16-20552137-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20552137
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 20552137
    reference: chr 16
allele count: 1
allele frequency: 8.257092842751923e-6
allele num: 121108
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000454995
  ensembl transcript: ENST00000565232
  gene symbol: ACSM2B
  hgvsc: ENST00000565232.1:c.1510-42A>C
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000457377
  ensembl transcript: ENST00000565322
  gene symbol: ACSM2B
  hgvsc: ENST00000565322.1:c.1273-42A>C
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000327453
  ensembl transcript: ENST00000329697
  gene symbol: ACSM2B
  hgvsc: ENST00000329697.6:c.1510-42A>C
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000456378
  ensembl transcript: ENST00000567001
  gene symbol: ACSM2B
  hgvsc: ENST00000567001.1:c.1510-42A>C
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000564849
  gene symbol: ACSM2B
  hgvsc: ENST00000564849.1:n.502A>C
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000455137
  ensembl transcript: ENST00000568098
  gene symbol: ACSM2B
  hgvsc: ENST00000568098.1:c.117-51A>C
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000566998
  gene symbol: ACSM2B
  hgvsc: ENST00000566998.1:n.1705-42A>C
  variant of: http://identifiers.org/hgnc/30931
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2721
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 945
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1232
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3031
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 859
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1613
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3701
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1273
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1668
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3375
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2146
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 917
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34927
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1460
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 150
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 645
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54932
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 343
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 126
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
population: African
reference allele: T
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ

16-20552138-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20552138
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 20552138
    reference: chr 16
allele count: 2
allele frequency: 1.652073352056831e-5
allele num: 121060
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000327453
  ensembl transcript: ENST00000329697
  gene symbol: ACSM2B
  hgvsc: ENST00000329697.6:c.1510-43C>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000457377
  ensembl transcript: ENST00000565322
  gene symbol: ACSM2B
  hgvsc: ENST00000565322.1:c.1273-43C>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000456378
  ensembl transcript: ENST00000567001
  gene symbol: ACSM2B
  hgvsc: ENST00000567001.1:c.1510-43C>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000566998
  gene symbol: ACSM2B
  hgvsc: ENST00000566998.1:n.1705-43C>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000454995
  ensembl transcript: ENST00000565232
  gene symbol: ACSM2B
  hgvsc: ENST00000565232.1:c.1510-43C>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000455137
  ensembl transcript: ENST00000568098
  gene symbol: ACSM2B
  hgvsc: ENST00000568098.1:c.117-52C>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000564849
  gene symbol: ACSM2B
  hgvsc: ENST00000564849.1:n.501C>T
  variant of: http://identifiers.org/hgnc/30931
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1233
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 916
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 862
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 585
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1265
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3376
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2721
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3031
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1611
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1661
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 956
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3701
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34926
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2147
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54932
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 555
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 140
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 349
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 680
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 115
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
population: Other
population: African
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum

16-20552142-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20552142
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 20552142
    reference: chr 16
allele count: 1
allele frequency: 8.262687356435807e-6
allele num: 121026
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000454995
  ensembl transcript: ENST00000565232
  gene symbol: ACSM2B
  hgvsc: ENST00000565232.1:c.1510-47A>G
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000566998
  gene symbol: ACSM2B
  hgvsc: ENST00000566998.1:n.1705-47A>G
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000457377
  ensembl transcript: ENST00000565322
  gene symbol: ACSM2B
  hgvsc: ENST00000565322.1:c.1273-47A>G
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000456378
  ensembl transcript: ENST00000567001
  gene symbol: ACSM2B
  hgvsc: ENST00000567001.1:c.1510-47A>G
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000327453
  ensembl transcript: ENST00000329697
  gene symbol: ACSM2B
  hgvsc: ENST00000329697.6:c.1510-47A>G
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000564849
  gene symbol: ACSM2B
  hgvsc: ENST00000564849.1:n.497A>G
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000455137
  ensembl transcript: ENST00000568098
  gene symbol: ACSM2B
  hgvsc: ENST00000568098.1:c.117-56A>G
  variant of: http://identifiers.org/hgnc/30931
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1282
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3376
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1007
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2145
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 855
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34925
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3031
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1611
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 585
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2722
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3701
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1235
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 916
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1641
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 246
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 670
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 342
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 523
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 135
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 734
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 583
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD

16-20552144-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20552144
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 20552144
    reference: chr 16
allele count: 1
allele frequency: 8.270888127967181e-6
allele num: 120906
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000566998
  gene symbol: ACSM2B
  hgvsc: ENST00000566998.1:n.1705-49T>C
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000455137
  ensembl transcript: ENST00000568098
  gene symbol: ACSM2B
  hgvsc: ENST00000568098.1:c.117-58T>C
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000454995
  ensembl transcript: ENST00000565232
  gene symbol: ACSM2B
  hgvsc: ENST00000565232.1:c.1510-49T>C
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000564849
  gene symbol: ACSM2B
  hgvsc: ENST00000564849.1:n.495T>C
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000456378
  ensembl transcript: ENST00000567001
  gene symbol: ACSM2B
  hgvsc: ENST00000567001.1:c.1510-49T>C
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000457377
  ensembl transcript: ENST00000565322
  gene symbol: ACSM2B
  hgvsc: ENST00000565322.1:c.1273-49T>C
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000327453
  ensembl transcript: ENST00000329697
  gene symbol: ACSM2B
  hgvsc: ENST00000329697.6:c.1510-49T>C
  variant of: http://identifiers.org/hgnc/30931
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 585
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1633
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1409
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1611
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 916
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1235
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3031
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 845
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3701
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34925
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2722
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2145
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3376
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 933
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 145
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 402
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54933
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 676
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 459
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 157
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 525
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 339
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: DP
site quality: BaseQRankSum

http://identifiers.org/exac.variant/16-20552146-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20552146
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 20552146
    reference: chr 16
allele count: 70
allele frequency: 5.789334391954479e-4
allele num: 120912
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000566998
  gene symbol: ACSM2B
  hgvsc: ENST00000566998.1:n.1705-51G>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000564849
  gene symbol: ACSM2B
  hgvsc: ENST00000564849.1:n.493G>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000457377
  ensembl transcript: ENST00000565322
  gene symbol: ACSM2B
  hgvsc: ENST00000565322.1:c.1273-51G>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000455137
  ensembl transcript: ENST00000568098
  gene symbol: ACSM2B
  hgvsc: ENST00000568098.1:c.117-60G>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000327453
  ensembl transcript: ENST00000329697
  gene symbol: ACSM2B
  hgvsc: ENST00000329697.6:c.1510-51G>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000454995
  ensembl transcript: ENST00000565232
  gene symbol: ACSM2B
  hgvsc: ENST00000565232.1:c.1510-51G>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000456378
  ensembl transcript: ENST00000567001
  gene symbol: ACSM2B
  hgvsc: ENST00000567001.1:c.1510-51G>T
  variant of: http://identifiers.org/hgnc/30931
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1236
  bin: 6.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 846
  bin: 1.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3701
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1409
  bin: 2.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1630
  bin: 1.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3375
  bin: 8.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 1610
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2146
  bin: 7.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 2721
  bin: 7.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 585
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 938
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34925
  bin: 9.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 916
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3032
  bin: 8.25e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 676
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 737
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 145
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 506
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54952
  bin: 9.75e1
  variant carriers: 70
genotype quality: GenotypeQuality
  all individuals: 95
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 127
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 116
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 334
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: Latino
reference allele: C
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ

