14-23533264-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23533264
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23533264
    reference: chr 14
allele count: 2
allele frequency: 1.662399840409615e-5
allele num: 120308
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000555807
  gene symbol: ACIN1
  hgvsc: ENST00000555807.1:n.815+50C>G
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000405677
  ensembl transcript: ENST00000457657
  gene symbol: ACIN1
  hgvsc: ENST00000457657.1:c.2649+50C>G
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451138
  ensembl transcript: ENST00000557515
  gene symbol: ACIN1
  hgvsc: ENST00000557515.1:c.492+50C>G
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000350073
  ensembl transcript: ENST00000357481
  gene symbol: ACIN1
  hgvsc: ENST00000357481.2:c.495+50C>G
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000380502
  ensembl transcript: ENST00000397341
  gene symbol: ACIN1
  hgvsc: ENST00000397341.3:c.495+50C>G
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000345541
  ensembl transcript: ENST00000338631
  gene symbol: ACIN1
  hgvsc: ENST00000338631.6:c.588+50C>G
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000473758
  gene symbol: ACIN1
  hgvsc: ENST00000473758.1:n.1702+50C>G
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451410
  ensembl transcript: ENST00000555566
  gene symbol: ACIN1
  hgvsc: ENST00000555566.1:c.459+50C>G
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000474349
  ensembl transcript: ENST00000605057
  gene symbol: ACIN1
  hgvsc: ENST00000605057.1:c.2595+50C>G
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000262710
  ensembl transcript: ENST00000262710
  gene symbol: ACIN1
  hgvsc: ENST00000262710.1:c.2769+50C>G
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451328
  ensembl transcript: ENST00000555053
  gene symbol: ACIN1
  hgvsc: ENST00000555053.1:c.2730+50C>G
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000557039
  gene symbol: ACIN1
  hgvsc: ENST00000557039.1:n.609+50C>G
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000553790
  gene symbol: ACIN1
  hgvsc: ENST00000553790.1:n.218+50C>G
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000556052
  gene symbol: ACIN1
  hgvsc: ENST00000556052.1:n.600+50C>G
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000555478
  gene symbol: ACIN1
  hgvsc: ENST00000555478.1:n.392+50C>G
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000554680
  gene symbol: ACIN1
  hgvsc: ENST00000554680.1:n.509+50C>G
  variant of: http://identifiers.org/hgnc/17066
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4917
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6798
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2521
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6718
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3056
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2689
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1559
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 862
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1145
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum

14-23533274-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23533274
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23533274
    reference: chr 14
allele count: 1
allele frequency: 8.309098462816784e-6
allele num: 120350
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000262710
  ensembl transcript: ENST00000262710
  gene symbol: ACIN1
  hgvsc: ENST00000262710.1:c.2769+40G>A
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000553790
  gene symbol: ACIN1
  hgvsc: ENST00000553790.1:n.218+40G>A
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000380502
  ensembl transcript: ENST00000397341
  gene symbol: ACIN1
  hgvsc: ENST00000397341.3:c.495+40G>A
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000557039
  gene symbol: ACIN1
  hgvsc: ENST00000557039.1:n.609+40G>A
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451138
  ensembl transcript: ENST00000557515
  gene symbol: ACIN1
  hgvsc: ENST00000557515.1:c.492+40G>A
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000345541
  ensembl transcript: ENST00000338631
  gene symbol: ACIN1
  hgvsc: ENST00000338631.6:c.588+40G>A
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000474349
  ensembl transcript: ENST00000605057
  gene symbol: ACIN1
  hgvsc: ENST00000605057.1:c.2595+40G>A
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451410
  ensembl transcript: ENST00000555566
  gene symbol: ACIN1
  hgvsc: ENST00000555566.1:c.459+40G>A
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000350073
  ensembl transcript: ENST00000357481
  gene symbol: ACIN1
  hgvsc: ENST00000357481.2:c.495+40G>A
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000405677
  ensembl transcript: ENST00000457657
  gene symbol: ACIN1
  hgvsc: ENST00000457657.1:c.2649+40G>A
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000555807
  gene symbol: ACIN1
  hgvsc: ENST00000555807.1:n.815+40G>A
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000473758
  gene symbol: ACIN1
  hgvsc: ENST00000473758.1:n.1702+40G>A
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451328
  ensembl transcript: ENST00000555053
  gene symbol: ACIN1
  hgvsc: ENST00000555053.1:c.2730+40G>A
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000554680
  gene symbol: ACIN1
  hgvsc: ENST00000554680.1:n.509+40G>A
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000555478
  gene symbol: ACIN1
  hgvsc: ENST00000555478.1:n.392+40G>A
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000556052
  gene symbol: ACIN1
  hgvsc: ENST00000556052.1:n.600+40G>A
  variant of: http://identifiers.org/hgnc/17066
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5938
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1233
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1146
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6728
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1652
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3602
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1433
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1738
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ

http://identifiers.org/exac.variant/14-23533279-AC-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23533279
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23533278
    reference: chr 14
allele count: 3
allele frequency: 2.489667878305034e-5
allele num: 120498
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000474349
  ensembl transcript: ENST00000605057
  gene symbol: ACIN1
  hgvsc: ENST00000605057.1:c.2595+34delG
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000555807
  gene symbol: ACIN1
  hgvsc: ENST00000555807.1:n.815+34delG
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000556052
  gene symbol: ACIN1
  hgvsc: ENST00000556052.1:n.600+34delG
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000350073
  ensembl transcript: ENST00000357481
  gene symbol: ACIN1
  hgvsc: ENST00000357481.2:c.495+34delG
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451328
  ensembl transcript: ENST00000555053
  gene symbol: ACIN1
  hgvsc: ENST00000555053.1:c.2730+34delG
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000554680
  gene symbol: ACIN1
  hgvsc: ENST00000554680.1:n.509+34delG
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000557039
  gene symbol: ACIN1
  hgvsc: ENST00000557039.1:n.609+34delG
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000345541
  ensembl transcript: ENST00000338631
  gene symbol: ACIN1
  hgvsc: ENST00000338631.6:c.588+34delG
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000555478
  gene symbol: ACIN1
  hgvsc: ENST00000555478.1:n.392+34delG
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000473758
  gene symbol: ACIN1
  hgvsc: ENST00000473758.1:n.1702+34delG
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000262710
  ensembl transcript: ENST00000262710
  gene symbol: ACIN1
  hgvsc: ENST00000262710.1:c.2769+34delG
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451410
  ensembl transcript: ENST00000555566
  gene symbol: ACIN1
  hgvsc: ENST00000555566.1:c.459+34delG
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000380502
  ensembl transcript: ENST00000397341
  gene symbol: ACIN1
  hgvsc: ENST00000397341.3:c.495+34delG
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000405677
  ensembl transcript: ENST00000457657
  gene symbol: ACIN1
  hgvsc: ENST00000457657.1:c.2649+34delG
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451138
  ensembl transcript: ENST00000557515
  gene symbol: ACIN1
  hgvsc: ENST00000557515.1:c.492+34delG
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000553790
  gene symbol: ACIN1
  hgvsc: ENST00000553790.1:n.218+34delG
  variant of: http://identifiers.org/hgnc/17066
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6047
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1253
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5942
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4917
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3696
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3603
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1737
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6801
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: AC
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ

http://identifiers.org/exac.variant/14-23533280-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23533280
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23533280
    reference: chr 14
allele count: 1
allele frequency: 8.301097405076952e-6
allele num: 120466
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000405677
  ensembl transcript: ENST00000457657
  gene symbol: ACIN1
  hgvsc: ENST00000457657.1:c.2649+34G>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451328
  ensembl transcript: ENST00000555053
  gene symbol: ACIN1
  hgvsc: ENST00000555053.1:c.2730+34G>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000350073
  ensembl transcript: ENST00000357481
  gene symbol: ACIN1
  hgvsc: ENST00000357481.2:c.495+34G>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000473758
  gene symbol: ACIN1
  hgvsc: ENST00000473758.1:n.1702+34G>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000380502
  ensembl transcript: ENST00000397341
  gene symbol: ACIN1
  hgvsc: ENST00000397341.3:c.495+34G>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000556052
  gene symbol: ACIN1
  hgvsc: ENST00000556052.1:n.600+34G>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000555807
  gene symbol: ACIN1
  hgvsc: ENST00000555807.1:n.815+34G>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000553790
  gene symbol: ACIN1
  hgvsc: ENST00000553790.1:n.218+34G>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451410
  ensembl transcript: ENST00000555566
  gene symbol: ACIN1
  hgvsc: ENST00000555566.1:c.459+34G>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000474349
  ensembl transcript: ENST00000605057
  gene symbol: ACIN1
  hgvsc: ENST00000605057.1:c.2595+34G>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000262710
  ensembl transcript: ENST00000262710
  gene symbol: ACIN1
  hgvsc: ENST00000262710.1:c.2769+34G>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451138
  ensembl transcript: ENST00000557515
  gene symbol: ACIN1
  hgvsc: ENST00000557515.1:c.492+34G>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000557039
  gene symbol: ACIN1
  hgvsc: ENST00000557039.1:n.609+34G>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000345541
  ensembl transcript: ENST00000338631
  gene symbol: ACIN1
  hgvsc: ENST00000338631.6:c.588+34G>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000555478
  gene symbol: ACIN1
  hgvsc: ENST00000555478.1:n.392+34G>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000554680
  gene symbol: ACIN1
  hgvsc: ENST00000554680.1:n.509+34G>T
  variant of: http://identifiers.org/hgnc/17066
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 862
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4527
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1206
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1146
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3715
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4917
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6047
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2521
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: C
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum

14-23533287-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23533287
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23533287
    reference: chr 14
allele count: 1
allele frequency: 8.2917364554485e-6
allele num: 120602
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451410
  ensembl transcript: ENST00000555566
  gene symbol: ACIN1
  hgvsc: ENST00000555566.1:c.459+27G>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000555807
  gene symbol: ACIN1
  hgvsc: ENST00000555807.1:n.815+27G>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000556052
  gene symbol: ACIN1
  hgvsc: ENST00000556052.1:n.600+27G>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000473758
  gene symbol: ACIN1
  hgvsc: ENST00000473758.1:n.1702+27G>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000405677
  ensembl transcript: ENST00000457657
  gene symbol: ACIN1
  hgvsc: ENST00000457657.1:c.2649+27G>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451328
  ensembl transcript: ENST00000555053
  gene symbol: ACIN1
  hgvsc: ENST00000555053.1:c.2730+27G>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000474349
  ensembl transcript: ENST00000605057
  gene symbol: ACIN1
  hgvsc: ENST00000605057.1:c.2595+27G>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000557039
  gene symbol: ACIN1
  hgvsc: ENST00000557039.1:n.609+27G>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000553790
  gene symbol: ACIN1
  hgvsc: ENST00000553790.1:n.218+27G>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000262710
  ensembl transcript: ENST00000262710
  gene symbol: ACIN1
  hgvsc: ENST00000262710.1:c.2769+27G>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000350073
  ensembl transcript: ENST00000357481
  gene symbol: ACIN1
  hgvsc: ENST00000357481.2:c.495+27G>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451138
  ensembl transcript: ENST00000557515
  gene symbol: ACIN1
  hgvsc: ENST00000557515.1:c.492+27G>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000554680
  gene symbol: ACIN1
  hgvsc: ENST00000554680.1:n.509+27G>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000555478
  gene symbol: ACIN1
  hgvsc: ENST00000555478.1:n.392+27G>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000345541
  ensembl transcript: ENST00000338631
  gene symbol: ACIN1
  hgvsc: ENST00000338631.6:c.588+27G>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000380502
  ensembl transcript: ENST00000397341
  gene symbol: ACIN1
  hgvsc: ENST00000397341.3:c.495+27G>C
  variant of: http://identifiers.org/hgnc/17066
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4537
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3581
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6048
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 862
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 892
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3602
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1146
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2524
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Latino
population: East Asian
population: Other
reference allele: C
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff

14-23533287-CCT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23533287
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23533285
    reference: chr 14
allele count: 2
allele frequency: 1.6583472910897e-5
allele num: 120602
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000554680
  gene symbol: ACIN1
  hgvsc: ENST00000554680.1:n.509+25_509+26delAG
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000350073
  ensembl transcript: ENST00000357481
  gene symbol: ACIN1
  hgvsc: ENST00000357481.2:c.495+25_495+26delAG
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000380502
  ensembl transcript: ENST00000397341
  gene symbol: ACIN1
  hgvsc: ENST00000397341.3:c.495+25_495+26delAG
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000553790
  gene symbol: ACIN1
  hgvsc: ENST00000553790.1:n.218+25_218+26delAG
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000345541
  ensembl transcript: ENST00000338631
  gene symbol: ACIN1
  hgvsc: ENST00000338631.6:c.588+25_588+26delAG
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000555807
  gene symbol: ACIN1
  hgvsc: ENST00000555807.1:n.815+25_815+26delAG
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000262710
  ensembl transcript: ENST00000262710
  gene symbol: ACIN1
  hgvsc: ENST00000262710.1:c.2769+25_2769+26delAG
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000473758
  gene symbol: ACIN1
  hgvsc: ENST00000473758.1:n.1702+25_1702+26delAG
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451328
  ensembl transcript: ENST00000555053
  gene symbol: ACIN1
  hgvsc: ENST00000555053.1:c.2730+25_2730+26delAG
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451138
  ensembl transcript: ENST00000557515
  gene symbol: ACIN1
  hgvsc: ENST00000557515.1:c.492+25_492+26delAG
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000405677
  ensembl transcript: ENST00000457657
  gene symbol: ACIN1
  hgvsc: ENST00000457657.1:c.2649+25_2649+26delAG
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000555478
  gene symbol: ACIN1
  hgvsc: ENST00000555478.1:n.392+25_392+26delAG
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000557039
  gene symbol: ACIN1
  hgvsc: ENST00000557039.1:n.609+25_609+26delAG
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451410
  ensembl transcript: ENST00000555566
  gene symbol: ACIN1
  hgvsc: ENST00000555566.1:c.459+25_459+26delAG
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000474349
  ensembl transcript: ENST00000605057
  gene symbol: ACIN1
  hgvsc: ENST00000605057.1:c.2595+25_2595+26delAG
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000556052
  gene symbol: ACIN1
  hgvsc: ENST00000556052.1:n.600+25_600+26delAG
  variant of: http://identifiers.org/hgnc/17066
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5950
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1146
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4537
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4537
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3752
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6048
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6805
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 892
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 862
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: CCT
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP

14-23533296-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23533296
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23533296
    reference: chr 14
allele count: 1
allele frequency: 8.279653579294243e-6
allele num: 120778
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000556052
  gene symbol: ACIN1
  hgvsc: ENST00000556052.1:n.600+18C>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000555807
  gene symbol: ACIN1
  hgvsc: ENST00000555807.1:n.815+18C>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000350073
  ensembl transcript: ENST00000357481
  gene symbol: ACIN1
  hgvsc: ENST00000357481.2:c.495+18C>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000553790
  gene symbol: ACIN1
  hgvsc: ENST00000553790.1:n.218+18C>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000554680
  gene symbol: ACIN1
  hgvsc: ENST00000554680.1:n.509+18C>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000405677
  ensembl transcript: ENST00000457657
  gene symbol: ACIN1
  hgvsc: ENST00000457657.1:c.2649+18C>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000473758
  gene symbol: ACIN1
  hgvsc: ENST00000473758.1:n.1702+18C>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000345541
  ensembl transcript: ENST00000338631
  gene symbol: ACIN1
  hgvsc: ENST00000338631.6:c.588+18C>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451410
  ensembl transcript: ENST00000555566
  gene symbol: ACIN1
  hgvsc: ENST00000555566.1:c.459+18C>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000557039
  gene symbol: ACIN1
  hgvsc: ENST00000557039.1:n.609+18C>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000474349
  ensembl transcript: ENST00000605057
  gene symbol: ACIN1
  hgvsc: ENST00000605057.1:c.2595+18C>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000262710
  ensembl transcript: ENST00000262710
  gene symbol: ACIN1
  hgvsc: ENST00000262710.1:c.2769+18C>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000380502
  ensembl transcript: ENST00000397341
  gene symbol: ACIN1
  hgvsc: ENST00000397341.3:c.495+18C>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451138
  ensembl transcript: ENST00000557515
  gene symbol: ACIN1
  hgvsc: ENST00000557515.1:c.492+18C>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000555478
  gene symbol: ACIN1
  hgvsc: ENST00000555478.1:n.392+18C>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451328
  ensembl transcript: ENST00000555053
  gene symbol: ACIN1
  hgvsc: ENST00000555053.1:c.2730+18C>T
  variant of: http://identifiers.org/hgnc/17066
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5954
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6804
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3884
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4544
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2523
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum

14-23533298-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23533298
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23533298
    reference: chr 14
allele count: 3
allele frequency: 2.482703829984442e-5
allele num: 120836
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000380502
  ensembl transcript: ENST00000397341
  gene symbol: ACIN1
  hgvsc: ENST00000397341.3:c.495+16C>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000555807
  gene symbol: ACIN1
  hgvsc: ENST00000555807.1:n.815+16C>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000555478
  gene symbol: ACIN1
  hgvsc: ENST00000555478.1:n.392+16C>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000405677
  ensembl transcript: ENST00000457657
  gene symbol: ACIN1
  hgvsc: ENST00000457657.1:c.2649+16C>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451138
  ensembl transcript: ENST00000557515
  gene symbol: ACIN1
  hgvsc: ENST00000557515.1:c.492+16C>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000474349
  ensembl transcript: ENST00000605057
  gene symbol: ACIN1
  hgvsc: ENST00000605057.1:c.2595+16C>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451328
  ensembl transcript: ENST00000555053
  gene symbol: ACIN1
  hgvsc: ENST00000555053.1:c.2730+16C>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000262710
  ensembl transcript: ENST00000262710
  gene symbol: ACIN1
  hgvsc: ENST00000262710.1:c.2769+16C>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000350073
  ensembl transcript: ENST00000357481
  gene symbol: ACIN1
  hgvsc: ENST00000357481.2:c.495+16C>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000553790
  gene symbol: ACIN1
  hgvsc: ENST00000553790.1:n.218+16C>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000556052
  gene symbol: ACIN1
  hgvsc: ENST00000556052.1:n.600+16C>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000345541
  ensembl transcript: ENST00000338631
  gene symbol: ACIN1
  hgvsc: ENST00000338631.6:c.588+16C>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000557039
  gene symbol: ACIN1
  hgvsc: ENST00000557039.1:n.609+16C>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000554680
  gene symbol: ACIN1
  hgvsc: ENST00000554680.1:n.509+16C>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451410
  ensembl transcript: ENST00000555566
  gene symbol: ACIN1
  hgvsc: ENST00000555566.1:c.459+16C>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000473758
  gene symbol: ACIN1
  hgvsc: ENST00000473758.1:n.1702+16C>T
  variant of: http://identifiers.org/hgnc/17066
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5955
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1738
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4546
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1652
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6045
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6805
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4901
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: Other
population: European (Finnish)
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum

14-23533299-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23533299
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23533299
    reference: chr 14
allele count: 2
allele frequency: 1.654807214959457e-5
allele num: 120860
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451410
  ensembl transcript: ENST00000555566
  gene symbol: ACIN1
  hgvsc: ENST00000555566.1:c.459+15C>G
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000556052
  gene symbol: ACIN1
  hgvsc: ENST00000556052.1:n.600+15C>G
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000555807
  gene symbol: ACIN1
  hgvsc: ENST00000555807.1:n.815+15C>G
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000380502
  ensembl transcript: ENST00000397341
  gene symbol: ACIN1
  hgvsc: ENST00000397341.3:c.495+15C>G
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000262710
  ensembl transcript: ENST00000262710
  gene symbol: ACIN1
  hgvsc: ENST00000262710.1:c.2769+15C>G
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000350073
  ensembl transcript: ENST00000357481
  gene symbol: ACIN1
  hgvsc: ENST00000357481.2:c.495+15C>G
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000557039
  gene symbol: ACIN1
  hgvsc: ENST00000557039.1:n.609+15C>G
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000555478
  gene symbol: ACIN1
  hgvsc: ENST00000555478.1:n.392+15C>G
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000474349
  ensembl transcript: ENST00000605057
  gene symbol: ACIN1
  hgvsc: ENST00000605057.1:c.2595+15C>G
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000345541
  ensembl transcript: ENST00000338631
  gene symbol: ACIN1
  hgvsc: ENST00000338631.6:c.588+15C>G
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451328
  ensembl transcript: ENST00000555053
  gene symbol: ACIN1
  hgvsc: ENST00000555053.1:c.2730+15C>G
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000554680
  gene symbol: ACIN1
  hgvsc: ENST00000554680.1:n.509+15C>G
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000473758
  gene symbol: ACIN1
  hgvsc: ENST00000473758.1:n.1702+15C>G
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451138
  ensembl transcript: ENST00000557515
  gene symbol: ACIN1
  hgvsc: ENST00000557515.1:c.492+15C>G
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000405677
  ensembl transcript: ENST00000457657
  gene symbol: ACIN1
  hgvsc: ENST00000457657.1:c.2649+15C>G
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000553790
  gene symbol: ACIN1
  hgvsc: ENST00000553790.1:n.218+15C>G
  variant of: http://identifiers.org/hgnc/17066
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6044
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3825
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4919
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3603
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3937
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4917
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: Other
population: East Asian
reference allele: G
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: QD

14-23533343-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23533343
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23533343
    reference: chr 14
allele count: 1
allele frequency: 8.239404126293587e-6
allele num: 121368
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451138
  ensembl transcript: ENST00000557515
  gene symbol: ACIN1
  hgvsc: ENST00000557515.1:c.463G>C
  hgvsp: ENSP00000451138.1:p.Gly155Arg
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000553790
  gene symbol: ACIN1
  hgvsc: ENST00000553790.1:n.189G>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451328
  ensembl transcript: ENST00000555053
  gene symbol: ACIN1
  hgvsc: ENST00000555053.1:c.2701G>C
  hgvsp: ENSP00000451328.1:p.Gly901Arg
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000474349
  ensembl transcript: ENST00000605057
  gene symbol: ACIN1
  hgvsc: ENST00000605057.1:c.2566G>C
  hgvsp: ENSP00000474349.1:p.Gly856Arg
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000555807
  gene symbol: ACIN1
  hgvsc: ENST00000555807.1:n.786G>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000345541
  ensembl transcript: ENST00000338631
  gene symbol: ACIN1
  hgvsc: ENST00000338631.6:c.559G>C
  hgvsp: ENSP00000345541.6:p.Gly187Arg
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000555478
  gene symbol: ACIN1
  hgvsc: ENST00000555478.1:n.363G>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000350073
  ensembl transcript: ENST00000357481
  gene symbol: ACIN1
  hgvsc: ENST00000357481.2:c.466G>C
  hgvsp: ENSP00000350073.2:p.Gly156Arg
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000557039
  gene symbol: ACIN1
  hgvsc: ENST00000557039.1:n.580G>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000473758
  gene symbol: ACIN1
  hgvsc: ENST00000473758.1:n.1673G>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000405677
  ensembl transcript: ENST00000457657
  gene symbol: ACIN1
  hgvsc: ENST00000457657.1:c.2620G>C
  hgvsp: ENSP00000405677.1:p.Gly874Arg
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451410
  ensembl transcript: ENST00000555566
  gene symbol: ACIN1
  hgvsc: ENST00000555566.1:c.430G>C
  hgvsp: ENSP00000451410.1:p.Gly144Arg
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000380502
  ensembl transcript: ENST00000397341
  gene symbol: ACIN1
  hgvsc: ENST00000397341.3:c.466G>C
  hgvsp: ENSP00000380502.3:p.Gly156Arg
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000554680
  gene symbol: ACIN1
  hgvsc: ENST00000554680.1:n.480G>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000556052
  gene symbol: ACIN1
  hgvsc: ENST00000556052.1:n.571G>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000262710
  ensembl transcript: ENST00000262710
  gene symbol: ACIN1
  hgvsc: ENST00000262710.1:c.2740G>C
  hgvsp: ENSP00000262710.1:p.Gly914Arg
  variant of: http://identifiers.org/hgnc/17066
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4920
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 862
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6805
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4553
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly914Arg
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: Other
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum

