13delT
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl transcript: ENST00000519371
  gene symbol: DYNC1I1
  hgvsc: ENST00000519371.1:n.239-13delT
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000438377
  ensembl transcript: ENST00000537881
  gene symbol: DYNC1I1
  hgvsc: ENST00000537881.1:c.521-13delT
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000412444
  ensembl transcript: ENST00000457059
  gene symbol: DYNC1I1
  hgvsc: ENST00000457059.1:c.581-13delT
  variant of: http://identifiers.org/hgnc/2963
canonical: true
consequence: intron
filter: VQSRTrancheINDEL95.00to96.00
genotype depth: GenotypeDepth
  all individuals: 1371
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1515
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22043
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9645
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 709
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 653
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 868
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 788
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5255
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12649
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2844
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3245
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1409
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 596
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 170
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 180
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2818
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4147
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4823
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: African
reference allele: AT
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: QD

7-95614114-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95614114
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 95614114
    reference: chr 7
allele count: 1
allele frequency: 8.539126276599378e-6
allele num: 117108
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000412444
  ensembl transcript: ENST00000457059
  gene symbol: DYNC1I1
  hgvsc: ENST00000457059.1:c.581-13T>G
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000398118
  ensembl transcript: ENST00000437599
  gene symbol: DYNC1I1
  hgvsc: ENST00000437599.1:c.572-13T>G
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000392337
  ensembl transcript: ENST00000447467
  gene symbol: DYNC1I1
  hgvsc: ENST00000447467.2:c.581-13T>G
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000352348
  ensembl transcript: ENST00000359388
  gene symbol: DYNC1I1
  hgvsc: ENST00000359388.4:c.521-13T>G
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl transcript: ENST00000519371
  gene symbol: DYNC1I1
  hgvsc: ENST00000519371.1:n.239-13T>G
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000320130
  ensembl transcript: ENST00000324972
  gene symbol: DYNC1I1
  hgvsc: ENST00000324972.6:c.632-13T>G
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000438377
  ensembl transcript: ENST00000537881
  gene symbol: DYNC1I1
  hgvsc: ENST00000537881.1:c.521-13T>G
  variant of: http://identifiers.org/hgnc/2963
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1516
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2849
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5265
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 656
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22107
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1313
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12674
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 787
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9684
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 868
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 252
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4151
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 156
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2041
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4823
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7044
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 585
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 329
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: South Asian
population: Latino
population: European (Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD

7-95614115-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95614115
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 95614115
    reference: chr 7
allele count: 3
allele frequency: 2.557283142389525e-5
allele num: 117312
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000320130
  ensembl transcript: ENST00000324972
  gene symbol: DYNC1I1
  hgvsc: ENST00000324972.6:c.632-12A>G
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000438377
  ensembl transcript: ENST00000537881
  gene symbol: DYNC1I1
  hgvsc: ENST00000537881.1:c.521-12A>G
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000398118
  ensembl transcript: ENST00000437599
  gene symbol: DYNC1I1
  hgvsc: ENST00000437599.1:c.572-12A>G
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000412444
  ensembl transcript: ENST00000457059
  gene symbol: DYNC1I1
  hgvsc: ENST00000457059.1:c.581-12A>G
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000392337
  ensembl transcript: ENST00000447467
  gene symbol: DYNC1I1
  hgvsc: ENST00000447467.2:c.581-12A>G
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl transcript: ENST00000519371
  gene symbol: DYNC1I1
  hgvsc: ENST00000519371.1:n.239-12A>G
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000352348
  ensembl transcript: ENST00000359388
  gene symbol: DYNC1I1
  hgvsc: ENST00000359388.4:c.521-12A>G
  variant of: http://identifiers.org/hgnc/2963
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2851
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 617
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5259
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 869
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9705
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1519
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1253
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12713
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22194
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 611
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 788
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 228
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10687
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 223
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2822
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22431
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 160
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4834
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3266
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 297
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: A
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: InbreedingCoeff

7-95614120-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95614120
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 95614120
    reference: chr 7
allele count: 1
allele frequency: 8.458376330079678e-6
allele num: 118226
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000438377
  ensembl transcript: ENST00000537881
  gene symbol: DYNC1I1
  hgvsc: ENST00000537881.1:c.521-7A>G
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000398118
  ensembl transcript: ENST00000437599
  gene symbol: DYNC1I1
  hgvsc: ENST00000437599.1:c.572-7A>G
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000320130
  ensembl transcript: ENST00000324972
  gene symbol: DYNC1I1
  hgvsc: ENST00000324972.6:c.632-7A>G
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000392337
  ensembl transcript: ENST00000447467
  gene symbol: DYNC1I1
  hgvsc: ENST00000447467.2:c.581-7A>G
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl transcript: ENST00000519371
  gene symbol: DYNC1I1
  hgvsc: ENST00000519371.1:n.239-7A>G
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000352348
  ensembl transcript: ENST00000359388
  gene symbol: DYNC1I1
  hgvsc: ENST00000359388.4:c.521-7A>G
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000412444
  ensembl transcript: ENST00000457059
  gene symbol: DYNC1I1
  hgvsc: ENST00000457059.1:c.581-7A>G
  variant of: http://identifiers.org/hgnc/2963
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 869
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12931
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9848
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5292
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 968
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2857
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1517
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 787
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22618
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3285
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2057
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10702
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4880
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 139
  bin: 2.75e1
  variant carriers: 0
hgvs: c.632-7A>G
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
population: Latino
population: European (Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: FS

7-95614126-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95614126
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 95614126
    reference: chr 7
allele count: 1
allele frequency: 8.398703240219711e-6
allele num: 119066
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000412444
  ensembl transcript: ENST00000457059
  gene symbol: DYNC1I1
  hgvsc: ENST00000457059.1:c.581-1G>A
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000398118
  ensembl transcript: ENST00000437599
  gene symbol: DYNC1I1
  hgvsc: ENST00000437599.1:c.572-1G>A
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000352348
  ensembl transcript: ENST00000359388
  gene symbol: DYNC1I1
  hgvsc: ENST00000359388.4:c.521-1G>A
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000158560
  ensembl transcript: ENST00000519371
  gene symbol: DYNC1I1
  hgvsc: ENST00000519371.1:n.239-1G>A
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: true
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000320130
  ensembl transcript: ENST00000324972
  gene symbol: DYNC1I1
  hgvsc: ENST00000324972.6:c.632-1G>A
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000438377
  ensembl transcript: ENST00000537881
  gene symbol: DYNC1I1
  hgvsc: ENST00000537881.1:c.521-1G>A
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000392337
  ensembl transcript: ENST00000447467
  gene symbol: DYNC1I1
  hgvsc: ENST00000447467.2:c.581-1G>A
  variant of: http://identifiers.org/hgnc/2963
canonical: true
consequence: splice acceptor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9925
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13119
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5303
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 817
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1517
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2863
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 870
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23034
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 788
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4198
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 811
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2848
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3307
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2063
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 313
  bin: 7.5e0
  variant carriers: 0
hgvs: c.632-1G>A
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: Latino
population: East Asian
population: African
reference allele: G
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: DP

7-95614130-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95614130
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 95614130
    reference: chr 7
allele count: 1
allele frequency: 8.377173876620983e-6
allele num: 119372
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000320130
  ensembl transcript: ENST00000324972
  gene symbol: DYNC1I1
  hgvsc: ENST00000324972.6:c.635C>T
  hgvsp: ENSP00000320130.6:p.Pro212Leu
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000352348
  ensembl transcript: ENST00000359388
  gene symbol: DYNC1I1
  hgvsc: ENST00000359388.4:c.524C>T
  hgvsp: ENSP00000352348.4:p.Pro175Leu
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000438377
  ensembl transcript: ENST00000537881
  gene symbol: DYNC1I1
  hgvsc: ENST00000537881.1:c.524C>T
  hgvsp: ENSP00000438377.1:p.Pro175Leu
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158560
  ensembl transcript: ENST00000519371
  gene symbol: DYNC1I1
  hgvsc: ENST00000519371.1:n.242C>T
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000398118
  ensembl transcript: ENST00000437599
  gene symbol: DYNC1I1
  hgvsc: ENST00000437599.1:c.575C>T
  hgvsp: ENSP00000398118.1:p.Pro192Leu
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000392337
  ensembl transcript: ENST00000447467
  gene symbol: DYNC1I1
  hgvsc: ENST00000447467.2:c.584C>T
  hgvsp: ENSP00000392337.2:p.Pro195Leu
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000412444
  ensembl transcript: ENST00000457059
  gene symbol: DYNC1I1
  hgvsc: ENST00000457059.1:c.584C>T
  hgvsp: ENSP00000412444.1:p.Pro195Leu
  variant of: http://identifiers.org/hgnc/2963
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2870
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 773
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13157
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 870
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23132
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9955
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 788
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5320
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1522
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2070
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2852
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4906
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Pro212Leu
num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
reference allele: C
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: QD

7-95614134-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95614134
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 95614134
    reference: chr 7
allele count: 1
allele frequency: 8.357570287166115e-6
allele num: 119652
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000438377
  ensembl transcript: ENST00000537881
  gene symbol: DYNC1I1
  hgvsc: ENST00000537881.1:c.528A>G
  hgvsp: ENST00000537881.1:c.528A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000412444
  ensembl transcript: ENST00000457059
  gene symbol: DYNC1I1
  hgvsc: ENST00000457059.1:c.588A>G
  hgvsp: ENST00000457059.1:c.588A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000320130
  ensembl transcript: ENST00000324972
  gene symbol: DYNC1I1
  hgvsc: ENST00000324972.6:c.639A>G
  hgvsp: ENST00000324972.6:c.639A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000352348
  ensembl transcript: ENST00000359388
  gene symbol: DYNC1I1
  hgvsc: ENST00000359388.4:c.528A>G
  hgvsp: ENST00000359388.4:c.528A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000392337
  ensembl transcript: ENST00000447467
  gene symbol: DYNC1I1
  hgvsc: ENST00000447467.2:c.588A>G
  hgvsp: ENST00000447467.2:c.588A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000398118
  ensembl transcript: ENST00000437599
  gene symbol: DYNC1I1
  hgvsc: ENST00000437599.1:c.579A>G
  hgvsp: ENST00000437599.1:c.579A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158560
  ensembl transcript: ENST00000519371
  gene symbol: DYNC1I1
  hgvsc: ENST00000519371.1:n.246A>G
  variant of: http://identifiers.org/hgnc/2963
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 870
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5322
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2876
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23246
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1524
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9973
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 731
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 789
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13178
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2855
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10725
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 139
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4225
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 740
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2072
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Pro213Pro
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
population: Latino
reference allele: A
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum

7-95614141-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95614141
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 95614141
    reference: chr 7
allele count: 1
allele frequency: 8.330001332800213e-6
allele num: 120048
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000438377
  ensembl transcript: ENST00000537881
  gene symbol: DYNC1I1
  hgvsc: ENST00000537881.1:c.535T>C
  hgvsp: ENST00000537881.1:c.535T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000398118
  ensembl transcript: ENST00000437599
  gene symbol: DYNC1I1
  hgvsc: ENST00000437599.1:c.586T>C
  hgvsp: ENST00000437599.1:c.586T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000392337
  ensembl transcript: ENST00000447467
  gene symbol: DYNC1I1
  hgvsc: ENST00000447467.2:c.595T>C
  hgvsp: ENST00000447467.2:c.595T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158560
  ensembl transcript: ENST00000519371
  gene symbol: DYNC1I1
  hgvsc: ENST00000519371.1:n.253T>C
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000320130
  ensembl transcript: ENST00000324972
  gene symbol: DYNC1I1
  hgvsc: ENST00000324972.6:c.646T>C
  hgvsp: ENST00000324972.6:c.646T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000412444
  ensembl transcript: ENST00000457059
  gene symbol: DYNC1I1
  hgvsc: ENST00000457059.1:c.595T>C
  hgvsp: ENST00000457059.1:c.595T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000352348
  ensembl transcript: ENST00000359388
  gene symbol: DYNC1I1
  hgvsc: ENST00000359388.4:c.535T>C
  hgvsp: ENST00000359388.4:c.535T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2963
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1526
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23385
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2880
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5320
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13231
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 872
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9995
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 789
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4916
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7402
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 583
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Leu216Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: South Asian
reference allele: T
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum

7-95614159-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95614159
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 95614159
    reference: chr 7
allele count: 2
allele frequency: 1.658044833532299e-5
allele num: 120624
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000412444
  ensembl transcript: ENST00000457059
  gene symbol: DYNC1I1
  hgvsc: ENST00000457059.1:c.613C>G
  hgvsp: ENSP00000412444.1:p.Gln205Glu
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000438377
  ensembl transcript: ENST00000537881
  gene symbol: DYNC1I1
  hgvsc: ENST00000537881.1:c.553C>G
  hgvsp: ENSP00000438377.1:p.Gln185Glu
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000392337
  ensembl transcript: ENST00000447467
  gene symbol: DYNC1I1
  hgvsc: ENST00000447467.2:c.613C>G
  hgvsp: ENSP00000392337.2:p.Gln205Glu
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158560
  ensembl transcript: ENST00000519371
  gene symbol: DYNC1I1
  hgvsc: ENST00000519371.1:n.271C>G
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000320130
  ensembl transcript: ENST00000324972
  gene symbol: DYNC1I1
  hgvsc: ENST00000324972.6:c.664C>G
  hgvsp: ENSP00000320130.6:p.Gln222Glu
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000398118
  ensembl transcript: ENST00000437599
  gene symbol: DYNC1I1
  hgvsc: ENST00000437599.1:c.604C>G
  hgvsp: ENSP00000398118.1:p.Gln202Glu
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000352348
  ensembl transcript: ENST00000359388
  gene symbol: DYNC1I1
  hgvsc: ENST00000359388.4:c.553C>G
  hgvsp: ENSP00000352348.4:p.Gln185Glu
  variant of: http://identifiers.org/hgnc/2963
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 872
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13302
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5328
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10003
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2882
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1526
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23587
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 790
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4229
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7436
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2856
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3348
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4918
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Gln222Glu
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
population: Other
population: Latino
reference allele: C
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: MQ
site quality: ReadPosRankSum

7-95614160-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95614160
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 95614160
    reference: chr 7
allele count: 1
allele frequency: 8.288025460814215e-6
allele num: 120656
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000438377
  ensembl transcript: ENST00000537881
  gene symbol: DYNC1I1
  hgvsc: ENST00000537881.1:c.554A>G
  hgvsp: ENSP00000438377.1:p.Gln185Arg
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000352348
  ensembl transcript: ENST00000359388
  gene symbol: DYNC1I1
  hgvsc: ENST00000359388.4:c.554A>G
  hgvsp: ENSP00000352348.4:p.Gln185Arg
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000320130
  ensembl transcript: ENST00000324972
  gene symbol: DYNC1I1
  hgvsc: ENST00000324972.6:c.665A>G
  hgvsp: ENSP00000320130.6:p.Gln222Arg
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000392337
  ensembl transcript: ENST00000447467
  gene symbol: DYNC1I1
  hgvsc: ENST00000447467.2:c.614A>G
  hgvsp: ENSP00000392337.2:p.Gln205Arg
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158560
  ensembl transcript: ENST00000519371
  gene symbol: DYNC1I1
  hgvsc: ENST00000519371.1:n.272A>G
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000398118
  ensembl transcript: ENST00000437599
  gene symbol: DYNC1I1
  hgvsc: ENST00000437599.1:c.605A>G
  hgvsp: ENSP00000398118.1:p.Gln202Arg
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000412444
  ensembl transcript: ENST00000457059
  gene symbol: DYNC1I1
  hgvsc: ENST00000457059.1:c.614A>G
  hgvsp: ENSP00000412444.1:p.Gln205Arg
  variant of: http://identifiers.org/hgnc/2963
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1527
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10005
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23596
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 872
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2880
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 790
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5328
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13302
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2857
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10726
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Gln222Arg
num of homozygotes: 0
population: Other
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
reference allele: A
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: QD

7-95614165-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95614165
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 95614165
    reference: chr 7
allele count: 2
allele frequency: 1.656150113446283e-5
allele num: 120762
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000398118
  ensembl transcript: ENST00000437599
  gene symbol: DYNC1I1
  hgvsc: ENST00000437599.1:c.610A>G
  hgvsp: ENSP00000398118.1:p.Ile204Val
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158560
  ensembl transcript: ENST00000519371
  gene symbol: DYNC1I1
  hgvsc: ENST00000519371.1:n.277A>G
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000352348
  ensembl transcript: ENST00000359388
  gene symbol: DYNC1I1
  hgvsc: ENST00000359388.4:c.559A>G
  hgvsp: ENSP00000352348.4:p.Ile187Val
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000392337
  ensembl transcript: ENST00000447467
  gene symbol: DYNC1I1
  hgvsc: ENST00000447467.2:c.619A>G
  hgvsp: ENSP00000392337.2:p.Ile207Val
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000320130
  ensembl transcript: ENST00000324972
  gene symbol: DYNC1I1
  hgvsc: ENST00000324972.6:c.670A>G
  hgvsp: ENSP00000320130.6:p.Ile224Val
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000412444
  ensembl transcript: ENST00000457059
  gene symbol: DYNC1I1
  hgvsc: ENST00000457059.1:c.619A>G
  hgvsp: ENSP00000412444.1:p.Ile207Val
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000438377
  ensembl transcript: ENST00000537881
  gene symbol: DYNC1I1
  hgvsc: ENST00000537881.1:c.559A>G
  hgvsp: ENSP00000438377.1:p.Ile187Val
  variant of: http://identifiers.org/hgnc/2963
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 791
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5327
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1527
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2882
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10007
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13315
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 873
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23645
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3346
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24644
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Ile224Val
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP

7-95614166-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95614166
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 95614166
    reference: chr 7
allele count: 1
allele frequency: 8.280202036929701e-6
allele num: 120770
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000412444
  ensembl transcript: ENST00000457059
  gene symbol: DYNC1I1
  hgvsc: ENST00000457059.1:c.620T>G
  hgvsp: ENSP00000412444.1:p.Ile207Ser
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000438377
  ensembl transcript: ENST00000537881
  gene symbol: DYNC1I1
  hgvsc: ENST00000537881.1:c.560T>G
  hgvsp: ENSP00000438377.1:p.Ile187Ser
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000392337
  ensembl transcript: ENST00000447467
  gene symbol: DYNC1I1
  hgvsc: ENST00000447467.2:c.620T>G
  hgvsp: ENSP00000392337.2:p.Ile207Ser
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000398118
  ensembl transcript: ENST00000437599
  gene symbol: DYNC1I1
  hgvsc: ENST00000437599.1:c.611T>G
  hgvsp: ENSP00000398118.1:p.Ile204Ser
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000320130
  ensembl transcript: ENST00000324972
  gene symbol: DYNC1I1
  hgvsc: ENST00000324972.6:c.671T>G
  hgvsp: ENSP00000320130.6:p.Ile224Ser
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158560
  ensembl transcript: ENST00000519371
  gene symbol: DYNC1I1
  hgvsc: ENST00000519371.1:n.278T>G
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000352348
  ensembl transcript: ENST00000359388
  gene symbol: DYNC1I1
  hgvsc: ENST00000359388.4:c.560T>G
  hgvsp: ENSP00000352348.4:p.Ile187Ser
  variant of: http://identifiers.org/hgnc/2963
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1528
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23649
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5327
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2881
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 873
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 790
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10008
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13318
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3346
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4923
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Ile224Ser
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: South Asian
population: East Asian
reference allele: T
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP

7-95614174-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95614174
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 95614174
    reference: chr 7
allele count: 1
allele frequency: 8.268426187759421e-6
allele num: 120942
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000398118
  ensembl transcript: ENST00000437599
  gene symbol: DYNC1I1
  hgvsc: ENST00000437599.1:c.619T>A
  hgvsp: ENSP00000398118.1:p.Ser207Thr
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000412444
  ensembl transcript: ENST00000457059
  gene symbol: DYNC1I1
  hgvsc: ENST00000457059.1:c.628T>A
  hgvsp: ENSP00000412444.1:p.Ser210Thr
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000392337
  ensembl transcript: ENST00000447467
  gene symbol: DYNC1I1
  hgvsc: ENST00000447467.2:c.628T>A
  hgvsp: ENSP00000392337.2:p.Ser210Thr
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000438377
  ensembl transcript: ENST00000537881
  gene symbol: DYNC1I1
  hgvsc: ENST00000537881.1:c.568T>A
  hgvsp: ENSP00000438377.1:p.Ser190Thr
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000352348
  ensembl transcript: ENST00000359388
  gene symbol: DYNC1I1
  hgvsc: ENST00000359388.4:c.568T>A
  hgvsp: ENSP00000352348.4:p.Ser190Thr
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000320130
  ensembl transcript: ENST00000324972
  gene symbol: DYNC1I1
  hgvsc: ENST00000324972.6:c.679T>A
  hgvsp: ENSP00000320130.6:p.Ser227Thr
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158560
  ensembl transcript: ENST00000519371
  gene symbol: DYNC1I1
  hgvsc: ENST00000519371.1:n.286T>A
  variant of: http://identifiers.org/hgnc/2963
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10011
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5325
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 790
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 874
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1528
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13337
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23730
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2883
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10728
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 7455
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24742
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4233
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 213
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Ser227Thr
num of homozygotes: 0
population: European (Finnish)
population: Other
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
reference allele: T
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: QD

7-95614188-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95614188
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 95614188
    reference: chr 7
allele count: 1
allele frequency: 8.256411103221652e-6
allele num: 121118
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158560
  ensembl transcript: ENST00000519371
  gene symbol: DYNC1I1
  hgvsc: ENST00000519371.1:n.300C>G
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000412444
  ensembl transcript: ENST00000457059
  gene symbol: DYNC1I1
  hgvsc: ENST00000457059.1:c.642C>G
  hgvsp: ENST00000457059.1:c.642C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000438377
  ensembl transcript: ENST00000537881
  gene symbol: DYNC1I1
  hgvsc: ENST00000537881.1:c.582C>G
  hgvsp: ENST00000537881.1:c.582C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000352348
  ensembl transcript: ENST00000359388
  gene symbol: DYNC1I1
  hgvsc: ENST00000359388.4:c.582C>G
  hgvsp: ENST00000359388.4:c.582C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000320130
  ensembl transcript: ENST00000324972
  gene symbol: DYNC1I1
  hgvsc: ENST00000324972.6:c.693C>G
  hgvsp: ENST00000324972.6:c.693C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000398118
  ensembl transcript: ENST00000437599
  gene symbol: DYNC1I1
  hgvsc: ENST00000437599.1:c.633C>G
  hgvsp: ENST00000437599.1:c.633C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000392337
  ensembl transcript: ENST00000447467
  gene symbol: DYNC1I1
  hgvsc: ENST00000447467.2:c.642C>G
  hgvsp: ENST00000447467.2:c.642C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2963
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2885
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23789
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 875
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13363
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1528
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5326
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10023
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 789
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10729
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3349
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 136
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4919
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7457
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Leu231Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
population: African
population: Latino
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: ReadPosRankSum

7-95614191-C-CT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95614191
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 95614192
    reference: chr 7
allele count: 1
allele frequency: 8.255184255712587e-6
allele num: 121136
alternate allele: CT
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000392337
  ensembl transcript: ENST00000447467
  gene symbol: DYNC1I1
  hgvsc: ENST00000447467.2:c.651dupT
  hgvsp: ENSP00000392337.2:p.Asp218Ter
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000398118
  ensembl transcript: ENST00000437599
  gene symbol: DYNC1I1
  hgvsc: ENST00000437599.1:c.642dupT
  hgvsp: ENSP00000398118.1:p.Asp215Ter
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000320130
  ensembl transcript: ENST00000324972
  gene symbol: DYNC1I1
  hgvsc: ENST00000324972.6:c.702dupT
  hgvsp: ENSP00000320130.6:p.Asp235Ter
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000352348
  ensembl transcript: ENST00000359388
  gene symbol: DYNC1I1
  hgvsc: ENST00000359388.4:c.591dupT
  hgvsp: ENSP00000352348.4:p.Asp198Ter
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000438377
  ensembl transcript: ENST00000537881
  gene symbol: DYNC1I1
  hgvsc: ENST00000537881.1:c.591dupT
  hgvsp: ENSP00000438377.1:p.Asp198Ter
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158560
  ensembl transcript: ENST00000519371
  gene symbol: DYNC1I1
  hgvsc: ENST00000519371.1:n.309dupT
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000412444
  ensembl transcript: ENST00000457059
  gene symbol: DYNC1I1
  hgvsc: ENST00000457059.1:c.651dupT
  hgvsp: ENSP00000412444.1:p.Asp218Ter
  variant of: http://identifiers.org/hgnc/2963
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 23795
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1528
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10022
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 874
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5328
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13365
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 790
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2883
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10729
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2075
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 125
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Asp235Ter
num of homozygotes: 0
population: Other
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
reference allele: C
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum

7-95614192-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95614192
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 95614192
    reference: chr 7
allele count: 1
allele frequency: 8.254775387561705e-6
allele num: 121142
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158560
  ensembl transcript: ENST00000519371
  gene symbol: DYNC1I1
  hgvsc: ENST00000519371.1:n.304T>C
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000352348
  ensembl transcript: ENST00000359388
  gene symbol: DYNC1I1
  hgvsc: ENST00000359388.4:c.586T>C
  hgvsp: ENSP00000352348.4:p.Phe196Leu
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000392337
  ensembl transcript: ENST00000447467
  gene symbol: DYNC1I1
  hgvsc: ENST00000447467.2:c.646T>C
  hgvsp: ENSP00000392337.2:p.Phe216Leu
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000412444
  ensembl transcript: ENST00000457059
  gene symbol: DYNC1I1
  hgvsc: ENST00000457059.1:c.646T>C
  hgvsp: ENSP00000412444.1:p.Phe216Leu
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000438377
  ensembl transcript: ENST00000537881
  gene symbol: DYNC1I1
  hgvsc: ENST00000537881.1:c.586T>C
  hgvsp: ENSP00000438377.1:p.Phe196Leu
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000398118
  ensembl transcript: ENST00000437599
  gene symbol: DYNC1I1
  hgvsc: ENST00000437599.1:c.637T>C
  hgvsp: ENSP00000398118.1:p.Phe213Leu
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000320130
  ensembl transcript: ENST00000324972
  gene symbol: DYNC1I1
  hgvsc: ENST00000324972.6:c.697T>C
  hgvsp: ENSP00000320130.6:p.Phe233Leu
  variant of: http://identifiers.org/hgnc/2963
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 791
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 874
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10027
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1528
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13361
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2883
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5327
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23798
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24827
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7460
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 126
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Phe233Leu
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: Other
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum

7-95614193-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95614193
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 95614193
    reference: chr 7
allele count: 1
allele frequency: 8.254094030639197e-6
allele num: 121152
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000398118
  ensembl transcript: ENST00000437599
  gene symbol: DYNC1I1
  hgvsc: ENST00000437599.1:c.638T>C
  hgvsp: ENSP00000398118.1:p.Phe213Ser
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000352348
  ensembl transcript: ENST00000359388
  gene symbol: DYNC1I1
  hgvsc: ENST00000359388.4:c.587T>C
  hgvsp: ENSP00000352348.4:p.Phe196Ser
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000438377
  ensembl transcript: ENST00000537881
  gene symbol: DYNC1I1
  hgvsc: ENST00000537881.1:c.587T>C
  hgvsp: ENSP00000438377.1:p.Phe196Ser
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000320130
  ensembl transcript: ENST00000324972
  gene symbol: DYNC1I1
  hgvsc: ENST00000324972.6:c.698T>C
  hgvsp: ENSP00000320130.6:p.Phe233Ser
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000412444
  ensembl transcript: ENST00000457059
  gene symbol: DYNC1I1
  hgvsc: ENST00000457059.1:c.647T>C
  hgvsp: ENSP00000412444.1:p.Phe216Ser
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000392337
  ensembl transcript: ENST00000447467
  gene symbol: DYNC1I1
  hgvsc: ENST00000447467.2:c.647T>C
  hgvsp: ENSP00000392337.2:p.Phe216Ser
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158560
  ensembl transcript: ENST00000519371
  gene symbol: DYNC1I1
  hgvsc: ENST00000519371.1:n.305T>C
  variant of: http://identifiers.org/hgnc/2963
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5327
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10024
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2883
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 790
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1529
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13362
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 874
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23801
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4918
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10730
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2075
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 126
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Phe233Ser
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
population: Other
population: African
population: European (Non-Finnish)
reference allele: T
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff

7-95614201-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95614201
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 95614201
    reference: chr 7
allele count: 2
allele frequency: 1.650464605786529e-5
allele num: 121178
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000320130
  ensembl transcript: ENST00000324972
  gene symbol: DYNC1I1
  hgvsc: ENST00000324972.6:c.706C>T
  hgvsp: ENSP00000320130.6:p.Arg236Trp
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000352348
  ensembl transcript: ENST00000359388
  gene symbol: DYNC1I1
  hgvsc: ENST00000359388.4:c.595C>T
  hgvsp: ENSP00000352348.4:p.Arg199Trp
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158560
  ensembl transcript: ENST00000519371
  gene symbol: DYNC1I1
  hgvsc: ENST00000519371.1:n.313C>T
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000398118
  ensembl transcript: ENST00000437599
  gene symbol: DYNC1I1
  hgvsc: ENST00000437599.1:c.646C>T
  hgvsp: ENSP00000398118.1:p.Arg216Trp
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000412444
  ensembl transcript: ENST00000457059
  gene symbol: DYNC1I1
  hgvsc: ENST00000457059.1:c.655C>T
  hgvsp: ENSP00000412444.1:p.Arg219Trp
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000392337
  ensembl transcript: ENST00000447467
  gene symbol: DYNC1I1
  hgvsc: ENST00000447467.2:c.655C>T
  hgvsp: ENSP00000392337.2:p.Arg219Trp
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000438377
  ensembl transcript: ENST00000537881
  gene symbol: DYNC1I1
  hgvsc: ENST00000537881.1:c.595C>T
  hgvsp: ENSP00000438377.1:p.Arg199Trp
  variant of: http://identifiers.org/hgnc/2963
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10026
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13367
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23820
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2882
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 790
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1529
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5328
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 873
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24839
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3348
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4916
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Arg236Trp
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
population: East Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP

7-95614202-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95614202
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 95614202
    reference: chr 7
allele count: 2
allele frequency: 1.650464605786529e-5
allele num: 121178
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000352348
  ensembl transcript: ENST00000359388
  gene symbol: DYNC1I1
  hgvsc: ENST00000359388.4:c.596G>A
  hgvsp: ENSP00000352348.4:p.Arg199Gln
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000320130
  ensembl transcript: ENST00000324972
  gene symbol: DYNC1I1
  hgvsc: ENST00000324972.6:c.707G>A
  hgvsp: ENSP00000320130.6:p.Arg236Gln
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158560
  ensembl transcript: ENST00000519371
  gene symbol: DYNC1I1
  hgvsc: ENST00000519371.1:n.314G>A
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000438377
  ensembl transcript: ENST00000537881
  gene symbol: DYNC1I1
  hgvsc: ENST00000537881.1:c.596G>A
  hgvsp: ENSP00000438377.1:p.Arg199Gln
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000392337
  ensembl transcript: ENST00000447467
  gene symbol: DYNC1I1
  hgvsc: ENST00000447467.2:c.656G>A
  hgvsp: ENSP00000392337.2:p.Arg219Gln
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000412444
  ensembl transcript: ENST00000457059
  gene symbol: DYNC1I1
  hgvsc: ENST00000457059.1:c.656G>A
  hgvsp: ENSP00000412444.1:p.Arg219Gln
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000398118
  ensembl transcript: ENST00000437599
  gene symbol: DYNC1I1
  hgvsc: ENST00000437599.1:c.647G>A
  hgvsp: ENSP00000398118.1:p.Arg216Gln
  variant of: http://identifiers.org/hgnc/2963
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 23818
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1530
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 873
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13367
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5331
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10025
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2886
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 790
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4238
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10732
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4915
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Arg236Gln
num of homozygotes: 0
population: Other
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD

7-95614210-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95614210
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 95614210
    reference: chr 7
allele count: 4
allele frequency: 3.3000033000033e-5
allele num: 121212
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000438377
  ensembl transcript: ENST00000537881
  gene symbol: DYNC1I1
  hgvsc: ENST00000537881.1:c.604C>T
  hgvsp: ENSP00000438377.1:p.Arg202Trp
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000352348
  ensembl transcript: ENST00000359388
  gene symbol: DYNC1I1
  hgvsc: ENST00000359388.4:c.604C>T
  hgvsp: ENSP00000352348.4:p.Arg202Trp
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000412444
  ensembl transcript: ENST00000457059
  gene symbol: DYNC1I1
  hgvsc: ENST00000457059.1:c.664C>T
  hgvsp: ENSP00000412444.1:p.Arg222Trp
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000392337
  ensembl transcript: ENST00000447467
  gene symbol: DYNC1I1
  hgvsc: ENST00000447467.2:c.664C>T
  hgvsp: ENSP00000392337.2:p.Arg222Trp
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000398118
  ensembl transcript: ENST00000437599
  gene symbol: DYNC1I1
  hgvsc: ENST00000437599.1:c.655C>T
  hgvsp: ENSP00000398118.1:p.Arg219Trp
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000320130
  ensembl transcript: ENST00000324972
  gene symbol: DYNC1I1
  hgvsc: ENST00000324972.6:c.715C>T
  hgvsp: ENSP00000320130.6:p.Arg239Trp
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158560
  ensembl transcript: ENST00000519371
  gene symbol: DYNC1I1
  hgvsc: ENST00000519371.1:n.322C>T
  variant of: http://identifiers.org/hgnc/2963
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13377
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10026
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23821
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 873
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 793
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5331
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1530
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2884
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2856
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10735
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Arg239Trp
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum

7-95614211-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95614211
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 95614211
    reference: chr 7
allele count: 2
allele frequency: 1.65000165000165e-5
allele num: 121212
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000438377
  ensembl transcript: ENST00000537881
  gene symbol: DYNC1I1
  hgvsc: ENST00000537881.1:c.605G>A
  hgvsp: ENSP00000438377.1:p.Arg202Gln
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000352348
  ensembl transcript: ENST00000359388
  gene symbol: DYNC1I1
  hgvsc: ENST00000359388.4:c.605G>A
  hgvsp: ENSP00000352348.4:p.Arg202Gln
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000392337
  ensembl transcript: ENST00000447467
  gene symbol: DYNC1I1
  hgvsc: ENST00000447467.2:c.665G>A
  hgvsp: ENSP00000392337.2:p.Arg222Gln
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000412444
  ensembl transcript: ENST00000457059
  gene symbol: DYNC1I1
  hgvsc: ENST00000457059.1:c.665G>A
  hgvsp: ENSP00000412444.1:p.Arg222Gln
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158560
  ensembl transcript: ENST00000519371
  gene symbol: DYNC1I1
  hgvsc: ENST00000519371.1:n.323G>A
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000398118
  ensembl transcript: ENST00000437599
  gene symbol: DYNC1I1
  hgvsc: ENST00000437599.1:c.656G>A
  hgvsp: ENSP00000398118.1:p.Arg219Gln
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000320130
  ensembl transcript: ENST00000324972
  gene symbol: DYNC1I1
  hgvsc: ENST00000324972.6:c.716G>A
  hgvsp: ENSP00000320130.6:p.Arg239Gln
  variant of: http://identifiers.org/hgnc/2963
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2884
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23817
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13378
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10033
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1530
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 873
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5330
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 791
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4918
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2856
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Arg239Gln
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
population: Latino
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: FS

7-95614211-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95614211
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 95614211
    reference: chr 7
allele count: 1
allele frequency: 8.25000825000825e-6
allele num: 121212
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000352348
  ensembl transcript: ENST00000359388
  gene symbol: DYNC1I1
  hgvsc: ENST00000359388.4:c.605G>T
  hgvsp: ENSP00000352348.4:p.Arg202Leu
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000412444
  ensembl transcript: ENST00000457059
  gene symbol: DYNC1I1
  hgvsc: ENST00000457059.1:c.665G>T
  hgvsp: ENSP00000412444.1:p.Arg222Leu
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000398118
  ensembl transcript: ENST00000437599
  gene symbol: DYNC1I1
  hgvsc: ENST00000437599.1:c.656G>T
  hgvsp: ENSP00000398118.1:p.Arg219Leu
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000320130
  ensembl transcript: ENST00000324972
  gene symbol: DYNC1I1
  hgvsc: ENST00000324972.6:c.716G>T
  hgvsp: ENSP00000320130.6:p.Arg239Leu
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000438377
  ensembl transcript: ENST00000537881
  gene symbol: DYNC1I1
  hgvsc: ENST00000537881.1:c.605G>T
  hgvsp: ENSP00000438377.1:p.Arg202Leu
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000392337
  ensembl transcript: ENST00000447467
  gene symbol: DYNC1I1
  hgvsc: ENST00000447467.2:c.665G>T
  hgvsp: ENSP00000392337.2:p.Arg222Leu
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158560
  ensembl transcript: ENST00000519371
  gene symbol: DYNC1I1
  hgvsc: ENST00000519371.1:n.323G>T
  variant of: http://identifiers.org/hgnc/2963
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 791
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23817
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1530
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10033
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13378
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 873
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2884
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5330
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4242
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7458
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Arg239Leu
num of homozygotes: 0
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: DP

7-95614234-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95614234
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 95614234
    reference: chr 7
allele count: 2
allele frequency: 1.649566164098842e-5
allele num: 121244
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000438377
  ensembl transcript: ENST00000537881
  gene symbol: DYNC1I1
  hgvsc: ENST00000537881.1:c.628G>C
  hgvsp: ENSP00000438377.1:p.Glu210Gln
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000320130
  ensembl transcript: ENST00000324972
  gene symbol: DYNC1I1
  hgvsc: ENST00000324972.6:c.739G>C
  hgvsp: ENSP00000320130.6:p.Glu247Gln
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000352348
  ensembl transcript: ENST00000359388
  gene symbol: DYNC1I1
  hgvsc: ENST00000359388.4:c.628G>C
  hgvsp: ENSP00000352348.4:p.Glu210Gln
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158560
  ensembl transcript: ENST00000519371
  gene symbol: DYNC1I1
  hgvsc: ENST00000519371.1:n.346G>C
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000392337
  ensembl transcript: ENST00000447467
  gene symbol: DYNC1I1
  hgvsc: ENST00000447467.2:c.688G>C
  hgvsp: ENSP00000392337.2:p.Glu230Gln
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000398118
  ensembl transcript: ENST00000437599
  gene symbol: DYNC1I1
  hgvsc: ENST00000437599.1:c.679G>C
  hgvsp: ENSP00000398118.1:p.Glu227Gln
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000412444
  ensembl transcript: ENST00000457059
  gene symbol: DYNC1I1
  hgvsc: ENST00000457059.1:c.688G>C
  hgvsp: ENSP00000412444.1:p.Glu230Gln
  variant of: http://identifiers.org/hgnc/2963
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10019
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1529
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 873
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13390
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2886
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23796
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 791
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5328
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3349
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7474
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Glu247Gln
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ

7-95614242-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95614242
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 95614242
    reference: chr 7
allele count: 1
allele frequency: 8.246742536698004e-6
allele num: 121260
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000392337
  ensembl transcript: ENST00000447467
  gene symbol: DYNC1I1
  hgvsc: ENST00000447467.2:c.696C>G
  hgvsp: ENST00000447467.2:c.696C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000398118
  ensembl transcript: ENST00000437599
  gene symbol: DYNC1I1
  hgvsc: ENST00000437599.1:c.687C>G
  hgvsp: ENST00000437599.1:c.687C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000352348
  ensembl transcript: ENST00000359388
  gene symbol: DYNC1I1
  hgvsc: ENST00000359388.4:c.636C>G
  hgvsp: ENST00000359388.4:c.636C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000320130
  ensembl transcript: ENST00000324972
  gene symbol: DYNC1I1
  hgvsc: ENST00000324972.6:c.747C>G
  hgvsp: ENST00000324972.6:c.747C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000438377
  ensembl transcript: ENST00000537881
  gene symbol: DYNC1I1
  hgvsc: ENST00000537881.1:c.636C>G
  hgvsp: ENST00000537881.1:c.636C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000412444
  ensembl transcript: ENST00000457059
  gene symbol: DYNC1I1
  hgvsc: ENST00000457059.1:c.696C>G
  hgvsp: ENST00000457059.1:c.696C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158560
  ensembl transcript: ENST00000519371
  gene symbol: DYNC1I1
  hgvsc: ENST00000519371.1:n.354C>G
  variant of: http://identifiers.org/hgnc/2963
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5321
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23796
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10019
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13380
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 811
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2883
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1528
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 873
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2856
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24844
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4917
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7466
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Ser249Ser
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
population: European (Finnish)
reference allele: C
site quality: FS
site quality: DP
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum

7-95614242-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95614242
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 95614242
    reference: chr 7
allele count: 24
allele frequency: 1.979218208807521e-4
allele num: 121260
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000438377
  ensembl transcript: ENST00000537881
  gene symbol: DYNC1I1
  hgvsc: ENST00000537881.1:c.636C>T
  hgvsp: ENST00000537881.1:c.636C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000398118
  ensembl transcript: ENST00000437599
  gene symbol: DYNC1I1
  hgvsc: ENST00000437599.1:c.687C>T
  hgvsp: ENST00000437599.1:c.687C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158560
  ensembl transcript: ENST00000519371
  gene symbol: DYNC1I1
  hgvsc: ENST00000519371.1:n.354C>T
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000412444
  ensembl transcript: ENST00000457059
  gene symbol: DYNC1I1
  hgvsc: ENST00000457059.1:c.696C>T
  hgvsp: ENST00000457059.1:c.696C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000392337
  ensembl transcript: ENST00000447467
  gene symbol: DYNC1I1
  hgvsc: ENST00000447467.2:c.696C>T
  hgvsp: ENST00000447467.2:c.696C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000352348
  ensembl transcript: ENST00000359388
  gene symbol: DYNC1I1
  hgvsc: ENST00000359388.4:c.636C>T
  hgvsp: ENST00000359388.4:c.636C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000320130
  ensembl transcript: ENST00000324972
  gene symbol: DYNC1I1
  hgvsc: ENST00000324972.6:c.747C>T
  hgvsp: ENST00000324972.6:c.747C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2963
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1528
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10019
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2883
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 811
  bin: 9.75e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 873
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13380
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5321
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23796
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2075
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3346
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2856
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4237
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10749
  bin: 9.75e1
  variant carriers: 24
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7466
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Ser249Ser
num of homozygotes: 0
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
population: East Asian
reference allele: C
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: DP

7-95614243-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95614243
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 95614243
    reference: chr 7
allele count: 1
allele frequency: 8.247014580721778e-6
allele num: 121256
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000398118
  ensembl transcript: ENST00000437599
  gene symbol: DYNC1I1
  hgvsc: ENST00000437599.1:c.688G>A
  hgvsp: ENSP00000398118.1:p.Asp230Asn
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000438377
  ensembl transcript: ENST00000537881
  gene symbol: DYNC1I1
  hgvsc: ENST00000537881.1:c.637G>A
  hgvsp: ENSP00000438377.1:p.Asp213Asn
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158560
  ensembl transcript: ENST00000519371
  gene symbol: DYNC1I1
  hgvsc: ENST00000519371.1:n.355G>A
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000320130
  ensembl transcript: ENST00000324972
  gene symbol: DYNC1I1
  hgvsc: ENST00000324972.6:c.748G>A
  hgvsp: ENSP00000320130.6:p.Asp250Asn
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000352348
  ensembl transcript: ENST00000359388
  gene symbol: DYNC1I1
  hgvsc: ENST00000359388.4:c.637G>A
  hgvsp: ENSP00000352348.4:p.Asp213Asn
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000412444
  ensembl transcript: ENST00000457059
  gene symbol: DYNC1I1
  hgvsc: ENST00000457059.1:c.697G>A
  hgvsp: ENSP00000412444.1:p.Asp233Asn
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000392337
  ensembl transcript: ENST00000447467
  gene symbol: DYNC1I1
  hgvsc: ENST00000447467.2:c.697G>A
  hgvsp: ENSP00000392337.2:p.Asp233Asn
  variant of: http://identifiers.org/hgnc/2963
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13381
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 877
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5323
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10026
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2888
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1535
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 791
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23790
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3347
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 95
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2859
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Asp250Asn
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
reference allele: G
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum

7-95614247-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95614247
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 95614247
    reference: chr 7
allele count: 1
allele frequency: 8.246878556466378e-6
allele num: 121258
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000398118
  ensembl transcript: ENST00000437599
  gene symbol: DYNC1I1
  hgvsc: ENST00000437599.1:c.692T>C
  hgvsp: ENSP00000398118.1:p.Ile231Thr
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000412444
  ensembl transcript: ENST00000457059
  gene symbol: DYNC1I1
  hgvsc: ENST00000457059.1:c.701T>C
  hgvsp: ENSP00000412444.1:p.Ile234Thr
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000392337
  ensembl transcript: ENST00000447467
  gene symbol: DYNC1I1
  hgvsc: ENST00000447467.2:c.701T>C
  hgvsp: ENSP00000392337.2:p.Ile234Thr
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000438377
  ensembl transcript: ENST00000537881
  gene symbol: DYNC1I1
  hgvsc: ENST00000537881.1:c.641T>C
  hgvsp: ENSP00000438377.1:p.Ile214Thr
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000352348
  ensembl transcript: ENST00000359388
  gene symbol: DYNC1I1
  hgvsc: ENST00000359388.4:c.641T>C
  hgvsp: ENSP00000352348.4:p.Ile214Thr
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000320130
  ensembl transcript: ENST00000324972
  gene symbol: DYNC1I1
  hgvsc: ENST00000324972.6:c.752T>C
  hgvsp: ENSP00000320130.6:p.Ile251Thr
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158560
  ensembl transcript: ENST00000519371
  gene symbol: DYNC1I1
  hgvsc: ENST00000519371.1:n.359T>C
  variant of: http://identifiers.org/hgnc/2963
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10026
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13382
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1534
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2889
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23795
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 877
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5321
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 790
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 101
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2859
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2077
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Ile251Thr
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: T
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum

7-95614261-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95614261
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 95614261
    reference: chr 7
allele count: 8
allele frequency: 6.599679915524098e-5
allele num: 121218
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000352348
  ensembl transcript: ENST00000359388
  gene symbol: DYNC1I1
  hgvsc: ENST00000359388.4:c.655A>G
  hgvsp: ENSP00000352348.4:p.Ser219Gly
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000398118
  ensembl transcript: ENST00000437599
  gene symbol: DYNC1I1
  hgvsc: ENST00000437599.1:c.706A>G
  hgvsp: ENSP00000398118.1:p.Ser236Gly
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000320130
  ensembl transcript: ENST00000324972
  gene symbol: DYNC1I1
  hgvsc: ENST00000324972.6:c.766A>G
  hgvsp: ENSP00000320130.6:p.Ser256Gly
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158560
  ensembl transcript: ENST00000519371
  gene symbol: DYNC1I1
  hgvsc: ENST00000519371.1:n.373A>G
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000438377
  ensembl transcript: ENST00000537881
  gene symbol: DYNC1I1
  hgvsc: ENST00000537881.1:c.655A>G
  hgvsp: ENSP00000438377.1:p.Ser219Gly
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000392337
  ensembl transcript: ENST00000447467
  gene symbol: DYNC1I1
  hgvsc: ENST00000447467.2:c.715A>G
  hgvsp: ENSP00000392337.2:p.Ser239Gly
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000412444
  ensembl transcript: ENST00000457059
  gene symbol: DYNC1I1
  hgvsc: ENST00000457059.1:c.715A>G
  hgvsp: ENSP00000412444.1:p.Ser239Gly
  variant of: http://identifiers.org/hgnc/2963
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2889
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 877
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5323
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10021
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13375
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 796
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1533
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23758
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10744
  bin: 9.75e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ser256Gly
num of homozygotes: 0
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum

7-95614263-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95614263
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 95614263
    reference: chr 7
allele count: 5
allele frequency: 4.124731892426992e-5
allele num: 121220
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000392337
  ensembl transcript: ENST00000447467
  gene symbol: DYNC1I1
  hgvsc: ENST00000447467.2:c.717C>T
  hgvsp: ENST00000447467.2:c.717C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000398118
  ensembl transcript: ENST00000437599
  gene symbol: DYNC1I1
  hgvsc: ENST00000437599.1:c.708C>T
  hgvsp: ENST00000437599.1:c.708C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158560
  ensembl transcript: ENST00000519371
  gene symbol: DYNC1I1
  hgvsc: ENST00000519371.1:n.375C>T
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000320130
  ensembl transcript: ENST00000324972
  gene symbol: DYNC1I1
  hgvsc: ENST00000324972.6:c.768C>T
  hgvsp: ENST00000324972.6:c.768C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000352348
  ensembl transcript: ENST00000359388
  gene symbol: DYNC1I1
  hgvsc: ENST00000359388.4:c.657C>T
  hgvsp: ENST00000359388.4:c.657C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000438377
  ensembl transcript: ENST00000537881
  gene symbol: DYNC1I1
  hgvsc: ENST00000537881.1:c.657C>T
  hgvsp: ENST00000537881.1:c.657C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000412444
  ensembl transcript: ENST00000457059
  gene symbol: DYNC1I1
  hgvsc: ENST00000457059.1:c.717C>T
  hgvsp: ENST00000457059.1:c.717C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2963
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1532
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13375
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5324
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10018
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23761
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2889
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 878
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4235
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2077
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Ser256Ser
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: QD

7-95614268-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95614268
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 95614268
    reference: chr 7
allele count: 1
allele frequency: 8.250688932525866e-6
allele num: 121202
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000438377
  ensembl transcript: ENST00000537881
  gene symbol: DYNC1I1
  hgvsc: ENST00000537881.1:c.662G>T
  hgvsp: ENSP00000438377.1:p.Arg221Leu
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000398118
  ensembl transcript: ENST00000437599
  gene symbol: DYNC1I1
  hgvsc: ENST00000437599.1:c.713G>T
  hgvsp: ENSP00000398118.1:p.Arg238Leu
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000392337
  ensembl transcript: ENST00000447467
  gene symbol: DYNC1I1
  hgvsc: ENST00000447467.2:c.722G>T
  hgvsp: ENSP00000392337.2:p.Arg241Leu
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000320130
  ensembl transcript: ENST00000324972
  gene symbol: DYNC1I1
  hgvsc: ENST00000324972.6:c.773G>T
  hgvsp: ENSP00000320130.6:p.Arg258Leu
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000352348
  ensembl transcript: ENST00000359388
  gene symbol: DYNC1I1
  hgvsc: ENST00000359388.4:c.662G>T
  hgvsp: ENSP00000352348.4:p.Arg221Leu
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158560
  ensembl transcript: ENST00000519371
  gene symbol: DYNC1I1
  hgvsc: ENST00000519371.1:n.380G>T
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000412444
  ensembl transcript: ENST00000457059
  gene symbol: DYNC1I1
  hgvsc: ENST00000457059.1:c.722G>T
  hgvsp: ENSP00000412444.1:p.Arg241Leu
  variant of: http://identifiers.org/hgnc/2963
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1532
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23758
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 878
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13360
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2890
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10013
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5324
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4906
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10746
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 155
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4236
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Arg258Leu
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD

7-95614268-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95614268
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 95614268
    reference: chr 7
allele count: 1
allele frequency: 8.250688932525866e-6
allele num: 121202
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000320130
  ensembl transcript: ENST00000324972
  gene symbol: DYNC1I1
  hgvsc: ENST00000324972.6:c.773G>A
  hgvsp: ENSP00000320130.6:p.Arg258Gln
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000438377
  ensembl transcript: ENST00000537881
  gene symbol: DYNC1I1
  hgvsc: ENST00000537881.1:c.662G>A
  hgvsp: ENSP00000438377.1:p.Arg221Gln
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000352348
  ensembl transcript: ENST00000359388
  gene symbol: DYNC1I1
  hgvsc: ENST00000359388.4:c.662G>A
  hgvsp: ENSP00000352348.4:p.Arg221Gln
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000398118
  ensembl transcript: ENST00000437599
  gene symbol: DYNC1I1
  hgvsc: ENST00000437599.1:c.713G>A
  hgvsp: ENSP00000398118.1:p.Arg238Gln
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000412444
  ensembl transcript: ENST00000457059
  gene symbol: DYNC1I1
  hgvsc: ENST00000457059.1:c.722G>A
  hgvsp: ENSP00000412444.1:p.Arg241Gln
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000392337
  ensembl transcript: ENST00000447467
  gene symbol: DYNC1I1
  hgvsc: ENST00000447467.2:c.722G>A
  hgvsp: ENSP00000392337.2:p.Arg241Gln
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158560
  ensembl transcript: ENST00000519371
  gene symbol: DYNC1I1
  hgvsc: ENST00000519371.1:n.380G>A
  variant of: http://identifiers.org/hgnc/2963
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 878
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5324
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2890
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23758
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13360
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10013
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1532
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 155
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4906
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24787
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Arg258Gln
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: Latino
reference allele: G
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ

7-95614272-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95614272
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 95614272
    reference: chr 7
allele count: 140
allele frequency: 1.155058330445688e-3
allele num: 121206
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158560
  ensembl transcript: ENST00000519371
  gene symbol: DYNC1I1
  hgvsc: ENST00000519371.1:n.384G>A
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000352348
  ensembl transcript: ENST00000359388
  gene symbol: DYNC1I1
  hgvsc: ENST00000359388.4:c.666G>A
  hgvsp: ENST00000359388.4:c.666G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000438377
  ensembl transcript: ENST00000537881
  gene symbol: DYNC1I1
  hgvsc: ENST00000537881.1:c.666G>A
  hgvsp: ENST00000537881.1:c.666G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000398118
  ensembl transcript: ENST00000437599
  gene symbol: DYNC1I1
  hgvsc: ENST00000437599.1:c.717G>A
  hgvsp: ENST00000437599.1:c.717G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000392337
  ensembl transcript: ENST00000447467
  gene symbol: DYNC1I1
  hgvsc: ENST00000447467.2:c.726G>A
  hgvsp: ENST00000447467.2:c.726G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000412444
  ensembl transcript: ENST00000457059
  gene symbol: DYNC1I1
  hgvsc: ENST00000457059.1:c.726G>A
  hgvsp: ENST00000457059.1:c.726G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000320130
  ensembl transcript: ENST00000324972
  gene symbol: DYNC1I1
  hgvsc: ENST00000324972.6:c.777G>A
  hgvsp: ENST00000324972.6:c.777G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2963
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 877
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1527
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 9.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 8.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13316
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 887
  bin: 9.75e1
  variant carriers: 98
genotype depth: GenotypeDepth
  all individuals: 9992
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 7.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5324
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2883
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23707
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 8.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 24747
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10852
  bin: 9.75e1
  variant carriers: 137
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4900
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4220
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 161
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Glu259Glu
num of homozygotes: 3
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: South Asian
population: African
population: East Asian
population: Latino
reference allele: G
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

7-95614290-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95614290
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 95614290
    reference: chr 7
allele count: 1
allele frequency: 8.256547442121603e-6
allele num: 121116
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000392337
  ensembl transcript: ENST00000447467
  gene symbol: DYNC1I1
  hgvsc: ENST00000447467.2:c.743+1G>A
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000398118
  ensembl transcript: ENST00000437599
  gene symbol: DYNC1I1
  hgvsc: ENST00000437599.1:c.734+1G>A
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000352348
  ensembl transcript: ENST00000359388
  gene symbol: DYNC1I1
  hgvsc: ENST00000359388.4:c.683+1G>A
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: true
  consequence: splice_donor_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000320130
  ensembl transcript: ENST00000324972
  gene symbol: DYNC1I1
  hgvsc: ENST00000324972.6:c.794+1G>A
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000412444
  ensembl transcript: ENST00000457059
  gene symbol: DYNC1I1
  hgvsc: ENST00000457059.1:c.743+1G>A
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000438377
  ensembl transcript: ENST00000537881
  gene symbol: DYNC1I1
  hgvsc: ENST00000537881.1:c.683+1G>A
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000158560
  ensembl transcript: ENST00000519371
  gene symbol: DYNC1I1
  hgvsc: ENST00000519371.1:n.401+1G>A
  variant of: http://identifiers.org/hgnc/2963
canonical: true
consequence: splice donor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13316
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23602
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10006
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 887
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5342
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1541
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 795
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2899
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10769
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3325
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2081
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 4.75e1
  variant carriers: 0
hgvs: c.794+1G>A
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum

7-95614298-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95614298
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 95614298
    reference: chr 7
allele count: 2
allele frequency: 1.651554938975045e-5
allele num: 121098
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000352348
  ensembl transcript: ENST00000359388
  gene symbol: DYNC1I1
  hgvsc: ENST00000359388.4:c.683+9C>G
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000320130
  ensembl transcript: ENST00000324972
  gene symbol: DYNC1I1
  hgvsc: ENST00000324972.6:c.794+9C>G
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000438377
  ensembl transcript: ENST00000537881
  gene symbol: DYNC1I1
  hgvsc: ENST00000537881.1:c.683+9C>G
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000398118
  ensembl transcript: ENST00000437599
  gene symbol: DYNC1I1
  hgvsc: ENST00000437599.1:c.734+9C>G
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000392337
  ensembl transcript: ENST00000447467
  gene symbol: DYNC1I1
  hgvsc: ENST00000447467.2:c.743+9C>G
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000412444
  ensembl transcript: ENST00000457059
  gene symbol: DYNC1I1
  hgvsc: ENST00000457059.1:c.743+9C>G
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl transcript: ENST00000519371
  gene symbol: DYNC1I1
  hgvsc: ENST00000519371.1:n.401+9C>G
  variant of: http://identifiers.org/hgnc/2963
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9991
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1541
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13295
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 887
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2899
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23502
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5342
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 795
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3322
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4228
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7413
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: European (Finnish)
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum

7-95614300-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95614300
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 95614300
    reference: chr 7
allele count: 1
allele frequency: 8.259138737012504e-6
allele num: 121078
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000392337
  ensembl transcript: ENST00000447467
  gene symbol: DYNC1I1
  hgvsc: ENST00000447467.2:c.743+11T>C
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000352348
  ensembl transcript: ENST00000359388
  gene symbol: DYNC1I1
  hgvsc: ENST00000359388.4:c.683+11T>C
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000438377
  ensembl transcript: ENST00000537881
  gene symbol: DYNC1I1
  hgvsc: ENST00000537881.1:c.683+11T>C
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000412444
  ensembl transcript: ENST00000457059
  gene symbol: DYNC1I1
  hgvsc: ENST00000457059.1:c.743+11T>C
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000398118
  ensembl transcript: ENST00000437599
  gene symbol: DYNC1I1
  hgvsc: ENST00000437599.1:c.734+11T>C
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl transcript: ENST00000519371
  gene symbol: DYNC1I1
  hgvsc: ENST00000519371.1:n.401+11T>C
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000320130
  ensembl transcript: ENST00000324972
  gene symbol: DYNC1I1
  hgvsc: ENST00000324972.6:c.794+11T>C
  variant of: http://identifiers.org/hgnc/2963
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5339
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2898
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9990
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13283
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23453
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 888
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1542
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3322
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4228
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD

7-95614301-GT-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95614301
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 95614300
    reference: chr 7
allele count: 1
allele frequency: 8.260503229856763e-6
allele num: 121058
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000398118
  ensembl transcript: ENST00000437599
  gene symbol: DYNC1I1
  hgvsc: ENST00000437599.1:c.734+13delT
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl transcript: ENST00000519371
  gene symbol: DYNC1I1
  hgvsc: ENST00000519371.1:n.401+13delT
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000412444
  ensembl transcript: ENST00000457059
  gene symbol: DYNC1I1
  hgvsc: ENST00000457059.1:c.743+13delT
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000392337
  ensembl transcript: ENST00000447467
  gene symbol: DYNC1I1
  hgvsc: ENST00000447467.2:c.743+13delT
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000352348
  ensembl transcript: ENST00000359388
  gene symbol: DYNC1I1
  hgvsc: ENST00000359388.4:c.683+13delT
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000320130
  ensembl transcript: ENST00000324972
  gene symbol: DYNC1I1
  hgvsc: ENST00000324972.6:c.794+13delT
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000438377
  ensembl transcript: ENST00000537881
  gene symbol: DYNC1I1
  hgvsc: ENST00000537881.1:c.683+13delT
  variant of: http://identifiers.org/hgnc/2963
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 888
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13279
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2899
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23415
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5340
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9991
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1542
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2865
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7402
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3322
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24457
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: GT
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: ReadPosRankSum

7-95614303-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95614303
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 95614303
    reference: chr 7
allele count: 2
allele frequency: 1.652919882973272e-5
allele num: 120998
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000392337
  ensembl transcript: ENST00000447467
  gene symbol: DYNC1I1
  hgvsc: ENST00000447467.2:c.743+14G>A
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000438377
  ensembl transcript: ENST00000537881
  gene symbol: DYNC1I1
  hgvsc: ENST00000537881.1:c.683+14G>A
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000398118
  ensembl transcript: ENST00000437599
  gene symbol: DYNC1I1
  hgvsc: ENST00000437599.1:c.734+14G>A
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl transcript: ENST00000519371
  gene symbol: DYNC1I1
  hgvsc: ENST00000519371.1:n.401+14G>A
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000412444
  ensembl transcript: ENST00000457059
  gene symbol: DYNC1I1
  hgvsc: ENST00000457059.1:c.743+14G>A
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000352348
  ensembl transcript: ENST00000359388
  gene symbol: DYNC1I1
  hgvsc: ENST00000359388.4:c.683+14G>A
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000320130
  ensembl transcript: ENST00000324972
  gene symbol: DYNC1I1
  hgvsc: ENST00000324972.6:c.794+14G>A
  variant of: http://identifiers.org/hgnc/2963
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23355
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1543
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9989
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2905
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5337
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13258
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 796
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 890
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3319
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 404
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2863
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4226
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 107
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

7-95614318-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95614318
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 95614318
    reference: chr 7
allele count: 1
allele frequency: 8.273351534706709e-6
allele num: 120870
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000320130
  ensembl transcript: ENST00000324972
  gene symbol: DYNC1I1
  hgvsc: ENST00000324972.6:c.794+29A>G
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000392337
  ensembl transcript: ENST00000447467
  gene symbol: DYNC1I1
  hgvsc: ENST00000447467.2:c.743+29A>G
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl transcript: ENST00000519371
  gene symbol: DYNC1I1
  hgvsc: ENST00000519371.1:n.401+29A>G
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000398118
  ensembl transcript: ENST00000437599
  gene symbol: DYNC1I1
  hgvsc: ENST00000437599.1:c.734+29A>G
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000438377
  ensembl transcript: ENST00000537881
  gene symbol: DYNC1I1
  hgvsc: ENST00000537881.1:c.683+29A>G
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000352348
  ensembl transcript: ENST00000359388
  gene symbol: DYNC1I1
  hgvsc: ENST00000359388.4:c.683+29A>G
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000412444
  ensembl transcript: ENST00000457059
  gene symbol: DYNC1I1
  hgvsc: ENST00000457059.1:c.743+29A>G
  variant of: http://identifiers.org/hgnc/2963
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 575
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9978
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22899
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 891
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2907
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 712
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13172
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5346
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1544
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 797
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3314
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 616
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 106
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2865
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10771
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2079
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: ClippingRankSum

7-95614323-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95614323
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 95614323
    reference: chr 7
allele count: 1
allele frequency: 8.278968109414843e-6
allele num: 120788
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000398118
  ensembl transcript: ENST00000437599
  gene symbol: DYNC1I1
  hgvsc: ENST00000437599.1:c.734+34C>T
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000392337
  ensembl transcript: ENST00000447467
  gene symbol: DYNC1I1
  hgvsc: ENST00000447467.2:c.743+34C>T
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl transcript: ENST00000519371
  gene symbol: DYNC1I1
  hgvsc: ENST00000519371.1:n.401+34C>T
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000438377
  ensembl transcript: ENST00000537881
  gene symbol: DYNC1I1
  hgvsc: ENST00000537881.1:c.683+34C>T
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000412444
  ensembl transcript: ENST00000457059
  gene symbol: DYNC1I1
  hgvsc: ENST00000457059.1:c.743+34C>T
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000352348
  ensembl transcript: ENST00000359388
  gene symbol: DYNC1I1
  hgvsc: ENST00000359388.4:c.683+34C>T
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000320130
  ensembl transcript: ENST00000324972
  gene symbol: DYNC1I1
  hgvsc: ENST00000324972.6:c.794+34C>T
  variant of: http://identifiers.org/hgnc/2963
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5351
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1548
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 863
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 894
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2908
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9988
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22497
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13087
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7299
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2865
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 208
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 285
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 705
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
population: Other
population: South Asian
reference allele: C
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD

7-95614324-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95614324
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 95614324
    reference: chr 7
allele count: 3
allele frequency: 2.484389751064147e-5
allele num: 120754
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000398118
  ensembl transcript: ENST00000437599
  gene symbol: DYNC1I1
  hgvsc: ENST00000437599.1:c.734+35G>A
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000392337
  ensembl transcript: ENST00000447467
  gene symbol: DYNC1I1
  hgvsc: ENST00000447467.2:c.743+35G>A
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000352348
  ensembl transcript: ENST00000359388
  gene symbol: DYNC1I1
  hgvsc: ENST00000359388.4:c.683+35G>A
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000438377
  ensembl transcript: ENST00000537881
  gene symbol: DYNC1I1
  hgvsc: ENST00000537881.1:c.683+35G>A
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl transcript: ENST00000519371
  gene symbol: DYNC1I1
  hgvsc: ENST00000519371.1:n.401+35G>A
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000412444
  ensembl transcript: ENST00000457059
  gene symbol: DYNC1I1
  hgvsc: ENST00000457059.1:c.743+35G>A
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000320130
  ensembl transcript: ENST00000324972
  gene symbol: DYNC1I1
  hgvsc: ENST00000324972.6:c.794+35G>A
  variant of: http://identifiers.org/hgnc/2963
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9990
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22462
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2910
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 895
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13092
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 870
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5353
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 795
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1550
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2077
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23373
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4219
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 208
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
reference allele: G
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum

7-95614324-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95614324
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 95614324
    reference: chr 7
allele count: 2
allele frequency: 1.656259834042764e-5
allele num: 120754
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000398118
  ensembl transcript: ENST00000437599
  gene symbol: DYNC1I1
  hgvsc: ENST00000437599.1:c.734+35G>T
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000392337
  ensembl transcript: ENST00000447467
  gene symbol: DYNC1I1
  hgvsc: ENST00000447467.2:c.743+35G>T
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000412444
  ensembl transcript: ENST00000457059
  gene symbol: DYNC1I1
  hgvsc: ENST00000457059.1:c.743+35G>T
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000320130
  ensembl transcript: ENST00000324972
  gene symbol: DYNC1I1
  hgvsc: ENST00000324972.6:c.794+35G>T
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000352348
  ensembl transcript: ENST00000359388
  gene symbol: DYNC1I1
  hgvsc: ENST00000359388.4:c.683+35G>T
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000438377
  ensembl transcript: ENST00000537881
  gene symbol: DYNC1I1
  hgvsc: ENST00000537881.1:c.683+35G>T
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl transcript: ENST00000519371
  gene symbol: DYNC1I1
  hgvsc: ENST00000519371.1:n.401+35G>T
  variant of: http://identifiers.org/hgnc/2963
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13092
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 870
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 795
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 895
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1550
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2910
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5353
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22462
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9990
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2077
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4895
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 208
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10771
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 3310
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 295
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: African
reference allele: G
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD

7-95614325-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95614325
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 95614325
    reference: chr 7
allele count: 6
allele frequency: 4.967627626633108e-5
allele num: 120782
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000392337
  ensembl transcript: ENST00000447467
  gene symbol: DYNC1I1
  hgvsc: ENST00000447467.2:c.743+36T>C
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000438377
  ensembl transcript: ENST00000537881
  gene symbol: DYNC1I1
  hgvsc: ENST00000537881.1:c.683+36T>C
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000412444
  ensembl transcript: ENST00000457059
  gene symbol: DYNC1I1
  hgvsc: ENST00000457059.1:c.743+36T>C
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000352348
  ensembl transcript: ENST00000359388
  gene symbol: DYNC1I1
  hgvsc: ENST00000359388.4:c.683+36T>C
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000398118
  ensembl transcript: ENST00000437599
  gene symbol: DYNC1I1
  hgvsc: ENST00000437599.1:c.734+36T>C
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl transcript: ENST00000519371
  gene symbol: DYNC1I1
  hgvsc: ENST00000519371.1:n.401+36T>C
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000320130
  ensembl transcript: ENST00000324972
  gene symbol: DYNC1I1
  hgvsc: ENST00000324972.6:c.794+36T>C
  variant of: http://identifiers.org/hgnc/2963
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9981
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22346
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 883
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 891
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 698
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13077
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1544
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5351
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2912
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4221
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3315
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10779
  bin: 9.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7299
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 335
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
population: European (Finnish)
reference allele: T
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: DP

http://identifiers.org/exac.variant/7-95614326-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95614326
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 95614326
    reference: chr 7
allele count: 1
allele frequency: 8.281847845891375e-6
allele num: 120746
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl transcript: ENST00000519371
  gene symbol: DYNC1I1
  hgvsc: ENST00000519371.1:n.401+37A>C
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000398118
  ensembl transcript: ENST00000437599
  gene symbol: DYNC1I1
  hgvsc: ENST00000437599.1:c.734+37A>C
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000412444
  ensembl transcript: ENST00000457059
  gene symbol: DYNC1I1
  hgvsc: ENST00000457059.1:c.743+37A>C
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000438377
  ensembl transcript: ENST00000537881
  gene symbol: DYNC1I1
  hgvsc: ENST00000537881.1:c.683+37A>C
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000320130
  ensembl transcript: ENST00000324972
  gene symbol: DYNC1I1
  hgvsc: ENST00000324972.6:c.794+37A>C
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000352348
  ensembl transcript: ENST00000359388
  gene symbol: DYNC1I1
  hgvsc: ENST00000359388.4:c.683+37A>C
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000392337
  ensembl transcript: ENST00000447467
  gene symbol: DYNC1I1
  hgvsc: ENST00000447467.2:c.743+37A>C
  variant of: http://identifiers.org/hgnc/2963
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2910
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13046
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 803
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 575
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 895
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22258
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5355
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 891
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1544
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9975
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10771
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 7294
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 321
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 724
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
population: African
reference allele: A
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: FS

7-95614338-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95614338
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 95614338
    reference: chr 7
allele count: 1
allele frequency: 8.311446524153063e-6
allele num: 120316
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000320130
  ensembl transcript: ENST00000324972
  gene symbol: DYNC1I1
  hgvsc: ENST00000324972.6:c.794+49A>G
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000392337
  ensembl transcript: ENST00000447467
  gene symbol: DYNC1I1
  hgvsc: ENST00000447467.2:c.743+49A>G
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000412444
  ensembl transcript: ENST00000457059
  gene symbol: DYNC1I1
  hgvsc: ENST00000457059.1:c.743+49A>G
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000398118
  ensembl transcript: ENST00000437599
  gene symbol: DYNC1I1
  hgvsc: ENST00000437599.1:c.734+49A>G
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl transcript: ENST00000519371
  gene symbol: DYNC1I1
  hgvsc: ENST00000519371.1:n.401+49A>G
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000352348
  ensembl transcript: ENST00000359388
  gene symbol: DYNC1I1
  hgvsc: ENST00000359388.4:c.683+49A>G
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000438377
  ensembl transcript: ENST00000537881
  gene symbol: DYNC1I1
  hgvsc: ENST00000537881.1:c.683+49A>G
  variant of: http://identifiers.org/hgnc/2963
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 21215
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1541
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 889
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 817
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1488
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13340
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9935
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5359
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2910
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 825
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7024
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2076
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 153
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 914
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2868
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 625
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 374
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19789
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: East Asian
reference allele: A
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: MQ
site quality: ClippingRankSum

7-95616319-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95616319
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 95616319
    reference: chr 7
allele count: 1
allele frequency: 8.305233958440609e-6
allele num: 120406
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000438377
  ensembl transcript: ENST00000537881
  gene symbol: DYNC1I1
  hgvsc: ENST00000537881.1:c.684-49G>T
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl transcript: ENST00000519371
  gene symbol: DYNC1I1
  hgvsc: ENST00000519371.1:n.402-49G>T
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000412444
  ensembl transcript: ENST00000457059
  gene symbol: DYNC1I1
  hgvsc: ENST00000457059.1:c.744-49G>T
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000398118
  ensembl transcript: ENST00000437599
  gene symbol: DYNC1I1
  hgvsc: ENST00000437599.1:c.735-49G>T
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000352348
  ensembl transcript: ENST00000359388
  gene symbol: DYNC1I1
  hgvsc: ENST00000359388.4:c.684-49G>T
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000392337
  ensembl transcript: ENST00000447467
  gene symbol: DYNC1I1
  hgvsc: ENST00000447467.2:c.744-49G>T
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000320130
  ensembl transcript: ENST00000324972
  gene symbol: DYNC1I1
  hgvsc: ENST00000324972.6:c.795-49G>T
  variant of: http://identifiers.org/hgnc/2963
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1018
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 829
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1469
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 856
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1500
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28931
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2066
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1654
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1042
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3470
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3496
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1216
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2482
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1819
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 872
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2932
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1430
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3173
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50993
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 337
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 417
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 412
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 556
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 544
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 474
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: African
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/7-95616328-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95616328
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 95616328
    reference: chr 7
allele count: 1
allele frequency: 8.298066550493736e-6
allele num: 120510
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000320130
  ensembl transcript: ENST00000324972
  gene symbol: DYNC1I1
  hgvsc: ENST00000324972.6:c.795-40A>C
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000352348
  ensembl transcript: ENST00000359388
  gene symbol: DYNC1I1
  hgvsc: ENST00000359388.4:c.684-40A>C
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000392337
  ensembl transcript: ENST00000447467
  gene symbol: DYNC1I1
  hgvsc: ENST00000447467.2:c.744-40A>C
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000398118
  ensembl transcript: ENST00000437599
  gene symbol: DYNC1I1
  hgvsc: ENST00000437599.1:c.735-40A>C
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000412444
  ensembl transcript: ENST00000457059
  gene symbol: DYNC1I1
  hgvsc: ENST00000457059.1:c.744-40A>C
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl transcript: ENST00000519371
  gene symbol: DYNC1I1
  hgvsc: ENST00000519371.1:n.402-40A>C
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000438377
  ensembl transcript: ENST00000537881
  gene symbol: DYNC1I1
  hgvsc: ENST00000537881.1:c.684-40A>C
  variant of: http://identifiers.org/hgnc/2963
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1359
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2932
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1430
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1654
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1018
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 929
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2382
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 831
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2482
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1216
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1154
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 896
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3173
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2066
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 856
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3470
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28931
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3496
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 283
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1029
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 426
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 354
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 553
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50992
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 630
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum

7-95616330-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95616330
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 95616330
    reference: chr 7
allele count: 10538
allele frequency: 8.736383081029994e-2
allele num: 120622
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000412444
  ensembl transcript: ENST00000457059
  gene symbol: DYNC1I1
  hgvsc: ENST00000457059.1:c.744-38G>A
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000320130
  ensembl transcript: ENST00000324972
  gene symbol: DYNC1I1
  hgvsc: ENST00000324972.6:c.795-38G>A
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl transcript: ENST00000519371
  gene symbol: DYNC1I1
  hgvsc: ENST00000519371.1:n.402-38G>A
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000438377
  ensembl transcript: ENST00000537881
  gene symbol: DYNC1I1
  hgvsc: ENST00000537881.1:c.684-38G>A
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000398118
  ensembl transcript: ENST00000437599
  gene symbol: DYNC1I1
  hgvsc: ENST00000437599.1:c.735-38G>A
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000352348
  ensembl transcript: ENST00000359388
  gene symbol: DYNC1I1
  hgvsc: ENST00000359388.4:c.684-38G>A
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000392337
  ensembl transcript: ENST00000447467
  gene symbol: DYNC1I1
  hgvsc: ENST00000447467.2:c.744-38G>A
  variant of: http://identifiers.org/hgnc/2963
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 986
  bin: 4.75e1
  variant carriers: 47
genotype depth: GenotypeDepth
  all individuals: 1646
  bin: 6.25e1
  variant carriers: 48
genotype depth: GenotypeDepth
  all individuals: 1198
  bin: 5.25e1
  variant carriers: 53
genotype depth: GenotypeDepth
  all individuals: 3129
  bin: 8.25e1
  variant carriers: 34
genotype depth: GenotypeDepth
  all individuals: 3443
  bin: 8.75e1
  variant carriers: 46
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 7.5e0
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 3385
  bin: 9.25e1
  variant carriers: 38
genotype depth: GenotypeDepth
  all individuals: 969
  bin: 3.25e1
  variant carriers: 130
genotype depth: GenotypeDepth
  all individuals: 840
  bin: 3.75e1
  variant carriers: 68
genotype depth: GenotypeDepth
  all individuals: 1440
  bin: 5.75e1
  variant carriers: 64
genotype depth: GenotypeDepth
  all individuals: 2397
  bin: 2.25e1
  variant carriers: 325
genotype depth: GenotypeDepth
  all individuals: 1164
  bin: 1.25e1
  variant carriers: 112
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2906
  bin: 7.75e1
  variant carriers: 37
genotype depth: GenotypeDepth
  all individuals: 916
  bin: 1.75e1
  variant carriers: 301
genotype depth: GenotypeDepth
  all individuals: 2049
  bin: 6.75e1
  variant carriers: 57
genotype depth: GenotypeDepth
  all individuals: 855
  bin: 4.25e1
  variant carriers: 48
genotype depth: GenotypeDepth
  all individuals: 29290
  bin: 9.75e1
  variant carriers: 8271
genotype depth: GenotypeDepth
  all individuals: 1254
  bin: 2.75e1
  variant carriers: 224
genotype depth: GenotypeDepth
  all individuals: 2472
  bin: 7.25e1
  variant carriers: 34
genotype quality: GenotypeQuality
  all individuals: 3131
  bin: 6.25e1
  variant carriers: 14
genotype quality: GenotypeQuality
  all individuals: 52076
  bin: 9.75e1
  variant carriers: 9840
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 455
  bin: 3.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 403
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 531
  bin: 7.75e1
  variant carriers: 11
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 1.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 238
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 1.75e1
  variant carriers: 2
num of homozygotes: 602
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/7-95616345-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95616345
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 95616345
    reference: chr 7
allele count: 1
allele frequency: 8.275268532463878e-6
allele num: 120842
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000320130
  ensembl transcript: ENST00000324972
  gene symbol: DYNC1I1
  hgvsc: ENST00000324972.6:c.795-23C>A
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000398118
  ensembl transcript: ENST00000437599
  gene symbol: DYNC1I1
  hgvsc: ENST00000437599.1:c.735-23C>A
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000412444
  ensembl transcript: ENST00000457059
  gene symbol: DYNC1I1
  hgvsc: ENST00000457059.1:c.744-23C>A
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000392337
  ensembl transcript: ENST00000447467
  gene symbol: DYNC1I1
  hgvsc: ENST00000447467.2:c.744-23C>A
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000438377
  ensembl transcript: ENST00000537881
  gene symbol: DYNC1I1
  hgvsc: ENST00000537881.1:c.684-23C>A
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000352348
  ensembl transcript: ENST00000359388
  gene symbol: DYNC1I1
  hgvsc: ENST00000359388.4:c.684-23C>A
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl transcript: ENST00000519371
  gene symbol: DYNC1I1
  hgvsc: ENST00000519371.1:n.402-23C>A
  variant of: http://identifiers.org/hgnc/2963
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2409
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1142
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3666
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1644
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2906
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1917
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1673
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3577
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 952
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25091
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 919
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3975
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3417
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1094
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1371
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4087
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 292
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 125
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5124
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: Other
population: Latino
population: South Asian
reference allele: C
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD

7-95616363-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95616363
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 95616363
    reference: chr 7
allele count: 1
allele frequency: 8.248239000973292e-6
allele num: 121238
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000392337
  ensembl transcript: ENST00000447467
  gene symbol: DYNC1I1
  hgvsc: ENST00000447467.2:c.744-5C>T
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000412444
  ensembl transcript: ENST00000457059
  gene symbol: DYNC1I1
  hgvsc: ENST00000457059.1:c.744-5C>T
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000438377
  ensembl transcript: ENST00000537881
  gene symbol: DYNC1I1
  hgvsc: ENST00000537881.1:c.684-5C>T
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000352348
  ensembl transcript: ENST00000359388
  gene symbol: DYNC1I1
  hgvsc: ENST00000359388.4:c.684-5C>T
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000398118
  ensembl transcript: ENST00000437599
  gene symbol: DYNC1I1
  hgvsc: ENST00000437599.1:c.735-5C>T
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl transcript: ENST00000519371
  gene symbol: DYNC1I1
  hgvsc: ENST00000519371.1:n.402-5C>T
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000320130
  ensembl transcript: ENST00000324972
  gene symbol: DYNC1I1
  hgvsc: ENST00000324972.6:c.795-5C>T
  variant of: http://identifiers.org/hgnc/2963
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1370
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1094
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1196
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2906
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1644
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1950
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3949
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 954
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1917
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3975
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4087
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3418
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25090
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 922
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3666
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2409
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 634
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1396
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5808
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
hgvs: c.795-5C>T
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
reference allele: C
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: QD

7-95616372-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95616372
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 95616372
    reference: chr 7
allele count: 1
allele frequency: 8.243751236562685e-6
allele num: 121304
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000398118
  ensembl transcript: ENST00000437599
  gene symbol: DYNC1I1
  hgvsc: ENST00000437599.1:c.739G>A
  hgvsp: ENSP00000398118.1:p.Val247Ile
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000320130
  ensembl transcript: ENST00000324972
  gene symbol: DYNC1I1
  hgvsc: ENST00000324972.6:c.799G>A
  hgvsp: ENSP00000320130.6:p.Val267Ile
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158560
  ensembl transcript: ENST00000519371
  gene symbol: DYNC1I1
  hgvsc: ENST00000519371.1:n.406G>A
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000352348
  ensembl transcript: ENST00000359388
  gene symbol: DYNC1I1
  hgvsc: ENST00000359388.4:c.688G>A
  hgvsp: ENSP00000352348.4:p.Val230Ile
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000412444
  ensembl transcript: ENST00000457059
  gene symbol: DYNC1I1
  hgvsc: ENST00000457059.1:c.748G>A
  hgvsp: ENSP00000412444.1:p.Val250Ile
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000438377
  ensembl transcript: ENST00000537881
  gene symbol: DYNC1I1
  hgvsc: ENST00000537881.1:c.688G>A
  hgvsp: ENSP00000438377.1:p.Val230Ile
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000392337
  ensembl transcript: ENST00000447467
  gene symbol: DYNC1I1
  hgvsc: ENST00000447467.2:c.748G>A
  hgvsp: ENSP00000392337.2:p.Val250Ile
  variant of: http://identifiers.org/hgnc/2963
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1093
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1209
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1999
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 923
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1644
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2906
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1371
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25089
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2409
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3976
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 951
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4087
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3962
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1917
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3666
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3418
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 637
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5895
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Val267Ile
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum

7-95616372-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95616372
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 95616372
    reference: chr 7
allele count: 1
allele frequency: 8.243751236562685e-6
allele num: 121304
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000392337
  ensembl transcript: ENST00000447467
  gene symbol: DYNC1I1
  hgvsc: ENST00000447467.2:c.748G>C
  hgvsp: ENSP00000392337.2:p.Val250Leu
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158560
  ensembl transcript: ENST00000519371
  gene symbol: DYNC1I1
  hgvsc: ENST00000519371.1:n.406G>C
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000352348
  ensembl transcript: ENST00000359388
  gene symbol: DYNC1I1
  hgvsc: ENST00000359388.4:c.688G>C
  hgvsp: ENSP00000352348.4:p.Val230Leu
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000412444
  ensembl transcript: ENST00000457059
  gene symbol: DYNC1I1
  hgvsc: ENST00000457059.1:c.748G>C
  hgvsp: ENSP00000412444.1:p.Val250Leu
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000438377
  ensembl transcript: ENST00000537881
  gene symbol: DYNC1I1
  hgvsc: ENST00000537881.1:c.688G>C
  hgvsp: ENSP00000438377.1:p.Val230Leu
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000320130
  ensembl transcript: ENST00000324972
  gene symbol: DYNC1I1
  hgvsc: ENST00000324972.6:c.799G>C
  hgvsp: ENSP00000320130.6:p.Val267Leu
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000398118
  ensembl transcript: ENST00000437599
  gene symbol: DYNC1I1
  hgvsc: ENST00000437599.1:c.739G>C
  hgvsp: ENSP00000398118.1:p.Val247Leu
  variant of: http://identifiers.org/hgnc/2963
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1917
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25089
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1371
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3418
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1999
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 923
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4087
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 951
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1209
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1093
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2409
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2906
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3666
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1644
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3962
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3976
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1406
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5895
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Val267Leu
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: QD

7-95616378-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95616378
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 95616378
    reference: chr 7
allele count: 1
allele frequency: 8.242120532770671e-6
allele num: 121328
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000320130
  ensembl transcript: ENST00000324972
  gene symbol: DYNC1I1
  hgvsc: ENST00000324972.6:c.805G>A
  hgvsp: ENSP00000320130.6:p.Ala269Thr
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000412444
  ensembl transcript: ENST00000457059
  gene symbol: DYNC1I1
  hgvsc: ENST00000457059.1:c.754G>A
  hgvsp: ENSP00000412444.1:p.Ala252Thr
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158560
  ensembl transcript: ENST00000519371
  gene symbol: DYNC1I1
  hgvsc: ENST00000519371.1:n.412G>A
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000392337
  ensembl transcript: ENST00000447467
  gene symbol: DYNC1I1
  hgvsc: ENST00000447467.2:c.754G>A
  hgvsp: ENSP00000392337.2:p.Ala252Thr
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000398118
  ensembl transcript: ENST00000437599
  gene symbol: DYNC1I1
  hgvsc: ENST00000437599.1:c.745G>A
  hgvsp: ENSP00000398118.1:p.Ala249Thr
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000352348
  ensembl transcript: ENST00000359388
  gene symbol: DYNC1I1
  hgvsc: ENST00000359388.4:c.694G>A
  hgvsp: ENSP00000352348.4:p.Ala232Thr
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000438377
  ensembl transcript: ENST00000537881
  gene symbol: DYNC1I1
  hgvsc: ENST00000537881.1:c.694G>A
  hgvsp: ENSP00000438377.1:p.Ala232Thr
  variant of: http://identifiers.org/hgnc/2963
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3666
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2408
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1644
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2021
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25088
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1093
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1205
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 952
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 923
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1370
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3961
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3977
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1917
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2906
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4088
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3418
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 331
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50482
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Ala269Thr
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
population: Other
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD

7-95616378-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95616378
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 95616378
    reference: chr 7
allele count: 2
allele frequency: 1.648424106554134e-5
allele num: 121328
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000352348
  ensembl transcript: ENST00000359388
  gene symbol: DYNC1I1
  hgvsc: ENST00000359388.4:c.694G>C
  hgvsp: ENSP00000352348.4:p.Ala232Pro
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158560
  ensembl transcript: ENST00000519371
  gene symbol: DYNC1I1
  hgvsc: ENST00000519371.1:n.412G>C
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000412444
  ensembl transcript: ENST00000457059
  gene symbol: DYNC1I1
  hgvsc: ENST00000457059.1:c.754G>C
  hgvsp: ENSP00000412444.1:p.Ala252Pro
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000320130
  ensembl transcript: ENST00000324972
  gene symbol: DYNC1I1
  hgvsc: ENST00000324972.6:c.805G>C
  hgvsp: ENSP00000320130.6:p.Ala269Pro
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000398118
  ensembl transcript: ENST00000437599
  gene symbol: DYNC1I1
  hgvsc: ENST00000437599.1:c.745G>C
  hgvsp: ENSP00000398118.1:p.Ala249Pro
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000392337
  ensembl transcript: ENST00000447467
  gene symbol: DYNC1I1
  hgvsc: ENST00000447467.2:c.754G>C
  hgvsp: ENSP00000392337.2:p.Ala252Pro
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000438377
  ensembl transcript: ENST00000537881
  gene symbol: DYNC1I1
  hgvsc: ENST00000537881.1:c.694G>C
  hgvsp: ENSP00000438377.1:p.Ala232Pro
  variant of: http://identifiers.org/hgnc/2963
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1370
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3961
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2906
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 923
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2408
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1205
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1644
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2021
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3418
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3977
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1093
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3666
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1917
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 952
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4088
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25088
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 530
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 634
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5923
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Ala269Pro
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum

7-95616382-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95616382
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 95616382
    reference: chr 7
allele count: 2
allele frequency: 1.648206751054852e-5
allele num: 121344
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000412444
  ensembl transcript: ENST00000457059
  gene symbol: DYNC1I1
  hgvsc: ENST00000457059.1:c.758G>C
  hgvsp: ENSP00000412444.1:p.Gly253Ala
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000438377
  ensembl transcript: ENST00000537881
  gene symbol: DYNC1I1
  hgvsc: ENST00000537881.1:c.698G>C
  hgvsp: ENSP00000438377.1:p.Gly233Ala
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000352348
  ensembl transcript: ENST00000359388
  gene symbol: DYNC1I1
  hgvsc: ENST00000359388.4:c.698G>C
  hgvsp: ENSP00000352348.4:p.Gly233Ala
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158560
  ensembl transcript: ENST00000519371
  gene symbol: DYNC1I1
  hgvsc: ENST00000519371.1:n.416G>C
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000398118
  ensembl transcript: ENST00000437599
  gene symbol: DYNC1I1
  hgvsc: ENST00000437599.1:c.749G>C
  hgvsp: ENSP00000398118.1:p.Gly250Ala
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000320130
  ensembl transcript: ENST00000324972
  gene symbol: DYNC1I1
  hgvsc: ENST00000324972.6:c.809G>C
  hgvsp: ENSP00000320130.6:p.Gly270Ala
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000392337
  ensembl transcript: ENST00000447467
  gene symbol: DYNC1I1
  hgvsc: ENST00000447467.2:c.758G>C
  hgvsp: ENSP00000392337.2:p.Gly253Ala
  variant of: http://identifiers.org/hgnc/2963
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1917
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2408
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3964
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1210
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3666
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 953
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2906
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1093
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2023
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 923
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3976
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25088
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1644
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1370
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3418
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4088
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5933
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1401
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Gly270Ala
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP

7-95616400-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95616400
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 95616400
    reference: chr 7
allele count: 2
allele frequency: 1.647826516824309e-5
allele num: 121372
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000352348
  ensembl transcript: ENST00000359388
  gene symbol: DYNC1I1
  hgvsc: ENST00000359388.4:c.716A>G
  hgvsp: ENSP00000352348.4:p.Asn239Ser
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000438377
  ensembl transcript: ENST00000537881
  gene symbol: DYNC1I1
  hgvsc: ENST00000537881.1:c.716A>G
  hgvsp: ENSP00000438377.1:p.Asn239Ser
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158560
  ensembl transcript: ENST00000519371
  gene symbol: DYNC1I1
  hgvsc: ENST00000519371.1:n.434A>G
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000412444
  ensembl transcript: ENST00000457059
  gene symbol: DYNC1I1
  hgvsc: ENST00000457059.1:c.776A>G
  hgvsp: ENSP00000412444.1:p.Asn259Ser
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000392337
  ensembl transcript: ENST00000447467
  gene symbol: DYNC1I1
  hgvsc: ENST00000447467.2:c.776A>G
  hgvsp: ENSP00000392337.2:p.Asn259Ser
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000398118
  ensembl transcript: ENST00000437599
  gene symbol: DYNC1I1
  hgvsc: ENST00000437599.1:c.767A>G
  hgvsp: ENSP00000398118.1:p.Asn256Ser
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000320130
  ensembl transcript: ENST00000324972
  gene symbol: DYNC1I1
  hgvsc: ENST00000324972.6:c.827A>G
  hgvsp: ENSP00000320130.6:p.Asn276Ser
  variant of: http://identifiers.org/hgnc/2963
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3666
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 921
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3984
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4088
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1644
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1093
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 953
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2408
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1207
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3418
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1370
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2906
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25088
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2035
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3976
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1917
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 535
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 634
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 662
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 661
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50481
  bin: 9.75e1
  variant carriers: 2
hgvs: p.Asn276Ser
num of homozygotes: 0
population: East Asian
population: Other
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
reference allele: A
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum

7-95616412-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95616412
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 95616412
    reference: chr 7
allele count: 4
allele frequency: 3.295164346321773e-5
allele num: 121390
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000398118
  ensembl transcript: ENST00000437599
  gene symbol: DYNC1I1
  hgvsc: ENST00000437599.1:c.779A>G
  hgvsp: ENSP00000398118.1:p.Tyr260Cys
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000438377
  ensembl transcript: ENST00000537881
  gene symbol: DYNC1I1
  hgvsc: ENST00000537881.1:c.728A>G
  hgvsp: ENSP00000438377.1:p.Tyr243Cys
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000352348
  ensembl transcript: ENST00000359388
  gene symbol: DYNC1I1
  hgvsc: ENST00000359388.4:c.728A>G
  hgvsp: ENSP00000352348.4:p.Tyr243Cys
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000412444
  ensembl transcript: ENST00000457059
  gene symbol: DYNC1I1
  hgvsc: ENST00000457059.1:c.788A>G
  hgvsp: ENSP00000412444.1:p.Tyr263Cys
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158560
  ensembl transcript: ENST00000519371
  gene symbol: DYNC1I1
  hgvsc: ENST00000519371.1:n.446A>G
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000320130
  ensembl transcript: ENST00000324972
  gene symbol: DYNC1I1
  hgvsc: ENST00000324972.6:c.839A>G
  hgvsp: ENSP00000320130.6:p.Tyr280Cys
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000392337
  ensembl transcript: ENST00000447467
  gene symbol: DYNC1I1
  hgvsc: ENST00000447467.2:c.788A>G
  hgvsp: ENSP00000392337.2:p.Tyr263Cys
  variant of: http://identifiers.org/hgnc/2963
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1644
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1093
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1917
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3976
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3667
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3991
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2408
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2032
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25086
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4088
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 921
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3419
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 953
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1371
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2908
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1207
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 331
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1404
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Tyr280Cys
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
population: Other
reference allele: A
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP

7-95616431-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95616431
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 95616431
    reference: chr 7
allele count: 1
allele frequency: 8.238453806989504e-6
allele num: 121382
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000352348
  ensembl transcript: ENST00000359388
  gene symbol: DYNC1I1
  hgvsc: ENST00000359388.4:c.747G>A
  hgvsp: ENST00000359388.4:c.747G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000398118
  ensembl transcript: ENST00000437599
  gene symbol: DYNC1I1
  hgvsc: ENST00000437599.1:c.798G>A
  hgvsp: ENST00000437599.1:c.798G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000412444
  ensembl transcript: ENST00000457059
  gene symbol: DYNC1I1
  hgvsc: ENST00000457059.1:c.807G>A
  hgvsp: ENST00000457059.1:c.807G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000320130
  ensembl transcript: ENST00000324972
  gene symbol: DYNC1I1
  hgvsc: ENST00000324972.6:c.858G>A
  hgvsp: ENST00000324972.6:c.858G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000392337
  ensembl transcript: ENST00000447467
  gene symbol: DYNC1I1
  hgvsc: ENST00000447467.2:c.807G>A
  hgvsp: ENST00000447467.2:c.807G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000438377
  ensembl transcript: ENST00000537881
  gene symbol: DYNC1I1
  hgvsc: ENST00000537881.1:c.747G>A
  hgvsp: ENST00000537881.1:c.747G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158560
  ensembl transcript: ENST00000519371
  gene symbol: DYNC1I1
  hgvsc: ENST00000519371.1:n.465G>A
  variant of: http://identifiers.org/hgnc/2963
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3667
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1644
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3969
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 953
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1093
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1917
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1209
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 923
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3976
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2035
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4088
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2906
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25086
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2408
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1371
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3418
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 659
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 662
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Lys286Lys
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum

7-95616433-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95616433
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 95616433
    reference: chr 7
allele count: 1
allele frequency: 8.238589553468446e-6
allele num: 121380
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000412444
  ensembl transcript: ENST00000457059
  gene symbol: DYNC1I1
  hgvsc: ENST00000457059.1:c.809A>G
  hgvsp: ENSP00000412444.1:p.His270Arg
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158560
  ensembl transcript: ENST00000519371
  gene symbol: DYNC1I1
  hgvsc: ENST00000519371.1:n.467A>G
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000352348
  ensembl transcript: ENST00000359388
  gene symbol: DYNC1I1
  hgvsc: ENST00000359388.4:c.749A>G
  hgvsp: ENSP00000352348.4:p.His250Arg
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000398118
  ensembl transcript: ENST00000437599
  gene symbol: DYNC1I1
  hgvsc: ENST00000437599.1:c.800A>G
  hgvsp: ENSP00000398118.1:p.His267Arg
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000320130
  ensembl transcript: ENST00000324972
  gene symbol: DYNC1I1
  hgvsc: ENST00000324972.6:c.860A>G
  hgvsp: ENSP00000320130.6:p.His287Arg
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000438377
  ensembl transcript: ENST00000537881
  gene symbol: DYNC1I1
  hgvsc: ENST00000537881.1:c.749A>G
  hgvsp: ENSP00000438377.1:p.His250Arg
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000392337
  ensembl transcript: ENST00000447467
  gene symbol: DYNC1I1
  hgvsc: ENST00000447467.2:c.809A>G
  hgvsp: ENSP00000392337.2:p.His270Arg
  variant of: http://identifiers.org/hgnc/2963
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1644
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25086
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3969
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1093
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2408
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2034
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1209
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4088
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1371
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1917
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 953
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3976
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3667
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 923
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2906
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3418
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 662
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50481
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 635
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1402
  bin: 6.75e1
  variant carriers: 0
hgvs: p.His287Arg
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum

7-95616440-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95616440
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 95616440
    reference: chr 7
allele count: 1
allele frequency: 8.239268352970255e-6
allele num: 121370
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000392337
  ensembl transcript: ENST00000447467
  gene symbol: DYNC1I1
  hgvsc: ENST00000447467.2:c.816G>A
  hgvsp: ENST00000447467.2:c.816G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000352348
  ensembl transcript: ENST00000359388
  gene symbol: DYNC1I1
  hgvsc: ENST00000359388.4:c.756G>A
  hgvsp: ENST00000359388.4:c.756G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000438377
  ensembl transcript: ENST00000537881
  gene symbol: DYNC1I1
  hgvsc: ENST00000537881.1:c.756G>A
  hgvsp: ENST00000537881.1:c.756G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000412444
  ensembl transcript: ENST00000457059
  gene symbol: DYNC1I1
  hgvsc: ENST00000457059.1:c.816G>A
  hgvsp: ENST00000457059.1:c.816G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000320130
  ensembl transcript: ENST00000324972
  gene symbol: DYNC1I1
  hgvsc: ENST00000324972.6:c.867G>A
  hgvsp: ENST00000324972.6:c.867G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158560
  ensembl transcript: ENST00000519371
  gene symbol: DYNC1I1
  hgvsc: ENST00000519371.1:n.474G>A
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000398118
  ensembl transcript: ENST00000437599
  gene symbol: DYNC1I1
  hgvsc: ENST00000437599.1:c.807G>A
  hgvsp: ENST00000437599.1:c.807G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2963
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1371
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4088
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2906
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 955
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1644
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2034
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3976
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1208
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3666
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25086
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3964
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3419
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 923
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2408
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1093
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1917
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50481
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Val289Val
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum

7-95616442-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95616442
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 95616442
    reference: chr 7
allele count: 1
allele frequency: 8.239404126293587e-6
allele num: 121368
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000412444
  ensembl transcript: ENST00000457059
  gene symbol: DYNC1I1
  hgvsc: ENST00000457059.1:c.818T>C
  hgvsp: ENSP00000412444.1:p.Val273Ala
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000352348
  ensembl transcript: ENST00000359388
  gene symbol: DYNC1I1
  hgvsc: ENST00000359388.4:c.758T>C
  hgvsp: ENSP00000352348.4:p.Val253Ala
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000438377
  ensembl transcript: ENST00000537881
  gene symbol: DYNC1I1
  hgvsc: ENST00000537881.1:c.758T>C
  hgvsp: ENSP00000438377.1:p.Val253Ala
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158560
  ensembl transcript: ENST00000519371
  gene symbol: DYNC1I1
  hgvsc: ENST00000519371.1:n.476T>C
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000320130
  ensembl transcript: ENST00000324972
  gene symbol: DYNC1I1
  hgvsc: ENST00000324972.6:c.869T>C
  hgvsp: ENSP00000320130.6:p.Val290Ala
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000398118
  ensembl transcript: ENST00000437599
  gene symbol: DYNC1I1
  hgvsc: ENST00000437599.1:c.809T>C
  hgvsp: ENSP00000398118.1:p.Val270Ala
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000392337
  ensembl transcript: ENST00000447467
  gene symbol: DYNC1I1
  hgvsc: ENST00000447467.2:c.818T>C
  hgvsp: ENSP00000392337.2:p.Val273Ala
  variant of: http://identifiers.org/hgnc/2963
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 25085
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3666
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2033
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 923
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1644
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 955
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2408
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1207
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3963
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4088
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3419
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2906
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1093
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3976
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1371
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1917
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50480
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 634
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 529
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Val290Ala
num of homozygotes: 0
population: Other
population: South Asian
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
population: European (Finnish)
reference allele: T
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff

7-95616446-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95616446
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 95616446
    reference: chr 7
allele count: 2
allele frequency: 1.647962294622699e-5
allele num: 121362
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000412444
  ensembl transcript: ENST00000457059
  gene symbol: DYNC1I1
  hgvsc: ENST00000457059.1:c.822T>C
  hgvsp: ENST00000457059.1:c.822T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000352348
  ensembl transcript: ENST00000359388
  gene symbol: DYNC1I1
  hgvsc: ENST00000359388.4:c.762T>C
  hgvsp: ENST00000359388.4:c.762T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000398118
  ensembl transcript: ENST00000437599
  gene symbol: DYNC1I1
  hgvsc: ENST00000437599.1:c.813T>C
  hgvsp: ENST00000437599.1:c.813T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158560
  ensembl transcript: ENST00000519371
  gene symbol: DYNC1I1
  hgvsc: ENST00000519371.1:n.480T>C
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000320130
  ensembl transcript: ENST00000324972
  gene symbol: DYNC1I1
  hgvsc: ENST00000324972.6:c.873T>C
  hgvsp: ENST00000324972.6:c.873T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000392337
  ensembl transcript: ENST00000447467
  gene symbol: DYNC1I1
  hgvsc: ENST00000447467.2:c.822T>C
  hgvsp: ENST00000447467.2:c.822T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000438377
  ensembl transcript: ENST00000537881
  gene symbol: DYNC1I1
  hgvsc: ENST00000537881.1:c.762T>C
  hgvsp: ENST00000537881.1:c.762T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2963
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 924
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2034
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3666
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1206
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2408
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 955
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3976
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1917
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4088
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1371
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1644
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3955
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25085
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2906
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1093
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3419
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 660
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1397
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Thr291Thr
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
reference allele: T
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: DP

7-95616455-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95616455
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 95616455
    reference: chr 7
allele count: 1
allele frequency: 8.240762105679534e-6
allele num: 121348
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000438377
  ensembl transcript: ENST00000537881
  gene symbol: DYNC1I1
  hgvsc: ENST00000537881.1:c.771C>T
  hgvsp: ENST00000537881.1:c.771C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000352348
  ensembl transcript: ENST00000359388
  gene symbol: DYNC1I1
  hgvsc: ENST00000359388.4:c.771C>T
  hgvsp: ENST00000359388.4:c.771C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000412444
  ensembl transcript: ENST00000457059
  gene symbol: DYNC1I1
  hgvsc: ENST00000457059.1:c.831C>T
  hgvsp: ENST00000457059.1:c.831C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000320130
  ensembl transcript: ENST00000324972
  gene symbol: DYNC1I1
  hgvsc: ENST00000324972.6:c.882C>T
  hgvsp: ENST00000324972.6:c.882C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000398118
  ensembl transcript: ENST00000437599
  gene symbol: DYNC1I1
  hgvsc: ENST00000437599.1:c.822C>T
  hgvsp: ENST00000437599.1:c.822C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000392337
  ensembl transcript: ENST00000447467
  gene symbol: DYNC1I1
  hgvsc: ENST00000447467.2:c.831C>T
  hgvsp: ENST00000447467.2:c.831C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158560
  ensembl transcript: ENST00000519371
  gene symbol: DYNC1I1
  hgvsc: ENST00000519371.1:n.489C>T
  variant of: http://identifiers.org/hgnc/2963
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2906
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1093
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 955
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2409
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 923
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3666
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3419
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4088
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1644
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3942
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2029
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1204
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1371
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1917
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3975
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25085
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1392
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 527
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 660
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Asp294Asp
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: African
population: East Asian
population: South Asian
reference allele: C
site quality: FS
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD

7-95616486-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95616486
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 95616486
    reference: chr 7
allele count: 2
allele frequency: 1.649484536082474e-5
allele num: 121250
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000438377
  ensembl transcript: ENST00000537881
  gene symbol: DYNC1I1
  hgvsc: ENST00000537881.1:c.783+19C>T
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000352348
  ensembl transcript: ENST00000359388
  gene symbol: DYNC1I1
  hgvsc: ENST00000359388.4:c.783+19C>T
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000392337
  ensembl transcript: ENST00000447467
  gene symbol: DYNC1I1
  hgvsc: ENST00000447467.2:c.843+19C>T
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl transcript: ENST00000519371
  gene symbol: DYNC1I1
  hgvsc: ENST00000519371.1:n.501+19C>T
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000398118
  ensembl transcript: ENST00000437599
  gene symbol: DYNC1I1
  hgvsc: ENST00000437599.1:c.834+19C>T
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000320130
  ensembl transcript: ENST00000324972
  gene symbol: DYNC1I1
  hgvsc: ENST00000324972.6:c.894+19C>T
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000412444
  ensembl transcript: ENST00000457059
  gene symbol: DYNC1I1
  hgvsc: ENST00000457059.1:c.843+19C>T
  variant of: http://identifiers.org/hgnc/2963
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3666
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4088
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1644
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 927
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1211
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2907
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3419
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3567
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1371
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1092
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1917
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2409
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25084
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3975
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1988
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 953
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 632
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 199
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50478
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ

7-95616496-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95616496
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 95616496
    reference: chr 7
allele count: 2
allele frequency: 1.650028875505322e-5
allele num: 121210
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000438377
  ensembl transcript: ENST00000537881
  gene symbol: DYNC1I1
  hgvsc: ENST00000537881.1:c.783+29C>T
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000412444
  ensembl transcript: ENST00000457059
  gene symbol: DYNC1I1
  hgvsc: ENST00000457059.1:c.843+29C>T
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl transcript: ENST00000519371
  gene symbol: DYNC1I1
  hgvsc: ENST00000519371.1:n.501+29C>T
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000398118
  ensembl transcript: ENST00000437599
  gene symbol: DYNC1I1
  hgvsc: ENST00000437599.1:c.834+29C>T
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000352348
  ensembl transcript: ENST00000359388
  gene symbol: DYNC1I1
  hgvsc: ENST00000359388.4:c.783+29C>T
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000392337
  ensembl transcript: ENST00000447467
  gene symbol: DYNC1I1
  hgvsc: ENST00000447467.2:c.843+29C>T
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000320130
  ensembl transcript: ENST00000324972
  gene symbol: DYNC1I1
  hgvsc: ENST00000324972.6:c.894+29C>T
  variant of: http://identifiers.org/hgnc/2963
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1917
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25083
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2907
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3667
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1090
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3419
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3360
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 954
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1644
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3975
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 929
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2409
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1199
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2023
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1372
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4088
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 645
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5297
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 503
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 323
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 624
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum

7-95616497-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95616497
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 95616497
    reference: chr 7
allele count: 1
allele frequency: 8.248647221855616e-6
allele num: 121232
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000392337
  ensembl transcript: ENST00000447467
  gene symbol: DYNC1I1
  hgvsc: ENST00000447467.2:c.843+30T>A
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000320130
  ensembl transcript: ENST00000324972
  gene symbol: DYNC1I1
  hgvsc: ENST00000324972.6:c.894+30T>A
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000438377
  ensembl transcript: ENST00000537881
  gene symbol: DYNC1I1
  hgvsc: ENST00000537881.1:c.783+30T>A
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl transcript: ENST00000519371
  gene symbol: DYNC1I1
  hgvsc: ENST00000519371.1:n.501+30T>A
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000352348
  ensembl transcript: ENST00000359388
  gene symbol: DYNC1I1
  hgvsc: ENST00000359388.4:c.783+30T>A
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000398118
  ensembl transcript: ENST00000437599
  gene symbol: DYNC1I1
  hgvsc: ENST00000437599.1:c.834+30T>A
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000412444
  ensembl transcript: ENST00000457059
  gene symbol: DYNC1I1
  hgvsc: ENST00000457059.1:c.843+30T>A
  variant of: http://identifiers.org/hgnc/2963
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 950
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3312
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1371
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3975
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1644
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 925
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1190
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2009
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3667
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2410
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1091
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2908
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25082
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4087
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3419
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1917
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 325
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1336
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 287
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 661
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 180
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5244
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 626
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
reference allele: T
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD

7-95616503-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95616503
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 95616503
    reference: chr 7
allele count: 1
allele frequency: 8.25218682950982e-6
allele num: 121180
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000392337
  ensembl transcript: ENST00000447467
  gene symbol: DYNC1I1
  hgvsc: ENST00000447467.2:c.843+36T>G
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000438377
  ensembl transcript: ENST00000537881
  gene symbol: DYNC1I1
  hgvsc: ENST00000537881.1:c.783+36T>G
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000398118
  ensembl transcript: ENST00000437599
  gene symbol: DYNC1I1
  hgvsc: ENST00000437599.1:c.834+36T>G
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000412444
  ensembl transcript: ENST00000457059
  gene symbol: DYNC1I1
  hgvsc: ENST00000457059.1:c.843+36T>G
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000320130
  ensembl transcript: ENST00000324972
  gene symbol: DYNC1I1
  hgvsc: ENST00000324972.6:c.894+36T>G
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl transcript: ENST00000519371
  gene symbol: DYNC1I1
  hgvsc: ENST00000519371.1:n.501+36T>G
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000352348
  ensembl transcript: ENST00000359388
  gene symbol: DYNC1I1
  hgvsc: ENST00000359388.4:c.783+36T>G
  variant of: http://identifiers.org/hgnc/2963
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1149
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3418
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2908
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2410
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4086
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2792
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25082
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 937
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 937
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 926
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1643
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1370
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3668
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3975
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1881
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1093
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1917
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 364
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 115
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 460
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 222
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50476
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 319
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4543
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 619
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
population: South Asian
reference allele: T
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum

7-95616504-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95616504
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 95616504
    reference: chr 7
allele count: 3
allele frequency: 2.475982965237199e-5
allele num: 121164
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000392337
  ensembl transcript: ENST00000447467
  gene symbol: DYNC1I1
  hgvsc: ENST00000447467.2:c.843+37G>A
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000438377
  ensembl transcript: ENST00000537881
  gene symbol: DYNC1I1
  hgvsc: ENST00000537881.1:c.783+37G>A
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000398118
  ensembl transcript: ENST00000437599
  gene symbol: DYNC1I1
  hgvsc: ENST00000437599.1:c.834+37G>A
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000352348
  ensembl transcript: ENST00000359388
  gene symbol: DYNC1I1
  hgvsc: ENST00000359388.4:c.783+37G>A
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000412444
  ensembl transcript: ENST00000457059
  gene symbol: DYNC1I1
  hgvsc: ENST00000457059.1:c.843+37G>A
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl transcript: ENST00000519371
  gene symbol: DYNC1I1
  hgvsc: ENST00000519371.1:n.501+37G>A
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000320130
  ensembl transcript: ENST00000324972
  gene symbol: DYNC1I1
  hgvsc: ENST00000324972.6:c.894+37G>A
  variant of: http://identifiers.org/hgnc/2963
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 25082
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3975
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1895
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2781
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 937
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2410
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1145
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 939
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4086
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1093
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3418
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1370
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2908
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1645
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3667
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 922
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1917
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 320
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 223
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4575
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 364
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 322
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD

7-95616505-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95616505
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 95616505
    reference: chr 7
allele count: 8
allele frequency: 6.601749463607856e-5
allele num: 121180
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl transcript: ENST00000519371
  gene symbol: DYNC1I1
  hgvsc: ENST00000519371.1:n.501+38T>C
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000320130
  ensembl transcript: ENST00000324972
  gene symbol: DYNC1I1
  hgvsc: ENST00000324972.6:c.894+38T>C
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000392337
  ensembl transcript: ENST00000447467
  gene symbol: DYNC1I1
  hgvsc: ENST00000447467.2:c.843+38T>C
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000398118
  ensembl transcript: ENST00000437599
  gene symbol: DYNC1I1
  hgvsc: ENST00000437599.1:c.834+38T>C
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000352348
  ensembl transcript: ENST00000359388
  gene symbol: DYNC1I1
  hgvsc: ENST00000359388.4:c.783+38T>C
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000412444
  ensembl transcript: ENST00000457059
  gene symbol: DYNC1I1
  hgvsc: ENST00000457059.1:c.843+38T>C
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000438377
  ensembl transcript: ENST00000537881
  gene symbol: DYNC1I1
  hgvsc: ENST00000537881.1:c.783+38T>C
  variant of: http://identifiers.org/hgnc/2963
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 436
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1091
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2908
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2410
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 938
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1917
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25082
  bin: 9.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 1644
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1895
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3667
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2776
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 918
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1150
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1368
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 943
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4086
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3418
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3975
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 620
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 463
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 366
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 399
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1214
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 220
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
population: European (Finnish)
population: Other
reference allele: T
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: DP

7-95616505-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95616505
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 95616505
    reference: chr 7
allele count: 1
allele frequency: 8.25218682950982e-6
allele num: 121180
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000438377
  ensembl transcript: ENST00000537881
  gene symbol: DYNC1I1
  hgvsc: ENST00000537881.1:c.783+38T>G
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000398118
  ensembl transcript: ENST00000437599
  gene symbol: DYNC1I1
  hgvsc: ENST00000437599.1:c.834+38T>G
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl transcript: ENST00000519371
  gene symbol: DYNC1I1
  hgvsc: ENST00000519371.1:n.501+38T>G
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000352348
  ensembl transcript: ENST00000359388
  gene symbol: DYNC1I1
  hgvsc: ENST00000359388.4:c.783+38T>G
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000392337
  ensembl transcript: ENST00000447467
  gene symbol: DYNC1I1
  hgvsc: ENST00000447467.2:c.843+38T>G
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000412444
  ensembl transcript: ENST00000457059
  gene symbol: DYNC1I1
  hgvsc: ENST00000457059.1:c.843+38T>G
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000320130
  ensembl transcript: ENST00000324972
  gene symbol: DYNC1I1
  hgvsc: ENST00000324972.6:c.894+38T>G
  variant of: http://identifiers.org/hgnc/2963
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 938
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3667
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1895
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2776
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1150
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2410
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 436
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3975
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 943
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25082
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 918
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1368
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1091
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3418
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2908
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1644
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1917
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4086
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1214
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 624
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 658
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 399
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4622
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: Other
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS

7-95616508-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95616508
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 95616508
    reference: chr 7
allele count: 1
allele frequency: 8.254502831294471e-6
allele num: 121146
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000398118
  ensembl transcript: ENST00000437599
  gene symbol: DYNC1I1
  hgvsc: ENST00000437599.1:c.834+41T>A
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000352348
  ensembl transcript: ENST00000359388
  gene symbol: DYNC1I1
  hgvsc: ENST00000359388.4:c.783+41T>A
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl transcript: ENST00000519371
  gene symbol: DYNC1I1
  hgvsc: ENST00000519371.1:n.501+41T>A
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000412444
  ensembl transcript: ENST00000457059
  gene symbol: DYNC1I1
  hgvsc: ENST00000457059.1:c.843+41T>A
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000438377
  ensembl transcript: ENST00000537881
  gene symbol: DYNC1I1
  hgvsc: ENST00000537881.1:c.783+41T>A
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000320130
  ensembl transcript: ENST00000324972
  gene symbol: DYNC1I1
  hgvsc: ENST00000324972.6:c.894+41T>A
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000392337
  ensembl transcript: ENST00000447467
  gene symbol: DYNC1I1
  hgvsc: ENST00000447467.2:c.843+41T>A
  variant of: http://identifiers.org/hgnc/2963
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1687
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25079
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1370
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4086
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2907
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1291
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1916
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1095
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1641
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2705
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 936
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3666
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3419
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1090
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2413
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 898
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3975
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 657
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 235
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 618
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 484
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 618
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 430
  bin: 2.25e1
  variant carriers: 0
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: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ

7-95616511-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95616511
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 95616511
    reference: chr 7
allele count: 2
allele frequency: 1.651909607506277e-5
allele num: 121072
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000320130
  ensembl transcript: ENST00000324972
  gene symbol: DYNC1I1
  hgvsc: ENST00000324972.6:c.894+44C>T
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000352348
  ensembl transcript: ENST00000359388
  gene symbol: DYNC1I1
  hgvsc: ENST00000359388.4:c.783+44C>T
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl transcript: ENST00000519371
  gene symbol: DYNC1I1
  hgvsc: ENST00000519371.1:n.501+44C>T
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000398118
  ensembl transcript: ENST00000437599
  gene symbol: DYNC1I1
  hgvsc: ENST00000437599.1:c.834+44C>T
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000438377
  ensembl transcript: ENST00000537881
  gene symbol: DYNC1I1
  hgvsc: ENST00000537881.1:c.783+44C>T
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000392337
  ensembl transcript: ENST00000447467
  gene symbol: DYNC1I1
  hgvsc: ENST00000447467.2:c.843+44C>T
  variant of: http://identifiers.org/hgnc/2963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158560
  ensembl protein: ENSP00000412444
  ensembl transcript: ENST00000457059
  gene symbol: DYNC1I1
  hgvsc: ENST00000457059.1:c.843+44C>T
  variant of: http://identifiers.org/hgnc/2963
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 919
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1088
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1914
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1031
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1600
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1284
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1642
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 866
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3419
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2908
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1365
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2412
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25079
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2907
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
reference allele: C

GenotypeQuality
all individuals: 82
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 7005
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10683
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 612
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 103
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3239
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1594
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4802
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2813
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2027
bin: 8.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6548
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11328
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16202
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9368
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8016
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.114391603600237e-5
allele num: 64218
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -3.63e-1

MQ
type: SiteQuality
SIO_000300: 5.931e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.31e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.48e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.82e0

DP
type: SiteQuality
SIO_000300: 1.821765e6

FS
type: SiteQuality
SIO_000300: 7.25e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.1e-3

QD
type: SiteQuality
SIO_000300: 1.518e1

MQRankSum
type: SiteQuality
SIO_000300: -2.2e-1

GenotypeQuality
all individuals: 252
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 86
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 267
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2039
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 347
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22123
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7035
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10680
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 125
bin: 4.25e1
variant carriers: 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: 6552
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11342
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64450
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8062
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16272
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.062699256110521e-4
allele num: 9410
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.74e-1

DP
type: SiteQuality
SIO_000300: 1.827661e6

VQSLOD
type: SiteQuality
SIO_000300: 1.09e0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.88e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.29e0

FS
type: SiteQuality
SIO_000300: 9.651999999999999e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.73e-1

QD
type: SiteQuality
SIO_000300: 1.402e1

GenotypeQuality
all individuals: 193
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2819
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1346
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 245
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10679
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 121
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3247
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 73
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22237
bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64558
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9416
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8076
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.140997297961189e-5
allele num: 16284
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11346
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6554
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.27e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

QD
type: SiteQuality
SIO_000300: 1.059e1

MQRankSum
type: SiteQuality
SIO_000300: -1.84e-1

MQ
type: SiteQuality
SIO_000300: 5.952e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.0e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.830085e6

ClippingRankSum
type: SiteQuality
SIO_000300: 5.01e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.419999999999999e-1

GenotypeQuality
all individuals: 569
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2042
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1312
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7087
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 103
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 109
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4166
bin: 8.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9430
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8124
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6558
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 876
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.63922308477407e-5
allele num: 64666
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11350
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16308
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.76e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -3.45e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.3e-1

DP
type: SiteQuality
SIO_000300: 1.832894e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.5e-2

VQSLOD
type: SiteQuality
SIO_000300: 2.05e0

QD
type: SiteQuality
SIO_000300: 1.458e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

GenotypeQuality
all individuals: 4193
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 140
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1034
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 494
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 23231
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2843
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7250
bin: 6.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8244
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16398
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.533319022355791e-5
allele num: 65218
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9538
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
allele num: 11374
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6572
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.52e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.28e0

MQ
type: SiteQuality
SIO_000300: 5.925e1

DP
type: SiteQuality
SIO_000300: 1.845964e6

MQRankSum
type: SiteQuality
SIO_000300: -1.007e0

VQSLOD
type: SiteQuality
SIO_000300: -9.878e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.82e0

QD
type: SiteQuality
SIO_000300: 1.742e1

FS
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
all individuals: 33
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10707
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4894
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23850
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7336
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 5.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16426
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.52114390021296e-5
allele num: 65740
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6574
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11406
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8352
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9678
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.36e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.5e-2

FS
type: SiteQuality
SIO_000300: 8.7e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.321e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -2.372e0

VQSLOD
type: SiteQuality
SIO_000300: -8.24e-2

QD
type: SiteQuality
SIO_000300: 1.497e1

DP
type: SiteQuality
SIO_000300: 1.857879e6

GenotypeQuality
all individuals: 776
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3323
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 219
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 7361
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4217
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10721
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 23994
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 4.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6578
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 894
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11416
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9738
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.517404631118934e-5
allele num: 65902
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16450
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8394
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 5.600000000000001e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.1e0

VQSLOD
type: SiteQuality
SIO_000300: 6.68e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.91e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.247e0

MQ
type: SiteQuality
SIO_000300: 5.943e1

FS
type: SiteQuality
SIO_000300: 4.263e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-3

DP
type: SiteQuality
SIO_000300: 1.862178e6

QD
type: SiteQuality
SIO_000300: 1.489e1

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

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

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

GenotypeQuality
all individuals: 39
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3330
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24135
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7382
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4906
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9806
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.514187941007238e-5
allele num: 66042
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16462
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8426
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6584
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: 11434
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.03e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.8e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -7.009e0

QD
type: SiteQuality
SIO_000300: 1.144e1

MQ
type: SiteQuality
SIO_000300: 5.947e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-3

DP
type: SiteQuality
SIO_000300: 1.86527e6

MQRankSum
type: SiteQuality
SIO_000300: -2.27e-1

FS
type: SiteQuality
SIO_000300: 9.340000000000001e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.72e-1

GenotypeQuality
all individuals: 8
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2071
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2855
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24307
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66204
num of homozygotes: 0

Other
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allele frequency: 0.0e0
allele num: 900
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6584
num of homozygotes: 0

East Asian
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allele frequency: 1.182033096926714e-4
allele num: 8460
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9988
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Latino
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allele frequency: 0.0e0
allele num: 11448
num of homozygotes: 0

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

DP
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ClippingRankSum
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InbreedingCoeff
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MQ
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SIO_000300: 6.0e1

QD
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VQSLOD
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SIO_000300: 1.66e0

BaseQRankSum
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SIO_000300: 2.43e0

FS
type: SiteQuality
SIO_000300: 4.774e0

MQRankSum
type: SiteQuality
SIO_000300: 5.09e-1

ReadPosRankSum
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SIO_000300: -1.3e-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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GenotypeQuality
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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
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allele frequency: 0.0e0
allele num: 8526
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.505208019748329e-5
allele num: 66436
num of homozygotes: 0

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

African
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allele frequency: 9.79431929480901e-5
allele num: 10210
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
allele num: 16474
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Other
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allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

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

VQSLOD
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ClippingRankSum
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BaseQRankSum
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DP
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MQRankSum
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SIO_000300: 4.42e-1

InbreedingCoeff
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FS
type: SiteQuality
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QD
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MQ
type: SiteQuality
SIO_000300: 5.9e1

ReadPosRankSum
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SIO_000300: -1.57e-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

Other
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allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16472
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6596
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.504709741490866e-5
allele num: 66458
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11478
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African
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allele count: 0
allele frequency: 0.0e0
allele num: 10214
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East Asian
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

InbreedingCoeff
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MQRankSum
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MQ
type: SiteQuality
SIO_000300: 5.987e1

VQSLOD
type: SiteQuality
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BaseQRankSum
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SIO_000300: -4.219e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.04e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.916e0

DP
type: SiteQuality
SIO_000300: 1.874395e6

QD
type: SiteQuality
SIO_000300: 1.088e1

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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bin: 9.75e1
variant carriers: 2

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11492
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.339728591483388e-4
allele num: 8548
num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 904
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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10246
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6596
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66496
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 5.22e-1

QD
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MQRankSum
type: SiteQuality
SIO_000300: -5.16e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.04e0

FS
type: SiteQuality
SIO_000300: 1.704e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.379999999999999e-1

MQ
type: SiteQuality
SIO_000300: 5.962e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 3.3e0

DP
type: SiteQuality
SIO_000300: 1.875484e6

GenotypeQuality
all individuals: 4
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
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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bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11492
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.759906304899473e-5
allele num: 10246
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6596
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66502
num of homozygotes: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8550
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.444e1

MQ
type: SiteQuality
SIO_000300: 5.989e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.4e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.82e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.994e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 2.046e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.18e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.647e0

DP
type: SiteQuality
SIO_000300: 1.875563e6

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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bin: 9.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6602
num of homozygotes: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8578
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501862309263487e-5
allele num: 66584
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11506
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16482
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African
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allele count: 0
allele frequency: 0.0e0
allele num: 10284
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BaseQRankSum
type: SiteQuality
SIO_000300: -4.5e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.262e0

DP
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SIO_000300: 1.877082e6

MQ
type: SiteQuality
SIO_000300: 5.944e1

FS
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
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MQRankSum
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.517e1

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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variant carriers: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.500060002400096e-5
allele num: 66664
num of homozygotes: 0

South Asian
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allele num: 16490
num of homozygotes: 0

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

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

African
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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: 11534
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
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VQSLOD
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QD
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MQRankSum
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InbreedingCoeff
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ClippingRankSum
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FS
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.817e1

DP
type: SiteQuality
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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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Other
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allele num: 906
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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South Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.499880009599232e-5
allele num: 66672
num of homozygotes: 0

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

Latino
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ReadPosRankSum
type: SiteQuality
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ClippingRankSum
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VQSLOD
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InbreedingCoeff
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DP
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FS
type: SiteQuality
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MQ
type: SiteQuality
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MQRankSum
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QD
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BaseQRankSum
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

European (Finnish)
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num of homozygotes: 0

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

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

Latino
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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 frequency: 0.0e0
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South Asian
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InbreedingCoeff
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DP
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ReadPosRankSum
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BaseQRankSum
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FS
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MQ
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MQRankSum
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QD
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VQSLOD
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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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variant carriers: 0

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

Latino
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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: 8594
num of homozygotes: 0

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

Other
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African
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
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allele num: 66672
num of homozygotes: 0

QD
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ClippingRankSum
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DP
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SIO_000300: 1.879044e6

FS
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MQRankSum
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BaseQRankSum
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VQSLOD
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MQ
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SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

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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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66690
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11540
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.062810719049351e-5
allele num: 16494
num of homozygotes: 0

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

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

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.512401693889897e-4
allele num: 6612
num of homozygotes: 0

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

VQSLOD
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ReadPosRankSum
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MQ
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SIO_000300: 5.971e1

BaseQRankSum
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ClippingRankSum
type: SiteQuality
SIO_000300: 3.91e-1

QD
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FS
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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MQRankSum
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DP
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GenotypeQuality
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bin: 8.75e1
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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variant carriers: 0

Other
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allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

African
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allele frequency: 9.665571235260003e-5
allele num: 10346
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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allele frequency: 6.062810719049351e-5
allele num: 16494
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 66696
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8594
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
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MQ
type: SiteQuality
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BaseQRankSum
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FS
type: SiteQuality
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InbreedingCoeff
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SIO_000300: -1.0e-4

DP
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ClippingRankSum
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SIO_000300: 1.84e0

MQRankSum
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SIO_000300: 1.57e0

QD
type: SiteQuality
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VQSLOD
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11530
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: 8600
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 5.996641880546894e-5
allele num: 66704
num of homozygotes: 0

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

VQSLOD
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SIO_000300: 2.1e0

InbreedingCoeff
type: SiteQuality
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MQRankSum
type: SiteQuality
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QD
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FS
type: SiteQuality
SIO_000300: 0.0e0

DP
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SIO_000300: 1.880163e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.43e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.0e-2

MQ
type: SiteQuality
SIO_000300: 5.971e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.11e-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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variant carriers: 0

European (Finnish)
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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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num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66704
num of homozygotes: 0

African
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allele count: 2
allele frequency: 1.93050193050193e-4
allele num: 10360
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
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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

InbreedingCoeff
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SIO_000300: 1.0e-4

ClippingRankSum
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.346e1

ReadPosRankSum
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SIO_000300: 1.13e0

MQRankSum
type: SiteQuality
SIO_000300: -1.041e0

DP
type: SiteQuality
SIO_000300: 1.880255e6

VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.981e1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.04e0

FS
type: SiteQuality
SIO_000300: 5.31e-1

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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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: 8598
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
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.499160470136723e-5
allele num: 66704
num of homozygotes: 0

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

South Asian
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allele frequency: 0.0e0
allele num: 16496
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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MQRankSum
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QD
type: SiteQuality
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FS
type: SiteQuality
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ReadPosRankSum
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ClippingRankSum
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MQ
type: SiteQuality
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BaseQRankSum
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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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Other
type: Population
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allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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African
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East Asian
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allele frequency: 2.323420074349442e-4
allele num: 8608
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66702
num of homozygotes: 0

Latino
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South Asian
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ReadPosRankSum
type: SiteQuality
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FS
type: SiteQuality
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BaseQRankSum
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VQSLOD
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DP
type: SiteQuality
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QD
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InbreedingCoeff
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ClippingRankSum
type: SiteQuality
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MQRankSum
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MQ
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
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allele num: 10380
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.499160470136723e-5
allele num: 66704
num of homozygotes: 0

East Asian
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Other
type: Population
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num of homozygotes: 0

European (Finnish)
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FS
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DP
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QD
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MQ
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VQSLOD
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MQRankSum
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ReadPosRankSum
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InbreedingCoeff
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BaseQRankSum
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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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variant carriers: 0

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

Other
type: Population
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European (Non-Finnish)
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allele frequency: 2.398656752218757e-4
allele num: 66704
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African
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South Asian
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Latino
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allele frequency: 6.064806792583608e-4
allele num: 11542
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East Asian
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BaseQRankSum
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ReadPosRankSum
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MQRankSum
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MQ
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ClippingRankSum
type: SiteQuality
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InbreedingCoeff
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VQSLOD
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FS
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QD
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DP
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele num: 66706
num of homozygotes: 0

Latino
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European (Finnish)
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Other
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QD
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VQSLOD
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ClippingRankSum
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DP
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MQRankSum
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InbreedingCoeff
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MQ
type: SiteQuality
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FS
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BaseQRankSum
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ReadPosRankSum
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11538
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8606
num of homozygotes: 0

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

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

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10386
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.499160470136723e-5
allele num: 66704
num of homozygotes: 0

VQSLOD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
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MQRankSum
type: SiteQuality
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DP
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SIO_000300: 1.88032e6

MQ
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.227e1

ReadPosRankSum
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SIO_000300: 1.29e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.646e0

GenotypeQuality
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bin: 6.25e1
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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bin: 4.75e1
variant carriers: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8602
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11532
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10374
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66690
num of homozygotes: 0

South Asian
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allele count: 8
allele frequency: 4.848484848484848e-4
allele num: 16500
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.72e0

FS
type: SiteQuality
SIO_000300: 5.36e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.600000000000001e-1

MQRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.880723e6

MQ
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SIO_000300: 5.955e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.329e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

QD
type: SiteQuality
SIO_000300: 1.306e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.79e-1

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
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GenotypeQuality
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GenotypeQuality
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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: 5

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10372
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8602
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11534
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: 6612
num of homozygotes: 0

European (Non-Finnish)
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allele count: 4
allele frequency: 5.997720866070893e-5
allele num: 66692
num of homozygotes: 0

South Asian
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allele count: 1
allele frequency: 6.06060606060606e-5
allele num: 16500
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 6.68e-1

MQ
type: SiteQuality
SIO_000300: 5.972e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.53e0

VQSLOD
type: SiteQuality
SIO_000300: 1.88e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.98e-1

FS
type: SiteQuality
SIO_000300: 1.144e0

MQRankSum
type: SiteQuality
SIO_000300: 2.16e-1

DP
type: SiteQuality
SIO_000300: 1.880511e6

QD
type: SiteQuality
SIO_000300: 1.255e1

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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bin: 8.75e1
variant carriers: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11530
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.06060606060606e-5
allele num: 16500
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66682
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8600
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

DP
type: SiteQuality
SIO_000300: 1.879854e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.92e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.06e-1

FS
type: SiteQuality
SIO_000300: 1.126e0

MQRankSum
type: SiteQuality
SIO_000300: 5.26e-1

MQ
type: SiteQuality
SIO_000300: 5.985e1

VQSLOD
type: SiteQuality
SIO_000300: 1.54e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.41e-1

QD
type: SiteQuality
SIO_000300: 1.205e1

GenotypeQuality
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bin: 2.5e0
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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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: 1
allele frequency: 1.499655079331754e-5
allele num: 66682
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: 6612
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8600
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16500
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11530
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.205e1

FS
type: SiteQuality
SIO_000300: 1.126e0

VQSLOD
type: SiteQuality
SIO_000300: 1.54e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.41e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.06e-1

DP
type: SiteQuality
SIO_000300: 1.879854e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.92e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.26e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.985e1

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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bin: 4.25e1
variant carriers: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66678
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16498
num of homozygotes: 0

African
type: Population
allele count: 130
allele frequency: 1.253616200578592e-2
allele num: 10370
num of homozygotes: 3

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8604
num of homozygotes: 0

Latino
type: Population
allele count: 10
allele frequency: 8.668515950069349e-4
allele num: 11536
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.53e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.782e0

MQ
type: SiteQuality
SIO_000300: 5.962e1

DP
type: SiteQuality
SIO_000300: 1.89252e6

VQSLOD
type: SiteQuality
SIO_000300: 6.31e0

QD
type: SiteQuality
SIO_000300: 1.318e1

MQRankSum
type: SiteQuality
SIO_000300: 3.07e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.89e-2

ClippingRankSum
type: SiteQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500285054160291e-5
allele num: 66654
num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16494
num of homozygotes: 0

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

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

ClippingRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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DP
type: SiteQuality
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QD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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MQRankSum
type: SiteQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
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GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

Latino
type: Population
allele count: 2
allele frequency: 1.73550850399167e-4
allele num: 11524
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16496
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10336
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8578
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66646
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.981e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

QD
type: SiteQuality
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MQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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DP
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FS
type: SiteQuality
SIO_000300: 1.178e0

VQSLOD
type: SiteQuality
SIO_000300: 1.14e0

ReadPosRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10326
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16494
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8578
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.500555205426008e-5
allele num: 66642
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
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VQSLOD
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MQ
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MQRankSum
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InbreedingCoeff
type: SiteQuality
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FS
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DP
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 6.97e-1

QD
type: SiteQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10320
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8574
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: 11520
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: 1.500690317546071e-5
allele num: 66636
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16494
num of homozygotes: 0

InbreedingCoeff
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SIO_000300: 3.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -8.98e-1

QD
type: SiteQuality
SIO_000300: 3.52e0

FS
type: SiteQuality
SIO_000300: 4.772e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.68e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.25e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.059e-1

MQ
type: SiteQuality
SIO_000300: 3.772e1

DP
type: SiteQuality
SIO_000300: 1.877164e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.98e-1

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 10768
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 2080
bin: 8.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6604
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8564
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: 11504
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.002371873780286e-5
allele num: 66614
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16488
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 8.500000000000001e-2

VQSLOD
type: SiteQuality
SIO_000300: -2.799e0

FS
type: SiteQuality
SIO_000300: 1.3778e1

QD
type: SiteQuality
SIO_000300: 2.07e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.79e-1