16-20552147-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20552147
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 20552147
    reference: chr 16
allele count: 9
allele frequency: 7.444538190480918e-5
allele num: 120894
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000327453
  ensembl transcript: ENST00000329697
  gene symbol: ACSM2B
  hgvsc: ENST00000329697.6:c.1510-52A>G
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000455137
  ensembl transcript: ENST00000568098
  gene symbol: ACSM2B
  hgvsc: ENST00000568098.1:c.117-61A>G
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000457377
  ensembl transcript: ENST00000565322
  gene symbol: ACSM2B
  hgvsc: ENST00000565322.1:c.1273-52A>G
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000454995
  ensembl transcript: ENST00000565232
  gene symbol: ACSM2B
  hgvsc: ENST00000565232.1:c.1510-52A>G
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000564849
  gene symbol: ACSM2B
  hgvsc: ENST00000564849.1:n.492A>G
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000566998
  gene symbol: ACSM2B
  hgvsc: ENST00000566998.1:n.1705-52A>G
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000456378
  ensembl transcript: ENST00000567001
  gene symbol: ACSM2B
  hgvsc: ENST00000567001.1:c.1510-52A>G
  variant of: http://identifiers.org/hgnc/30931
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1235
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3703
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 943
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1611
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3031
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3375
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1411
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2145
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2722
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34925
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 916
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 849
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1627
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 520
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 454
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 608
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 744
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 211
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 129
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: T
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQ

16-20554172-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20554172
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 20554172
    reference: chr 16
allele count: 356
allele frequency: 3.645598656453529e-3
allele num: 97652
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000327453
  ensembl transcript: ENST00000329697
  gene symbol: ACSM2B
  hgvsc: ENST00000329697.6:c.1509+64G>A
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000566998
  gene symbol: ACSM2B
  hgvsc: ENST00000566998.1:n.1704+64G>A
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000569364
  gene symbol: ACSM2B
  hgvsc: ENST00000569364.1:n.1748G>A
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000457377
  ensembl transcript: ENST00000565322
  gene symbol: ACSM2B
  hgvsc: ENST00000565322.1:c.1272+64G>A
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000563943
  gene symbol: ACSM2B
  hgvsc: ENST00000563943.1:n.1502G>A
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000456378
  ensembl transcript: ENST00000567001
  gene symbol: ACSM2B
  hgvsc: ENST00000567001.1:c.1509+64G>A
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000569131
  gene symbol: ACSM2B
  hgvsc: ENST00000569131.1:n.1317G>A
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000454995
  ensembl transcript: ENST00000565232
  gene symbol: ACSM2B
  hgvsc: ENST00000565232.1:c.1509+64G>A
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000455137
  ensembl transcript: ENST00000568098
  gene symbol: ACSM2B
  hgvsc: ENST00000568098.1:c.116+311G>A
  variant of: http://identifiers.org/hgnc/30931
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1018
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 5.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 4.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18672
  bin: 1.25e1
  variant carriers: 50
genotype depth: GenotypeDepth
  all individuals: 9012
  bin: 7.5e0
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 10338
  bin: 2.25e1
  variant carriers: 65
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 4.75e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 5.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 788
  bin: 3.75e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 13200
  bin: 1.75e1
  variant carriers: 66
genotype depth: GenotypeDepth
  all individuals: 1421
  bin: 3.25e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 3265
  bin: 2.75e1
  variant carriers: 46
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 7.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 9.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 9.75e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 6.25e1
  variant carriers: 9
genotype quality: GenotypeQuality
  all individuals: 6796
  bin: 2.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 2600
  bin: 6.75e1
  variant carriers: 12
genotype quality: GenotypeQuality
  all individuals: 7425
  bin: 6.25e1
  variant carriers: 9
genotype quality: GenotypeQuality
  all individuals: 3775
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3741
  bin: 4.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 1153
  bin: 7.75e1
  variant carriers: 10
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: DP

16-20554175-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20554175
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 20554175
    reference: chr 16
allele count: 353
allele frequency: 3.58615925391633e-3
allele num: 98434
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000456378
  ensembl transcript: ENST00000567001
  gene symbol: ACSM2B
  hgvsc: ENST00000567001.1:c.1509+61A>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000454995
  ensembl transcript: ENST00000565232
  gene symbol: ACSM2B
  hgvsc: ENST00000565232.1:c.1509+61A>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000569131
  gene symbol: ACSM2B
  hgvsc: ENST00000569131.1:n.1314A>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000457377
  ensembl transcript: ENST00000565322
  gene symbol: ACSM2B
  hgvsc: ENST00000565322.1:c.1272+61A>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000327453
  ensembl transcript: ENST00000329697
  gene symbol: ACSM2B
  hgvsc: ENST00000329697.6:c.1509+61A>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000455137
  ensembl transcript: ENST00000568098
  gene symbol: ACSM2B
  hgvsc: ENST00000568098.1:c.116+308A>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000563943
  gene symbol: ACSM2B
  hgvsc: ENST00000563943.1:n.1499A>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000569364
  gene symbol: ACSM2B
  hgvsc: ENST00000569364.1:n.1745A>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000566998
  gene symbol: ACSM2B
  hgvsc: ENST00000566998.1:n.1704+61A>T
  variant of: http://identifiers.org/hgnc/30931
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 4.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 13750
  bin: 2.25e1
  variant carriers: 59
genotype depth: GenotypeDepth
  all individuals: 896
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 5.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 4.75e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 798
  bin: 3.75e1
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 9.75e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 5.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 3452
  bin: 2.75e1
  variant carriers: 45
genotype depth: GenotypeDepth
  all individuals: 8968
  bin: 7.5e0
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 10016
  bin: 1.75e1
  variant carriers: 71
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 6.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 6.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 9.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1554
  bin: 3.25e1
  variant carriers: 34
genotype depth: GenotypeDepth
  all individuals: 18253
  bin: 1.25e1
  variant carriers: 31
genotype quality: GenotypeQuality
  all individuals: 819
  bin: 8.25e1
  variant carriers: 12
genotype quality: GenotypeQuality
  all individuals: 4931
  bin: 4.75e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 7170
  bin: 3.25e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 255
  bin: 5.75e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 7298
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3535
  bin: 4.25e1
  variant carriers: 3
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
population: African
reference allele: T
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD

16-20554190-CT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20554190
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 20554189
    reference: chr 16
allele count: 2
allele frequency: 1.887575974932991e-5
allele num: 105956
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000569364
  gene symbol: ACSM2B
  hgvsc: ENST00000569364.1:n.1729delA
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000569131
  gene symbol: ACSM2B
  hgvsc: ENST00000569131.1:n.1298delA
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000563943
  gene symbol: ACSM2B
  hgvsc: ENST00000563943.1:n.1483delA
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000327453
  ensembl transcript: ENST00000329697
  gene symbol: ACSM2B
  hgvsc: ENST00000329697.6:c.1509+45delA
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000457377
  ensembl transcript: ENST00000565322
  gene symbol: ACSM2B
  hgvsc: ENST00000565322.1:c.1272+45delA
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000454995
  ensembl transcript: ENST00000565232
  gene symbol: ACSM2B
  hgvsc: ENST00000565232.1:c.1509+45delA
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000456378
  ensembl transcript: ENST00000567001
  gene symbol: ACSM2B
  hgvsc: ENST00000567001.1:c.1509+45delA
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000455137
  ensembl transcript: ENST00000568098
  gene symbol: ACSM2B
  hgvsc: ENST00000568098.1:c.116+292delA
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000566998
  gene symbol: ACSM2B
  hgvsc: ENST00000566998.1:n.1704+45delA
  variant of: http://identifiers.org/hgnc/30931
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7303
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5447
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34273
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 820
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1079
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2275
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6240
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 606
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1636
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 511
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 491
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1325
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 197
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
reference allele: CT
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum

16-20554195-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20554195
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 20554195
    reference: chr 16
allele count: 2
allele frequency: 1.831434745980001e-5
allele num: 109204
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000456378
  ensembl transcript: ENST00000567001
  gene symbol: ACSM2B
  hgvsc: ENST00000567001.1:c.1509+41C>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000569364
  gene symbol: ACSM2B
  hgvsc: ENST00000569364.1:n.1725C>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000454995
  ensembl transcript: ENST00000565232
  gene symbol: ACSM2B
  hgvsc: ENST00000565232.1:c.1509+41C>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000457377
  ensembl transcript: ENST00000565322
  gene symbol: ACSM2B
  hgvsc: ENST00000565322.1:c.1272+41C>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000327453
  ensembl transcript: ENST00000329697
  gene symbol: ACSM2B
  hgvsc: ENST00000329697.6:c.1509+41C>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000569131
  gene symbol: ACSM2B
  hgvsc: ENST00000569131.1:n.1294C>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000563943
  gene symbol: ACSM2B
  hgvsc: ENST00000563943.1:n.1479C>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000566998
  gene symbol: ACSM2B
  hgvsc: ENST00000566998.1:n.1704+41C>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000455137
  ensembl transcript: ENST00000568098
  gene symbol: ACSM2B
  hgvsc: ENST00000568098.1:c.116+288C>T
  variant of: http://identifiers.org/hgnc/30931
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 37260
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5818
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3891
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2652
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6298
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 848
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 747
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 606
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5314
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 646
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1524
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1032
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5528
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum

16-20554195-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20554195
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 20554195
    reference: chr 16
allele count: 1
allele frequency: 9.157173729900004e-6
allele num: 109204
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000327453
  ensembl transcript: ENST00000329697
  gene symbol: ACSM2B
  hgvsc: ENST00000329697.6:c.1509+41C>G
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000563943
  gene symbol: ACSM2B
  hgvsc: ENST00000563943.1:n.1479C>G
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000569364
  gene symbol: ACSM2B
  hgvsc: ENST00000569364.1:n.1725C>G
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000454995
  ensembl transcript: ENST00000565232
  gene symbol: ACSM2B
  hgvsc: ENST00000565232.1:c.1509+41C>G
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000457377
  ensembl transcript: ENST00000565322
  gene symbol: ACSM2B
  hgvsc: ENST00000565322.1:c.1272+41C>G
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000569131
  gene symbol: ACSM2B
  hgvsc: ENST00000569131.1:n.1294C>G
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000455137
  ensembl transcript: ENST00000568098
  gene symbol: ACSM2B
  hgvsc: ENST00000568098.1:c.116+288C>G
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000566998
  gene symbol: ACSM2B
  hgvsc: ENST00000566998.1:n.1704+41C>G
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000456378
  ensembl transcript: ENST00000567001
  gene symbol: ACSM2B
  hgvsc: ENST00000567001.1:c.1509+41C>G
  variant of: http://identifiers.org/hgnc/30931
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37260
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5818
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 848
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 747
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 606
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3891
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6298
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2652
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3602
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2280
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5314
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1499
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 639
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
population: Other
population: African
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: DP

16-20554203-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20554203
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 20554203
    reference: chr 16
allele count: 57
allele frequency: 5.000087720837208e-4
allele num: 113998
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000455137
  ensembl transcript: ENST00000568098
  gene symbol: ACSM2B
  hgvsc: ENST00000568098.1:c.116+280G>C
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000457377
  ensembl transcript: ENST00000565322
  gene symbol: ACSM2B
  hgvsc: ENST00000565322.1:c.1272+33G>C
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000569131
  gene symbol: ACSM2B
  hgvsc: ENST00000569131.1:n.1286G>C
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000563943
  gene symbol: ACSM2B
  hgvsc: ENST00000563943.1:n.1471G>C
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000569364
  gene symbol: ACSM2B
  hgvsc: ENST00000569364.1:n.1717G>C
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000454995
  ensembl transcript: ENST00000565232
  gene symbol: ACSM2B
  hgvsc: ENST00000565232.1:c.1509+33G>C
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000456378
  ensembl transcript: ENST00000567001
  gene symbol: ACSM2B
  hgvsc: ENST00000567001.1:c.1509+33G>C
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000327453
  ensembl transcript: ENST00000329697
  gene symbol: ACSM2B
  hgvsc: ENST00000329697.6:c.1509+33G>C
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000566998
  gene symbol: ACSM2B
  hgvsc: ENST00000566998.1:n.1704+33G>C
  variant of: http://identifiers.org/hgnc/30931
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 7173
  bin: 2.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41069
  bin: 2.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3076
  bin: 3.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1526
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3391
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 1.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 620
  bin: 9.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 894
  bin: 3.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 5.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 3273
  bin: 2.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 173
  bin: 4.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 2102
  bin: 7.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 1720
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 7.5e0
  variant carriers: 2
num of homozygotes: 2
population: South Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum

16-20554214-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20554214
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 20554214
    reference: chr 16
allele count: 3
allele frequency: 2.574444349094654e-5
allele num: 116530
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000454995
  ensembl transcript: ENST00000565232
  gene symbol: ACSM2B
  hgvsc: ENST00000565232.1:c.1509+22G>A
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000569364
  gene symbol: ACSM2B
  hgvsc: ENST00000569364.1:n.1706G>A
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000327453
  ensembl transcript: ENST00000329697
  gene symbol: ACSM2B
  hgvsc: ENST00000329697.6:c.1509+22G>A
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000456378
  ensembl transcript: ENST00000567001
  gene symbol: ACSM2B
  hgvsc: ENST00000567001.1:c.1509+22G>A
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000455137
  ensembl transcript: ENST00000568098
  gene symbol: ACSM2B
  hgvsc: ENST00000568098.1:c.116+269G>A
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000569131
  gene symbol: ACSM2B
  hgvsc: ENST00000569131.1:n.1275G>A
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000457377
  ensembl transcript: ENST00000565322
  gene symbol: ACSM2B
  hgvsc: ENST00000565322.1:c.1272+22G>A
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000563943
  gene symbol: ACSM2B
  hgvsc: ENST00000563943.1:n.1460G>A
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000566998
  gene symbol: ACSM2B
  hgvsc: ENST00000566998.1:n.1704+22G>A
  variant of: http://identifiers.org/hgnc/30931
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2318
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3742
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 968
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40731
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8314
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 965
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 620
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 262
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 286
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3798
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 172
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 402
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: Other
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: C
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: VQSLOD