14-23533354-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23533354
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23533354
    reference: chr 14
allele count: 3
allele frequency: 2.471291826614165e-5
allele num: 121394
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000473758
  gene symbol: ACIN1
  hgvsc: ENST00000473758.1:n.1662C>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000554680
  gene symbol: ACIN1
  hgvsc: ENST00000554680.1:n.469C>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000555807
  gene symbol: ACIN1
  hgvsc: ENST00000555807.1:n.775C>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000405677
  ensembl transcript: ENST00000457657
  gene symbol: ACIN1
  hgvsc: ENST00000457657.1:c.2609C>T
  hgvsp: ENSP00000405677.1:p.Thr870Ile
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451410
  ensembl transcript: ENST00000555566
  gene symbol: ACIN1
  hgvsc: ENST00000555566.1:c.419C>T
  hgvsp: ENSP00000451410.1:p.Thr140Ile
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451328
  ensembl transcript: ENST00000555053
  gene symbol: ACIN1
  hgvsc: ENST00000555053.1:c.2690C>T
  hgvsp: ENSP00000451328.1:p.Thr897Ile
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000474349
  ensembl transcript: ENST00000605057
  gene symbol: ACIN1
  hgvsc: ENST00000605057.1:c.2555C>T
  hgvsp: ENSP00000474349.1:p.Thr852Ile
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000556052
  gene symbol: ACIN1
  hgvsc: ENST00000556052.1:n.560C>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000557039
  gene symbol: ACIN1
  hgvsc: ENST00000557039.1:n.569C>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451138
  ensembl transcript: ENST00000557515
  gene symbol: ACIN1
  hgvsc: ENST00000557515.1:c.452C>T
  hgvsp: ENSP00000451138.1:p.Thr151Ile
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000555478
  gene symbol: ACIN1
  hgvsc: ENST00000555478.1:n.352C>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000262710
  ensembl transcript: ENST00000262710
  gene symbol: ACIN1
  hgvsc: ENST00000262710.1:c.2729C>T
  hgvsp: ENSP00000262710.1:p.Thr910Ile
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000345541
  ensembl transcript: ENST00000338631
  gene symbol: ACIN1
  hgvsc: ENST00000338631.6:c.548C>T
  hgvsp: ENSP00000345541.6:p.Thr183Ile
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000380502
  ensembl transcript: ENST00000397341
  gene symbol: ACIN1
  hgvsc: ENST00000397341.3:c.455C>T
  hgvsp: ENSP00000380502.3:p.Thr152Ile
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000350073
  ensembl transcript: ENST00000357481
  gene symbol: ACIN1
  hgvsc: ENST00000357481.2:c.455C>T
  hgvsp: ENSP00000350073.2:p.Thr152Ile
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000553790
  gene symbol: ACIN1
  hgvsc: ENST00000553790.1:n.178C>T
  variant of: http://identifiers.org/hgnc/17066
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1653
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6739
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6043
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 862
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3948
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4554
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 596
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Thr910Ile
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: Other
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum

14-23533358-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23533358
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23533358
    reference: chr 14
allele count: 1
allele frequency: 8.237367996177861e-6
allele num: 121398
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000345541
  ensembl transcript: ENST00000338631
  gene symbol: ACIN1
  hgvsc: ENST00000338631.6:c.544G>A
  hgvsp: ENSP00000345541.6:p.Gly182Arg
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451328
  ensembl transcript: ENST00000555053
  gene symbol: ACIN1
  hgvsc: ENST00000555053.1:c.2686G>A
  hgvsp: ENSP00000451328.1:p.Gly896Arg
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451410
  ensembl transcript: ENST00000555566
  gene symbol: ACIN1
  hgvsc: ENST00000555566.1:c.415G>A
  hgvsp: ENSP00000451410.1:p.Gly139Arg
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000555807
  gene symbol: ACIN1
  hgvsc: ENST00000555807.1:n.771G>A
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000553790
  gene symbol: ACIN1
  hgvsc: ENST00000553790.1:n.174G>A
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000473758
  gene symbol: ACIN1
  hgvsc: ENST00000473758.1:n.1658G>A
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000262710
  ensembl transcript: ENST00000262710
  gene symbol: ACIN1
  hgvsc: ENST00000262710.1:c.2725G>A
  hgvsp: ENSP00000262710.1:p.Gly909Arg
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000380502
  ensembl transcript: ENST00000397341
  gene symbol: ACIN1
  hgvsc: ENST00000397341.3:c.451G>A
  hgvsp: ENSP00000380502.3:p.Gly151Arg
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000557039
  gene symbol: ACIN1
  hgvsc: ENST00000557039.1:n.565G>A
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000350073
  ensembl transcript: ENST00000357481
  gene symbol: ACIN1
  hgvsc: ENST00000357481.2:c.451G>A
  hgvsp: ENSP00000350073.2:p.Gly151Arg
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000474349
  ensembl transcript: ENST00000605057
  gene symbol: ACIN1
  hgvsc: ENST00000605057.1:c.2551G>A
  hgvsp: ENSP00000474349.1:p.Gly851Arg
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451138
  ensembl transcript: ENST00000557515
  gene symbol: ACIN1
  hgvsc: ENST00000557515.1:c.448G>A
  hgvsp: ENSP00000451138.1:p.Gly150Arg
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000554680
  gene symbol: ACIN1
  hgvsc: ENST00000554680.1:n.465G>A
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000556052
  gene symbol: ACIN1
  hgvsc: ENST00000556052.1:n.556G>A
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000405677
  ensembl transcript: ENST00000457657
  gene symbol: ACIN1
  hgvsc: ENST00000457657.1:c.2605G>A
  hgvsp: ENSP00000405677.1:p.Gly869Arg
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000555478
  gene symbol: ACIN1
  hgvsc: ENST00000555478.1:n.348G>A
  variant of: http://identifiers.org/hgnc/17066
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6043
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4425
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5961
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1653
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 862
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly909Arg
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
population: European (Finnish)
population: Latino
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP

14-23533360-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23533360
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23533360
    reference: chr 14
allele count: 1
allele frequency: 8.236960890909689e-6
allele num: 121404
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000553790
  gene symbol: ACIN1
  hgvsc: ENST00000553790.1:n.172A>G
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000474349
  ensembl transcript: ENST00000605057
  gene symbol: ACIN1
  hgvsc: ENST00000605057.1:c.2549A>G
  hgvsp: ENSP00000474349.1:p.Asp850Gly
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451410
  ensembl transcript: ENST00000555566
  gene symbol: ACIN1
  hgvsc: ENST00000555566.1:c.413A>G
  hgvsp: ENSP00000451410.1:p.Asp138Gly
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000557039
  gene symbol: ACIN1
  hgvsc: ENST00000557039.1:n.563A>G
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000405677
  ensembl transcript: ENST00000457657
  gene symbol: ACIN1
  hgvsc: ENST00000457657.1:c.2603A>G
  hgvsp: ENSP00000405677.1:p.Asp868Gly
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000350073
  ensembl transcript: ENST00000357481
  gene symbol: ACIN1
  hgvsc: ENST00000357481.2:c.449A>G
  hgvsp: ENSP00000350073.2:p.Asp150Gly
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000380502
  ensembl transcript: ENST00000397341
  gene symbol: ACIN1
  hgvsc: ENST00000397341.3:c.449A>G
  hgvsp: ENSP00000380502.3:p.Asp150Gly
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000345541
  ensembl transcript: ENST00000338631
  gene symbol: ACIN1
  hgvsc: ENST00000338631.6:c.542A>G
  hgvsp: ENSP00000345541.6:p.Asp181Gly
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451138
  ensembl transcript: ENST00000557515
  gene symbol: ACIN1
  hgvsc: ENST00000557515.1:c.446A>G
  hgvsp: ENSP00000451138.1:p.Asp149Gly
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000473758
  gene symbol: ACIN1
  hgvsc: ENST00000473758.1:n.1656A>G
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000555478
  gene symbol: ACIN1
  hgvsc: ENST00000555478.1:n.346A>G
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000556052
  gene symbol: ACIN1
  hgvsc: ENST00000556052.1:n.554A>G
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000554680
  gene symbol: ACIN1
  hgvsc: ENST00000554680.1:n.463A>G
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000555807
  gene symbol: ACIN1
  hgvsc: ENST00000555807.1:n.769A>G
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000262710
  ensembl transcript: ENST00000262710
  gene symbol: ACIN1
  hgvsc: ENST00000262710.1:c.2723A>G
  hgvsp: ENSP00000262710.1:p.Asp908Gly
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451328
  ensembl transcript: ENST00000555053
  gene symbol: ACIN1
  hgvsc: ENST00000555053.1:c.2684A>G
  hgvsp: ENSP00000451328.1:p.Asp895Gly
  variant of: http://identifiers.org/hgnc/17066
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 2524
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6806
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5155
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1148
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1654
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5961
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4555
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4919
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp908Gly
num of homozygotes: 0
population: Other
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: DP
site quality: ReadPosRankSum

14-23533364-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23533364
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23533364
    reference: chr 14
allele count: 1
allele frequency: 8.236825198095647e-6
allele num: 121406
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000473758
  gene symbol: ACIN1
  hgvsc: ENST00000473758.1:n.1652G>A
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451138
  ensembl transcript: ENST00000557515
  gene symbol: ACIN1
  hgvsc: ENST00000557515.1:c.442G>A
  hgvsp: ENSP00000451138.1:p.Asp148Asn
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000555478
  gene symbol: ACIN1
  hgvsc: ENST00000555478.1:n.342G>A
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000555807
  gene symbol: ACIN1
  hgvsc: ENST00000555807.1:n.765G>A
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451328
  ensembl transcript: ENST00000555053
  gene symbol: ACIN1
  hgvsc: ENST00000555053.1:c.2680G>A
  hgvsp: ENSP00000451328.1:p.Asp894Asn
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000553790
  gene symbol: ACIN1
  hgvsc: ENST00000553790.1:n.168G>A
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000262710
  ensembl transcript: ENST00000262710
  gene symbol: ACIN1
  hgvsc: ENST00000262710.1:c.2719G>A
  hgvsp: ENSP00000262710.1:p.Asp907Asn
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000345541
  ensembl transcript: ENST00000338631
  gene symbol: ACIN1
  hgvsc: ENST00000338631.6:c.538G>A
  hgvsp: ENSP00000345541.6:p.Asp180Asn
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000554680
  gene symbol: ACIN1
  hgvsc: ENST00000554680.1:n.459G>A
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000350073
  ensembl transcript: ENST00000357481
  gene symbol: ACIN1
  hgvsc: ENST00000357481.2:c.445G>A
  hgvsp: ENSP00000350073.2:p.Asp149Asn
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000405677
  ensembl transcript: ENST00000457657
  gene symbol: ACIN1
  hgvsc: ENST00000457657.1:c.2599G>A
  hgvsp: ENSP00000405677.1:p.Asp867Asn
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451410
  ensembl transcript: ENST00000555566
  gene symbol: ACIN1
  hgvsc: ENST00000555566.1:c.409G>A
  hgvsp: ENSP00000451410.1:p.Asp137Asn
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000557039
  gene symbol: ACIN1
  hgvsc: ENST00000557039.1:n.559G>A
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000474349
  ensembl transcript: ENST00000605057
  gene symbol: ACIN1
  hgvsc: ENST00000605057.1:c.2545G>A
  hgvsp: ENSP00000474349.1:p.Asp849Asn
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000556052
  gene symbol: ACIN1
  hgvsc: ENST00000556052.1:n.550G>A
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000380502
  ensembl transcript: ENST00000397341
  gene symbol: ACIN1
  hgvsc: ENST00000397341.3:c.445G>A
  hgvsp: ENSP00000380502.3:p.Asp149Asn
  variant of: http://identifiers.org/hgnc/17066
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1739
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4556
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1654
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6738
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6043
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp907Asn
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Other
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
reference allele: C
site quality: FS
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP

14-23533365-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23533365
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23533365
    reference: chr 14
allele count: 4
allele frequency: 3.294621530351701e-5
allele num: 121410
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451328
  ensembl transcript: ENST00000555053
  gene symbol: ACIN1
  hgvsc: ENST00000555053.1:c.2679C>T
  hgvsp: ENST00000555053.1:c.2679C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000473758
  gene symbol: ACIN1
  hgvsc: ENST00000473758.1:n.1651C>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000557039
  gene symbol: ACIN1
  hgvsc: ENST00000557039.1:n.558C>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000555478
  gene symbol: ACIN1
  hgvsc: ENST00000555478.1:n.341C>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000405677
  ensembl transcript: ENST00000457657
  gene symbol: ACIN1
  hgvsc: ENST00000457657.1:c.2598C>T
  hgvsp: ENST00000457657.1:c.2598C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451410
  ensembl transcript: ENST00000555566
  gene symbol: ACIN1
  hgvsc: ENST00000555566.1:c.408C>T
  hgvsp: ENST00000555566.1:c.408C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000345541
  ensembl transcript: ENST00000338631
  gene symbol: ACIN1
  hgvsc: ENST00000338631.6:c.537C>T
  hgvsp: ENST00000338631.6:c.537C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000350073
  ensembl transcript: ENST00000357481
  gene symbol: ACIN1
  hgvsc: ENST00000357481.2:c.444C>T
  hgvsp: ENST00000357481.2:c.444C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000474349
  ensembl transcript: ENST00000605057
  gene symbol: ACIN1
  hgvsc: ENST00000605057.1:c.2544C>T
  hgvsp: ENST00000605057.1:c.2544C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000380502
  ensembl transcript: ENST00000397341
  gene symbol: ACIN1
  hgvsc: ENST00000397341.3:c.444C>T
  hgvsp: ENST00000397341.3:c.444C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000556052
  gene symbol: ACIN1
  hgvsc: ENST00000556052.1:n.549C>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000553790
  gene symbol: ACIN1
  hgvsc: ENST00000553790.1:n.167C>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000554680
  gene symbol: ACIN1
  hgvsc: ENST00000554680.1:n.458C>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451138
  ensembl transcript: ENST00000557515
  gene symbol: ACIN1
  hgvsc: ENST00000557515.1:c.441C>T
  hgvsp: ENST00000557515.1:c.441C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000262710
  ensembl transcript: ENST00000262710
  gene symbol: ACIN1
  hgvsc: ENST00000262710.1:c.2718C>T
  hgvsp: ENST00000262710.1:c.2718C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000555807
  gene symbol: ACIN1
  hgvsc: ENST00000555807.1:n.764C>T
  variant of: http://identifiers.org/hgnc/17066
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1148
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6806
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3604
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5960
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3957
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 864
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4554
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly906Gly
num of homozygotes: 0
population: Latino
population: Other
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

14-23533368-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23533368
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23533368
    reference: chr 14
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000557039
  gene symbol: ACIN1
  hgvsc: ENST00000557039.1:n.555T>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000553790
  gene symbol: ACIN1
  hgvsc: ENST00000553790.1:n.164T>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000474349
  ensembl transcript: ENST00000605057
  gene symbol: ACIN1
  hgvsc: ENST00000605057.1:c.2541T>C
  hgvsp: ENST00000605057.1:c.2541T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451138
  ensembl transcript: ENST00000557515
  gene symbol: ACIN1
  hgvsc: ENST00000557515.1:c.438T>C
  hgvsp: ENST00000557515.1:c.438T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000554680
  gene symbol: ACIN1
  hgvsc: ENST00000554680.1:n.455T>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000405677
  ensembl transcript: ENST00000457657
  gene symbol: ACIN1
  hgvsc: ENST00000457657.1:c.2595T>C
  hgvsp: ENST00000457657.1:c.2595T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000262710
  ensembl transcript: ENST00000262710
  gene symbol: ACIN1
  hgvsc: ENST00000262710.1:c.2715T>C
  hgvsp: ENST00000262710.1:c.2715T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000380502
  ensembl transcript: ENST00000397341
  gene symbol: ACIN1
  hgvsc: ENST00000397341.3:c.441T>C
  hgvsp: ENST00000397341.3:c.441T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000350073
  ensembl transcript: ENST00000357481
  gene symbol: ACIN1
  hgvsc: ENST00000357481.2:c.441T>C
  hgvsp: ENST00000357481.2:c.441T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000473758
  gene symbol: ACIN1
  hgvsc: ENST00000473758.1:n.1648T>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451410
  ensembl transcript: ENST00000555566
  gene symbol: ACIN1
  hgvsc: ENST00000555566.1:c.405T>C
  hgvsp: ENST00000555566.1:c.405T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000345541
  ensembl transcript: ENST00000338631
  gene symbol: ACIN1
  hgvsc: ENST00000338631.6:c.534T>C
  hgvsp: ENST00000338631.6:c.534T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000555478
  gene symbol: ACIN1
  hgvsc: ENST00000555478.1:n.338T>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000555807
  gene symbol: ACIN1
  hgvsc: ENST00000555807.1:n.761T>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451328
  ensembl transcript: ENST00000555053
  gene symbol: ACIN1
  hgvsc: ENST00000555053.1:c.2676T>C
  hgvsp: ENST00000555053.1:c.2676T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000556052
  gene symbol: ACIN1
  hgvsc: ENST00000556052.1:n.546T>C
  variant of: http://identifiers.org/hgnc/17066
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5960
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1148
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3960
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6041
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1740
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn905Asn
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
population: Latino
reference allele: A
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ

14-23533369-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23533369
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23533369
    reference: chr 14
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451328
  ensembl transcript: ENST00000555053
  gene symbol: ACIN1
  hgvsc: ENST00000555053.1:c.2675A>G
  hgvsp: ENSP00000451328.1:p.Asn892Ser
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000553790
  gene symbol: ACIN1
  hgvsc: ENST00000553790.1:n.163A>G
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000555478
  gene symbol: ACIN1
  hgvsc: ENST00000555478.1:n.337A>G
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000350073
  ensembl transcript: ENST00000357481
  gene symbol: ACIN1
  hgvsc: ENST00000357481.2:c.440A>G
  hgvsp: ENSP00000350073.2:p.Asn147Ser
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000474349
  ensembl transcript: ENST00000605057
  gene symbol: ACIN1
  hgvsc: ENST00000605057.1:c.2540A>G
  hgvsp: ENSP00000474349.1:p.Asn847Ser
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000556052
  gene symbol: ACIN1
  hgvsc: ENST00000556052.1:n.545A>G
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451410
  ensembl transcript: ENST00000555566
  gene symbol: ACIN1
  hgvsc: ENST00000555566.1:c.404A>G
  hgvsp: ENSP00000451410.1:p.Asn135Ser
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000554680
  gene symbol: ACIN1
  hgvsc: ENST00000554680.1:n.454A>G
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000262710
  ensembl transcript: ENST00000262710
  gene symbol: ACIN1
  hgvsc: ENST00000262710.1:c.2714A>G
  hgvsp: ENSP00000262710.1:p.Asn905Ser
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451138
  ensembl transcript: ENST00000557515
  gene symbol: ACIN1
  hgvsc: ENST00000557515.1:c.437A>G
  hgvsp: ENSP00000451138.1:p.Asn146Ser
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000557039
  gene symbol: ACIN1
  hgvsc: ENST00000557039.1:n.554A>G
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000345541
  ensembl transcript: ENST00000338631
  gene symbol: ACIN1
  hgvsc: ENST00000338631.6:c.533A>G
  hgvsp: ENSP00000345541.6:p.Asn178Ser
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000405677
  ensembl transcript: ENST00000457657
  gene symbol: ACIN1
  hgvsc: ENST00000457657.1:c.2594A>G
  hgvsp: ENSP00000405677.1:p.Asn865Ser
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000473758
  gene symbol: ACIN1
  hgvsc: ENST00000473758.1:n.1647A>G
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000380502
  ensembl transcript: ENST00000397341
  gene symbol: ACIN1
  hgvsc: ENST00000397341.3:c.440A>G
  hgvsp: ENSP00000380502.3:p.Asn147Ser
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000555807
  gene symbol: ACIN1
  hgvsc: ENST00000555807.1:n.760A>G
  variant of: http://identifiers.org/hgnc/17066
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3604
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5146
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6737
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3960
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4434
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4554
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn905Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
population: Latino
reference allele: T
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ

14-23533372-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23533372
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23533372
    reference: chr 14
allele count: 4
allele frequency: 3.294621530351701e-5
allele num: 121410
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000473758
  gene symbol: ACIN1
  hgvsc: ENST00000473758.1:n.1644G>A
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000554680
  gene symbol: ACIN1
  hgvsc: ENST00000554680.1:n.451G>A
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000474349
  ensembl transcript: ENST00000605057
  gene symbol: ACIN1
  hgvsc: ENST00000605057.1:c.2537G>A
  hgvsp: ENSP00000474349.1:p.Arg846His
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000555478
  gene symbol: ACIN1
  hgvsc: ENST00000555478.1:n.334G>A
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000553790
  gene symbol: ACIN1
  hgvsc: ENST00000553790.1:n.160G>A
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451410
  ensembl transcript: ENST00000555566
  gene symbol: ACIN1
  hgvsc: ENST00000555566.1:c.401G>A
  hgvsp: ENSP00000451410.1:p.Arg134His
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000345541
  ensembl transcript: ENST00000338631
  gene symbol: ACIN1
  hgvsc: ENST00000338631.6:c.530G>A
  hgvsp: ENSP00000345541.6:p.Arg177His
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000405677
  ensembl transcript: ENST00000457657
  gene symbol: ACIN1
  hgvsc: ENST00000457657.1:c.2591G>A
  hgvsp: ENSP00000405677.1:p.Arg864His
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000350073
  ensembl transcript: ENST00000357481
  gene symbol: ACIN1
  hgvsc: ENST00000357481.2:c.437G>A
  hgvsp: ENSP00000350073.2:p.Arg146His
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451328
  ensembl transcript: ENST00000555053
  gene symbol: ACIN1
  hgvsc: ENST00000555053.1:c.2672G>A
  hgvsp: ENSP00000451328.1:p.Arg891His
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000262710
  ensembl transcript: ENST00000262710
  gene symbol: ACIN1
  hgvsc: ENST00000262710.1:c.2711G>A
  hgvsp: ENSP00000262710.1:p.Arg904His
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000380502
  ensembl transcript: ENST00000397341
  gene symbol: ACIN1
  hgvsc: ENST00000397341.3:c.437G>A
  hgvsp: ENSP00000380502.3:p.Arg146His
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451138
  ensembl transcript: ENST00000557515
  gene symbol: ACIN1
  hgvsc: ENST00000557515.1:c.434G>A
  hgvsp: ENSP00000451138.1:p.Arg145His
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000555807
  gene symbol: ACIN1
  hgvsc: ENST00000555807.1:n.757G>A
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000557039
  gene symbol: ACIN1
  hgvsc: ENST00000557039.1:n.551G>A
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000556052
  gene symbol: ACIN1
  hgvsc: ENST00000556052.1:n.542G>A
  variant of: http://identifiers.org/hgnc/17066
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1657
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6737
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2527
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3959
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5144
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 863
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4918
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg904His
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
population: South Asian
reference allele: C
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff

14-23533396-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23533396
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23533396
    reference: chr 14
allele count: 4
allele frequency: 3.294621530351701e-5
allele num: 121410
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451138
  ensembl transcript: ENST00000557515
  gene symbol: ACIN1
  hgvsc: ENST00000557515.1:c.410G>A
  hgvsp: ENSP00000451138.1:p.Arg137His
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451328
  ensembl transcript: ENST00000555053
  gene symbol: ACIN1
  hgvsc: ENST00000555053.1:c.2648G>A
  hgvsp: ENSP00000451328.1:p.Arg883His
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000350073
  ensembl transcript: ENST00000357481
  gene symbol: ACIN1
  hgvsc: ENST00000357481.2:c.413G>A
  hgvsp: ENSP00000350073.2:p.Arg138His
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000405677
  ensembl transcript: ENST00000457657
  gene symbol: ACIN1
  hgvsc: ENST00000457657.1:c.2567G>A
  hgvsp: ENSP00000405677.1:p.Arg856His
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000474349
  ensembl transcript: ENST00000605057
  gene symbol: ACIN1
  hgvsc: ENST00000605057.1:c.2513G>A
  hgvsp: ENSP00000474349.1:p.Arg838His
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000473758
  gene symbol: ACIN1
  hgvsc: ENST00000473758.1:n.1620G>A
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000345541
  ensembl transcript: ENST00000338631
  gene symbol: ACIN1
  hgvsc: ENST00000338631.6:c.506G>A
  hgvsp: ENSP00000345541.6:p.Arg169His
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000555478
  gene symbol: ACIN1
  hgvsc: ENST00000555478.1:n.310G>A
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000555807
  gene symbol: ACIN1
  hgvsc: ENST00000555807.1:n.733G>A
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000553790
  gene symbol: ACIN1
  hgvsc: ENST00000553790.1:n.136G>A
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000557039
  gene symbol: ACIN1
  hgvsc: ENST00000557039.1:n.527G>A
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000380502
  ensembl transcript: ENST00000397341
  gene symbol: ACIN1
  hgvsc: ENST00000397341.3:c.413G>A
  hgvsp: ENSP00000380502.3:p.Arg138His
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000554680
  gene symbol: ACIN1
  hgvsc: ENST00000554680.1:n.427G>A
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451410
  ensembl transcript: ENST00000555566
  gene symbol: ACIN1
  hgvsc: ENST00000555566.1:c.377G>A
  hgvsp: ENSP00000451410.1:p.Arg126His
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000262710
  ensembl transcript: ENST00000262710
  gene symbol: ACIN1
  hgvsc: ENST00000262710.1:c.2687G>A
  hgvsp: ENSP00000262710.1:p.Arg896His
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000556052
  gene symbol: ACIN1
  hgvsc: ENST00000556052.1:n.518G>A
  variant of: http://identifiers.org/hgnc/17066
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3974
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1740
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 863
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4435
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4560
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg896His
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS

14-23533399-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23533399
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23533399
    reference: chr 14
allele count: 1
allele frequency: 8.236418146476461e-6
allele num: 121412
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000473758
  gene symbol: ACIN1
  hgvsc: ENST00000473758.1:n.1617C>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000262710
  ensembl transcript: ENST00000262710
  gene symbol: ACIN1
  hgvsc: ENST00000262710.1:c.2684C>T
  hgvsp: ENSP00000262710.1:p.Ser895Phe
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451328
  ensembl transcript: ENST00000555053
  gene symbol: ACIN1
  hgvsc: ENST00000555053.1:c.2645C>T
  hgvsp: ENSP00000451328.1:p.Ser882Phe
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000474349
  ensembl transcript: ENST00000605057
  gene symbol: ACIN1
  hgvsc: ENST00000605057.1:c.2510C>T
  hgvsp: ENSP00000474349.1:p.Ser837Phe
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000556052
  gene symbol: ACIN1
  hgvsc: ENST00000556052.1:n.515C>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451410
  ensembl transcript: ENST00000555566
  gene symbol: ACIN1
  hgvsc: ENST00000555566.1:c.374C>T
  hgvsp: ENSP00000451410.1:p.Ser125Phe
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000345541
  ensembl transcript: ENST00000338631
  gene symbol: ACIN1
  hgvsc: ENST00000338631.6:c.503C>T
  hgvsp: ENSP00000345541.6:p.Ser168Phe
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000555807
  gene symbol: ACIN1
  hgvsc: ENST00000555807.1:n.730C>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000557039
  gene symbol: ACIN1
  hgvsc: ENST00000557039.1:n.524C>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000555478
  gene symbol: ACIN1
  hgvsc: ENST00000555478.1:n.307C>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451138
  ensembl transcript: ENST00000557515
  gene symbol: ACIN1
  hgvsc: ENST00000557515.1:c.407C>T
  hgvsp: ENSP00000451138.1:p.Ser136Phe
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000553790
  gene symbol: ACIN1
  hgvsc: ENST00000553790.1:n.133C>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000380502
  ensembl transcript: ENST00000397341
  gene symbol: ACIN1
  hgvsc: ENST00000397341.3:c.410C>T
  hgvsp: ENSP00000380502.3:p.Ser137Phe
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000350073
  ensembl transcript: ENST00000357481
  gene symbol: ACIN1
  hgvsc: ENST00000357481.2:c.410C>T
  hgvsp: ENSP00000350073.2:p.Ser137Phe
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000405677
  ensembl transcript: ENST00000457657
  gene symbol: ACIN1
  hgvsc: ENST00000457657.1:c.2564C>T
  hgvsp: ENSP00000405677.1:p.Ser855Phe
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000554680
  gene symbol: ACIN1
  hgvsc: ENST00000554680.1:n.424C>T
  variant of: http://identifiers.org/hgnc/17066
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3605
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4918
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5960
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6041
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3980
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser895Phe
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: Other
population: African
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum

14-23533402-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23533402
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23533402
    reference: chr 14
allele count: 1
allele frequency: 8.236418146476461e-6
allele num: 121412
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000262710
  ensembl transcript: ENST00000262710
  gene symbol: ACIN1
  hgvsc: ENST00000262710.1:c.2681A>C
  hgvsp: ENSP00000262710.1:p.Asp894Ala
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000473758
  gene symbol: ACIN1
  hgvsc: ENST00000473758.1:n.1614A>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000350073
  ensembl transcript: ENST00000357481
  gene symbol: ACIN1
  hgvsc: ENST00000357481.2:c.407A>C
  hgvsp: ENSP00000350073.2:p.Asp136Ala
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000405677
  ensembl transcript: ENST00000457657
  gene symbol: ACIN1
  hgvsc: ENST00000457657.1:c.2561A>C
  hgvsp: ENSP00000405677.1:p.Asp854Ala
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000380502
  ensembl transcript: ENST00000397341
  gene symbol: ACIN1
  hgvsc: ENST00000397341.3:c.407A>C
  hgvsp: ENSP00000380502.3:p.Asp136Ala
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000345541
  ensembl transcript: ENST00000338631
  gene symbol: ACIN1
  hgvsc: ENST00000338631.6:c.500A>C
  hgvsp: ENSP00000345541.6:p.Asp167Ala
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000556052
  gene symbol: ACIN1
  hgvsc: ENST00000556052.1:n.512A>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000553790
  gene symbol: ACIN1
  hgvsc: ENST00000553790.1:n.130A>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451328
  ensembl transcript: ENST00000555053
  gene symbol: ACIN1
  hgvsc: ENST00000555053.1:c.2642A>C
  hgvsp: ENSP00000451328.1:p.Asp881Ala
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000474349
  ensembl transcript: ENST00000605057
  gene symbol: ACIN1
  hgvsc: ENST00000605057.1:c.2507A>C
  hgvsp: ENSP00000474349.1:p.Asp836Ala
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000557039
  gene symbol: ACIN1
  hgvsc: ENST00000557039.1:n.521A>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000555807
  gene symbol: ACIN1
  hgvsc: ENST00000555807.1:n.727A>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000555478
  gene symbol: ACIN1
  hgvsc: ENST00000555478.1:n.304A>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000554680
  gene symbol: ACIN1
  hgvsc: ENST00000554680.1:n.421A>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451410
  ensembl transcript: ENST00000555566
  gene symbol: ACIN1
  hgvsc: ENST00000555566.1:c.371A>C
  hgvsp: ENSP00000451410.1:p.Asp124Ala
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451138
  ensembl transcript: ENST00000557515
  gene symbol: ACIN1
  hgvsc: ENST00000557515.1:c.404A>C
  hgvsp: ENSP00000451138.1:p.Asp135Ala
  variant of: http://identifiers.org/hgnc/17066
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1740
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5959
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5118
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6041
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4918
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp894Ala
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
population: European (Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: QD

14-23533422-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23533422
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23533422
    reference: chr 14
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000555478
  gene symbol: ACIN1
  hgvsc: ENST00000555478.1:n.284T>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000473758
  gene symbol: ACIN1
  hgvsc: ENST00000473758.1:n.1594T>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000380502
  ensembl transcript: ENST00000397341
  gene symbol: ACIN1
  hgvsc: ENST00000397341.3:c.387T>C
  hgvsp: ENST00000397341.3:c.387T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451328
  ensembl transcript: ENST00000555053
  gene symbol: ACIN1
  hgvsc: ENST00000555053.1:c.2622T>C
  hgvsp: ENST00000555053.1:c.2622T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000262710
  ensembl transcript: ENST00000262710
  gene symbol: ACIN1
  hgvsc: ENST00000262710.1:c.2661T>C
  hgvsp: ENST00000262710.1:c.2661T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000345541
  ensembl transcript: ENST00000338631
  gene symbol: ACIN1
  hgvsc: ENST00000338631.6:c.480T>C
  hgvsp: ENST00000338631.6:c.480T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000556052
  gene symbol: ACIN1
  hgvsc: ENST00000556052.1:n.492T>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000557039
  gene symbol: ACIN1
  hgvsc: ENST00000557039.1:n.501T>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000405677
  ensembl transcript: ENST00000457657
  gene symbol: ACIN1
  hgvsc: ENST00000457657.1:c.2541T>C
  hgvsp: ENST00000457657.1:c.2541T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000350073
  ensembl transcript: ENST00000357481
  gene symbol: ACIN1
  hgvsc: ENST00000357481.2:c.387T>C
  hgvsp: ENST00000357481.2:c.387T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000553790
  gene symbol: ACIN1
  hgvsc: ENST00000553790.1:n.110T>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451138
  ensembl transcript: ENST00000557515
  gene symbol: ACIN1
  hgvsc: ENST00000557515.1:c.384T>C
  hgvsp: ENST00000557515.1:c.384T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000474349
  ensembl transcript: ENST00000605057
  gene symbol: ACIN1
  hgvsc: ENST00000605057.1:c.2487T>C
  hgvsp: ENST00000605057.1:c.2487T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000555807
  gene symbol: ACIN1
  hgvsc: ENST00000555807.1:n.707T>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451410
  ensembl transcript: ENST00000555566
  gene symbol: ACIN1
  hgvsc: ENST00000555566.1:c.351T>C
  hgvsp: ENST00000555566.1:c.351T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000554680
  gene symbol: ACIN1
  hgvsc: ENST00000554680.1:n.401T>C
  variant of: http://identifiers.org/hgnc/17066
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1150
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6041
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6806
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5960
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 864
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2526
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val887Val
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: Other
reference allele: A
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD

14-23533438-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23533438
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23533438
    reference: chr 14
allele count: 3
allele frequency: 2.471251112063001e-5
allele num: 121396
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000473758
  gene symbol: ACIN1
  hgvsc: ENST00000473758.1:n.1586-8C>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000380502
  ensembl transcript: ENST00000397341
  gene symbol: ACIN1
  hgvsc: ENST00000397341.3:c.371C>T
  hgvsp: ENSP00000380502.3:p.Ala124Val
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451328
  ensembl transcript: ENST00000555053
  gene symbol: ACIN1
  hgvsc: ENST00000555053.1:c.2614-8C>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000554680
  gene symbol: ACIN1
  hgvsc: ENST00000554680.1:n.385C>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000350073
  ensembl transcript: ENST00000357481
  gene symbol: ACIN1
  hgvsc: ENST00000357481.2:c.371C>T
  hgvsp: ENSP00000350073.2:p.Ala124Val
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000345541
  ensembl transcript: ENST00000338631
  gene symbol: ACIN1
  hgvsc: ENST00000338631.6:c.464C>T
  hgvsp: ENSP00000345541.6:p.Ala155Val
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000262710
  ensembl transcript: ENST00000262710
  gene symbol: ACIN1
  hgvsc: ENST00000262710.1:c.2645C>T
  hgvsp: ENSP00000262710.1:p.Ala882Val
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000405677
  ensembl transcript: ENST00000457657
  gene symbol: ACIN1
  hgvsc: ENST00000457657.1:c.2525C>T
  hgvsp: ENSP00000405677.1:p.Ala842Val
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451138
  ensembl transcript: ENST00000557515
  gene symbol: ACIN1
  hgvsc: ENST00000557515.1:c.368C>T
  hgvsp: ENSP00000451138.1:p.Ala123Val
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000557039
  gene symbol: ACIN1
  hgvsc: ENST00000557039.1:n.493-8C>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000555807
  gene symbol: ACIN1
  hgvsc: ENST00000555807.1:n.691C>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000556052
  gene symbol: ACIN1
  hgvsc: ENST00000556052.1:n.476C>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000474349
  ensembl transcript: ENST00000605057
  gene symbol: ACIN1
  hgvsc: ENST00000605057.1:c.2471C>T
  hgvsp: ENSP00000474349.1:p.Ala824Val
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000553790
  gene symbol: ACIN1
  hgvsc: ENST00000553790.1:n.94C>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451410
  ensembl transcript: ENST00000555566
  gene symbol: ACIN1
  hgvsc: ENST00000555566.1:c.343-8C>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000555478
  gene symbol: ACIN1
  hgvsc: ENST00000555478.1:n.276-8C>T
  variant of: http://identifiers.org/hgnc/17066
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3603
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 864
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1662
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 6743
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5961
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala882Val
num of homozygotes: 0
population: South Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff

14-23533438-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23533438
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23533438
    reference: chr 14
allele count: 2
allele frequency: 1.647500741375333e-5
allele num: 121396
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000350073
  ensembl transcript: ENST00000357481
  gene symbol: ACIN1
  hgvsc: ENST00000357481.2:c.371C>A
  hgvsp: ENSP00000350073.2:p.Ala124Glu
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000473758
  gene symbol: ACIN1
  hgvsc: ENST00000473758.1:n.1586-8C>A
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451328
  ensembl transcript: ENST00000555053
  gene symbol: ACIN1
  hgvsc: ENST00000555053.1:c.2614-8C>A
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000557039
  gene symbol: ACIN1
  hgvsc: ENST00000557039.1:n.493-8C>A
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451138
  ensembl transcript: ENST00000557515
  gene symbol: ACIN1
  hgvsc: ENST00000557515.1:c.368C>A
  hgvsp: ENSP00000451138.1:p.Ala123Glu
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000405677
  ensembl transcript: ENST00000457657
  gene symbol: ACIN1
  hgvsc: ENST00000457657.1:c.2525C>A
  hgvsp: ENSP00000405677.1:p.Ala842Glu
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451410
  ensembl transcript: ENST00000555566
  gene symbol: ACIN1
  hgvsc: ENST00000555566.1:c.343-8C>A
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000262710
  ensembl transcript: ENST00000262710
  gene symbol: ACIN1
  hgvsc: ENST00000262710.1:c.2645C>A
  hgvsp: ENSP00000262710.1:p.Ala882Glu
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000555478
  gene symbol: ACIN1
  hgvsc: ENST00000555478.1:n.276-8C>A
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000380502
  ensembl transcript: ENST00000397341
  gene symbol: ACIN1
  hgvsc: ENST00000397341.3:c.371C>A
  hgvsp: ENSP00000380502.3:p.Ala124Glu
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000553790
  gene symbol: ACIN1
  hgvsc: ENST00000553790.1:n.94C>A
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000345541
  ensembl transcript: ENST00000338631
  gene symbol: ACIN1
  hgvsc: ENST00000338631.6:c.464C>A
  hgvsp: ENSP00000345541.6:p.Ala155Glu
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000474349
  ensembl transcript: ENST00000605057
  gene symbol: ACIN1
  hgvsc: ENST00000605057.1:c.2471C>A
  hgvsp: ENSP00000474349.1:p.Ala824Glu
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000554680
  gene symbol: ACIN1
  hgvsc: ENST00000554680.1:n.385C>A
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000556052
  gene symbol: ACIN1
  hgvsc: ENST00000556052.1:n.476C>A
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000555807
  gene symbol: ACIN1
  hgvsc: ENST00000555807.1:n.691C>A
  variant of: http://identifiers.org/hgnc/17066
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 864
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4919
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1662
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5961
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5088
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala882Glu
num of homozygotes: 0
population: Other
population: South Asian
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD

14-23533447-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23533447
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23533447
    reference: chr 14
allele count: 1
allele frequency: 8.237639422047218e-6
allele num: 121394
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000262710
  ensembl transcript: ENST00000262710
  gene symbol: ACIN1
  hgvsc: ENST00000262710.1:c.2636A>G
  hgvsp: ENSP00000262710.1:p.Lys879Arg
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000405677
  ensembl transcript: ENST00000457657
  gene symbol: ACIN1
  hgvsc: ENST00000457657.1:c.2516A>G
  hgvsp: ENSP00000405677.1:p.Lys839Arg
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000473758
  gene symbol: ACIN1
  hgvsc: ENST00000473758.1:n.1586-17A>G
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000474349
  ensembl transcript: ENST00000605057
  gene symbol: ACIN1
  hgvsc: ENST00000605057.1:c.2462A>G
  hgvsp: ENSP00000474349.1:p.Lys821Arg
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000345541
  ensembl transcript: ENST00000338631
  gene symbol: ACIN1
  hgvsc: ENST00000338631.6:c.455A>G
  hgvsp: ENSP00000345541.6:p.Lys152Arg
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000556052
  gene symbol: ACIN1
  hgvsc: ENST00000556052.1:n.467A>G
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000554680
  gene symbol: ACIN1
  hgvsc: ENST00000554680.1:n.376A>G
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000350073
  ensembl transcript: ENST00000357481
  gene symbol: ACIN1
  hgvsc: ENST00000357481.2:c.362A>G
  hgvsp: ENSP00000350073.2:p.Lys121Arg
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451328
  ensembl transcript: ENST00000555053
  gene symbol: ACIN1
  hgvsc: ENST00000555053.1:c.2614-17A>G
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000380502
  ensembl transcript: ENST00000397341
  gene symbol: ACIN1
  hgvsc: ENST00000397341.3:c.362A>G
  hgvsp: ENSP00000380502.3:p.Lys121Arg
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451138
  ensembl transcript: ENST00000557515
  gene symbol: ACIN1
  hgvsc: ENST00000557515.1:c.359A>G
  hgvsp: ENSP00000451138.1:p.Lys120Arg
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451410
  ensembl transcript: ENST00000555566
  gene symbol: ACIN1
  hgvsc: ENST00000555566.1:c.343-17A>G
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000553790
  gene symbol: ACIN1
  hgvsc: ENST00000553790.1:n.85A>G
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000557039
  gene symbol: ACIN1
  hgvsc: ENST00000557039.1:n.493-17A>G
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000555478
  gene symbol: ACIN1
  hgvsc: ENST00000555478.1:n.276-17A>G
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000555807
  gene symbol: ACIN1
  hgvsc: ENST00000555807.1:n.682A>G
  variant of: http://identifiers.org/hgnc/17066
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3602
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1151
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5063
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2526
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6742
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4919
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6041
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys879Arg
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: T
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum

14-23533454-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23533454
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23533454
    reference: chr 14
allele count: 1
allele frequency: 8.237775141689733e-6
allele num: 121392
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000350073
  ensembl transcript: ENST00000357481
  gene symbol: ACIN1
  hgvsc: ENST00000357481.2:c.355G>A
  hgvsp: ENSP00000350073.2:p.Asp119Asn
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000555807
  gene symbol: ACIN1
  hgvsc: ENST00000555807.1:n.675G>A
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000345541
  ensembl transcript: ENST00000338631
  gene symbol: ACIN1
  hgvsc: ENST00000338631.6:c.448G>A
  hgvsp: ENSP00000345541.6:p.Asp150Asn
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000557039
  gene symbol: ACIN1
  hgvsc: ENST00000557039.1:n.493-24G>A
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451410
  ensembl transcript: ENST00000555566
  gene symbol: ACIN1
  hgvsc: ENST00000555566.1:c.343-24G>A
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000262710
  ensembl transcript: ENST00000262710
  gene symbol: ACIN1
  hgvsc: ENST00000262710.1:c.2629G>A
  hgvsp: ENSP00000262710.1:p.Asp877Asn
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000473758
  gene symbol: ACIN1
  hgvsc: ENST00000473758.1:n.1586-24G>A
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000380502
  ensembl transcript: ENST00000397341
  gene symbol: ACIN1
  hgvsc: ENST00000397341.3:c.355G>A
  hgvsp: ENSP00000380502.3:p.Asp119Asn
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000554680
  gene symbol: ACIN1
  hgvsc: ENST00000554680.1:n.369G>A
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000405677
  ensembl transcript: ENST00000457657
  gene symbol: ACIN1
  hgvsc: ENST00000457657.1:c.2509G>A
  hgvsp: ENSP00000405677.1:p.Asp837Asn
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000474349
  ensembl transcript: ENST00000605057
  gene symbol: ACIN1
  hgvsc: ENST00000605057.1:c.2455G>A
  hgvsp: ENSP00000474349.1:p.Asp819Asn
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000556052
  gene symbol: ACIN1
  hgvsc: ENST00000556052.1:n.460G>A
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000553790
  gene symbol: ACIN1
  hgvsc: ENST00000553790.1:n.78G>A
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451138
  ensembl transcript: ENST00000557515
  gene symbol: ACIN1
  hgvsc: ENST00000557515.1:c.352G>A
  hgvsp: ENSP00000451138.1:p.Asp118Asn
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451328
  ensembl transcript: ENST00000555053
  gene symbol: ACIN1
  hgvsc: ENST00000555053.1:c.2614-24G>A
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000555478
  gene symbol: ACIN1
  hgvsc: ENST00000555478.1:n.276-24G>A
  variant of: http://identifiers.org/hgnc/17066
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5959
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6803
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4427
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6742
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4557
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp877Asn
num of homozygotes: 0
population: Other
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
reference allele: C
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD

14-23533455-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23533455
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23533455
    reference: chr 14
allele count: 2
allele frequency: 1.647609318878308e-5
allele num: 121388
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000555478
  gene symbol: ACIN1
  hgvsc: ENST00000555478.1:n.276-25C>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000474349
  ensembl transcript: ENST00000605057
  gene symbol: ACIN1
  hgvsc: ENST00000605057.1:c.2454C>T
  hgvsp: ENST00000605057.1:c.2454C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000553790
  gene symbol: ACIN1
  hgvsc: ENST00000553790.1:n.77C>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000350073
  ensembl transcript: ENST00000357481
  gene symbol: ACIN1
  hgvsc: ENST00000357481.2:c.354C>T
  hgvsp: ENST00000357481.2:c.354C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451328
  ensembl transcript: ENST00000555053
  gene symbol: ACIN1
  hgvsc: ENST00000555053.1:c.2614-25C>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000345541
  ensembl transcript: ENST00000338631
  gene symbol: ACIN1
  hgvsc: ENST00000338631.6:c.447C>T
  hgvsp: ENST00000338631.6:c.447C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000262710
  ensembl transcript: ENST00000262710
  gene symbol: ACIN1
  hgvsc: ENST00000262710.1:c.2628C>T
  hgvsp: ENST00000262710.1:c.2628C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000473758
  gene symbol: ACIN1
  hgvsc: ENST00000473758.1:n.1586-25C>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451410
  ensembl transcript: ENST00000555566
  gene symbol: ACIN1
  hgvsc: ENST00000555566.1:c.343-25C>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000380502
  ensembl transcript: ENST00000397341
  gene symbol: ACIN1
  hgvsc: ENST00000397341.3:c.354C>T
  hgvsp: ENST00000397341.3:c.354C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000405677
  ensembl transcript: ENST00000457657
  gene symbol: ACIN1
  hgvsc: ENST00000457657.1:c.2508C>T
  hgvsp: ENST00000457657.1:c.2508C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000554680
  gene symbol: ACIN1
  hgvsc: ENST00000554680.1:n.368C>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451138
  ensembl transcript: ENST00000557515
  gene symbol: ACIN1
  hgvsc: ENST00000557515.1:c.351C>T
  hgvsp: ENST00000557515.1:c.351C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000555807
  gene symbol: ACIN1
  hgvsc: ENST00000555807.1:n.674C>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000556052
  gene symbol: ACIN1
  hgvsc: ENST00000556052.1:n.459C>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000557039
  gene symbol: ACIN1
  hgvsc: ENST00000557039.1:n.493-25C>T
  variant of: http://identifiers.org/hgnc/17066
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4422
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5959
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 864
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3602
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6803
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro876Pro
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: African
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ

14-23533461-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23533461
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23533461
    reference: chr 14
allele count: 1
allele frequency: 8.238182327451271e-6
allele num: 121386
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000350073
  ensembl transcript: ENST00000357481
  gene symbol: ACIN1
  hgvsc: ENST00000357481.2:c.348C>T
  hgvsp: ENST00000357481.2:c.348C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451410
  ensembl transcript: ENST00000555566
  gene symbol: ACIN1
  hgvsc: ENST00000555566.1:c.343-31C>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000553790
  gene symbol: ACIN1
  hgvsc: ENST00000553790.1:n.71C>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000474349
  ensembl transcript: ENST00000605057
  gene symbol: ACIN1
  hgvsc: ENST00000605057.1:c.2448C>T
  hgvsp: ENST00000605057.1:c.2448C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000555478
  gene symbol: ACIN1
  hgvsc: ENST00000555478.1:n.276-31C>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451138
  ensembl transcript: ENST00000557515
  gene symbol: ACIN1
  hgvsc: ENST00000557515.1:c.345C>T
  hgvsp: ENST00000557515.1:c.345C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000262710
  ensembl transcript: ENST00000262710
  gene symbol: ACIN1
  hgvsc: ENST00000262710.1:c.2622C>T
  hgvsp: ENST00000262710.1:c.2622C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000405677
  ensembl transcript: ENST00000457657
  gene symbol: ACIN1
  hgvsc: ENST00000457657.1:c.2502C>T
  hgvsp: ENST00000457657.1:c.2502C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000380502
  ensembl transcript: ENST00000397341
  gene symbol: ACIN1
  hgvsc: ENST00000397341.3:c.348C>T
  hgvsp: ENST00000397341.3:c.348C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000473758
  gene symbol: ACIN1
  hgvsc: ENST00000473758.1:n.1586-31C>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000345541
  ensembl transcript: ENST00000338631
  gene symbol: ACIN1
  hgvsc: ENST00000338631.6:c.441C>T
  hgvsp: ENST00000338631.6:c.441C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000557039
  gene symbol: ACIN1
  hgvsc: ENST00000557039.1:n.493-31C>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000556052
  gene symbol: ACIN1
  hgvsc: ENST00000556052.1:n.453C>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451328
  ensembl transcript: ENST00000555053
  gene symbol: ACIN1
  hgvsc: ENST00000555053.1:c.2614-31C>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000555807
  gene symbol: ACIN1
  hgvsc: ENST00000555807.1:n.668C>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000554680
  gene symbol: ACIN1
  hgvsc: ENST00000554680.1:n.362C>T
  variant of: http://identifiers.org/hgnc/17066
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3602
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 864
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6041
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4554
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6742
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1150
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2526
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu874Leu
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum

14-23533471-GAC-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23533471
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23533469
    reference: chr 14
allele count: 1
allele frequency: 8.2387253044209e-6
allele num: 121378
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000345541
  ensembl transcript: ENST00000338631
  gene symbol: ACIN1
  hgvsc: ENST00000338631.6:c.436-7_436-6delGT
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000474349
  ensembl transcript: ENST00000605057
  gene symbol: ACIN1
  hgvsc: ENST00000605057.1:c.2443-7_2443-6delGT
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000380502
  ensembl transcript: ENST00000397341
  gene symbol: ACIN1
  hgvsc: ENST00000397341.3:c.343-7_343-6delGT
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000350073
  ensembl transcript: ENST00000357481
  gene symbol: ACIN1
  hgvsc: ENST00000357481.2:c.343-7_343-6delGT
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000405677
  ensembl transcript: ENST00000457657
  gene symbol: ACIN1
  hgvsc: ENST00000457657.1:c.2497-7_2497-6delGT
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000555478
  gene symbol: ACIN1
  hgvsc: ENST00000555478.1:n.276-43_276-42delGT
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451138
  ensembl transcript: ENST00000557515
  gene symbol: ACIN1
  hgvsc: ENST00000557515.1:c.340-7_340-6delGT
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000262710
  ensembl transcript: ENST00000262710
  gene symbol: ACIN1
  hgvsc: ENST00000262710.1:c.2617-7_2617-6delGT
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000555807
  gene symbol: ACIN1
  hgvsc: ENST00000555807.1:n.663-7_663-6delGT
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000554680
  gene symbol: ACIN1
  hgvsc: ENST00000554680.1:n.357-7_357-6delGT
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000556052
  gene symbol: ACIN1
  hgvsc: ENST00000556052.1:n.441_442delGT
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000557039
  gene symbol: ACIN1
  hgvsc: ENST00000557039.1:n.493-43_493-42delGT
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000553790
  gene symbol: ACIN1
  hgvsc: ENST00000553790.1:n.66-7_66-6delGT
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451410
  ensembl transcript: ENST00000555566
  gene symbol: ACIN1
  hgvsc: ENST00000555566.1:c.343-43_343-42delGT
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451328
  ensembl transcript: ENST00000555053
  gene symbol: ACIN1
  hgvsc: ENST00000555053.1:c.2614-43_2614-42delGT
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000473758
  gene symbol: ACIN1
  hgvsc: ENST00000473758.1:n.1586-43_1586-42delGT
  variant of: http://identifiers.org/hgnc/17066
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6041
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6803
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1738
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2526
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4390
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6743
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3951
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.2617-7_2617-6delGT
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: GAC
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum

14-23533473-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23533473
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23533473
    reference: chr 14
allele count: 1
allele frequency: 8.238996819747227e-6
allele num: 121374
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000345541
  ensembl transcript: ENST00000338631
  gene symbol: ACIN1
  hgvsc: ENST00000338631.6:c.436-7G>A
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000554680
  gene symbol: ACIN1
  hgvsc: ENST00000554680.1:n.357-7G>A
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000553790
  gene symbol: ACIN1
  hgvsc: ENST00000553790.1:n.66-7G>A
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000555807
  gene symbol: ACIN1
  hgvsc: ENST00000555807.1:n.663-7G>A
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000262710
  ensembl transcript: ENST00000262710
  gene symbol: ACIN1
  hgvsc: ENST00000262710.1:c.2617-7G>A
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000474349
  ensembl transcript: ENST00000605057
  gene symbol: ACIN1
  hgvsc: ENST00000605057.1:c.2443-7G>A
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451410
  ensembl transcript: ENST00000555566
  gene symbol: ACIN1
  hgvsc: ENST00000555566.1:c.343-43G>A
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451328
  ensembl transcript: ENST00000555053
  gene symbol: ACIN1
  hgvsc: ENST00000555053.1:c.2614-43G>A
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000473758
  gene symbol: ACIN1
  hgvsc: ENST00000473758.1:n.1586-43G>A
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000555478
  gene symbol: ACIN1
  hgvsc: ENST00000555478.1:n.276-43G>A
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000405677
  ensembl transcript: ENST00000457657
  gene symbol: ACIN1
  hgvsc: ENST00000457657.1:c.2497-7G>A
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451138
  ensembl transcript: ENST00000557515
  gene symbol: ACIN1
  hgvsc: ENST00000557515.1:c.340-7G>A
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000380502
  ensembl transcript: ENST00000397341
  gene symbol: ACIN1
  hgvsc: ENST00000397341.3:c.343-7G>A
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000350073
  ensembl transcript: ENST00000357481
  gene symbol: ACIN1
  hgvsc: ENST00000357481.2:c.343-7G>A
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000556052
  gene symbol: ACIN1
  hgvsc: ENST00000556052.1:n.441G>A
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000557039
  gene symbol: ACIN1
  hgvsc: ENST00000557039.1:n.493-43G>A
  variant of: http://identifiers.org/hgnc/17066
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6743
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4384
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1738
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5960
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3602
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.2617-7G>A
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: DP

http://identifiers.org/exac.variant/14-23533480-A-AC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23533480
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23533481
    reference: chr 14
allele count: 5
allele frequency: 4.120516877637131e-5
allele num: 121344
alternate allele: AC
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000553790
  gene symbol: ACIN1
  hgvsc: ENST00000553790.1:n.66-15dupG
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000350073
  ensembl transcript: ENST00000357481
  gene symbol: ACIN1
  hgvsc: ENST00000357481.2:c.343-15dupG
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000555807
  gene symbol: ACIN1
  hgvsc: ENST00000555807.1:n.663-15dupG
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451138
  ensembl transcript: ENST00000557515
  gene symbol: ACIN1
  hgvsc: ENST00000557515.1:c.340-15dupG
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000554680
  gene symbol: ACIN1
  hgvsc: ENST00000554680.1:n.357-15dupG
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000473758
  gene symbol: ACIN1
  hgvsc: ENST00000473758.1:n.1586-51dupG
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000555478
  gene symbol: ACIN1
  hgvsc: ENST00000555478.1:n.276-51dupG
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000556052
  gene symbol: ACIN1
  hgvsc: ENST00000556052.1:n.433dupG
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000262710
  ensembl transcript: ENST00000262710
  gene symbol: ACIN1
  hgvsc: ENST00000262710.1:c.2617-15dupG
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451410
  ensembl transcript: ENST00000555566
  gene symbol: ACIN1
  hgvsc: ENST00000555566.1:c.343-51dupG
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000405677
  ensembl transcript: ENST00000457657
  gene symbol: ACIN1
  hgvsc: ENST00000457657.1:c.2497-15dupG
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000380502
  ensembl transcript: ENST00000397341
  gene symbol: ACIN1
  hgvsc: ENST00000397341.3:c.343-15dupG
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000345541
  ensembl transcript: ENST00000338631
  gene symbol: ACIN1
  hgvsc: ENST00000338631.6:c.436-15dupG
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000557039
  gene symbol: ACIN1
  hgvsc: ENST00000557039.1:n.493-51dupG
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451328
  ensembl transcript: ENST00000555053
  gene symbol: ACIN1
  hgvsc: ENST00000555053.1:c.2614-51dupG
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000474349
  ensembl transcript: ENST00000605057
  gene symbol: ACIN1
  hgvsc: ENST00000605057.1:c.2443-15dupG
  variant of: http://identifiers.org/hgnc/17066
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6743
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1668
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 4918
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2525
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4365
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5959
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1737
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4706
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: A
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/14-23533481-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23533481
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23533481
    reference: chr 14
allele count: 1
allele frequency: 8.240897928238261e-6
allele num: 121346
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000405677
  ensembl transcript: ENST00000457657
  gene symbol: ACIN1
  hgvsc: ENST00000457657.1:c.2497-15G>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451328
  ensembl transcript: ENST00000555053
  gene symbol: ACIN1
  hgvsc: ENST00000555053.1:c.2614-51G>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000557039
  gene symbol: ACIN1
  hgvsc: ENST00000557039.1:n.493-51G>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000473758
  gene symbol: ACIN1
  hgvsc: ENST00000473758.1:n.1586-51G>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451138
  ensembl transcript: ENST00000557515
  gene symbol: ACIN1
  hgvsc: ENST00000557515.1:c.340-15G>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000350073
  ensembl transcript: ENST00000357481
  gene symbol: ACIN1
  hgvsc: ENST00000357481.2:c.343-15G>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000555807
  gene symbol: ACIN1
  hgvsc: ENST00000555807.1:n.663-15G>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451410
  ensembl transcript: ENST00000555566
  gene symbol: ACIN1
  hgvsc: ENST00000555566.1:c.343-51G>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000262710
  ensembl transcript: ENST00000262710
  gene symbol: ACIN1
  hgvsc: ENST00000262710.1:c.2617-15G>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000553790
  gene symbol: ACIN1
  hgvsc: ENST00000553790.1:n.66-15G>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000556052
  gene symbol: ACIN1
  hgvsc: ENST00000556052.1:n.433G>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000345541
  ensembl transcript: ENST00000338631
  gene symbol: ACIN1
  hgvsc: ENST00000338631.6:c.436-15G>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000380502
  ensembl transcript: ENST00000397341
  gene symbol: ACIN1
  hgvsc: ENST00000397341.3:c.343-15G>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000474349
  ensembl transcript: ENST00000605057
  gene symbol: ACIN1
  hgvsc: ENST00000605057.1:c.2443-15G>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000555478
  gene symbol: ACIN1
  hgvsc: ENST00000555478.1:n.276-51G>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000554680
  gene symbol: ACIN1
  hgvsc: ENST00000554680.1:n.357-15G>T
  variant of: http://identifiers.org/hgnc/17066
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4683
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4918
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4576
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2525
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3962
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 864
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: Other
reference allele: C
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum

14-23533481-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23533481
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23533481
    reference: chr 14
allele count: 2
allele frequency: 1.648179585647652e-5
allele num: 121346
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000555478
  gene symbol: ACIN1
  hgvsc: ENST00000555478.1:n.276-51G>A
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000473758
  gene symbol: ACIN1
  hgvsc: ENST00000473758.1:n.1586-51G>A
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000262710
  ensembl transcript: ENST00000262710
  gene symbol: ACIN1
  hgvsc: ENST00000262710.1:c.2617-15G>A
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000350073
  ensembl transcript: ENST00000357481
  gene symbol: ACIN1
  hgvsc: ENST00000357481.2:c.343-15G>A
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000556052
  gene symbol: ACIN1
  hgvsc: ENST00000556052.1:n.433G>A
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451410
  ensembl transcript: ENST00000555566
  gene symbol: ACIN1
  hgvsc: ENST00000555566.1:c.343-51G>A
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000405677
  ensembl transcript: ENST00000457657
  gene symbol: ACIN1
  hgvsc: ENST00000457657.1:c.2497-15G>A
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000557039
  gene symbol: ACIN1
  hgvsc: ENST00000557039.1:n.493-51G>A
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451138
  ensembl transcript: ENST00000557515
  gene symbol: ACIN1
  hgvsc: ENST00000557515.1:c.340-15G>A
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451328
  ensembl transcript: ENST00000555053
  gene symbol: ACIN1
  hgvsc: ENST00000555053.1:c.2614-51G>A
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000474349
  ensembl transcript: ENST00000605057
  gene symbol: ACIN1
  hgvsc: ENST00000605057.1:c.2443-15G>A
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000380502
  ensembl transcript: ENST00000397341
  gene symbol: ACIN1
  hgvsc: ENST00000397341.3:c.343-15G>A
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000553790
  gene symbol: ACIN1
  hgvsc: ENST00000553790.1:n.66-15G>A
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000345541
  ensembl transcript: ENST00000338631
  gene symbol: ACIN1
  hgvsc: ENST00000338631.6:c.436-15G>A
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000555807
  gene symbol: ACIN1
  hgvsc: ENST00000555807.1:n.663-15G>A
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000554680
  gene symbol: ACIN1
  hgvsc: ENST00000554680.1:n.357-15G>A
  variant of: http://identifiers.org/hgnc/17066
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3602
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6743
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4576
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4390
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6803
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1737
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
population: African
population: Other
reference allele: C
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum

14-23533484-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23533484
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23533484
    reference: chr 14
allele count: 2
allele frequency: 1.648070932972955e-5
allele num: 121354
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000474349
  ensembl transcript: ENST00000605057
  gene symbol: ACIN1
  hgvsc: ENST00000605057.1:c.2443-18G>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000405677
  ensembl transcript: ENST00000457657
  gene symbol: ACIN1
  hgvsc: ENST00000457657.1:c.2497-18G>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000553790
  gene symbol: ACIN1
  hgvsc: ENST00000553790.1:n.66-18G>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000473758
  gene symbol: ACIN1
  hgvsc: ENST00000473758.1:n.1586-54G>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000555478
  gene symbol: ACIN1
  hgvsc: ENST00000555478.1:n.276-54G>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000380502
  ensembl transcript: ENST00000397341
  gene symbol: ACIN1
  hgvsc: ENST00000397341.3:c.343-18G>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000556052
  gene symbol: ACIN1
  hgvsc: ENST00000556052.1:n.430G>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451328
  ensembl transcript: ENST00000555053
  gene symbol: ACIN1
  hgvsc: ENST00000555053.1:c.2614-54G>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000350073
  ensembl transcript: ENST00000357481
  gene symbol: ACIN1
  hgvsc: ENST00000357481.2:c.343-18G>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000345541
  ensembl transcript: ENST00000338631
  gene symbol: ACIN1
  hgvsc: ENST00000338631.6:c.436-18G>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000557039
  gene symbol: ACIN1
  hgvsc: ENST00000557039.1:n.493-54G>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000554680
  gene symbol: ACIN1
  hgvsc: ENST00000554680.1:n.357-18G>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451410
  ensembl transcript: ENST00000555566
  gene symbol: ACIN1
  hgvsc: ENST00000555566.1:c.343-54G>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000555807
  gene symbol: ACIN1
  hgvsc: ENST00000555807.1:n.663-18G>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000262710
  ensembl transcript: ENST00000262710
  gene symbol: ACIN1
  hgvsc: ENST00000262710.1:c.2617-18G>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451138
  ensembl transcript: ENST00000557515
  gene symbol: ACIN1
  hgvsc: ENST00000557515.1:c.340-18G>C
  variant of: http://identifiers.org/hgnc/17066
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6743
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3963
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2525
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4619
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4571
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6803
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4918
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 864
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
population: African
population: Other
reference allele: C
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD

http://identifiers.org/exac.variant/14-23533486-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23533486
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23533486
    reference: chr 14
allele count: 5
allele frequency: 4.120652711389484e-5
allele num: 121340
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451410
  ensembl transcript: ENST00000555566
  gene symbol: ACIN1
  hgvsc: ENST00000555566.1:c.343-56G>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000555478
  gene symbol: ACIN1
  hgvsc: ENST00000555478.1:n.276-56G>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000473758
  gene symbol: ACIN1
  hgvsc: ENST00000473758.1:n.1586-56G>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000380502
  ensembl transcript: ENST00000397341
  gene symbol: ACIN1
  hgvsc: ENST00000397341.3:c.343-20G>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000553790
  gene symbol: ACIN1
  hgvsc: ENST00000553790.1:n.66-20G>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000405677
  ensembl transcript: ENST00000457657
  gene symbol: ACIN1
  hgvsc: ENST00000457657.1:c.2497-20G>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000350073
  ensembl transcript: ENST00000357481
  gene symbol: ACIN1
  hgvsc: ENST00000357481.2:c.343-20G>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000556052
  gene symbol: ACIN1
  hgvsc: ENST00000556052.1:n.428G>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000557039
  gene symbol: ACIN1
  hgvsc: ENST00000557039.1:n.493-56G>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000345541
  ensembl transcript: ENST00000338631
  gene symbol: ACIN1
  hgvsc: ENST00000338631.6:c.436-20G>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000555807
  gene symbol: ACIN1
  hgvsc: ENST00000555807.1:n.663-20G>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000474349
  ensembl transcript: ENST00000605057
  gene symbol: ACIN1
  hgvsc: ENST00000605057.1:c.2443-20G>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000262710
  ensembl transcript: ENST00000262710
  gene symbol: ACIN1
  hgvsc: ENST00000262710.1:c.2617-20G>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451138
  ensembl transcript: ENST00000557515
  gene symbol: ACIN1
  hgvsc: ENST00000557515.1:c.340-20G>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451328
  ensembl transcript: ENST00000555053
  gene symbol: ACIN1
  hgvsc: ENST00000555053.1:c.2614-56G>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000554680
  gene symbol: ACIN1
  hgvsc: ENST00000554680.1:n.357-20G>T
  variant of: http://identifiers.org/hgnc/17066
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6803
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1152
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3602
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1674
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 6041
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4529
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4573
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1737
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4918
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
population: African
population: European (Finnish)
population: East Asian
reference allele: C
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: DP

14-23533486-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23533486
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23533486
    reference: chr 14
allele count: 1
allele frequency: 8.241305422778968e-6
allele num: 121340
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000350073
  ensembl transcript: ENST00000357481
  gene symbol: ACIN1
  hgvsc: ENST00000357481.2:c.343-20G>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000555478
  gene symbol: ACIN1
  hgvsc: ENST00000555478.1:n.276-56G>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451410
  ensembl transcript: ENST00000555566
  gene symbol: ACIN1
  hgvsc: ENST00000555566.1:c.343-56G>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000473758
  gene symbol: ACIN1
  hgvsc: ENST00000473758.1:n.1586-56G>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000345541
  ensembl transcript: ENST00000338631
  gene symbol: ACIN1
  hgvsc: ENST00000338631.6:c.436-20G>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451328
  ensembl transcript: ENST00000555053
  gene symbol: ACIN1
  hgvsc: ENST00000555053.1:c.2614-56G>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000405677
  ensembl transcript: ENST00000457657
  gene symbol: ACIN1
  hgvsc: ENST00000457657.1:c.2497-20G>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000380502
  ensembl transcript: ENST00000397341
  gene symbol: ACIN1
  hgvsc: ENST00000397341.3:c.343-20G>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000262710
  ensembl transcript: ENST00000262710
  gene symbol: ACIN1
  hgvsc: ENST00000262710.1:c.2617-20G>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000557039
  gene symbol: ACIN1
  hgvsc: ENST00000557039.1:n.493-56G>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000556052
  gene symbol: ACIN1
  hgvsc: ENST00000556052.1:n.428G>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000474349
  ensembl transcript: ENST00000605057
  gene symbol: ACIN1
  hgvsc: ENST00000605057.1:c.2443-20G>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000555807
  gene symbol: ACIN1
  hgvsc: ENST00000555807.1:n.663-20G>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451138
  ensembl transcript: ENST00000557515
  gene symbol: ACIN1
  hgvsc: ENST00000557515.1:c.340-20G>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000554680
  gene symbol: ACIN1
  hgvsc: ENST00000554680.1:n.357-20G>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000553790
  gene symbol: ACIN1
  hgvsc: ENST00000553790.1:n.66-20G>C
  variant of: http://identifiers.org/hgnc/17066
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2524
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4444
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5960
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4529
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4918
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6803
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4573
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6743
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum

14-23533491-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23533491
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23533491
    reference: chr 14
allele count: 3
allele frequency: 2.472595400972554e-5
allele num: 121330
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000553790
  gene symbol: ACIN1
  hgvsc: ENST00000553790.1:n.66-25G>A
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451328
  ensembl transcript: ENST00000555053
  gene symbol: ACIN1
  hgvsc: ENST00000555053.1:c.2614-61G>A
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000473758
  gene symbol: ACIN1
  hgvsc: ENST00000473758.1:n.1586-61G>A
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000345541
  ensembl transcript: ENST00000338631
  gene symbol: ACIN1
  hgvsc: ENST00000338631.6:c.436-25G>A
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451138
  ensembl transcript: ENST00000557515
  gene symbol: ACIN1
  hgvsc: ENST00000557515.1:c.340-25G>A
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000380502
  ensembl transcript: ENST00000397341
  gene symbol: ACIN1
  hgvsc: ENST00000397341.3:c.343-25G>A
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451410
  ensembl transcript: ENST00000555566
  gene symbol: ACIN1
  hgvsc: ENST00000555566.1:c.343-61G>A
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000555807
  gene symbol: ACIN1
  hgvsc: ENST00000555807.1:n.663-25G>A
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000262710
  ensembl transcript: ENST00000262710
  gene symbol: ACIN1
  hgvsc: ENST00000262710.1:c.2617-25G>A
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000556052
  gene symbol: ACIN1
  hgvsc: ENST00000556052.1:n.423G>A
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000557039
  gene symbol: ACIN1
  hgvsc: ENST00000557039.1:n.493-61G>A
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000555478
  gene symbol: ACIN1
  hgvsc: ENST00000555478.1:n.276-61G>A
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000405677
  ensembl transcript: ENST00000457657
  gene symbol: ACIN1
  hgvsc: ENST00000457657.1:c.2497-25G>A
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000474349
  ensembl transcript: ENST00000605057
  gene symbol: ACIN1
  hgvsc: ENST00000605057.1:c.2443-25G>A
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000350073
  ensembl transcript: ENST00000357481
  gene symbol: ACIN1
  hgvsc: ENST00000357481.2:c.343-25G>A
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000554680
  gene symbol: ACIN1
  hgvsc: ENST00000554680.1:n.357-25G>A
  variant of: http://identifiers.org/hgnc/17066
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3601
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1154
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4483
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 864
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4498
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6802
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: MQ

14-23533507-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23533507
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23533507
    reference: chr 14
allele count: 1
allele frequency: 8.243751236562685e-6
allele num: 121304
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000405677
  ensembl transcript: ENST00000457657
  gene symbol: ACIN1
  hgvsc: ENST00000457657.1:c.2497-41A>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000474349
  ensembl transcript: ENST00000605057
  gene symbol: ACIN1
  hgvsc: ENST00000605057.1:c.2443-41A>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000557039
  gene symbol: ACIN1
  hgvsc: ENST00000557039.1:n.492+57A>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451328
  ensembl transcript: ENST00000555053
  gene symbol: ACIN1
  hgvsc: ENST00000555053.1:c.2613+57A>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000380502
  ensembl transcript: ENST00000397341
  gene symbol: ACIN1
  hgvsc: ENST00000397341.3:c.343-41A>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000555807
  gene symbol: ACIN1
  hgvsc: ENST00000555807.1:n.663-41A>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000350073
  ensembl transcript: ENST00000357481
  gene symbol: ACIN1
  hgvsc: ENST00000357481.2:c.343-41A>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000556052
  gene symbol: ACIN1
  hgvsc: ENST00000556052.1:n.407A>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000262710
  ensembl transcript: ENST00000262710
  gene symbol: ACIN1
  hgvsc: ENST00000262710.1:c.2617-41A>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000554680
  gene symbol: ACIN1
  hgvsc: ENST00000554680.1:n.357-41A>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000473758
  gene symbol: ACIN1
  hgvsc: ENST00000473758.1:n.1585+57A>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000345541
  ensembl transcript: ENST00000338631
  gene symbol: ACIN1
  hgvsc: ENST00000338631.6:c.436-41A>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000553790
  gene symbol: ACIN1
  hgvsc: ENST00000553790.1:n.66-41A>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000555478
  gene symbol: ACIN1
  hgvsc: ENST00000555478.1:n.275+57A>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451410
  ensembl transcript: ENST00000555566
  gene symbol: ACIN1
  hgvsc: ENST00000555566.1:c.342+57A>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451138
  ensembl transcript: ENST00000557515
  gene symbol: ACIN1
  hgvsc: ENST00000557515.1:c.340-41A>T
  variant of: http://identifiers.org/hgnc/17066
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5955
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6731
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4916
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2524
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4418
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3994
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6802
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4574
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: T
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: MQ

14-23533509-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23533509
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23533509
    reference: chr 14
allele count: 1
allele frequency: 8.245246615326264e-6
allele num: 121282
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000556052
  gene symbol: ACIN1
  hgvsc: ENST00000556052.1:n.405A>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000555478
  gene symbol: ACIN1
  hgvsc: ENST00000555478.1:n.275+55A>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000380502
  ensembl transcript: ENST00000397341
  gene symbol: ACIN1
  hgvsc: ENST00000397341.3:c.343-43A>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000553790
  gene symbol: ACIN1
  hgvsc: ENST00000553790.1:n.66-43A>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000345541
  ensembl transcript: ENST00000338631
  gene symbol: ACIN1
  hgvsc: ENST00000338631.6:c.436-43A>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000405677
  ensembl transcript: ENST00000457657
  gene symbol: ACIN1
  hgvsc: ENST00000457657.1:c.2497-43A>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451328
  ensembl transcript: ENST00000555053
  gene symbol: ACIN1
  hgvsc: ENST00000555053.1:c.2613+55A>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000350073
  ensembl transcript: ENST00000357481
  gene symbol: ACIN1
  hgvsc: ENST00000357481.2:c.343-43A>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451410
  ensembl transcript: ENST00000555566
  gene symbol: ACIN1
  hgvsc: ENST00000555566.1:c.342+55A>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000262710
  ensembl transcript: ENST00000262710
  gene symbol: ACIN1
  hgvsc: ENST00000262710.1:c.2617-43A>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000474349
  ensembl transcript: ENST00000605057
  gene symbol: ACIN1
  hgvsc: ENST00000605057.1:c.2443-43A>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000473758
  gene symbol: ACIN1
  hgvsc: ENST00000473758.1:n.1585+55A>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451138
  ensembl transcript: ENST00000557515
  gene symbol: ACIN1
  hgvsc: ENST00000557515.1:c.340-43A>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000554680
  gene symbol: ACIN1
  hgvsc: ENST00000554680.1:n.357-43A>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000557039
  gene symbol: ACIN1
  hgvsc: ENST00000557039.1:n.492+55A>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000555807
  gene symbol: ACIN1
  hgvsc: ENST00000555807.1:n.663-43A>T
  variant of: http://identifiers.org/hgnc/17066
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1676
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3600
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6801
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4491
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6732
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1738
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4396
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4576
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4916
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
reference allele: T
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

14-23533516-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23533516
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23533516
    reference: chr 14
allele count: 1
allele frequency: 8.246334504312833e-6
allele num: 121266
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000557039
  gene symbol: ACIN1
  hgvsc: ENST00000557039.1:n.492+48G>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000380502
  ensembl transcript: ENST00000397341
  gene symbol: ACIN1
  hgvsc: ENST00000397341.3:c.342+48G>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000474349
  ensembl transcript: ENST00000605057
  gene symbol: ACIN1
  hgvsc: ENST00000605057.1:c.2442+48G>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000345541
  ensembl transcript: ENST00000338631
  gene symbol: ACIN1
  hgvsc: ENST00000338631.6:c.435+48G>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451328
  ensembl transcript: ENST00000555053
  gene symbol: ACIN1
  hgvsc: ENST00000555053.1:c.2613+48G>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451138
  ensembl transcript: ENST00000557515
  gene symbol: ACIN1
  hgvsc: ENST00000557515.1:c.339+48G>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000556052
  gene symbol: ACIN1
  hgvsc: ENST00000556052.1:n.398G>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000350073
  ensembl transcript: ENST00000357481
  gene symbol: ACIN1
  hgvsc: ENST00000357481.2:c.342+48G>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000555478
  gene symbol: ACIN1
  hgvsc: ENST00000555478.1:n.275+48G>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000262710
  ensembl transcript: ENST00000262710
  gene symbol: ACIN1
  hgvsc: ENST00000262710.1:c.2616+48G>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000553790
  gene symbol: ACIN1
  hgvsc: ENST00000553790.1:n.65+48G>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000405677
  ensembl transcript: ENST00000457657
  gene symbol: ACIN1
  hgvsc: ENST00000457657.1:c.2496+48G>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000554680
  gene symbol: ACIN1
  hgvsc: ENST00000554680.1:n.356+48G>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000555807
  gene symbol: ACIN1
  hgvsc: ENST00000555807.1:n.662+48G>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000473758
  gene symbol: ACIN1
  hgvsc: ENST00000473758.1:n.1585+48G>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451410
  ensembl transcript: ENST00000555566
  gene symbol: ACIN1
  hgvsc: ENST00000555566.1:c.342+48G>C
  variant of: http://identifiers.org/hgnc/17066
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1154
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4580
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1677
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6038
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4314
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2524
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4008
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4561
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: Latino
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: African
population: European (Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: MQ

14-23533525-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23533525
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23533525
    reference: chr 14
allele count: 1
allele frequency: 8.244430886935875e-6
allele num: 121294
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000555478
  gene symbol: ACIN1
  hgvsc: ENST00000555478.1:n.275+39G>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000557039
  gene symbol: ACIN1
  hgvsc: ENST00000557039.1:n.492+39G>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000262710
  ensembl transcript: ENST00000262710
  gene symbol: ACIN1
  hgvsc: ENST00000262710.1:c.2616+39G>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000555807
  gene symbol: ACIN1
  hgvsc: ENST00000555807.1:n.662+39G>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000474349
  ensembl transcript: ENST00000605057
  gene symbol: ACIN1
  hgvsc: ENST00000605057.1:c.2442+39G>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451410
  ensembl transcript: ENST00000555566
  gene symbol: ACIN1
  hgvsc: ENST00000555566.1:c.342+39G>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000554680
  gene symbol: ACIN1
  hgvsc: ENST00000554680.1:n.356+39G>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451328
  ensembl transcript: ENST00000555053
  gene symbol: ACIN1
  hgvsc: ENST00000555053.1:c.2613+39G>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000556052
  gene symbol: ACIN1
  hgvsc: ENST00000556052.1:n.389G>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000553790
  gene symbol: ACIN1
  hgvsc: ENST00000553790.1:n.65+39G>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000345541
  ensembl transcript: ENST00000338631
  gene symbol: ACIN1
  hgvsc: ENST00000338631.6:c.435+39G>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000350073
  ensembl transcript: ENST00000357481
  gene symbol: ACIN1
  hgvsc: ENST00000357481.2:c.342+39G>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451138
  ensembl transcript: ENST00000557515
  gene symbol: ACIN1
  hgvsc: ENST00000557515.1:c.339+39G>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000473758
  gene symbol: ACIN1
  hgvsc: ENST00000473758.1:n.1585+39G>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000405677
  ensembl transcript: ENST00000457657
  gene symbol: ACIN1
  hgvsc: ENST00000457657.1:c.2496+39G>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000380502
  ensembl transcript: ENST00000397341
  gene symbol: ACIN1
  hgvsc: ENST00000397341.3:c.342+39G>C
  variant of: http://identifiers.org/hgnc/17066
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6037
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4025
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6731
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6801
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5963
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 865
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4618
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: African
population: East Asian
population: Latino
reference allele: C
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ

14-23533526-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23533526
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23533526
    reference: chr 14
allele count: 10
allele frequency: 8.244566830458728e-5
allele num: 121292
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451138
  ensembl transcript: ENST00000557515
  gene symbol: ACIN1
  hgvsc: ENST00000557515.1:c.339+38T>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000556052
  gene symbol: ACIN1
  hgvsc: ENST00000556052.1:n.388T>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000553790
  gene symbol: ACIN1
  hgvsc: ENST00000553790.1:n.65+38T>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000350073
  ensembl transcript: ENST00000357481
  gene symbol: ACIN1
  hgvsc: ENST00000357481.2:c.342+38T>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000473758
  gene symbol: ACIN1
  hgvsc: ENST00000473758.1:n.1585+38T>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000474349
  ensembl transcript: ENST00000605057
  gene symbol: ACIN1
  hgvsc: ENST00000605057.1:c.2442+38T>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451410
  ensembl transcript: ENST00000555566
  gene symbol: ACIN1
  hgvsc: ENST00000555566.1:c.342+38T>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000554680
  gene symbol: ACIN1
  hgvsc: ENST00000554680.1:n.356+38T>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000555478
  gene symbol: ACIN1
  hgvsc: ENST00000555478.1:n.275+38T>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000555807
  gene symbol: ACIN1
  hgvsc: ENST00000555807.1:n.662+38T>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000380502
  ensembl transcript: ENST00000397341
  gene symbol: ACIN1
  hgvsc: ENST00000397341.3:c.342+38T>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000405677
  ensembl transcript: ENST00000457657
  gene symbol: ACIN1
  hgvsc: ENST00000457657.1:c.2496+38T>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000557039
  gene symbol: ACIN1
  hgvsc: ENST00000557039.1:n.492+38T>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000345541
  ensembl transcript: ENST00000338631
  gene symbol: ACIN1
  hgvsc: ENST00000338631.6:c.435+38T>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000262710
  ensembl transcript: ENST00000262710
  gene symbol: ACIN1
  hgvsc: ENST00000262710.1:c.2616+38T>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451328
  ensembl transcript: ENST00000555053
  gene symbol: ACIN1
  hgvsc: ENST00000555053.1:c.2613+38T>C
  variant of: http://identifiers.org/hgnc/17066
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 864
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4288
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4641
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5961
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6036
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3599
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1739
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
population: Other
population: South Asian
reference allele: A
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum

14-23533527-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23533527
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23533527
    reference: chr 14
allele count: 140
allele frequency: 1.154144202074162e-3
allele num: 121302
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000473758
  gene symbol: ACIN1
  hgvsc: ENST00000473758.1:n.1585+37C>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000553790
  gene symbol: ACIN1
  hgvsc: ENST00000553790.1:n.65+37C>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000556052
  gene symbol: ACIN1
  hgvsc: ENST00000556052.1:n.387C>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000380502
  ensembl transcript: ENST00000397341
  gene symbol: ACIN1
  hgvsc: ENST00000397341.3:c.342+37C>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000405677
  ensembl transcript: ENST00000457657
  gene symbol: ACIN1
  hgvsc: ENST00000457657.1:c.2496+37C>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000555478
  gene symbol: ACIN1
  hgvsc: ENST00000555478.1:n.275+37C>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000474349
  ensembl transcript: ENST00000605057
  gene symbol: ACIN1
  hgvsc: ENST00000605057.1:c.2442+37C>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000262710
  ensembl transcript: ENST00000262710
  gene symbol: ACIN1
  hgvsc: ENST00000262710.1:c.2616+37C>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000557039
  gene symbol: ACIN1
  hgvsc: ENST00000557039.1:n.492+37C>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000350073
  ensembl transcript: ENST00000357481
  gene symbol: ACIN1
  hgvsc: ENST00000357481.2:c.342+37C>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451138
  ensembl transcript: ENST00000557515
  gene symbol: ACIN1
  hgvsc: ENST00000557515.1:c.339+37C>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451328
  ensembl transcript: ENST00000555053
  gene symbol: ACIN1
  hgvsc: ENST00000555053.1:c.2613+37C>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000555807
  gene symbol: ACIN1
  hgvsc: ENST00000555807.1:n.662+37C>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451410
  ensembl transcript: ENST00000555566
  gene symbol: ACIN1
  hgvsc: ENST00000555566.1:c.342+37C>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000345541
  ensembl transcript: ENST00000338631
  gene symbol: ACIN1
  hgvsc: ENST00000338631.6:c.435+37C>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000554680
  gene symbol: ACIN1
  hgvsc: ENST00000554680.1:n.356+37C>T
  variant of: http://identifiers.org/hgnc/17066
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4579
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1151
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1796
  bin: 9.75e1
  variant carriers: 122
genotype depth: GenotypeDepth
  all individuals: 3999
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4289
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4641
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 864
  bin: 8.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
num of homozygotes: 2
population: Latino
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: ClippingRankSum

14-23533552-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23533552
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23533552
    reference: chr 14
allele count: 1
allele frequency: 8.240490473993011e-6
allele num: 121352
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451410
  ensembl transcript: ENST00000555566
  gene symbol: ACIN1
  hgvsc: ENST00000555566.1:c.342+12G>A
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000405677
  ensembl transcript: ENST00000457657
  gene symbol: ACIN1
  hgvsc: ENST00000457657.1:c.2496+12G>A
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000553790
  gene symbol: ACIN1
  hgvsc: ENST00000553790.1:n.65+12G>A
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000556052
  gene symbol: ACIN1
  hgvsc: ENST00000556052.1:n.362G>A
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000555478
  gene symbol: ACIN1
  hgvsc: ENST00000555478.1:n.275+12G>A
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451138
  ensembl transcript: ENST00000557515
  gene symbol: ACIN1
  hgvsc: ENST00000557515.1:c.339+12G>A
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000350073
  ensembl transcript: ENST00000357481
  gene symbol: ACIN1
  hgvsc: ENST00000357481.2:c.342+12G>A
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000473758
  gene symbol: ACIN1
  hgvsc: ENST00000473758.1:n.1585+12G>A
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000262710
  ensembl transcript: ENST00000262710
  gene symbol: ACIN1
  hgvsc: ENST00000262710.1:c.2616+12G>A
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451328
  ensembl transcript: ENST00000555053
  gene symbol: ACIN1
  hgvsc: ENST00000555053.1:c.2613+12G>A
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000345541
  ensembl transcript: ENST00000338631
  gene symbol: ACIN1
  hgvsc: ENST00000338631.6:c.435+12G>A
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000380502
  ensembl transcript: ENST00000397341
  gene symbol: ACIN1
  hgvsc: ENST00000397341.3:c.342+12G>A
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000555807
  gene symbol: ACIN1
  hgvsc: ENST00000555807.1:n.662+12G>A
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000557039
  gene symbol: ACIN1
  hgvsc: ENST00000557039.1:n.492+12G>A
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000554680
  gene symbol: ACIN1
  hgvsc: ENST00000554680.1:n.356+12G>A
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000474349
  ensembl transcript: ENST00000605057
  gene symbol: ACIN1
  hgvsc: ENST00000605057.1:c.2442+12G>A
  variant of: http://identifiers.org/hgnc/17066
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6715
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4979
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4301
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6022
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4023
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1164
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4566
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 872
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD

14-23533554-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23533554
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23533554
    reference: chr 14
allele count: 64
allele frequency: 5.274000824062628e-4
allele num: 121350
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000555478
  gene symbol: ACIN1
  hgvsc: ENST00000555478.1:n.275+10G>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451410
  ensembl transcript: ENST00000555566
  gene symbol: ACIN1
  hgvsc: ENST00000555566.1:c.342+10G>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000557039
  gene symbol: ACIN1
  hgvsc: ENST00000557039.1:n.492+10G>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000553790
  gene symbol: ACIN1
  hgvsc: ENST00000553790.1:n.65+10G>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000405677
  ensembl transcript: ENST00000457657
  gene symbol: ACIN1
  hgvsc: ENST00000457657.1:c.2496+10G>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000262710
  ensembl transcript: ENST00000262710
  gene symbol: ACIN1
  hgvsc: ENST00000262710.1:c.2616+10G>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451328
  ensembl transcript: ENST00000555053
  gene symbol: ACIN1
  hgvsc: ENST00000555053.1:c.2613+10G>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000474349
  ensembl transcript: ENST00000605057
  gene symbol: ACIN1
  hgvsc: ENST00000605057.1:c.2442+10G>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000380502
  ensembl transcript: ENST00000397341
  gene symbol: ACIN1
  hgvsc: ENST00000397341.3:c.342+10G>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000350073
  ensembl transcript: ENST00000357481
  gene symbol: ACIN1
  hgvsc: ENST00000357481.2:c.342+10G>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000554680
  gene symbol: ACIN1
  hgvsc: ENST00000554680.1:n.356+10G>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451138
  ensembl transcript: ENST00000557515
  gene symbol: ACIN1
  hgvsc: ENST00000557515.1:c.339+10G>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000473758
  gene symbol: ACIN1
  hgvsc: ENST00000473758.1:n.1585+10G>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000556052
  gene symbol: ACIN1
  hgvsc: ENST00000556052.1:n.360G>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000345541
  ensembl transcript: ENST00000338631
  gene symbol: ACIN1
  hgvsc: ENST00000338631.6:c.435+10G>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000555807
  gene symbol: ACIN1
  hgvsc: ENST00000555807.1:n.662+10G>C
  variant of: http://identifiers.org/hgnc/17066
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6778
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1771
  bin: 9.75e1
  variant carriers: 60
genotype depth: GenotypeDepth
  all individuals: 4313
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6009
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4990
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 871
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1164
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 1
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
reference allele: C
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD

14-23533575-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23533575
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23533575
    reference: chr 14
allele count: 1
allele frequency: 8.238453806989504e-6
allele num: 121382
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451328
  ensembl transcript: ENST00000555053
  gene symbol: ACIN1
  hgvsc: ENST00000555053.1:c.2602G>C
  hgvsp: ENSP00000451328.1:p.Glu868Gln
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000345541
  ensembl transcript: ENST00000338631
  gene symbol: ACIN1
  hgvsc: ENST00000338631.6:c.424G>C
  hgvsp: ENSP00000345541.6:p.Glu142Gln
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451138
  ensembl transcript: ENST00000557515
  gene symbol: ACIN1
  hgvsc: ENST00000557515.1:c.328G>C
  hgvsp: ENSP00000451138.1:p.Glu110Gln
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451410
  ensembl transcript: ENST00000555566
  gene symbol: ACIN1
  hgvsc: ENST00000555566.1:c.331G>C
  hgvsp: ENSP00000451410.1:p.Glu111Gln
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000474349
  ensembl transcript: ENST00000605057
  gene symbol: ACIN1
  hgvsc: ENST00000605057.1:c.2431G>C
  hgvsp: ENSP00000474349.1:p.Glu811Gln
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000555478
  gene symbol: ACIN1
  hgvsc: ENST00000555478.1:n.264G>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000380502
  ensembl transcript: ENST00000397341
  gene symbol: ACIN1
  hgvsc: ENST00000397341.3:c.331G>C
  hgvsp: ENSP00000380502.3:p.Glu111Gln
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000555807
  gene symbol: ACIN1
  hgvsc: ENST00000555807.1:n.651G>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000553790
  gene symbol: ACIN1
  hgvsc: ENST00000553790.1:n.54G>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000350073
  ensembl transcript: ENST00000357481
  gene symbol: ACIN1
  hgvsc: ENST00000357481.2:c.331G>C
  hgvsp: ENSP00000350073.2:p.Glu111Gln
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000262710
  ensembl transcript: ENST00000262710
  gene symbol: ACIN1
  hgvsc: ENST00000262710.1:c.2605G>C
  hgvsp: ENSP00000262710.1:p.Glu869Gln
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000405677
  ensembl transcript: ENST00000457657
  gene symbol: ACIN1
  hgvsc: ENST00000457657.1:c.2485G>C
  hgvsp: ENSP00000405677.1:p.Glu829Gln
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000557039
  gene symbol: ACIN1
  hgvsc: ENST00000557039.1:n.481G>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000554680
  gene symbol: ACIN1
  hgvsc: ENST00000554680.1:n.345G>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000473758
  gene symbol: ACIN1
  hgvsc: ENST00000473758.1:n.1574G>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000556052
  gene symbol: ACIN1
  hgvsc: ENST00000556052.1:n.339G>C
  variant of: http://identifiers.org/hgnc/17066
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6008
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3602
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4052
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5937
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1753
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu869Gln
num of homozygotes: 0
population: East Asian
population: South Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
reference allele: C
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum

14-23533588-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23533588
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23533588
    reference: chr 14
allele count: 2
allele frequency: 1.647582173160887e-5
allele num: 121390
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000473758
  gene symbol: ACIN1
  hgvsc: ENST00000473758.1:n.1561C>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451410
  ensembl transcript: ENST00000555566
  gene symbol: ACIN1
  hgvsc: ENST00000555566.1:c.318C>T
  hgvsp: ENST00000555566.1:c.318C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000345541
  ensembl transcript: ENST00000338631
  gene symbol: ACIN1
  hgvsc: ENST00000338631.6:c.411C>T
  hgvsp: ENST00000338631.6:c.411C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451138
  ensembl transcript: ENST00000557515
  gene symbol: ACIN1
  hgvsc: ENST00000557515.1:c.315C>T
  hgvsp: ENST00000557515.1:c.315C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000553790
  gene symbol: ACIN1
  hgvsc: ENST00000553790.1:n.41C>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451328
  ensembl transcript: ENST00000555053
  gene symbol: ACIN1
  hgvsc: ENST00000555053.1:c.2589C>T
  hgvsp: ENST00000555053.1:c.2589C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000556052
  gene symbol: ACIN1
  hgvsc: ENST00000556052.1:n.326C>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000380502
  ensembl transcript: ENST00000397341
  gene symbol: ACIN1
  hgvsc: ENST00000397341.3:c.318C>T
  hgvsp: ENST00000397341.3:c.318C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000555478
  gene symbol: ACIN1
  hgvsc: ENST00000555478.1:n.251C>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000555807
  gene symbol: ACIN1
  hgvsc: ENST00000555807.1:n.638C>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000262710
  ensembl transcript: ENST00000262710
  gene symbol: ACIN1
  hgvsc: ENST00000262710.1:c.2592C>T
  hgvsp: ENST00000262710.1:c.2592C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000474349
  ensembl transcript: ENST00000605057
  gene symbol: ACIN1
  hgvsc: ENST00000605057.1:c.2418C>T
  hgvsp: ENST00000605057.1:c.2418C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000350073
  ensembl transcript: ENST00000357481
  gene symbol: ACIN1
  hgvsc: ENST00000357481.2:c.318C>T
  hgvsp: ENST00000357481.2:c.318C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000557039
  gene symbol: ACIN1
  hgvsc: ENST00000557039.1:n.468C>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000405677
  ensembl transcript: ENST00000457657
  gene symbol: ACIN1
  hgvsc: ENST00000457657.1:c.2472C>T
  hgvsp: ENST00000457657.1:c.2472C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000554680
  gene symbol: ACIN1
  hgvsc: ENST00000554680.1:n.332C>T
  variant of: http://identifiers.org/hgnc/17066
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6008
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3602
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6778
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6702
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4351
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1168
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile864Ile
num of homozygotes: 1
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
reference allele: G
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: FS

14-23533590-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23533590
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23533590
    reference: chr 14
allele count: 1
allele frequency: 8.237639422047218e-6
allele num: 121394
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000380502
  ensembl transcript: ENST00000397341
  gene symbol: ACIN1
  hgvsc: ENST00000397341.3:c.316A>G
  hgvsp: ENSP00000380502.3:p.Ile106Val
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000556052
  gene symbol: ACIN1
  hgvsc: ENST00000556052.1:n.324A>G
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451410
  ensembl transcript: ENST00000555566
  gene symbol: ACIN1
  hgvsc: ENST00000555566.1:c.316A>G
  hgvsp: ENSP00000451410.1:p.Ile106Val
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000553790
  gene symbol: ACIN1
  hgvsc: ENST00000553790.1:n.39A>G
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451328
  ensembl transcript: ENST00000555053
  gene symbol: ACIN1
  hgvsc: ENST00000555053.1:c.2587A>G
  hgvsp: ENSP00000451328.1:p.Ile863Val
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000405677
  ensembl transcript: ENST00000457657
  gene symbol: ACIN1
  hgvsc: ENST00000457657.1:c.2470A>G
  hgvsp: ENSP00000405677.1:p.Ile824Val
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000473758
  gene symbol: ACIN1
  hgvsc: ENST00000473758.1:n.1559A>G
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000350073
  ensembl transcript: ENST00000357481
  gene symbol: ACIN1
  hgvsc: ENST00000357481.2:c.316A>G
  hgvsp: ENSP00000350073.2:p.Ile106Val
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000474349
  ensembl transcript: ENST00000605057
  gene symbol: ACIN1
  hgvsc: ENST00000605057.1:c.2416A>G
  hgvsp: ENSP00000474349.1:p.Ile806Val
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000555807
  gene symbol: ACIN1
  hgvsc: ENST00000555807.1:n.636A>G
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000345541
  ensembl transcript: ENST00000338631
  gene symbol: ACIN1
  hgvsc: ENST00000338631.6:c.409A>G
  hgvsp: ENSP00000345541.6:p.Ile137Val
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000262710
  ensembl transcript: ENST00000262710
  gene symbol: ACIN1
  hgvsc: ENST00000262710.1:c.2590A>G
  hgvsp: ENSP00000262710.1:p.Ile864Val
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451138
  ensembl transcript: ENST00000557515
  gene symbol: ACIN1
  hgvsc: ENST00000557515.1:c.313A>G
  hgvsp: ENSP00000451138.1:p.Ile105Val
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000554680
  gene symbol: ACIN1
  hgvsc: ENST00000554680.1:n.330A>G
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000557039
  gene symbol: ACIN1
  hgvsc: ENST00000557039.1:n.466A>G
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000555478
  gene symbol: ACIN1
  hgvsc: ENST00000555478.1:n.249A>G
  variant of: http://identifiers.org/hgnc/17066
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6008
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3602
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4356
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4910
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5100
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1754
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile864Val
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: VQSLOD

14-23533607-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23533607
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23533607
    reference: chr 14
allele count: 1
allele frequency: 8.237096588194593e-6
allele num: 121402
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000553790
  gene symbol: ACIN1
  hgvsc: ENST00000553790.1:n.22C>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000345541
  ensembl transcript: ENST00000338631
  gene symbol: ACIN1
  hgvsc: ENST00000338631.6:c.392C>T
  hgvsp: ENSP00000345541.6:p.Thr131Ile
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000262710
  ensembl transcript: ENST00000262710
  gene symbol: ACIN1
  hgvsc: ENST00000262710.1:c.2573C>T
  hgvsp: ENSP00000262710.1:p.Thr858Ile
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000555478
  gene symbol: ACIN1
  hgvsc: ENST00000555478.1:n.232C>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451328
  ensembl transcript: ENST00000555053
  gene symbol: ACIN1
  hgvsc: ENST00000555053.1:c.2570C>T
  hgvsp: ENSP00000451328.1:p.Thr857Ile
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000380502
  ensembl transcript: ENST00000397341
  gene symbol: ACIN1
  hgvsc: ENST00000397341.3:c.299C>T
  hgvsp: ENSP00000380502.3:p.Thr100Ile
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000555807
  gene symbol: ACIN1
  hgvsc: ENST00000555807.1:n.619C>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451410
  ensembl transcript: ENST00000555566
  gene symbol: ACIN1
  hgvsc: ENST00000555566.1:c.299C>T
  hgvsp: ENSP00000451410.1:p.Thr100Ile
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000350073
  ensembl transcript: ENST00000357481
  gene symbol: ACIN1
  hgvsc: ENST00000357481.2:c.299C>T
  hgvsp: ENSP00000350073.2:p.Thr100Ile
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000474349
  ensembl transcript: ENST00000605057
  gene symbol: ACIN1
  hgvsc: ENST00000605057.1:c.2399C>T
  hgvsp: ENSP00000474349.1:p.Thr800Ile
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000557039
  gene symbol: ACIN1
  hgvsc: ENST00000557039.1:n.449C>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000473758
  gene symbol: ACIN1
  hgvsc: ENST00000473758.1:n.1542C>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451138
  ensembl transcript: ENST00000557515
  gene symbol: ACIN1
  hgvsc: ENST00000557515.1:c.296C>T
  hgvsp: ENSP00000451138.1:p.Thr99Ile
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000405677
  ensembl transcript: ENST00000457657
  gene symbol: ACIN1
  hgvsc: ENST00000457657.1:c.2453C>T
  hgvsp: ENSP00000405677.1:p.Thr818Ile
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000556052
  gene symbol: ACIN1
  hgvsc: ENST00000556052.1:n.307C>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000554680
  gene symbol: ACIN1
  hgvsc: ENST00000554680.1:n.313C>T
  variant of: http://identifiers.org/hgnc/17066
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6008
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 876
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4058
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1754
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4910
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5932
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr858Ile
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
population: Latino
population: European (Finnish)
population: South Asian
reference allele: G
site quality: DP
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum

14-23533624-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23533624
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23533624
    reference: chr 14
allele count: 1
allele frequency: 8.237232289950576e-6
allele num: 121400
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451410
  ensembl transcript: ENST00000555566
  gene symbol: ACIN1
  hgvsc: ENST00000555566.1:c.282A>T
  hgvsp: ENST00000555566.1:c.282A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000405677
  ensembl transcript: ENST00000457657
  gene symbol: ACIN1
  hgvsc: ENST00000457657.1:c.2436A>T
  hgvsp: ENST00000457657.1:c.2436A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000555478
  gene symbol: ACIN1
  hgvsc: ENST00000555478.1:n.215A>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000474349
  ensembl transcript: ENST00000605057
  gene symbol: ACIN1
  hgvsc: ENST00000605057.1:c.2382A>T
  hgvsp: ENST00000605057.1:c.2382A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000262710
  ensembl transcript: ENST00000262710
  gene symbol: ACIN1
  hgvsc: ENST00000262710.1:c.2556A>T
  hgvsp: ENST00000262710.1:c.2556A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000556052
  gene symbol: ACIN1
  hgvsc: ENST00000556052.1:n.290A>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451328
  ensembl transcript: ENST00000555053
  gene symbol: ACIN1
  hgvsc: ENST00000555053.1:c.2553A>T
  hgvsp: ENST00000555053.1:c.2553A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000553790
  gene symbol: ACIN1
  hgvsc: ENST00000553790.1:n.5A>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451138
  ensembl transcript: ENST00000557515
  gene symbol: ACIN1
  hgvsc: ENST00000557515.1:c.279A>T
  hgvsp: ENST00000557515.1:c.279A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000557039
  gene symbol: ACIN1
  hgvsc: ENST00000557039.1:n.432A>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000350073
  ensembl transcript: ENST00000357481
  gene symbol: ACIN1
  hgvsc: ENST00000357481.2:c.282A>T
  hgvsp: ENST00000357481.2:c.282A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000473758
  gene symbol: ACIN1
  hgvsc: ENST00000473758.1:n.1525A>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000345541
  ensembl transcript: ENST00000338631
  gene symbol: ACIN1
  hgvsc: ENST00000338631.6:c.375A>T
  hgvsp: ENST00000338631.6:c.375A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000380502
  ensembl transcript: ENST00000397341
  gene symbol: ACIN1
  hgvsc: ENST00000397341.3:c.282A>T
  hgvsp: ENST00000397341.3:c.282A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000555807
  gene symbol: ACIN1
  hgvsc: ENST00000555807.1:n.602A>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000554680
  gene symbol: ACIN1
  hgvsc: ENST00000554680.1:n.296A>T
  variant of: http://identifiers.org/hgnc/17066
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6008
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1754
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4909
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6701
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5933
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly852Gly
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
reference allele: T
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: QD

http://identifiers.org/exac.variant/14-23533643-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23533643
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23533643
    reference: chr 14
allele count: 1
allele frequency: 8.237503706876667e-6
allele num: 121396
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000262710
  ensembl transcript: ENST00000262710
  gene symbol: ACIN1
  hgvsc: ENST00000262710.1:c.2537G>T
  hgvsp: ENSP00000262710.1:p.Gly846Val
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000405677
  ensembl transcript: ENST00000457657
  gene symbol: ACIN1
  hgvsc: ENST00000457657.1:c.2417G>T
  hgvsp: ENSP00000405677.1:p.Gly806Val
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451410
  ensembl transcript: ENST00000555566
  gene symbol: ACIN1
  hgvsc: ENST00000555566.1:c.263G>T
  hgvsp: ENSP00000451410.1:p.Gly88Val
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000380502
  ensembl transcript: ENST00000397341
  gene symbol: ACIN1
  hgvsc: ENST00000397341.3:c.263G>T
  hgvsp: ENSP00000380502.3:p.Gly88Val
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000345541
  ensembl transcript: ENST00000338631
  gene symbol: ACIN1
  hgvsc: ENST00000338631.6:c.356G>T
  hgvsp: ENSP00000345541.6:p.Gly119Val
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000555478
  gene symbol: ACIN1
  hgvsc: ENST00000555478.1:n.196G>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451328
  ensembl transcript: ENST00000555053
  gene symbol: ACIN1
  hgvsc: ENST00000555053.1:c.2534G>T
  hgvsp: ENSP00000451328.1:p.Gly845Val
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000474349
  ensembl transcript: ENST00000605057
  gene symbol: ACIN1
  hgvsc: ENST00000605057.1:c.2363G>T
  hgvsp: ENSP00000474349.1:p.Gly788Val
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000350073
  ensembl transcript: ENST00000357481
  gene symbol: ACIN1
  hgvsc: ENST00000357481.2:c.263G>T
  hgvsp: ENSP00000350073.2:p.Gly88Val
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000473758
  gene symbol: ACIN1
  hgvsc: ENST00000473758.1:n.1506G>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451138
  ensembl transcript: ENST00000557515
  gene symbol: ACIN1
  hgvsc: ENST00000557515.1:c.260G>T
  hgvsp: ENSP00000451138.1:p.Gly87Val
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000556052
  gene symbol: ACIN1
  hgvsc: ENST00000556052.1:n.271G>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000554680
  gene symbol: ACIN1
  hgvsc: ENST00000554680.1:n.277G>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000555807
  gene symbol: ACIN1
  hgvsc: ENST00000555807.1:n.583G>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000557039
  gene symbol: ACIN1
  hgvsc: ENST00000557039.1:n.413G>T
  variant of: http://identifiers.org/hgnc/17066
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4058
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1169
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6008
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1754
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6778
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4345
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly846Val
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD

14-23533644-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23533644
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23533644
    reference: chr 14
allele count: 1
allele frequency: 8.237503706876667e-6
allele num: 121396
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000380502
  ensembl transcript: ENST00000397341
  gene symbol: ACIN1
  hgvsc: ENST00000397341.3:c.262G>A
  hgvsp: ENSP00000380502.3:p.Gly88Ser
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000262710
  ensembl transcript: ENST00000262710
  gene symbol: ACIN1
  hgvsc: ENST00000262710.1:c.2536G>A
  hgvsp: ENSP00000262710.1:p.Gly846Ser
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000474349
  ensembl transcript: ENST00000605057
  gene symbol: ACIN1
  hgvsc: ENST00000605057.1:c.2362G>A
  hgvsp: ENSP00000474349.1:p.Gly788Ser
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451410
  ensembl transcript: ENST00000555566
  gene symbol: ACIN1
  hgvsc: ENST00000555566.1:c.262G>A
  hgvsp: ENSP00000451410.1:p.Gly88Ser
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451328
  ensembl transcript: ENST00000555053
  gene symbol: ACIN1
  hgvsc: ENST00000555053.1:c.2533G>A
  hgvsp: ENSP00000451328.1:p.Gly845Ser
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451138
  ensembl transcript: ENST00000557515
  gene symbol: ACIN1
  hgvsc: ENST00000557515.1:c.259G>A
  hgvsp: ENSP00000451138.1:p.Gly87Ser
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000557039
  gene symbol: ACIN1
  hgvsc: ENST00000557039.1:n.412G>A
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000555807
  gene symbol: ACIN1
  hgvsc: ENST00000555807.1:n.582G>A
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000345541
  ensembl transcript: ENST00000338631
  gene symbol: ACIN1
  hgvsc: ENST00000338631.6:c.355G>A
  hgvsp: ENSP00000345541.6:p.Gly119Ser
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000554680
  gene symbol: ACIN1
  hgvsc: ENST00000554680.1:n.276G>A
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000555478
  gene symbol: ACIN1
  hgvsc: ENST00000555478.1:n.195G>A
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000350073
  ensembl transcript: ENST00000357481
  gene symbol: ACIN1
  hgvsc: ENST00000357481.2:c.262G>A
  hgvsp: ENSP00000350073.2:p.Gly88Ser
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000405677
  ensembl transcript: ENST00000457657
  gene symbol: ACIN1
  hgvsc: ENST00000457657.1:c.2416G>A
  hgvsp: ENSP00000405677.1:p.Gly806Ser
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000473758
  gene symbol: ACIN1
  hgvsc: ENST00000473758.1:n.1505G>A
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000556052
  gene symbol: ACIN1
  hgvsc: ENST00000556052.1:n.270G>A
  variant of: http://identifiers.org/hgnc/17066
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5109
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2531
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4345
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1743
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3602
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 876
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1169
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5934
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly846Ser
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: ReadPosRankSum

14-23533652-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23533652
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23533652
    reference: chr 14
allele count: 2
allele frequency: 1.648342591524222e-5
allele num: 121334
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000557039
  gene symbol: ACIN1
  hgvsc: ENST00000557039.1:n.404G>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000473758
  gene symbol: ACIN1
  hgvsc: ENST00000473758.1:n.1497G>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451138
  ensembl transcript: ENST00000557515
  gene symbol: ACIN1
  hgvsc: ENST00000557515.1:c.251G>C
  hgvsp: ENSP00000451138.1:p.Gly84Ala
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000556052
  gene symbol: ACIN1
  hgvsc: ENST00000556052.1:n.262G>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000345541
  ensembl transcript: ENST00000338631
  gene symbol: ACIN1
  hgvsc: ENST00000338631.6:c.347G>C
  hgvsp: ENSP00000345541.6:p.Gly116Ala
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000350073
  ensembl transcript: ENST00000357481
  gene symbol: ACIN1
  hgvsc: ENST00000357481.2:c.254G>C
  hgvsp: ENSP00000350073.2:p.Gly85Ala
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000380502
  ensembl transcript: ENST00000397341
  gene symbol: ACIN1
  hgvsc: ENST00000397341.3:c.254G>C
  hgvsp: ENSP00000380502.3:p.Gly85Ala
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451410
  ensembl transcript: ENST00000555566
  gene symbol: ACIN1
  hgvsc: ENST00000555566.1:c.254G>C
  hgvsp: ENSP00000451410.1:p.Gly85Ala
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000474349
  ensembl transcript: ENST00000605057
  gene symbol: ACIN1
  hgvsc: ENST00000605057.1:c.2354G>C
  hgvsp: ENSP00000474349.1:p.Gly785Ala
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000405677
  ensembl transcript: ENST00000457657
  gene symbol: ACIN1
  hgvsc: ENST00000457657.1:c.2408G>C
  hgvsp: ENSP00000405677.1:p.Gly803Ala
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451328
  ensembl transcript: ENST00000555053
  gene symbol: ACIN1
  hgvsc: ENST00000555053.1:c.2525G>C
  hgvsp: ENSP00000451328.1:p.Gly842Ala
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000262710
  ensembl transcript: ENST00000262710
  gene symbol: ACIN1
  hgvsc: ENST00000262710.1:c.2528G>C
  hgvsp: ENSP00000262710.1:p.Gly843Ala
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000555478
  gene symbol: ACIN1
  hgvsc: ENST00000555478.1:n.187G>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000554680
  gene symbol: ACIN1
  hgvsc: ENST00000554680.1:n.268G>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000555807
  gene symbol: ACIN1
  hgvsc: ENST00000555807.1:n.574G>C
  variant of: http://identifiers.org/hgnc/17066
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4559
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4328
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3599
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2528
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1753
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4905
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1769
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
hgvs: p.Gly843Ala
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Latino
population: African
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP

14-23533654-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23533654
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23533654
    reference: chr 14
allele count: 1
allele frequency: 8.238046594391538e-6
allele num: 121388
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000473758
  gene symbol: ACIN1
  hgvsc: ENST00000473758.1:n.1495G>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451328
  ensembl transcript: ENST00000555053
  gene symbol: ACIN1
  hgvsc: ENST00000555053.1:c.2523G>C
  hgvsp: ENST00000555053.1:c.2523G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451138
  ensembl transcript: ENST00000557515
  gene symbol: ACIN1
  hgvsc: ENST00000557515.1:c.249G>C
  hgvsp: ENST00000557515.1:c.249G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451410
  ensembl transcript: ENST00000555566
  gene symbol: ACIN1
  hgvsc: ENST00000555566.1:c.252G>C
  hgvsp: ENST00000555566.1:c.252G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000262710
  ensembl transcript: ENST00000262710
  gene symbol: ACIN1
  hgvsc: ENST00000262710.1:c.2526G>C
  hgvsp: ENST00000262710.1:c.2526G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000380502
  ensembl transcript: ENST00000397341
  gene symbol: ACIN1
  hgvsc: ENST00000397341.3:c.252G>C
  hgvsp: ENST00000397341.3:c.252G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000405677
  ensembl transcript: ENST00000457657
  gene symbol: ACIN1
  hgvsc: ENST00000457657.1:c.2406G>C
  hgvsp: ENST00000457657.1:c.2406G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000557039
  gene symbol: ACIN1
  hgvsc: ENST00000557039.1:n.402G>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000554680
  gene symbol: ACIN1
  hgvsc: ENST00000554680.1:n.266G>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000345541
  ensembl transcript: ENST00000338631
  gene symbol: ACIN1
  hgvsc: ENST00000338631.6:c.345G>C
  hgvsp: ENST00000338631.6:c.345G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000555478
  gene symbol: ACIN1
  hgvsc: ENST00000555478.1:n.185G>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000474349
  ensembl transcript: ENST00000605057
  gene symbol: ACIN1
  hgvsc: ENST00000605057.1:c.2352G>C
  hgvsp: ENST00000605057.1:c.2352G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000556052
  gene symbol: ACIN1
  hgvsc: ENST00000556052.1:n.260G>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000555807
  gene symbol: ACIN1
  hgvsc: ENST00000555807.1:n.572G>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000350073
  ensembl transcript: ENST00000357481
  gene symbol: ACIN1
  hgvsc: ENST00000357481.2:c.252G>C
  hgvsp: ENST00000357481.2:c.252G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17066
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6777
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5928
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 878
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1173
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2533
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6695
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly842Gly
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ

14-23533656-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23533656
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23533656
    reference: chr 14
allele count: 8
allele frequency: 6.590763045591603e-5
allele num: 121382
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000555478
  gene symbol: ACIN1
  hgvsc: ENST00000555478.1:n.183G>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000556052
  gene symbol: ACIN1
  hgvsc: ENST00000556052.1:n.258G>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000405677
  ensembl transcript: ENST00000457657
  gene symbol: ACIN1
  hgvsc: ENST00000457657.1:c.2404G>C
  hgvsp: ENSP00000405677.1:p.Gly802Arg
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000473758
  gene symbol: ACIN1
  hgvsc: ENST00000473758.1:n.1493G>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451138
  ensembl transcript: ENST00000557515
  gene symbol: ACIN1
  hgvsc: ENST00000557515.1:c.247G>C
  hgvsp: ENSP00000451138.1:p.Gly83Arg
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000350073
  ensembl transcript: ENST00000357481
  gene symbol: ACIN1
  hgvsc: ENST00000357481.2:c.250G>C
  hgvsp: ENSP00000350073.2:p.Gly84Arg
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000380502
  ensembl transcript: ENST00000397341
  gene symbol: ACIN1
  hgvsc: ENST00000397341.3:c.250G>C
  hgvsp: ENSP00000380502.3:p.Gly84Arg
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451328
  ensembl transcript: ENST00000555053
  gene symbol: ACIN1
  hgvsc: ENST00000555053.1:c.2521G>C
  hgvsp: ENSP00000451328.1:p.Gly841Arg
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451410
  ensembl transcript: ENST00000555566
  gene symbol: ACIN1
  hgvsc: ENST00000555566.1:c.250G>C
  hgvsp: ENSP00000451410.1:p.Gly84Arg
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000555807
  gene symbol: ACIN1
  hgvsc: ENST00000555807.1:n.570G>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000262710
  ensembl transcript: ENST00000262710
  gene symbol: ACIN1
  hgvsc: ENST00000262710.1:c.2524G>C
  hgvsp: ENSP00000262710.1:p.Gly842Arg
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000554680
  gene symbol: ACIN1
  hgvsc: ENST00000554680.1:n.264G>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000474349
  ensembl transcript: ENST00000605057
  gene symbol: ACIN1
  hgvsc: ENST00000605057.1:c.2350G>C
  hgvsp: ENSP00000474349.1:p.Gly784Arg
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000345541
  ensembl transcript: ENST00000338631
  gene symbol: ACIN1
  hgvsc: ENST00000338631.6:c.343G>C
  hgvsp: ENSP00000345541.6:p.Gly115Arg
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000557039
  gene symbol: ACIN1
  hgvsc: ENST00000557039.1:n.400G>C
  variant of: http://identifiers.org/hgnc/17066
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1755
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2532
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5110
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6003
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4319
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 608
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Gly842Arg
num of homozygotes: 0
population: Other
population: East Asian
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP

14-23533657-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23533657
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23533657
    reference: chr 14
allele count: 1
allele frequency: 8.238453806989504e-6
allele num: 121382
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451410
  ensembl transcript: ENST00000555566
  gene symbol: ACIN1
  hgvsc: ENST00000555566.1:c.249G>C
  hgvsp: ENSP00000451410.1:p.Glu83Asp
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000555478
  gene symbol: ACIN1
  hgvsc: ENST00000555478.1:n.182G>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451328
  ensembl transcript: ENST00000555053
  gene symbol: ACIN1
  hgvsc: ENST00000555053.1:c.2520G>C
  hgvsp: ENSP00000451328.1:p.Glu840Asp
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451138
  ensembl transcript: ENST00000557515
  gene symbol: ACIN1
  hgvsc: ENST00000557515.1:c.246G>C
  hgvsp: ENSP00000451138.1:p.Glu82Asp
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000473758
  gene symbol: ACIN1
  hgvsc: ENST00000473758.1:n.1492G>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000474349
  ensembl transcript: ENST00000605057
  gene symbol: ACIN1
  hgvsc: ENST00000605057.1:c.2349G>C
  hgvsp: ENSP00000474349.1:p.Glu783Asp
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000380502
  ensembl transcript: ENST00000397341
  gene symbol: ACIN1
  hgvsc: ENST00000397341.3:c.249G>C
  hgvsp: ENSP00000380502.3:p.Glu83Asp
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000556052
  gene symbol: ACIN1
  hgvsc: ENST00000556052.1:n.257G>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000405677
  ensembl transcript: ENST00000457657
  gene symbol: ACIN1
  hgvsc: ENST00000457657.1:c.2403G>C
  hgvsp: ENSP00000405677.1:p.Glu801Asp
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000554680
  gene symbol: ACIN1
  hgvsc: ENST00000554680.1:n.263G>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000350073
  ensembl transcript: ENST00000357481
  gene symbol: ACIN1
  hgvsc: ENST00000357481.2:c.249G>C
  hgvsp: ENSP00000350073.2:p.Glu83Asp
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000262710
  ensembl transcript: ENST00000262710
  gene symbol: ACIN1
  hgvsc: ENST00000262710.1:c.2523G>C
  hgvsp: ENSP00000262710.1:p.Glu841Asp
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000555807
  gene symbol: ACIN1
  hgvsc: ENST00000555807.1:n.569G>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000557039
  gene symbol: ACIN1
  hgvsc: ENST00000557039.1:n.399G>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000345541
  ensembl transcript: ENST00000338631
  gene symbol: ACIN1
  hgvsc: ENST00000338631.6:c.342G>C
  hgvsp: ENSP00000345541.6:p.Glu114Asp
  variant of: http://identifiers.org/hgnc/17066
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4557
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5927
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6003
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4315
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1175
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6777
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5107
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2532
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu841Asp
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
reference allele: C
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum

14-23533678-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23533678
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23533678
    reference: chr 14
allele count: 1
allele frequency: 8.248102936324645e-6
allele num: 121240
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451138
  ensembl transcript: ENST00000557515
  gene symbol: ACIN1
  hgvsc: ENST00000557515.1:c.225A>G
  hgvsp: ENST00000557515.1:c.225A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451328
  ensembl transcript: ENST00000555053
  gene symbol: ACIN1
  hgvsc: ENST00000555053.1:c.2499A>G
  hgvsp: ENST00000555053.1:c.2499A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000405677
  ensembl transcript: ENST00000457657
  gene symbol: ACIN1
  hgvsc: ENST00000457657.1:c.2382A>G
  hgvsp: ENST00000457657.1:c.2382A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000380502
  ensembl transcript: ENST00000397341
  gene symbol: ACIN1
  hgvsc: ENST00000397341.3:c.228A>G
  hgvsp: ENST00000397341.3:c.228A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451410
  ensembl transcript: ENST00000555566
  gene symbol: ACIN1
  hgvsc: ENST00000555566.1:c.228A>G
  hgvsp: ENST00000555566.1:c.228A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000262710
  ensembl transcript: ENST00000262710
  gene symbol: ACIN1
  hgvsc: ENST00000262710.1:c.2502A>G
  hgvsp: ENST00000262710.1:c.2502A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000555478
  gene symbol: ACIN1
  hgvsc: ENST00000555478.1:n.161A>G
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000350073
  ensembl transcript: ENST00000357481
  gene symbol: ACIN1
  hgvsc: ENST00000357481.2:c.228A>G
  hgvsp: ENST00000357481.2:c.228A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000554680
  gene symbol: ACIN1
  hgvsc: ENST00000554680.1:n.242A>G
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000474349
  ensembl transcript: ENST00000605057
  gene symbol: ACIN1
  hgvsc: ENST00000605057.1:c.2328A>G
  hgvsp: ENST00000605057.1:c.2328A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000556052
  gene symbol: ACIN1
  hgvsc: ENST00000556052.1:n.236A>G
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000473758
  gene symbol: ACIN1
  hgvsc: ENST00000473758.1:n.1471A>G
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000555807
  gene symbol: ACIN1
  hgvsc: ENST00000555807.1:n.548A>G
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000345541
  ensembl transcript: ENST00000338631
  gene symbol: ACIN1
  hgvsc: ENST00000338631.6:c.321A>G
  hgvsp: ENST00000338631.6:c.321A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000557039
  gene symbol: ACIN1
  hgvsc: ENST00000557039.1:n.378A>G
  variant of: http://identifiers.org/hgnc/17066
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6695
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 879
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3601
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6776
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6002
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5929
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2532
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5051
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro834Pro
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: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD

14-23533688-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23533688
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23533688
    reference: chr 14
allele count: 1
allele frequency: 8.261595148791329e-6
allele num: 121042
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451328
  ensembl transcript: ENST00000555053
  gene symbol: ACIN1
  hgvsc: ENST00000555053.1:c.2489A>G
  hgvsp: ENSP00000451328.1:p.Lys830Arg
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451410
  ensembl transcript: ENST00000555566
  gene symbol: ACIN1
  hgvsc: ENST00000555566.1:c.218A>G
  hgvsp: ENSP00000451410.1:p.Lys73Arg
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000350073
  ensembl transcript: ENST00000357481
  gene symbol: ACIN1
  hgvsc: ENST00000357481.2:c.218A>G
  hgvsp: ENSP00000350073.2:p.Lys73Arg
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000474349
  ensembl transcript: ENST00000605057
  gene symbol: ACIN1
  hgvsc: ENST00000605057.1:c.2318A>G
  hgvsp: ENSP00000474349.1:p.Lys773Arg
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000380502
  ensembl transcript: ENST00000397341
  gene symbol: ACIN1
  hgvsc: ENST00000397341.3:c.218A>G
  hgvsp: ENSP00000380502.3:p.Lys73Arg
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000555478
  gene symbol: ACIN1
  hgvsc: ENST00000555478.1:n.151A>G
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000262710
  ensembl transcript: ENST00000262710
  gene symbol: ACIN1
  hgvsc: ENST00000262710.1:c.2492A>G
  hgvsp: ENSP00000262710.1:p.Lys831Arg
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451138
  ensembl transcript: ENST00000557515
  gene symbol: ACIN1
  hgvsc: ENST00000557515.1:c.215A>G
  hgvsp: ENSP00000451138.1:p.Lys72Arg
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000557039
  gene symbol: ACIN1
  hgvsc: ENST00000557039.1:n.368A>G
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000345541
  ensembl transcript: ENST00000338631
  gene symbol: ACIN1
  hgvsc: ENST00000338631.6:c.311A>G
  hgvsp: ENSP00000345541.6:p.Lys104Arg
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000555807
  gene symbol: ACIN1
  hgvsc: ENST00000555807.1:n.538A>G
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000554680
  gene symbol: ACIN1
  hgvsc: ENST00000554680.1:n.232A>G
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000405677
  ensembl transcript: ENST00000457657
  gene symbol: ACIN1
  hgvsc: ENST00000457657.1:c.2372A>G
  hgvsp: ENSP00000405677.1:p.Lys791Arg
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000556052
  gene symbol: ACIN1
  hgvsc: ENST00000556052.1:n.226A>G
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000473758
  gene symbol: ACIN1
  hgvsc: ENST00000473758.1:n.1461A>G
  variant of: http://identifiers.org/hgnc/17066
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6777
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 879
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 608
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6694
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4014
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3601
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5929
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4904
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys831Arg
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: African
population: Latino
population: South Asian
reference allele: T
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD

http://identifiers.org/exac.variant/14-23533707-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23533707
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23533707
    reference: chr 14
allele count: 2
allele frequency: 1.658622348277521e-5
allele num: 120582
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000262710
  ensembl transcript: ENST00000262710
  gene symbol: ACIN1
  hgvsc: ENST00000262710.1:c.2483-10T>G
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000557039
  gene symbol: ACIN1
  hgvsc: ENST00000557039.1:n.359-10T>G
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000473758
  gene symbol: ACIN1
  hgvsc: ENST00000473758.1:n.1452-10T>G
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000405677
  ensembl transcript: ENST00000457657
  gene symbol: ACIN1
  hgvsc: ENST00000457657.1:c.2363-10T>G
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000554680
  gene symbol: ACIN1
  hgvsc: ENST00000554680.1:n.213T>G
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000555478
  gene symbol: ACIN1
  hgvsc: ENST00000555478.1:n.132T>G
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000555807
  gene symbol: ACIN1
  hgvsc: ENST00000555807.1:n.532-13T>G
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000474349
  ensembl transcript: ENST00000605057
  gene symbol: ACIN1
  hgvsc: ENST00000605057.1:c.2309-10T>G
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000556052
  gene symbol: ACIN1
  hgvsc: ENST00000556052.1:n.207T>G
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451410
  ensembl transcript: ENST00000555566
  gene symbol: ACIN1
  hgvsc: ENST00000555566.1:c.209-10T>G
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000345541
  ensembl transcript: ENST00000338631
  gene symbol: ACIN1
  hgvsc: ENST00000338631.6:c.302-10T>G
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000380502
  ensembl transcript: ENST00000397341
  gene symbol: ACIN1
  hgvsc: ENST00000397341.3:c.209-10T>G
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451328
  ensembl transcript: ENST00000555053
  gene symbol: ACIN1
  hgvsc: ENST00000555053.1:c.2483-13T>G
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451138
  ensembl transcript: ENST00000557515
  gene symbol: ACIN1
  hgvsc: ENST00000557515.1:c.209-13T>G
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000350073
  ensembl transcript: ENST00000357481
  gene symbol: ACIN1
  hgvsc: ENST00000357481.2:c.209-10T>G
  variant of: http://identifiers.org/hgnc/17066
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1761
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6693
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3546
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2531
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6001
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4245
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1175
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4904
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 608
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: QD
site quality: FS
site quality: ReadPosRankSum

14-23533713-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23533713
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23533713
    reference: chr 14
allele count: 34
allele frequency: 2.821904619623857e-4
allele num: 120486
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451328
  ensembl transcript: ENST00000555053
  gene symbol: ACIN1
  hgvsc: ENST00000555053.1:c.2483-19T>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000473758
  gene symbol: ACIN1
  hgvsc: ENST00000473758.1:n.1452-16T>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000554680
  gene symbol: ACIN1
  hgvsc: ENST00000554680.1:n.207T>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451410
  ensembl transcript: ENST00000555566
  gene symbol: ACIN1
  hgvsc: ENST00000555566.1:c.209-16T>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000405677
  ensembl transcript: ENST00000457657
  gene symbol: ACIN1
  hgvsc: ENST00000457657.1:c.2363-16T>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000555478
  gene symbol: ACIN1
  hgvsc: ENST00000555478.1:n.126T>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000474349
  ensembl transcript: ENST00000605057
  gene symbol: ACIN1
  hgvsc: ENST00000605057.1:c.2309-16T>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000380502
  ensembl transcript: ENST00000397341
  gene symbol: ACIN1
  hgvsc: ENST00000397341.3:c.209-16T>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451138
  ensembl transcript: ENST00000557515
  gene symbol: ACIN1
  hgvsc: ENST00000557515.1:c.209-19T>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000262710
  ensembl transcript: ENST00000262710
  gene symbol: ACIN1
  hgvsc: ENST00000262710.1:c.2483-16T>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000350073
  ensembl transcript: ENST00000357481
  gene symbol: ACIN1
  hgvsc: ENST00000357481.2:c.209-16T>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000555807
  gene symbol: ACIN1
  hgvsc: ENST00000555807.1:n.532-19T>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000556052
  gene symbol: ACIN1
  hgvsc: ENST00000556052.1:n.201T>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000345541
  ensembl transcript: ENST00000338631
  gene symbol: ACIN1
  hgvsc: ENST00000338631.6:c.302-16T>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000557039
  gene symbol: ACIN1
  hgvsc: ENST00000557039.1:n.359-16T>C
  variant of: http://identifiers.org/hgnc/17066
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1174
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1773
  bin: 9.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 4532
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1756
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6778
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6689
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6000
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4904
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3768
  bin: 3.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 3949
  bin: 2.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
num of homozygotes: 1
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
reference allele: A
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/14-23533716-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23533716
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23533716
    reference: chr 14
allele count: 1
allele frequency: 8.309650828472188e-6
allele num: 120342
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000380502
  ensembl transcript: ENST00000397341
  gene symbol: ACIN1
  hgvsc: ENST00000397341.3:c.209-19G>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000554680
  gene symbol: ACIN1
  hgvsc: ENST00000554680.1:n.204G>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000474349
  ensembl transcript: ENST00000605057
  gene symbol: ACIN1
  hgvsc: ENST00000605057.1:c.2309-19G>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000555807
  gene symbol: ACIN1
  hgvsc: ENST00000555807.1:n.532-22G>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000555478
  gene symbol: ACIN1
  hgvsc: ENST00000555478.1:n.123G>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000556052
  gene symbol: ACIN1
  hgvsc: ENST00000556052.1:n.198G>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000557039
  gene symbol: ACIN1
  hgvsc: ENST00000557039.1:n.359-19G>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000350073
  ensembl transcript: ENST00000357481
  gene symbol: ACIN1
  hgvsc: ENST00000357481.2:c.209-19G>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000262710
  ensembl transcript: ENST00000262710
  gene symbol: ACIN1
  hgvsc: ENST00000262710.1:c.2483-19G>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451328
  ensembl transcript: ENST00000555053
  gene symbol: ACIN1
  hgvsc: ENST00000555053.1:c.2483-22G>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000345541
  ensembl transcript: ENST00000338631
  gene symbol: ACIN1
  hgvsc: ENST00000338631.6:c.302-19G>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000405677
  ensembl transcript: ENST00000457657
  gene symbol: ACIN1
  hgvsc: ENST00000457657.1:c.2363-19G>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000473758
  gene symbol: ACIN1
  hgvsc: ENST00000473758.1:n.1452-19G>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451410
  ensembl transcript: ENST00000555566
  gene symbol: ACIN1
  hgvsc: ENST00000555566.1:c.209-19G>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451138
  ensembl transcript: ENST00000557515
  gene symbol: ACIN1
  hgvsc: ENST00000557515.1:c.209-22G>T
  variant of: http://identifiers.org/hgnc/17066
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1767
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4905
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1607
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 879
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3872
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1177
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6779
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3164
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5928
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: QD

14-23533718-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23533718
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23533718
    reference: chr 14
allele count: 7
allele frequency: 5.81781914893617e-5
allele num: 120320
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000405677
  ensembl transcript: ENST00000457657
  gene symbol: ACIN1
  hgvsc: ENST00000457657.1:c.2363-21G>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451328
  ensembl transcript: ENST00000555053
  gene symbol: ACIN1
  hgvsc: ENST00000555053.1:c.2483-24G>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000555478
  gene symbol: ACIN1
  hgvsc: ENST00000555478.1:n.121G>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000556052
  gene symbol: ACIN1
  hgvsc: ENST00000556052.1:n.196G>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000345541
  ensembl transcript: ENST00000338631
  gene symbol: ACIN1
  hgvsc: ENST00000338631.6:c.302-21G>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000555807
  gene symbol: ACIN1
  hgvsc: ENST00000555807.1:n.532-24G>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000380502
  ensembl transcript: ENST00000397341
  gene symbol: ACIN1
  hgvsc: ENST00000397341.3:c.209-21G>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000474349
  ensembl transcript: ENST00000605057
  gene symbol: ACIN1
  hgvsc: ENST00000605057.1:c.2309-21G>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451410
  ensembl transcript: ENST00000555566
  gene symbol: ACIN1
  hgvsc: ENST00000555566.1:c.209-21G>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000473758
  gene symbol: ACIN1
  hgvsc: ENST00000473758.1:n.1452-21G>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000554680
  gene symbol: ACIN1
  hgvsc: ENST00000554680.1:n.202G>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451138
  ensembl transcript: ENST00000557515
  gene symbol: ACIN1
  hgvsc: ENST00000557515.1:c.209-24G>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000262710
  ensembl transcript: ENST00000262710
  gene symbol: ACIN1
  hgvsc: ENST00000262710.1:c.2483-21G>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000557039
  gene symbol: ACIN1
  hgvsc: ENST00000557039.1:n.359-21G>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000350073
  ensembl transcript: ENST00000357481
  gene symbol: ACIN1
  hgvsc: ENST00000357481.2:c.209-21G>C
  variant of: http://identifiers.org/hgnc/17066
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1756
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3603
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 727
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6000
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1773
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 5923
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3801
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2531
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3746
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4530
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
population: African
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

14-23533720-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23533720
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23533720
    reference: chr 14
allele count: 1
allele frequency: 8.311308366163002e-6
allele num: 120318
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000473758
  gene symbol: ACIN1
  hgvsc: ENST00000473758.1:n.1452-23T>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000555478
  gene symbol: ACIN1
  hgvsc: ENST00000555478.1:n.119T>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000405677
  ensembl transcript: ENST00000457657
  gene symbol: ACIN1
  hgvsc: ENST00000457657.1:c.2363-23T>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000556052
  gene symbol: ACIN1
  hgvsc: ENST00000556052.1:n.194T>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000350073
  ensembl transcript: ENST00000357481
  gene symbol: ACIN1
  hgvsc: ENST00000357481.2:c.209-23T>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000345541
  ensembl transcript: ENST00000338631
  gene symbol: ACIN1
  hgvsc: ENST00000338631.6:c.302-23T>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000380502
  ensembl transcript: ENST00000397341
  gene symbol: ACIN1
  hgvsc: ENST00000397341.3:c.209-23T>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000474349
  ensembl transcript: ENST00000605057
  gene symbol: ACIN1
  hgvsc: ENST00000605057.1:c.2309-23T>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000555807
  gene symbol: ACIN1
  hgvsc: ENST00000555807.1:n.532-26T>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000262710
  ensembl transcript: ENST00000262710
  gene symbol: ACIN1
  hgvsc: ENST00000262710.1:c.2483-23T>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000554680
  gene symbol: ACIN1
  hgvsc: ENST00000554680.1:n.200T>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000557039
  gene symbol: ACIN1
  hgvsc: ENST00000557039.1:n.359-23T>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451328
  ensembl transcript: ENST00000555053
  gene symbol: ACIN1
  hgvsc: ENST00000555053.1:c.2483-26T>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451410
  ensembl transcript: ENST00000555566
  gene symbol: ACIN1
  hgvsc: ENST00000555566.1:c.209-23T>C
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451138
  ensembl transcript: ENST00000557515
  gene symbol: ACIN1
  hgvsc: ENST00000557515.1:c.209-26T>C
  variant of: http://identifiers.org/hgnc/17066
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1770
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1844
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2958
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3727
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3706
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6780
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 878
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6687
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2530
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4904
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3604
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD

14-23533723-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23533723
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 23533723
    reference: chr 14
allele count: 1
allele frequency: 8.316284949187499e-6
allele num: 120246
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000555807
  gene symbol: ACIN1
  hgvsc: ENST00000555807.1:n.532-29C>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000380502
  ensembl transcript: ENST00000397341
  gene symbol: ACIN1
  hgvsc: ENST00000397341.3:c.209-26C>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000554680
  gene symbol: ACIN1
  hgvsc: ENST00000554680.1:n.197C>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000405677
  ensembl transcript: ENST00000457657
  gene symbol: ACIN1
  hgvsc: ENST00000457657.1:c.2363-26C>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451410
  ensembl transcript: ENST00000555566
  gene symbol: ACIN1
  hgvsc: ENST00000555566.1:c.209-26C>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000474349
  ensembl transcript: ENST00000605057
  gene symbol: ACIN1
  hgvsc: ENST00000605057.1:c.2309-26C>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451138
  ensembl transcript: ENST00000557515
  gene symbol: ACIN1
  hgvsc: ENST00000557515.1:c.209-29C>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000555478
  gene symbol: ACIN1
  hgvsc: ENST00000555478.1:n.116C>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000345541
  ensembl transcript: ENST00000338631
  gene symbol: ACIN1
  hgvsc: ENST00000338631.6:c.302-26C>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000556052
  gene symbol: ACIN1
  hgvsc: ENST00000556052.1:n.191C>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000262710
  ensembl transcript: ENST00000262710
  gene symbol: ACIN1
  hgvsc: ENST00000262710.1:c.2483-26C>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000451328
  ensembl transcript: ENST00000555053
  gene symbol: ACIN1
  hgvsc: ENST00000555053.1:c.2483-29C>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl protein: ENSP00000350073
  ensembl transcript: ENST00000357481
  gene symbol: ACIN1
  hgvsc: ENST00000357481.2:c.209-26C>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000557039
  gene symbol: ACIN1
  hgvsc: ENST00000557039.1:n.359-26C>T
  variant of: http://identifiers.org/hgnc/17066
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100813
  ensembl transcript: ENST00000473758
  gene symbol: ACIN1
  hgvsc: ENST00000473758.1:n.1452-26C>T
  variant of: http://identifiers.org/hgnc/17066
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3563
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 608
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1966
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3711
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 878
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1756
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2818
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5921
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1178
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4524
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
reference allele: G