MQ
type: SiteQuality
SIO_000300: 4.037e1

DP
type: SiteQuality
SIO_000300: 1.877131e6

MQRankSum
type: SiteQuality
SIO_000300: -1.203e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 8.500000000000001e-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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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
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allele count: 0
allele frequency: 0.0e0
allele num: 8550
num of homozygotes: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16486
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10272
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.50253929140247e-5
allele num: 66554
num of homozygotes: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6604
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.79e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.567e0

QD
type: SiteQuality
SIO_000300: 1.643e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.5e-3

VQSLOD
type: SiteQuality
SIO_000300: -1.268e0

FS
type: SiteQuality
SIO_000300: 6.82e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.14e0

DP
type: SiteQuality
SIO_000300: 1.872232e6

MQ
type: SiteQuality
SIO_000300: 5.973e1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.31e-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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bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10232
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66526
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11496
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8544
num of homozygotes: 0

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

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

South Asian
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allele count: 1
allele frequency: 6.065752759917505e-5
allele num: 16486
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 4.401e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.21e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.58e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.035e0

DP
type: SiteQuality
SIO_000300: 1.868241e6

FS
type: SiteQuality
SIO_000300: 3.203e0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.51e-1

MQRankSum
type: SiteQuality
SIO_000300: -7.51e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.9e-3

QD
type: SiteQuality
SIO_000300: 1.246e1

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 3

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6592
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.065752759917505e-5
allele num: 16486
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10232
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.503533303262667e-5
allele num: 66510
num of homozygotes: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.170686022008897e-4
allele num: 8542
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.74e0

MQ
type: SiteQuality
SIO_000300: 4.843e1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.98e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.1e-3

DP
type: SiteQuality
SIO_000300: 1.868563e6

FS
type: SiteQuality
SIO_000300: 2.516e0

QD
type: SiteQuality
SIO_000300: 1.199e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.379e0

MQRankSum
type: SiteQuality
SIO_000300: -1.4e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.021e0

GenotypeQuality
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bin: 2.25e1
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: 0

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: 16486
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8542
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6592
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.007066606525334e-5
allele num: 66510
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: 10232
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.021e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.98e-1

DP
type: SiteQuality
SIO_000300: 1.868563e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.1e-3

QD
type: SiteQuality
SIO_000300: 1.199e1

FS
type: SiteQuality
SIO_000300: 2.516e0

MQ
type: SiteQuality
SIO_000300: 4.843e1

MQRankSum
type: SiteQuality
SIO_000300: -1.4e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.379e0

VQSLOD
type: SiteQuality
SIO_000300: 1.74e0

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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variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16486
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 6
allele frequency: 9.018216797931822e-5
allele num: 66532
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10224
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11492
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8548
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6596
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.963e1

MQRankSum
type: SiteQuality
SIO_000300: 1.75e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.43e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.19e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.26e-2

BaseQRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 7.1e-1

QD
type: SiteQuality
SIO_000300: 1.401e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.88e-1

DP
type: SiteQuality
SIO_000300: 1.867115e6

GenotypeQuality
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bin: 1.25e1
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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variant carriers: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8542
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16486
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66512
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6596
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11490
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 9.788566953797964e-5
allele num: 10216
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.6e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 3.69e0

ClippingRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.956e1

ReadPosRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.866087e6

MQRankSum
type: SiteQuality
SIO_000300: 7.3e-1

QD
type: SiteQuality
SIO_000300: 1.549e1

FS
type: SiteQuality
SIO_000300: 1.666e0

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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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.507068149621726e-5
allele num: 66354
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6586
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11458
num of homozygotes: 0

African
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allele frequency: 0.0e0
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South Asian
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allele num: 16466
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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8484
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.6e-1

VQSLOD
type: SiteQuality
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InbreedingCoeff
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BaseQRankSum
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FS
type: SiteQuality
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MQRankSum
type: SiteQuality
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QD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.862815e6

MQ
type: SiteQuality
SIO_000300: 5.942e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.8e-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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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: 0
allele frequency: 0.0e0
allele num: 11562
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8640
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South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 15886
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.505706628120577e-5
allele num: 66414
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
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num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.5e-2

FS
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.989e1

MQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 5.767133e6

QD
type: SiteQuality
SIO_000300: 1.407e1

ReadPosRankSum
type: SiteQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 304
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variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8644
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10396
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.505389293671343e-5
allele num: 66428
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15968
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 9.14e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.13e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.65e0

MQ
type: SiteQuality
SIO_000300: 5.98e1

DP
type: SiteQuality
SIO_000300: 5.77328e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 2.81e0

MQRankSum
type: SiteQuality
SIO_000300: 3.62e-1

QD
type: SiteQuality
SIO_000300: 1.496e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.22e-1

GenotypeQuality
all individuals: 291
bin: 8.75e1
variant carriers: 5

GenotypeQuality
all individuals: 582
bin: 9.25e1
variant carriers: 15

GenotypeQuality
all individuals: 195
bin: 4.25e1
variant carriers: 3

GenotypeQuality
all individuals: 240
bin: 4.75e1
variant carriers: 11

GenotypeQuality
all individuals: 405
bin: 7.25e1
variant carriers: 12

GenotypeQuality
all individuals: 57
bin: 5.75e1
variant carriers: 11

GenotypeQuality
all individuals: 946
bin: 6.75e1
variant carriers: 12

GenotypeQuality
all individuals: 98
bin: 5.25e1
variant carriers: 7

GenotypeQuality
all individuals: 524
bin: 8.25e1
variant carriers: 8

GenotypeQuality
all individuals: 471
bin: 3.25e1
variant carriers: 2

Latino
type: Population
allele count: 593
allele frequency: 5.129757785467128e-2
allele num: 11560
num of homozygotes: 19

European (Finnish)
type: Population
allele count: 584
allele frequency: 8.832425892316999e-2
allele num: 6612
num of homozygotes: 30

East Asian
type: Population
allele count: 3
allele frequency: 3.469812630117973e-4
allele num: 8646
num of homozygotes: 0

South Asian
type: Population
allele count: 1477
allele frequency: 9.209377727896247e-2
allele num: 16038
num of homozygotes: 97

African
type: Population
allele count: 324
allele frequency: 3.117182990186646e-2
allele num: 10394
num of homozygotes: 2

Other
type: Population
allele count: 80
allele frequency: 8.869179600886919e-2
allele num: 902
num of homozygotes: 4

European (Non-Finnish)
type: Population
allele count: 7477
allele frequency: 1.124868361666917e-1
allele num: 66470
num of homozygotes: 450

MQ
type: SiteQuality
SIO_000300: 5.976e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.49e-2

MQRankSum
type: SiteQuality
SIO_000300: 7.3e-2

QD
type: SiteQuality
SIO_000300: 1.56e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.97e-1

DP
type: SiteQuality
SIO_000300: 6.113163e6

VQSLOD
type: SiteQuality
SIO_000300: 4.4e0

FS
type: SiteQuality
SIO_000300: 8.48e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.48e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.1e-1

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

GenotypeQuality
all individuals: 636
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 132
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 220
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 506
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 50479
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 331
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1294
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 662
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 629
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.503307276007216e-5
allele num: 66520
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10398
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: 11572
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16188
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 3.772e0

QD
type: SiteQuality
SIO_000300: 2.161e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.0e-3

MQRankSum
type: SiteQuality
SIO_000300: 8.179999999999999e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.1e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.74e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.076e0

MQ
type: SiteQuality
SIO_000300: 5.979e1

DP
type: SiteQuality
SIO_000300: 5.283191e6

VQSLOD
type: SiteQuality
SIO_000300: -2.261e0

GenotypeQuality
all individuals: 523
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 37
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 661
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 50482
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 16
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 330
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 656
bin: 7.75e1
variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500870504892838e-5
allele num: 66628
num of homozygotes: 0

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

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

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

MQ
type: SiteQuality
SIO_000300: 5.97e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.93e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -6.934e0

MQRankSum
type: SiteQuality
SIO_000300: 9.3e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -4.98e-1

DP
type: SiteQuality
SIO_000300: 5.292268e6

VQSLOD
type: SiteQuality
SIO_000300: 8.0e-1

QD
type: SiteQuality
SIO_000300: 1.311e1

GenotypeQuality
all individuals: 3
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 661
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 2.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 50483
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1406
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 331
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 657
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 526
bin: 7.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.641548565502938e-5
allele num: 11572
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: 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: 6614
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16494
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 3.79e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.04e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

MQ
type: SiteQuality
SIO_000300: 5.979e1

DP
type: SiteQuality
SIO_000300: 5.293639e6

VQSLOD
type: SiteQuality
SIO_000300: 9.22e-1

FS
type: SiteQuality
SIO_000300: 3.495e0

QD
type: SiteQuality
SIO_000300: 1.38e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.85e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.277e0

GenotypeQuality
all individuals: 661
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 331
bin: 8.75e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 526
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 657
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 637
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 50483
bin: 9.75e1
variant carriers: 1

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16494
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.609840476648087e-5
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: 11572
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

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

ClippingRankSum
type: SiteQuality
SIO_000300: 3.79e-1

FS
type: SiteQuality
SIO_000300: 3.495e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.85e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -2.277e0

MQ
type: SiteQuality
SIO_000300: 5.979e1

MQRankSum
type: SiteQuality
SIO_000300: 1.04e0

DP
type: SiteQuality
SIO_000300: 5.293639e6

VQSLOD
type: SiteQuality
SIO_000300: 9.22e-1

QD
type: SiteQuality
SIO_000300: 1.38e1

GenotypeQuality
all individuals: 634
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 661
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 658
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5923
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1405
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 530
bin: 7.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8652
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: 1.499880009599232e-5
allele num: 66672
num of homozygotes: 0

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

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

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

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

FS
type: SiteQuality
SIO_000300: 1.163e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.52e0

MQ
type: SiteQuality
SIO_000300: 5.976e1

MQRankSum
type: SiteQuality
SIO_000300: 1.65e0

DP
type: SiteQuality
SIO_000300: 5.293547e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.5e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -7.35e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.02e0

VQSLOD
type: SiteQuality
SIO_000300: 6.5e-2

QD
type: SiteQuality
SIO_000300: 1.452e1

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

GenotypeQuality
all individuals: 658
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 331
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1405
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 5.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 50482
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 5
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 661
bin: 9.25e1
variant carriers: 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: 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

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.999760019198464e-5
allele num: 66672
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.5e-3

DP
type: SiteQuality
SIO_000300: 5.293547e6

FS
type: SiteQuality
SIO_000300: 1.163e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.02e0

MQRankSum
type: SiteQuality
SIO_000300: 1.65e0

QD
type: SiteQuality
SIO_000300: 1.452e1

MQ
type: SiteQuality
SIO_000300: 5.976e1

VQSLOD
type: SiteQuality
SIO_000300: 6.5e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.52e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.35e-1

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

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

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

GenotypeQuality
all individuals: 659
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 50481
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 634
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 532
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 331
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 662
bin: 9.25e1
variant carriers: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.999130252226854e-5
allele num: 66686
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: 16504
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.48e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.59e0

MQ
type: SiteQuality
SIO_000300: 5.944e1

FS
type: SiteQuality
SIO_000300: 5.4e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

QD
type: SiteQuality
SIO_000300: 1.297e1

MQRankSum
type: SiteQuality
SIO_000300: 5.87e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.06e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.613e0

DP
type: SiteQuality
SIO_000300: 5.293619e6

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

GenotypeQuality
all individuals: 1
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 331
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5959
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1404
bin: 6.75e1
variant carriers: 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: 908
num of homozygotes: 0

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

South Asian
type: Population
allele count: 2
allele frequency: 1.211827435773146e-4
allele num: 16504
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: 0
allele frequency: 0.0e0
allele num: 66714
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 1.42e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.72e0

VQSLOD
type: SiteQuality
SIO_000300: 2.51e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.308e1

MQ
type: SiteQuality
SIO_000300: 5.965e1

DP
type: SiteQuality
SIO_000300: 5.293716e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.38e-1

FS
type: SiteQuality
SIO_000300: 5.19e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.891e0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

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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bin: 3.75e1
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GenotypeQuality
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bin: 9.75e1
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GenotypeQuality
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GenotypeQuality
all individuals: 660
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variant carriers: 0

GenotypeQuality
all individuals: 5967
bin: 6.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 3
allele frequency: 1.817300702689605e-4
allele num: 16508
num of homozygotes: 0

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

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

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

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: -1.6e-2

FS
type: SiteQuality
SIO_000300: 1.09e0

QD
type: SiteQuality
SIO_000300: 1.378e1

VQSLOD
type: SiteQuality
SIO_000300: 7.82e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.18e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.952e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.6e-2

MQRankSum
type: SiteQuality
SIO_000300: 9.92e-1

DP
type: SiteQuality
SIO_000300: 5.293747e6

GenotypeQuality
all individuals: 23
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 8.25e1
variant carriers: 0

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

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11574
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: 16508
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.498756032493031e-5
allele num: 66722
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.7e-1

MQ
type: SiteQuality
SIO_000300: 5.954e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 5.293547e6

QD
type: SiteQuality
SIO_000300: 1.08e1

FS
type: SiteQuality
SIO_000300: 1.3239e1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.891e0

MQRankSum
type: SiteQuality
SIO_000300: -9.65e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.872e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.5e-2

GenotypeQuality
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bin: 2.5e0
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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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: 908
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: 11574
num of homozygotes: 0

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

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16508
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 4.9e-1

QD
type: SiteQuality
SIO_000300: 1.336e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.65e0

MQRankSum
type: SiteQuality
SIO_000300: 1.43e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.49e0

VQSLOD
type: SiteQuality
SIO_000300: 3.78e-1

MQ
type: SiteQuality
SIO_000300: 5.957e1

DP
type: SiteQuality
SIO_000300: 5.29342e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.23e-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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bin: 9.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11570
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

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: 16508
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498890820792613e-5
allele num: 66716
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.595e0

VQSLOD
type: SiteQuality
SIO_000300: 6.19e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.88e-1

QD
type: SiteQuality
SIO_000300: 1.191e1

DP
type: SiteQuality
SIO_000300: 5.293209e6

FS
type: SiteQuality
SIO_000300: 7.66e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.88e0

MQ
type: SiteQuality
SIO_000300: 5.927e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.24e-1

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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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 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: 16508
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498935755613514e-5
allele num: 66714
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11570
num of homozygotes: 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: 6614
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.548e1

MQRankSum
type: SiteQuality
SIO_000300: -1.82e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.28e-1

MQ
type: SiteQuality
SIO_000300: 5.938e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.25e0

FS
type: SiteQuality
SIO_000300: 5.45e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.2e0

DP
type: SiteQuality
SIO_000300: 5.293167e6

BaseQRankSum
type: SiteQuality
SIO_000300: 6.81e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 4.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.75e1
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: 2
allele frequency: 2.312673450508788e-4
allele num: 8648
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11568
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66710
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: 10406
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16508
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.13e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.48e-1

FS
type: SiteQuality
SIO_000300: 6.37e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.99e1

QD
type: SiteQuality
SIO_000300: 1.518e1

VQSLOD
type: SiteQuality
SIO_000300: 3.22e-1

DP
type: SiteQuality
SIO_000300: 5.293158e6

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.25e1
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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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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 8.644536652835408e-5
allele num: 11568
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: 0
allele frequency: 0.0e0
allele num: 66700
num of homozygotes: 0

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

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16508
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 7.28e-1

DP
type: SiteQuality
SIO_000300: 5.292632e6

MQ
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 5.1e-3

VQSLOD
type: SiteQuality
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MQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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QD
type: SiteQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
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: 11556
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8640
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.000840235265874e-5
allele num: 66648
num of homozygotes: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16484
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.48e-2

ReadPosRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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QD
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DP
type: SiteQuality
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MQRankSum
type: SiteQuality
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FS
type: SiteQuality
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ClippingRankSum
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BaseQRankSum
type: SiteQuality
SIO_000300: -8.433999999999999e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

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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variant carriers: 0

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

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

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16472
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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African
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 2
allele frequency: 3.001200480192077e-5
allele num: 66640
num of homozygotes: 0

FS
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.979e1

VQSLOD
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InbreedingCoeff
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QD
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BaseQRankSum
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MQRankSum
type: SiteQuality
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DP
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -1.132e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

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: 11544
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500420117632937e-5
allele num: 66648
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8636
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: 16480
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.3e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.02e0

FS
type: SiteQuality
SIO_000300: 5.378e0

DP
type: SiteQuality
SIO_000300: 5.287074e6

MQ
type: SiteQuality
SIO_000300: 5.962e1

VQSLOD
type: SiteQuality
SIO_000300: 7.82e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.75e-2

MQRankSum
type: SiteQuality
SIO_000300: 7.099999999999999e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.83e-1

QD
type: SiteQuality
SIO_000300: 1.431e1

GenotypeQuality
all individuals: 125
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 389
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 20
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 321
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1217
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 657
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 632
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 5.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6608
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: 1.500915558490679e-5
allele num: 66626
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8624
num of homozygotes: 0

Latino
type: Population
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: 10402
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 1.39e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.500000000000001e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 3.46e-1

QD
type: SiteQuality
SIO_000300: 1.473e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.63e0

DP
type: SiteQuality
SIO_000300: 5.28183e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.95e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.19e-1

GenotypeQuality
all individuals: 131
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 392
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 627
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 657
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 461
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 50475
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 1213
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 617
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 1.75e1
variant carriers: 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: 8614
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66624
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 1.822378811809015e-4
allele num: 16462
num of homozygotes: 0

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: -1.13e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 7.93e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.8e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 5.281838e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.0e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.63e0

MQRankSum
type: SiteQuality
SIO_000300: -4.93e-1

QD
type: SiteQuality
SIO_000300: 1.228e1

GenotypeQuality
all individuals: 318
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 624
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4622
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 50475
bin: 9.75e1
variant carriers: 8

GenotypeQuality
all individuals: 51
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 658
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 129
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 321
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 9.617234083477592e-5
allele num: 10398
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8622
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66626
num of homozygotes: 0

Latino
type: Population
allele count: 7
allele frequency: 6.060606060606061e-4
allele num: 11550
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16468
num of homozygotes: 0

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

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

VQSLOD
type: SiteQuality
SIO_000300: 4.33e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.987e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.9e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.5e-3

MQRankSum
type: SiteQuality
SIO_000300: 2.89e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.421e0

QD
type: SiteQuality
SIO_000300: 1.39e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.1e-2

DP
type: SiteQuality
SIO_000300: 5.281628e6

GenotypeQuality
all individuals: 366
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 220
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 620
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 463
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 321
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 129
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 50475
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 318
bin: 3.75e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 8.658008658008658e-5
allele num: 11550
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16468
num of homozygotes: 0

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

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8622
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66626
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -6.421e0

MQ
type: SiteQuality
SIO_000300: 5.987e1

VQSLOD
type: SiteQuality
SIO_000300: 4.33e0

MQRankSum
type: SiteQuality
SIO_000300: 2.89e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.9e-1

QD
type: SiteQuality
SIO_000300: 1.39e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.1e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.5e-3

DP
type: SiteQuality
SIO_000300: 5.281628e6

FS
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
all individuals: 457
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 212
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 50476
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 66
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1170
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 495
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 321
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4022
bin: 6.25e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66612
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8616
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.076072426783327e-5
allele num: 16458
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: -3.41e0

FS
type: SiteQuality
SIO_000300: 5.228e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.518e0

MQRankSum
type: SiteQuality
SIO_000300: 2.42e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.49e-1

QD
type: SiteQuality
SIO_000300: 1.638e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.21e0

DP
type: SiteQuality
SIO_000300: 5.277307e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.1e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1