GenotypeDepth
all individuals: 1737
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3564
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3604
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 24
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 594
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6047
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2308
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5932
bin: 4.25e1
variant carriers: 1

GenotypeDepth
all individuals: 4522
bin: 3.75e1
variant carriers: 1

GenotypeDepth
all individuals: 1652
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1564
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 409
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1263
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3214
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 596
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 438
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 959
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 648
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45021
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 829
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1334
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 93
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 825
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 291
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1506
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 856
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 770
bin: 3.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10332
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.652015919709292e-5
allele num: 11558
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: 898
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66328
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.269592476489028e-5
allele num: 15950
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.306e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 3.03e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.26e-1

MQRankSum
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SIO_000300: 2.55e-1

FS
type: SiteQuality
SIO_000300: 1.151e0

DP
type: SiteQuality
SIO_000300: 3.015082e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.24e-1

BaseQRankSum
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SIO_000300: -3.47e0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11558
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 15980
num of homozygotes: 0

African
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allele count: 1
allele frequency: 9.676795045480937e-5
allele num: 10334
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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66340
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
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allele frequency: 0.0e0
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num of homozygotes: 0

BaseQRankSum
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SIO_000300: -3.616e0

FS
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QD
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ClippingRankSum
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ReadPosRankSum
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VQSLOD
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MQRankSum
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InbreedingCoeff
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SIO_000300: -1.0e-4

DP
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MQ
type: SiteQuality
SIO_000300: 5.972e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 898
num of homozygotes: 0

African
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allele count: 1
allele frequency: 9.676795045480937e-5
allele num: 10334
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8636
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

European (Non-Finnish)
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allele count: 2
allele frequency: 3.011957471160507e-5
allele num: 66402
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11558
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 7.58e-1

BaseQRankSum
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SIO_000300: 2.84e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.86e-1

DP
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SIO_000300: 3.028501e6

QD
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MQRankSum
type: SiteQuality
SIO_000300: 6.919999999999999e-1

InbreedingCoeff
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SIO_000300: 2.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 3.84e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.1e-2

MQ
type: SiteQuality
SIO_000300: 6.049e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 8636
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
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num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.506477854775535e-5
allele num: 66380
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11558
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

DP
type: SiteQuality
SIO_000300: 3.029488e6

MQRankSum
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InbreedingCoeff
type: SiteQuality
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QD
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ReadPosRankSum
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VQSLOD
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FS
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MQ
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SIO_000300: 5.487e1

ClippingRankSum
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SIO_000300: 2.01e0

BaseQRankSum
type: SiteQuality
SIO_000300: -9.76e-1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 count: 1
allele frequency: 9.671179883945841e-5
allele num: 10340
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66430
num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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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
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num of homozygotes: 0

FS
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DP
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ClippingRankSum
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ReadPosRankSum
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MQ
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VQSLOD
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QD
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BaseQRankSum
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MQRankSum
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InbreedingCoeff
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11560
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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allele frequency: 0.0e0
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European (Non-Finnish)
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allele num: 66430
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East Asian
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allele num: 8636
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South Asian
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MQ
type: SiteQuality
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ClippingRankSum
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QD
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InbreedingCoeff
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FS
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BaseQRankSum
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ReadPosRankSum
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MQRankSum
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VQSLOD
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DP
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 6610
num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
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East Asian
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allele count: 0
allele frequency: 0.0e0
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South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16240
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.504302304591131e-5
allele num: 66476
num of homozygotes: 0

InbreedingCoeff
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MQ
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MQRankSum
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FS
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VQSLOD
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DP
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ReadPosRankSum
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BaseQRankSum
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QD
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ClippingRankSum
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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African
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East Asian
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South Asian
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European (Non-Finnish)
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FS
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VQSLOD
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MQ
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QD
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BaseQRankSum
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InbreedingCoeff
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DP
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ReadPosRankSum
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MQRankSum
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ClippingRankSum
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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African
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European (Non-Finnish)
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South Asian
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Other
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East Asian
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InbreedingCoeff
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BaseQRankSum
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MQ
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ClippingRankSum
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ReadPosRankSum
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FS
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MQRankSum
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VQSLOD
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DP
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QD
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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European (Finnish)
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Latino
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Other
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African
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European (Non-Finnish)
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South Asian
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InbreedingCoeff
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FS
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MQ
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BaseQRankSum
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QD
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ClippingRankSum
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MQRankSum
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VQSLOD
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DP
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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European (Finnish)
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Latino
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European (Non-Finnish)
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African
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Other
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FS
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MQRankSum
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ClippingRankSum
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VQSLOD
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QD
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DP
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ReadPosRankSum
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InbreedingCoeff
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MQ
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BaseQRankSum
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GenotypeQuality
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East Asian
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European (Non-Finnish)
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African
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Other
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European (Finnish)
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Latino
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South Asian
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VQSLOD
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QD
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FS
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MQ
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ClippingRankSum
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MQRankSum
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BaseQRankSum
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InbreedingCoeff
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ReadPosRankSum
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DP
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GenotypeDepth
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GenotypeQuality
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East Asian
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MQ
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FS
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QD
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DP
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MQ
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VQSLOD
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MQRankSum
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InbreedingCoeff
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ClippingRankSum
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African
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DP
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VQSLOD
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FS
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InbreedingCoeff
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MQ
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African
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GenotypeQuality
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European (Finnish)
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Latino
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East Asian
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South Asian
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African
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European (Non-Finnish)
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QD
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MQRankSum
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DP
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BaseQRankSum
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MQ
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ReadPosRankSum
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InbreedingCoeff
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ClippingRankSum
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VQSLOD
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FS
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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African
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South Asian
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East Asian
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European (Finnish)
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VQSLOD
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BaseQRankSum
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ClippingRankSum
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DP
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QD
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MQ
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FS
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InbreedingCoeff
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MQRankSum
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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African
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European (Non-Finnish)
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Latino
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South Asian
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European (Finnish)
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InbreedingCoeff
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BaseQRankSum
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ClippingRankSum
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ReadPosRankSum
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FS
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MQRankSum
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MQ
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VQSLOD
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DP
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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European (Non-Finnish)
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East Asian
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European (Finnish)
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Latino
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African
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Other
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BaseQRankSum
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MQRankSum
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InbreedingCoeff
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MQ
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QD
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FS
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ClippingRankSum
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DP
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ReadPosRankSum
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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European (Finnish)
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European (Non-Finnish)
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African
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Latino
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East Asian
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MQRankSum
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BaseQRankSum
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QD
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MQ
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ReadPosRankSum
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VQSLOD
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FS
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ClippingRankSum
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DP
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InbreedingCoeff
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South Asian
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East Asian
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African
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European (Finnish)
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Latino
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European (Non-Finnish)
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FS
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MQRankSum
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MQ
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VQSLOD
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ReadPosRankSum
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DP
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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East Asian
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South Asian
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European (Non-Finnish)
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European (Finnish)
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Other
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VQSLOD
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DP
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BaseQRankSum
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FS
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QD
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InbreedingCoeff
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MQRankSum
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MQ
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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European (Finnish)
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European (Non-Finnish)
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African
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South Asian
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Latino
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DP
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MQRankSum
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MQ
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FS
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InbreedingCoeff
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ReadPosRankSum
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ClippingRankSum
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QD
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BaseQRankSum
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VQSLOD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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Latino
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European (Non-Finnish)
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European (Finnish)
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South Asian
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African
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InbreedingCoeff
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FS
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MQRankSum
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VQSLOD
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QD
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ReadPosRankSum
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DP
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BaseQRankSum
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ClippingRankSum
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MQ
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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European (Finnish)
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African
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Other
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European (Non-Finnish)
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South Asian
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DP
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MQ
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VQSLOD
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ClippingRankSum
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InbreedingCoeff
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FS
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QD
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ReadPosRankSum
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BaseQRankSum
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GenotypeDepth
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African
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East Asian
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Latino
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European (Finnish)
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European (Non-Finnish)
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BaseQRankSum
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FS
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QD
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VQSLOD
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InbreedingCoeff
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DP
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MQRankSum
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MQ
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ReadPosRankSum
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European (Finnish)
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Latino
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African
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East Asian
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South Asian
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ClippingRankSum
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VQSLOD
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SIO_000300: -7.185e-1

MQRankSum
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FS
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QD
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InbreedingCoeff
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SIO_000300: -1.0e-4

ReadPosRankSum
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SIO_000300: 7.39e-1

MQ
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SIO_000300: 6.0e1

BaseQRankSum
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele frequency: 0.0e0
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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 num: 10406
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East Asian
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European (Non-Finnish)
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allele frequency: 5.997181324777355e-5
allele num: 66698
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

Other
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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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QD
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BaseQRankSum
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FS
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MQ
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MQRankSum
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ReadPosRankSum
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VQSLOD
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InbreedingCoeff
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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num of homozygotes: 0

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

Latino
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allele frequency: 8.637070305752289e-5
allele num: 11578
num of homozygotes: 0

European (Non-Finnish)
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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
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Other
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allele frequency: 0.0e0
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VQSLOD
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SIO_000300: 9.76e-1

MQ
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SIO_000300: 5.95e1

DP
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InbreedingCoeff
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SIO_000300: 1.0e-4

BaseQRankSum
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QD
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MQRankSum
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FS
type: SiteQuality
SIO_000300: 5.4e-1

ReadPosRankSum
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SIO_000300: 8.88e-1

ClippingRankSum
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 1.499430216517723e-5
allele num: 66692
num of homozygotes: 0

European (Finnish)
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num of homozygotes: 0

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

South Asian
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African
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Other
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DP
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SIO_000300: 3.060529e6

ClippingRankSum
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InbreedingCoeff
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MQRankSum
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VQSLOD
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QD
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ReadPosRankSum
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FS
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MQ
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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num of homozygotes: 0

European (Non-Finnish)
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East Asian
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South Asian
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allele frequency: 0.0e0
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European (Finnish)
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African
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Other
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MQ
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ClippingRankSum
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BaseQRankSum
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DP
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FS
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MQRankSum
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QD
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InbreedingCoeff
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ReadPosRankSum
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VQSLOD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele num: 11576
num of homozygotes: 0

Other
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European (Non-Finnish)
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South Asian
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African
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European (Finnish)
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East Asian
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BaseQRankSum
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InbreedingCoeff
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MQRankSum
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FS
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ReadPosRankSum
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ClippingRankSum
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QD
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MQ
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VQSLOD
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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Latino
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South Asian
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European (Non-Finnish)
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East Asian
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European (Finnish)
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Other
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FS
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DP
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VQSLOD
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InbreedingCoeff
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ReadPosRankSum
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MQ
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ClippingRankSum
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MQRankSum
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QD
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BaseQRankSum
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele count: 3
allele frequency: 4.498155756139982e-5
allele num: 66694
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

ReadPosRankSum
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FS
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BaseQRankSum
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InbreedingCoeff
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QD
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ClippingRankSum
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VQSLOD
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MQRankSum
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DP
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MQ
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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South Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.499565126113427e-5
allele num: 66686
num of homozygotes: 0

East Asian
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ReadPosRankSum
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MQRankSum
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VQSLOD
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BaseQRankSum
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InbreedingCoeff
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FS
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ClippingRankSum
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QD
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DP
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MQ
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 frequency: 0.0e0
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num of homozygotes: 0

Other
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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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num of homozygotes: 0

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

European (Finnish)
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FS
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QD
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BaseQRankSum
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DP
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MQ
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VQSLOD
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InbreedingCoeff
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MQRankSum
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ClippingRankSum
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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European (Non-Finnish)
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South Asian
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East Asian
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African
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European (Finnish)
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ClippingRankSum
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MQRankSum
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FS
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DP
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BaseQRankSum
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InbreedingCoeff
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VQSLOD
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QD
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ReadPosRankSum
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MQ
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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South Asian
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European (Finnish)
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African
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East Asian
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Latino
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QD
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MQRankSum
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InbreedingCoeff
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FS
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VQSLOD
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ReadPosRankSum
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DP
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BaseQRankSum
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ClippingRankSum
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MQ
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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East Asian
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European (Non-Finnish)
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Latino
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African
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allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16454
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.391e0

MQRankSum
type: SiteQuality
SIO_000300: 3.24e-1

MQ
type: SiteQuality
SIO_000300: 5.952e1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 3.063539e6

ClippingRankSum
type: SiteQuality
SIO_000300: -3.8e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.65e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

QD
type: SiteQuality
SIO_000300: 1.225e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.26e-1

GenotypeDepth
all individuals: 160
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1734
bin: 7.75e1
variant carriers: 0

GenotypeDepth
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bin: 4.25e1
variant carriers: 1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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bin: 7.25e1
variant carriers: 3

GenotypeDepth
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variant carriers: 1

GenotypeDepth
all individuals: 4907
bin: 6.25e1
variant carriers: 1

GenotypeDepth
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variant carriers: 1

GenotypeDepth
all individuals: 6711
bin: 4.75e1
variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
all individuals: 6
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variant carriers: 0

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

GenotypeQuality
all individuals: 1799
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variant carriers: 1

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

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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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 137

GenotypeQuality
all individuals: 141
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1550
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 12
allele frequency: 1.036448436690275e-3
allele num: 11578
num of homozygotes: 0

African
type: Population
allele count: 124
allele frequency: 1.191620219104363e-2
allele num: 10406
num of homozygotes: 1

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499610101373643e-5
allele num: 66684
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 3
allele frequency: 1.822600243013366e-4
allele num: 16460
num of homozygotes: 1

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

MQRankSum
type: SiteQuality
SIO_000300: 3.84e-1

FS
type: SiteQuality
SIO_000300: 5.27e-1

MQ
type: SiteQuality
SIO_000300: 5.959e1

VQSLOD
type: SiteQuality
SIO_000300: 4.06e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.090000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.46e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -2.71e0

DP
type: SiteQuality
SIO_000300: 3.082376e6

QD
type: SiteQuality
SIO_000300: 1.412e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.75e-1

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

GenotypeDepth
all individuals: 1748
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
all individuals: 34
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variant carriers: 0

GenotypeQuality
all individuals: 879
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variant carriers: 0

GenotypeQuality
all individuals: 1
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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
all individuals: 41
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 993
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variant carriers: 0

GenotypeQuality
all individuals: 11
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 45049
bin: 9.75e1
variant carriers: 1

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.49934029027228e-5
allele num: 66696
num of homozygotes: 0

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

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

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

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

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: 16500
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.974e0

MQRankSum
type: SiteQuality
SIO_000300: 1.24e0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.56e-1

FS
type: SiteQuality
SIO_000300: 1.76e0

MQ
type: SiteQuality
SIO_000300: 5.965e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 3.069583e6

VQSLOD
type: SiteQuality
SIO_000300: 7.72e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.97e-1

QD
type: SiteQuality
SIO_000300: 1.228e1

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

GenotypeDepth
all individuals: 4907
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
all individuals: 6704
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variant carriers: 1

GenotypeQuality
all individuals: 30
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variant carriers: 0

GenotypeQuality
all individuals: 879
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 32
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variant carriers: 0

GenotypeQuality
all individuals: 45056
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variant carriers: 63

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
all individuals: 25
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variant carriers: 0

GenotypeQuality
all individuals: 1339
bin: 7.75e1
variant carriers: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
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: 61
allele frequency: 9.145975770660909e-4
allele num: 66696
num of homozygotes: 1

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

African
type: Population
allele count: 3
allele frequency: 2.882952142994427e-4
allele num: 10406
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 3.079952e6

QD
type: SiteQuality
SIO_000300: 1.334e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.46e0

MQRankSum
type: SiteQuality
SIO_000300: 1.23e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.29e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.52e-2

MQ
type: SiteQuality
SIO_000300: 5.952e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.01e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.85e0

GenotypeDepth
all individuals: 4349
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5073
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variant carriers: 0

GenotypeDepth
all individuals: 1168
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6778
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 25
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 10
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 994
bin: 8.75e1
variant carriers: 0

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

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

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

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

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

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

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

DP
type: SiteQuality
SIO_000300: 3.074094e6

ClippingRankSum
type: SiteQuality
SIO_000300: 8.2e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.806e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 1.03e0

VQSLOD
type: SiteQuality
SIO_000300: -4.875e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.21e0

FS
type: SiteQuality
SIO_000300: 1.741e0

BaseQRankSum
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SIO_000300: -1.277e0

GenotypeDepth
all individuals: 4055
bin: 3.25e1
variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
all individuals: 1740
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variant carriers: 1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
all individuals: 4
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
all individuals: 5105
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
all individuals: 15
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GenotypeDepth
all individuals: 875
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variant carriers: 0

GenotypeDepth
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GenotypeQuality
all individuals: 17
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GenotypeQuality
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GenotypeQuality
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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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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 2.75e1
variant carriers: 0

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

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

South Asian
type: Population
allele count: 2
allele frequency: 1.211240310077519e-4
allele num: 16512
num of homozygotes: 1

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

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

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

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

QD
type: SiteQuality
SIO_000300: 3.317e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.92e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.34e0

MQ
type: SiteQuality
SIO_000300: 5.915e1

DP
type: SiteQuality
SIO_000300: 3.074418e6

FS
type: SiteQuality
SIO_000300: 0.0e0

GenotypeDepth
all individuals: 5932
bin: 4.25e1
variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
all individuals: 6702
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
all individuals: 4056
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variant carriers: 0

GenotypeQuality
all individuals: 0
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 7
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variant carriers: 0

GenotypeQuality
all individuals: 0
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
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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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: 7.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 881
bin: 7.25e1
variant carriers: 0

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

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

East Asian
type: Population
allele count: 1
allele frequency: 1.155535012710885e-4
allele num: 8654
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Other
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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 frequency: 0.0e0
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num of homozygotes: 0

South Asian
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MQ
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MQRankSum
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ReadPosRankSum
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ClippingRankSum
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QD
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InbreedingCoeff
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BaseQRankSum
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DP
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FS
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VQSLOD
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

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

European (Finnish)
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num of homozygotes: 0

South Asian
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DP
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FS
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QD
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MQRankSum
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MQ
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InbreedingCoeff
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ClippingRankSum
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VQSLOD
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ReadPosRankSum
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 10404
num of homozygotes: 0

Other
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European (Non-Finnish)
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European (Finnish)
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East Asian
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Latino
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South Asian
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VQSLOD
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ReadPosRankSum
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FS
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ClippingRankSum
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MQRankSum
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DP
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InbreedingCoeff
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BaseQRankSum
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MQ
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QD
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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Other
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European (Non-Finnish)
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Latino
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European (Finnish)
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East Asian
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South Asian
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BaseQRankSum
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InbreedingCoeff
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MQRankSum
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FS
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DP
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ClippingRankSum
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ReadPosRankSum
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QD
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MQ
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VQSLOD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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African
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South Asian
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East Asian
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European (Finnish)
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European (Non-Finnish)
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Other
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FS
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InbreedingCoeff
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MQRankSum
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VQSLOD
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QD
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BaseQRankSum
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ClippingRankSum
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DP
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MQ
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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European (Finnish)
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South Asian
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European (Non-Finnish)
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Latino
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African
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ClippingRankSum
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QD
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VQSLOD
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FS
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InbreedingCoeff
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MQ
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MQRankSum
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ReadPosRankSum
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DP
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Latino
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African
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South Asian
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European (Non-Finnish)
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East Asian
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European (Finnish)
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Other
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VQSLOD
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QD
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DP
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FS
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BaseQRankSum
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MQRankSum
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InbreedingCoeff
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ReadPosRankSum
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ClippingRankSum
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MQ
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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South Asian
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Latino
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African
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European (Finnish)
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European (Non-Finnish)
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ClippingRankSum
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VQSLOD
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InbreedingCoeff
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BaseQRankSum
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MQ
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QD
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FS
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MQRankSum
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ReadPosRankSum
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DP
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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European (Finnish)
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Other
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African
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European (Non-Finnish)
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East Asian
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Latino
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VQSLOD
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MQ
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ReadPosRankSum
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ClippingRankSum
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FS
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DP
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InbreedingCoeff
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MQRankSum
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QD
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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European (Finnish)
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East Asian
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African
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Latino
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South Asian
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ReadPosRankSum
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MQ
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QD
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MQRankSum
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BaseQRankSum
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ClippingRankSum
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FS
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InbreedingCoeff
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DP
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VQSLOD
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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European (Finnish)
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African
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Latino
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South Asian
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ReadPosRankSum
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ClippingRankSum
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MQRankSum
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DP
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FS
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MQ
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QD
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BaseQRankSum
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InbreedingCoeff
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VQSLOD
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African
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South Asian
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VQSLOD
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MQ
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QD
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FS
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ReadPosRankSum
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African
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allele frequency: 8.638562543192812e-5
allele num: 11576
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.505434618974498e-5
allele num: 66426
num of homozygotes: 0

South Asian
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allele count: 32
allele frequency: 2.010555415933651e-3
allele num: 15916
num of homozygotes: 1

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

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

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

FS
type: SiteQuality
SIO_000300: 1.51e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.46e-2

VQSLOD
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SIO_000300: 2.69e0

DP
type: SiteQuality
SIO_000300: 3.0442e6

BaseQRankSum
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SIO_000300: -2.7e-2

MQRankSum
type: SiteQuality
SIO_000300: -4.1e-2

MQ
type: SiteQuality
SIO_000300: 5.974e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.88e-1

QD
type: SiteQuality
SIO_000300: 1.356e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.07e-1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

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

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

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

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele count: 1
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allele num: 8654
num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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South Asian
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allele frequency: 0.0e0
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MQRankSum
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SIO_000300: 2.35e-1

ReadPosRankSum
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VQSLOD
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FS
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SIO_000300: 1.0506e1

DP
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InbreedingCoeff
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SIO_000300: 3.2e-3

BaseQRankSum
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SIO_000300: -4.46e-1

ClippingRankSum
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SIO_000300: -9.87e-1

MQ
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SIO_000300: 5.972e1

QD
type: SiteQuality
SIO_000300: 1.967e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 7

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
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 7
allele frequency: 1.054788740883612e-4
allele num: 66364
num of homozygotes: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 15820
num of homozygotes: 0

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

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

Other
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allele count: 0
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num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.87e-1

DP
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SIO_000300: 3.038976e6

BaseQRankSum
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SIO_000300: -1.002e0

FS
type: SiteQuality
SIO_000300: 4.434e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.5e-3

QD
type: SiteQuality
SIO_000300: 1.238e1

MQ
type: SiteQuality
SIO_000300: 5.94e1

MQRankSum
type: SiteQuality
SIO_000300: -4.88e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.43e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.98e-1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

South Asian
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allele frequency: 0.0e0
allele num: 15816
num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
allele num: 8654
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 count: 1
allele frequency: 1.506750241080039e-5
allele num: 66368
num of homozygotes: 0

Other
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QD
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SIO_000300: 8.640000000000001e0

FS
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InbreedingCoeff
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MQ
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ClippingRankSum
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MQRankSum
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ReadPosRankSum
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BaseQRankSum
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DP
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VQSLOD
type: SiteQuality
SIO_000300: -1.834e-1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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