16-20554217-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20554217
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 20554217
    reference: chr 16
allele count: 2
allele frequency: 1.7080877957127e-5
allele num: 117090
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000454995
  ensembl transcript: ENST00000565232
  gene symbol: ACSM2B
  hgvsc: ENST00000565232.1:c.1509+19C>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000569364
  gene symbol: ACSM2B
  hgvsc: ENST00000569364.1:n.1703C>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000569131
  gene symbol: ACSM2B
  hgvsc: ENST00000569131.1:n.1272C>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000456378
  ensembl transcript: ENST00000567001
  gene symbol: ACSM2B
  hgvsc: ENST00000567001.1:c.1509+19C>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000455137
  ensembl transcript: ENST00000568098
  gene symbol: ACSM2B
  hgvsc: ENST00000568098.1:c.116+266C>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000566998
  gene symbol: ACSM2B
  hgvsc: ENST00000566998.1:n.1704+19C>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000457377
  ensembl transcript: ENST00000565322
  gene symbol: ACSM2B
  hgvsc: ENST00000565322.1:c.1272+19C>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000563943
  gene symbol: ACSM2B
  hgvsc: ENST00000563943.1:n.1457C>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000327453
  ensembl transcript: ENST00000329697
  gene symbol: ACSM2B
  hgvsc: ENST00000329697.6:c.1509+19C>T
  variant of: http://identifiers.org/hgnc/30931
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 40753
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3874
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8515
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 874
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2050
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 620
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 972
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 423
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 245
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 257
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 148
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
reference allele: G
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD

16-20554217-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20554217
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 20554217
    reference: chr 16
allele count: 2
allele frequency: 1.7080877957127e-5
allele num: 117090
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000566998
  gene symbol: ACSM2B
  hgvsc: ENST00000566998.1:n.1704+19C>A
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000327453
  ensembl transcript: ENST00000329697
  gene symbol: ACSM2B
  hgvsc: ENST00000329697.6:c.1509+19C>A
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000563943
  gene symbol: ACSM2B
  hgvsc: ENST00000563943.1:n.1457C>A
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000455137
  ensembl transcript: ENST00000568098
  gene symbol: ACSM2B
  hgvsc: ENST00000568098.1:c.116+266C>A
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000569364
  gene symbol: ACSM2B
  hgvsc: ENST00000569364.1:n.1703C>A
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000569131
  gene symbol: ACSM2B
  hgvsc: ENST00000569131.1:n.1272C>A
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000456378
  ensembl transcript: ENST00000567001
  gene symbol: ACSM2B
  hgvsc: ENST00000567001.1:c.1509+19C>A
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000457377
  ensembl transcript: ENST00000565322
  gene symbol: ACSM2B
  hgvsc: ENST00000565322.1:c.1272+19C>A
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000454995
  ensembl transcript: ENST00000565232
  gene symbol: ACSM2B
  hgvsc: ENST00000565232.1:c.1509+19C>A
  variant of: http://identifiers.org/hgnc/30931
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 8515
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3874
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2050
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 874
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40753
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 972
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 620
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3816
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 423
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2064
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6536
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: African
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: DP

16-20554221-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20554221
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 20554221
    reference: chr 16
allele count: 1
allele frequency: 8.472565831836514e-6
allele num: 118028
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000569364
  gene symbol: ACSM2B
  hgvsc: ENST00000569364.1:n.1699G>C
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000569131
  gene symbol: ACSM2B
  hgvsc: ENST00000569131.1:n.1268G>C
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000457377
  ensembl transcript: ENST00000565322
  gene symbol: ACSM2B
  hgvsc: ENST00000565322.1:c.1272+15G>C
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000563943
  gene symbol: ACSM2B
  hgvsc: ENST00000563943.1:n.1453G>C
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000455137
  ensembl transcript: ENST00000568098
  gene symbol: ACSM2B
  hgvsc: ENST00000568098.1:c.116+262G>C
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000456378
  ensembl transcript: ENST00000567001
  gene symbol: ACSM2B
  hgvsc: ENST00000567001.1:c.1509+15G>C
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000327453
  ensembl transcript: ENST00000329697
  gene symbol: ACSM2B
  hgvsc: ENST00000329697.6:c.1509+15G>C
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000566998
  gene symbol: ACSM2B
  hgvsc: ENST00000566998.1:n.1704+15G>C
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000454995
  ensembl transcript: ENST00000565232
  gene symbol: ACSM2B
  hgvsc: ENST00000565232.1:c.1509+15G>C
  variant of: http://identifiers.org/hgnc/30931
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1630
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 983
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40961
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8842
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4048
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 620
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1650
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 135
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 200
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3160
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
reference allele: C
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum

16-20554224-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20554224
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 20554224
    reference: chr 16
allele count: 1
allele frequency: 8.41779184484326e-6
allele num: 118796
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000566998
  gene symbol: ACSM2B
  hgvsc: ENST00000566998.1:n.1704+12G>A
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000569131
  gene symbol: ACSM2B
  hgvsc: ENST00000569131.1:n.1265G>A
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000456378
  ensembl transcript: ENST00000567001
  gene symbol: ACSM2B
  hgvsc: ENST00000567001.1:c.1509+12G>A
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000563943
  gene symbol: ACSM2B
  hgvsc: ENST00000563943.1:n.1450G>A
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000457377
  ensembl transcript: ENST00000565322
  gene symbol: ACSM2B
  hgvsc: ENST00000565322.1:c.1272+12G>A
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000327453
  ensembl transcript: ENST00000329697
  gene symbol: ACSM2B
  hgvsc: ENST00000329697.6:c.1509+12G>A
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000569364
  gene symbol: ACSM2B
  hgvsc: ENST00000569364.1:n.1696G>A
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000454995
  ensembl transcript: ENST00000565232
  gene symbol: ACSM2B
  hgvsc: ENST00000565232.1:c.1509+12G>A
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000455137
  ensembl transcript: ENST00000568098
  gene symbol: ACSM2B
  hgvsc: ENST00000568098.1:c.116+259G>A
  variant of: http://identifiers.org/hgnc/30931
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1002
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1258
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41233
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4214
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9048
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 620
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2543
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3868
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 155
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 276
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3222
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: MQ

16-20554226-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20554226
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 20554226
    reference: chr 16
allele count: 1
allele frequency: 8.382370198997468e-6
allele num: 119298
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000455137
  ensembl transcript: ENST00000568098
  gene symbol: ACSM2B
  hgvsc: ENST00000568098.1:c.116+257A>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000563943
  gene symbol: ACSM2B
  hgvsc: ENST00000563943.1:n.1448A>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000454995
  ensembl transcript: ENST00000565232
  gene symbol: ACSM2B
  hgvsc: ENST00000565232.1:c.1509+10A>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000569131
  gene symbol: ACSM2B
  hgvsc: ENST00000569131.1:n.1263A>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000569364
  gene symbol: ACSM2B
  hgvsc: ENST00000569364.1:n.1694A>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000327453
  ensembl transcript: ENST00000329697
  gene symbol: ACSM2B
  hgvsc: ENST00000329697.6:c.1509+10A>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000456378
  ensembl transcript: ENST00000567001
  gene symbol: ACSM2B
  hgvsc: ENST00000567001.1:c.1509+10A>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000566998
  gene symbol: ACSM2B
  hgvsc: ENST00000566998.1:n.1704+10A>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000457377
  ensembl transcript: ENST00000565322
  gene symbol: ACSM2B
  hgvsc: ENST00000565322.1:c.1272+10A>T
  variant of: http://identifiers.org/hgnc/30931
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1024
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41506
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4255
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9133
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1006
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 620
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 184
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1055
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3256
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
reference allele: T
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum

16-20554229-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20554229
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 20554229
    reference: chr 16
allele count: 26
allele frequency: 2.171516386596733e-4
allele num: 119732
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000456378
  ensembl transcript: ENST00000567001
  gene symbol: ACSM2B
  hgvsc: ENST00000567001.1:c.1509+7G>A
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000327453
  ensembl transcript: ENST00000329697
  gene symbol: ACSM2B
  hgvsc: ENST00000329697.6:c.1509+7G>A
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000455137
  ensembl transcript: ENST00000568098
  gene symbol: ACSM2B
  hgvsc: ENST00000568098.1:c.116+254G>A
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000569364
  gene symbol: ACSM2B
  hgvsc: ENST00000569364.1:n.1691G>A
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000566998
  gene symbol: ACSM2B
  hgvsc: ENST00000566998.1:n.1704+7G>A
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000569131
  gene symbol: ACSM2B
  hgvsc: ENST00000569131.1:n.1260G>A
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000457377
  ensembl transcript: ENST00000565322
  gene symbol: ACSM2B
  hgvsc: ENST00000565322.1:c.1272+7G>A
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000454995
  ensembl transcript: ENST00000565232
  gene symbol: ACSM2B
  hgvsc: ENST00000565232.1:c.1509+7G>A
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000563943
  gene symbol: ACSM2B
  hgvsc: ENST00000563943.1:n.1445G>A
  variant of: http://identifiers.org/hgnc/30931
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41484
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9321
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 4.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 802
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 620
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4375
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1034
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 845
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6909
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2586
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
hgvs: c.1509+7G>A
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
population: South Asian
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: QD

16-20554230-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20554230
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 20554230
    reference: chr 16
allele count: 2
allele frequency: 1.668557698725222e-5
allele num: 119864
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000563943
  gene symbol: ACSM2B
  hgvsc: ENST00000563943.1:n.1444G>A
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000454995
  ensembl transcript: ENST00000565232
  gene symbol: ACSM2B
  hgvsc: ENST00000565232.1:c.1509+6G>A
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000456378
  ensembl transcript: ENST00000567001
  gene symbol: ACSM2B
  hgvsc: ENST00000567001.1:c.1509+6G>A
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000327453
  ensembl transcript: ENST00000329697
  gene symbol: ACSM2B
  hgvsc: ENST00000329697.6:c.1509+6G>A
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000457377
  ensembl transcript: ENST00000565322
  gene symbol: ACSM2B
  hgvsc: ENST00000565322.1:c.1272+6G>A
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000569131
  gene symbol: ACSM2B
  hgvsc: ENST00000569131.1:n.1259G>A
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000569364
  gene symbol: ACSM2B
  hgvsc: ENST00000569364.1:n.1690G>A
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000455137
  ensembl transcript: ENST00000568098
  gene symbol: ACSM2B
  hgvsc: ENST00000568098.1:c.116+253G>A
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000566998
  gene symbol: ACSM2B
  hgvsc: ENST00000566998.1:n.1704+6G>A
  variant of: http://identifiers.org/hgnc/30931
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 733
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1049
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4431
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41464
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9353
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 620
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1012
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 120
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3333
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2395
  bin: 8.25e1
  variant carriers: 0
hgvs: c.1509+6G>A
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: African
population: European (Finnish)
population: Other
population: Latino
reference allele: C
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: MQ

16-20554243-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20554243
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 20554243
    reference: chr 16
allele count: 8
allele frequency: 6.623174487531874e-5
allele num: 120788
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000563943
  gene symbol: ACSM2B
  hgvsc: ENST00000563943.1:n.1431G>A
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000455137
  ensembl transcript: ENST00000568098
  gene symbol: ACSM2B
  hgvsc: ENST00000568098.1:c.116+240G>A
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000454995
  ensembl transcript: ENST00000565232
  gene symbol: ACSM2B
  hgvsc: ENST00000565232.1:c.1502G>A
  hgvsp: ENSP00000454995.1:p.Arg501Gln
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000456378
  ensembl transcript: ENST00000567001
  gene symbol: ACSM2B
  hgvsc: ENST00000567001.1:c.1502G>A
  hgvsp: ENSP00000456378.1:p.Arg501Gln
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000569131
  gene symbol: ACSM2B
  hgvsc: ENST00000569131.1:n.1246G>A
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000457377
  ensembl transcript: ENST00000565322
  gene symbol: ACSM2B
  hgvsc: ENST00000565322.1:c.1265G>A
  hgvsp: ENSP00000457377.1:p.Arg422Gln
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000327453
  ensembl transcript: ENST00000329697
  gene symbol: ACSM2B
  hgvsc: ENST00000329697.6:c.1502G>A
  hgvsp: ENSP00000327453.6:p.Arg501Gln
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000566998
  gene symbol: ACSM2B
  hgvsc: ENST00000566998.1:n.1697G>A
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000569364
  gene symbol: ACSM2B
  hgvsc: ENST00000569364.1:n.1677G>A
  variant of: http://identifiers.org/hgnc/30931
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9692
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41461
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1150
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4694
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 615
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 620
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6947
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 168
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2494
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3406
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3984
  bin: 9.75e1
  variant carriers: 8
hgvs: p.Arg501Gln
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
population: East Asian
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP

16-20554244-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20554244
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 20554244
    reference: chr 16
allele count: 3
allele frequency: 2.481389578163772e-5
allele num: 120900
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000566998
  gene symbol: ACSM2B
  hgvsc: ENST00000566998.1:n.1696C>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000456378
  ensembl transcript: ENST00000567001
  gene symbol: ACSM2B
  hgvsc: ENST00000567001.1:c.1501C>T
  hgvsp: ENSP00000456378.1:p.Arg501Ter
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000569364
  gene symbol: ACSM2B
  hgvsc: ENST00000569364.1:n.1676C>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000457377
  ensembl transcript: ENST00000565322
  gene symbol: ACSM2B
  hgvsc: ENST00000565322.1:c.1264C>T
  hgvsp: ENSP00000457377.1:p.Arg422Ter
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000327453
  ensembl transcript: ENST00000329697
  gene symbol: ACSM2B
  hgvsc: ENST00000329697.6:c.1501C>T
  hgvsp: ENSP00000327453.6:p.Arg501Ter
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000569131
  gene symbol: ACSM2B
  hgvsc: ENST00000569131.1:n.1245C>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000454995
  ensembl transcript: ENST00000565232
  gene symbol: ACSM2B
  hgvsc: ENST00000565232.1:c.1501C>T
  hgvsp: ENSP00000454995.1:p.Arg501Ter
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000455137
  ensembl transcript: ENST00000568098
  gene symbol: ACSM2B
  hgvsc: ENST00000568098.1:c.116+239C>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000563943
  gene symbol: ACSM2B
  hgvsc: ENST00000563943.1:n.1430C>T
  variant of: http://identifiers.org/hgnc/30931
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 623
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41475
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1156
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9713
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4721
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 620
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 148
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37817
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Arg501Ter
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
population: African
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum

16-20554247-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20554247
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 20554247
    reference: chr 16
allele count: 1
allele frequency: 8.262141216517673e-6
allele num: 121034
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000455137
  ensembl transcript: ENST00000568098
  gene symbol: ACSM2B
  hgvsc: ENST00000568098.1:c.116+236G>A
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000456378
  ensembl transcript: ENST00000567001
  gene symbol: ACSM2B
  hgvsc: ENST00000567001.1:c.1498G>A
  hgvsp: ENSP00000456378.1:p.Val500Ile
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000569364
  gene symbol: ACSM2B
  hgvsc: ENST00000569364.1:n.1673G>A
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000454995
  ensembl transcript: ENST00000565232
  gene symbol: ACSM2B
  hgvsc: ENST00000565232.1:c.1498G>A
  hgvsp: ENSP00000454995.1:p.Val500Ile
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000563943
  gene symbol: ACSM2B
  hgvsc: ENST00000563943.1:n.1427G>A
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000566998
  gene symbol: ACSM2B
  hgvsc: ENST00000566998.1:n.1693G>A
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000327453
  ensembl transcript: ENST00000329697
  gene symbol: ACSM2B
  hgvsc: ENST00000329697.6:c.1498G>A
  hgvsp: ENSP00000327453.6:p.Val500Ile
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000457377
  ensembl transcript: ENST00000565322
  gene symbol: ACSM2B
  hgvsc: ENST00000565322.1:c.1261G>A
  hgvsp: ENSP00000457377.1:p.Val421Ile
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000569131
  gene symbol: ACSM2B
  hgvsc: ENST00000569131.1:n.1242G>A
  variant of: http://identifiers.org/hgnc/30931
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4738
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41478
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9691
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 665
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 620
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1199
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1239
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37952
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Val500Ile
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD

16-20554247-CG-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20554247
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 20554246
    reference: chr 16
allele count: 1
allele frequency: 8.262141216517673e-6
allele num: 121034
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000455137
  ensembl transcript: ENST00000568098
  gene symbol: ACSM2B
  hgvsc: ENST00000568098.1:c.116+235delC
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000454995
  ensembl transcript: ENST00000565232
  gene symbol: ACSM2B
  hgvsc: ENST00000565232.1:c.1497delC
  hgvsp: ENSP00000454995.1:p.Val500SerfsTer6
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000563943
  gene symbol: ACSM2B
  hgvsc: ENST00000563943.1:n.1426delC
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000569131
  gene symbol: ACSM2B
  hgvsc: ENST00000569131.1:n.1241delC
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000569364
  gene symbol: ACSM2B
  hgvsc: ENST00000569364.1:n.1672delC
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000566998
  gene symbol: ACSM2B
  hgvsc: ENST00000566998.1:n.1692delC
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000457377
  ensembl transcript: ENST00000565322
  gene symbol: ACSM2B
  hgvsc: ENST00000565322.1:c.1260delC
  hgvsp: ENSP00000457377.1:p.Val421SerfsTer6
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000327453
  ensembl transcript: ENST00000329697
  gene symbol: ACSM2B
  hgvsc: ENST00000329697.6:c.1497delC
  hgvsp: ENSP00000327453.6:p.Val500SerfsTer6
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000456378
  ensembl transcript: ENST00000567001
  gene symbol: ACSM2B
  hgvsc: ENST00000567001.1:c.1497delC
  hgvsp: ENSP00000456378.1:p.Val500SerfsTer6
  variant of: http://identifiers.org/hgnc/30931
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9691
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 620
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 665
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41478
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1199
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4738
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37952
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4004
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2519
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 115
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Val500SerfsTer6
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
population: African
population: South Asian
reference allele: CG
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum

16-20554248-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20554248
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 20554248
    reference: chr 16
allele count: 6536
allele frequency: 5.400403212479757e-2
allele num: 121028
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000457377
  ensembl transcript: ENST00000565322
  gene symbol: ACSM2B
  hgvsc: ENST00000565322.1:c.1260C>T
  hgvsp: ENST00000565322.1:c.1260C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000327453
  ensembl transcript: ENST00000329697
  gene symbol: ACSM2B
  hgvsc: ENST00000329697.6:c.1497C>T
  hgvsp: ENST00000329697.6:c.1497C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000456378
  ensembl transcript: ENST00000567001
  gene symbol: ACSM2B
  hgvsc: ENST00000567001.1:c.1497C>T
  hgvsp: ENST00000567001.1:c.1497C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000563943
  gene symbol: ACSM2B
  hgvsc: ENST00000563943.1:n.1426C>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000455137
  ensembl transcript: ENST00000568098
  gene symbol: ACSM2B
  hgvsc: ENST00000568098.1:c.116+235C>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000566998
  gene symbol: ACSM2B
  hgvsc: ENST00000566998.1:n.1692C>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000569131
  gene symbol: ACSM2B
  hgvsc: ENST00000569131.1:n.1241C>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000569364
  gene symbol: ACSM2B
  hgvsc: ENST00000569364.1:n.1672C>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000454995
  ensembl transcript: ENST00000565232
  gene symbol: ACSM2B
  hgvsc: ENST00000565232.1:c.1497C>T
  hgvsp: ENST00000565232.1:c.1497C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30931
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 1.75e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1163
  bin: 4.25e1
  variant carriers: 517
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 7.25e1
  variant carriers: 444
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 9.25e1
  variant carriers: 126
genotype depth: GenotypeDepth
  all individuals: 8783
  bin: 2.75e1
  variant carriers: 118
genotype depth: GenotypeDepth
  all individuals: 928
  bin: 5.75e1
  variant carriers: 704
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 1.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1490
  bin: 3.75e1
  variant carriers: 334
genotype depth: GenotypeDepth
  all individuals: 952
  bin: 5.25e1
  variant carriers: 678
genotype depth: GenotypeDepth
  all individuals: 37214
  bin: 2.25e1
  variant carriers: 63
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 8.25e1
  variant carriers: 207
genotype depth: GenotypeDepth
  all individuals: 994
  bin: 4.75e1
  variant carriers: 613
genotype depth: GenotypeDepth
  all individuals: 856
  bin: 6.25e1
  variant carriers: 670
genotype depth: GenotypeDepth
  all individuals: 1065
  bin: 9.75e1
  variant carriers: 522
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 6.75e1
  variant carriers: 527
genotype depth: GenotypeDepth
  all individuals: 4503
  bin: 3.25e1
  variant carriers: 220
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 7.75e1
  variant carriers: 285
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 8.75e1
  variant carriers: 145
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 4.75e1
  variant carriers: 9
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.25e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 182
  bin: 2.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 972
  bin: 8.75e1
  variant carriers: 11
genotype quality: GenotypeQuality
  all individuals: 34153
  bin: 6.25e1
  variant carriers: 9
hgvs: p.Pro499Pro
num of homozygotes: 364
population: South Asian
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS

16-20554256-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20554256
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 20554256
    reference: chr 16
allele count: 1
allele frequency: 8.248783304462591e-6
allele num: 121230
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000456378
  ensembl transcript: ENST00000567001
  gene symbol: ACSM2B
  hgvsc: ENST00000567001.1:c.1489C>A
  hgvsp: ENSP00000456378.1:p.Pro497Thr
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000454995
  ensembl transcript: ENST00000565232
  gene symbol: ACSM2B
  hgvsc: ENST00000565232.1:c.1489C>A
  hgvsp: ENSP00000454995.1:p.Pro497Thr
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000569364
  gene symbol: ACSM2B
  hgvsc: ENST00000569364.1:n.1664C>A
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000327453
  ensembl transcript: ENST00000329697
  gene symbol: ACSM2B
  hgvsc: ENST00000329697.6:c.1489C>A
  hgvsp: ENSP00000327453.6:p.Pro497Thr
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000457377
  ensembl transcript: ENST00000565322
  gene symbol: ACSM2B
  hgvsc: ENST00000565322.1:c.1252C>A
  hgvsp: ENSP00000457377.1:p.Pro418Thr
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000563943
  gene symbol: ACSM2B
  hgvsc: ENST00000563943.1:n.1418C>A
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000566998
  gene symbol: ACSM2B
  hgvsc: ENST00000566998.1:n.1684C>A
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000455137
  ensembl transcript: ENST00000568098
  gene symbol: ACSM2B
  hgvsc: ENST00000568098.1:c.116+227C>A
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000569131
  gene symbol: ACSM2B
  hgvsc: ENST00000569131.1:n.1233C>A
  variant of: http://identifiers.org/hgnc/30931
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 845
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9140
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 495
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4742
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37293
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1119
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 961
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1030
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 872
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1541
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34598
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Pro497Thr
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff

16-20554264-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20554264
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 20554264
    reference: chr 16
allele count: 1
allele frequency: 8.245926512302922e-6
allele num: 121272
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000563943
  gene symbol: ACSM2B
  hgvsc: ENST00000563943.1:n.1410T>C
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000456378
  ensembl transcript: ENST00000567001
  gene symbol: ACSM2B
  hgvsc: ENST00000567001.1:c.1481T>C
  hgvsp: ENSP00000456378.1:p.Ile494Thr
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000455137
  ensembl transcript: ENST00000568098
  gene symbol: ACSM2B
  hgvsc: ENST00000568098.1:c.116+219T>C
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000569364
  gene symbol: ACSM2B
  hgvsc: ENST00000569364.1:n.1656T>C
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000457377
  ensembl transcript: ENST00000565322
  gene symbol: ACSM2B
  hgvsc: ENST00000565322.1:c.1244T>C
  hgvsp: ENSP00000457377.1:p.Ile415Thr
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000454995
  ensembl transcript: ENST00000565232
  gene symbol: ACSM2B
  hgvsc: ENST00000565232.1:c.1481T>C
  hgvsp: ENSP00000454995.1:p.Ile494Thr
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000327453
  ensembl transcript: ENST00000329697
  gene symbol: ACSM2B
  hgvsc: ENST00000329697.6:c.1481T>C
  hgvsp: ENSP00000327453.6:p.Ile494Thr
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000566998
  gene symbol: ACSM2B
  hgvsc: ENST00000566998.1:n.1676T>C
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000569131
  gene symbol: ACSM2B
  hgvsc: ENST00000569131.1:n.1225T>C
  variant of: http://identifiers.org/hgnc/30931
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 495
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1117
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1030
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9162
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37299
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4760
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 961
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 873
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 846
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1546
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1047
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8694
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3289
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Ile494Thr
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: ClippingRankSum

http://identifiers.org/exac.variant/16-20554266-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20554266
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 20554266
    reference: chr 16
allele count: 1
allele frequency: 8.245382585751979e-6
allele num: 121280
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000455137
  ensembl transcript: ENST00000568098
  gene symbol: ACSM2B
  hgvsc: ENST00000568098.1:c.116+217G>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000454995
  ensembl transcript: ENST00000565232
  gene symbol: ACSM2B
  hgvsc: ENST00000565232.1:c.1479G>T
  hgvsp: ENST00000565232.1:c.1479G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000456378
  ensembl transcript: ENST00000567001
  gene symbol: ACSM2B
  hgvsc: ENST00000567001.1:c.1479G>T
  hgvsp: ENST00000567001.1:c.1479G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000569131
  gene symbol: ACSM2B
  hgvsc: ENST00000569131.1:n.1223G>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000457377
  ensembl transcript: ENST00000565322
  gene symbol: ACSM2B
  hgvsc: ENST00000565322.1:c.1242G>T
  hgvsp: ENST00000565322.1:c.1242G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000327453
  ensembl transcript: ENST00000329697
  gene symbol: ACSM2B
  hgvsc: ENST00000329697.6:c.1479G>T
  hgvsp: ENST00000329697.6:c.1479G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000563943
  gene symbol: ACSM2B
  hgvsc: ENST00000563943.1:n.1408G>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000569364
  gene symbol: ACSM2B
  hgvsc: ENST00000569364.1:n.1654G>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000566998
  gene symbol: ACSM2B
  hgvsc: ENST00000566998.1:n.1674G>T
  variant of: http://identifiers.org/hgnc/30931
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 873
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 846
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37298
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 961
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1546
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4764
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1116
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 495
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9165
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1030
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34632
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8695
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1047
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Val493Val
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Latino
population: Other
population: African
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP

16-20554272-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20554272
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 20554272
    reference: chr 16
allele count: 5
allele frequency: 4.121943578836293e-5
allele num: 121302
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000457377
  ensembl transcript: ENST00000565322
  gene symbol: ACSM2B
  hgvsc: ENST00000565322.1:c.1236G>A
  hgvsp: ENST00000565322.1:c.1236G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000456378
  ensembl transcript: ENST00000567001
  gene symbol: ACSM2B
  hgvsc: ENST00000567001.1:c.1473G>A
  hgvsp: ENST00000567001.1:c.1473G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000563943
  gene symbol: ACSM2B
  hgvsc: ENST00000563943.1:n.1402G>A
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000569131
  gene symbol: ACSM2B
  hgvsc: ENST00000569131.1:n.1217G>A
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000327453
  ensembl transcript: ENST00000329697
  gene symbol: ACSM2B
  hgvsc: ENST00000329697.6:c.1473G>A
  hgvsp: ENST00000329697.6:c.1473G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000566998
  gene symbol: ACSM2B
  hgvsc: ENST00000566998.1:n.1668G>A
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000454995
  ensembl transcript: ENST00000565232
  gene symbol: ACSM2B
  hgvsc: ENST00000565232.1:c.1473G>A
  hgvsp: ENST00000565232.1:c.1473G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000455137
  ensembl transcript: ENST00000568098
  gene symbol: ACSM2B
  hgvsc: ENST00000568098.1:c.116+211G>A
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000569364
  gene symbol: ACSM2B
  hgvsc: ENST00000569364.1:n.1648G>A
  variant of: http://identifiers.org/hgnc/30931
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 651
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37298
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1031
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 496
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9168
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1555
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 962
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 874
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4771
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 847
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1117
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 770
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1048
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2557
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1296
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8705
  bin: 9.75e1
  variant carriers: 5
hgvs: p.Thr491Thr
num of homozygotes: 0
population: Other
population: South Asian
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
population: European (Finnish)
reference allele: C
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ

16-20554273-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20554273
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 20554273
    reference: chr 16
allele count: 12
allele frequency: 9.891522964819151e-5
allele num: 121316
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000327453
  ensembl transcript: ENST00000329697
  gene symbol: ACSM2B
  hgvsc: ENST00000329697.6:c.1472C>T
  hgvsp: ENSP00000327453.6:p.Thr491Met
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000454995
  ensembl transcript: ENST00000565232
  gene symbol: ACSM2B
  hgvsc: ENST00000565232.1:c.1472C>T
  hgvsp: ENSP00000454995.1:p.Thr491Met
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000457377
  ensembl transcript: ENST00000565322
  gene symbol: ACSM2B
  hgvsc: ENST00000565322.1:c.1235C>T
  hgvsp: ENSP00000457377.1:p.Thr412Met
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000569364
  gene symbol: ACSM2B
  hgvsc: ENST00000569364.1:n.1647C>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000563943
  gene symbol: ACSM2B
  hgvsc: ENST00000563943.1:n.1401C>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000455137
  ensembl transcript: ENST00000568098
  gene symbol: ACSM2B
  hgvsc: ENST00000568098.1:c.116+210C>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000569131
  gene symbol: ACSM2B
  hgvsc: ENST00000569131.1:n.1216C>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000566998
  gene symbol: ACSM2B
  hgvsc: ENST00000566998.1:n.1667C>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000456378
  ensembl transcript: ENST00000567001
  gene symbol: ACSM2B
  hgvsc: ENST00000567001.1:c.1472C>T
  hgvsp: ENSP00000456378.1:p.Thr491Met
  variant of: http://identifiers.org/hgnc/30931
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37292
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 772
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 848
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1555
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 651
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1034
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9166
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 874
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1119
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4777
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 496
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 962
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2556
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6638
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Thr491Met
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD

16-20554273-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20554273
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 20554273
    reference: chr 16
allele count: 1
allele frequency: 8.242935804015958e-6
allele num: 121316
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000457377
  ensembl transcript: ENST00000565322
  gene symbol: ACSM2B
  hgvsc: ENST00000565322.1:c.1235C>G
  hgvsp: ENSP00000457377.1:p.Thr412Arg
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000327453
  ensembl transcript: ENST00000329697
  gene symbol: ACSM2B
  hgvsc: ENST00000329697.6:c.1472C>G
  hgvsp: ENSP00000327453.6:p.Thr491Arg
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000569131
  gene symbol: ACSM2B
  hgvsc: ENST00000569131.1:n.1216C>G
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000563943
  gene symbol: ACSM2B
  hgvsc: ENST00000563943.1:n.1401C>G
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000456378
  ensembl transcript: ENST00000567001
  gene symbol: ACSM2B
  hgvsc: ENST00000567001.1:c.1472C>G
  hgvsp: ENSP00000456378.1:p.Thr491Arg
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000454995
  ensembl transcript: ENST00000565232
  gene symbol: ACSM2B
  hgvsc: ENST00000565232.1:c.1472C>G
  hgvsp: ENSP00000454995.1:p.Thr491Arg
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000566998
  gene symbol: ACSM2B
  hgvsc: ENST00000566998.1:n.1667C>G
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000569364
  gene symbol: ACSM2B
  hgvsc: ENST00000569364.1:n.1647C>G
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000455137
  ensembl transcript: ENST00000568098
  gene symbol: ACSM2B
  hgvsc: ENST00000568098.1:c.116+210C>G
  variant of: http://identifiers.org/hgnc/30931
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 962
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37292
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4777
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 651
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 772
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 496
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1119
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9166
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 848
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1034
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 874
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1555
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34629
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2556
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Thr491Arg
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
reference allele: G
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: QD

16-20554283-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20554283
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 20554283
    reference: chr 16
allele count: 1
allele frequency: 8.241577108195424e-6
allele num: 121336
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000569131
  gene symbol: ACSM2B
  hgvsc: ENST00000569131.1:n.1206G>A
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000456378
  ensembl transcript: ENST00000567001
  gene symbol: ACSM2B
  hgvsc: ENST00000567001.1:c.1462G>A
  hgvsp: ENSP00000456378.1:p.Val488Met
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000566998
  gene symbol: ACSM2B
  hgvsc: ENST00000566998.1:n.1657G>A
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000457377
  ensembl transcript: ENST00000565322
  gene symbol: ACSM2B
  hgvsc: ENST00000565322.1:c.1225G>A
  hgvsp: ENSP00000457377.1:p.Val409Met
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000563943
  gene symbol: ACSM2B
  hgvsc: ENST00000563943.1:n.1391G>A
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000569364
  gene symbol: ACSM2B
  hgvsc: ENST00000569364.1:n.1637G>A
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000327453
  ensembl transcript: ENST00000329697
  gene symbol: ACSM2B
  hgvsc: ENST00000329697.6:c.1462G>A
  hgvsp: ENSP00000327453.6:p.Val488Met
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000454995
  ensembl transcript: ENST00000565232
  gene symbol: ACSM2B
  hgvsc: ENST00000565232.1:c.1462G>A
  hgvsp: ENSP00000454995.1:p.Val488Met
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000455137
  ensembl transcript: ENST00000568098
  gene symbol: ACSM2B
  hgvsc: ENST00000568098.1:c.116+200G>A
  variant of: http://identifiers.org/hgnc/30931
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37280
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1119
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9184
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1561
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 964
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 849
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 772
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 875
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 653
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1033
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 495
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4784
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8721
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Val488Met
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: C
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum

16-20554285-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20554285
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 20554285
    reference: chr 16
allele count: 1
allele frequency: 8.241305422778968e-6
allele num: 121340
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000454995
  ensembl transcript: ENST00000565232
  gene symbol: ACSM2B
  hgvsc: ENST00000565232.1:c.1460C>T
  hgvsp: ENSP00000454995.1:p.Ala487Val
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000569131
  gene symbol: ACSM2B
  hgvsc: ENST00000569131.1:n.1204C>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000455137
  ensembl transcript: ENST00000568098
  gene symbol: ACSM2B
  hgvsc: ENST00000568098.1:c.116+198C>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000569364
  gene symbol: ACSM2B
  hgvsc: ENST00000569364.1:n.1635C>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000456378
  ensembl transcript: ENST00000567001
  gene symbol: ACSM2B
  hgvsc: ENST00000567001.1:c.1460C>T
  hgvsp: ENSP00000456378.1:p.Ala487Val
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000563943
  gene symbol: ACSM2B
  hgvsc: ENST00000563943.1:n.1389C>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000457377
  ensembl transcript: ENST00000565322
  gene symbol: ACSM2B
  hgvsc: ENST00000565322.1:c.1223C>T
  hgvsp: ENSP00000457377.1:p.Ala408Val
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000327453
  ensembl transcript: ENST00000329697
  gene symbol: ACSM2B
  hgvsc: ENST00000329697.6:c.1460C>T
  hgvsp: ENSP00000327453.6:p.Ala487Val
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000566998
  gene symbol: ACSM2B
  hgvsc: ENST00000566998.1:n.1655C>T
  variant of: http://identifiers.org/hgnc/30931
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 772
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 849
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 495
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 963
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 653
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9187
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4786
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1033
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1562
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37278
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1119
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 875
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34630
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Ala487Val
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: Other
population: African
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: G
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum

16-20554286-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20554286
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 20554286
    reference: chr 16
allele count: 1
allele frequency: 8.241441263248117e-6
allele num: 121338
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000457377
  ensembl transcript: ENST00000565322
  gene symbol: ACSM2B
  hgvsc: ENST00000565322.1:c.1222G>A
  hgvsp: ENSP00000457377.1:p.Ala408Thr
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000563943
  gene symbol: ACSM2B
  hgvsc: ENST00000563943.1:n.1388G>A
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000569364
  gene symbol: ACSM2B
  hgvsc: ENST00000569364.1:n.1634G>A
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000456378
  ensembl transcript: ENST00000567001
  gene symbol: ACSM2B
  hgvsc: ENST00000567001.1:c.1459G>A
  hgvsp: ENSP00000456378.1:p.Ala487Thr
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000566998
  gene symbol: ACSM2B
  hgvsc: ENST00000566998.1:n.1654G>A
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000455137
  ensembl transcript: ENST00000568098
  gene symbol: ACSM2B
  hgvsc: ENST00000568098.1:c.116+197G>A
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000454995
  ensembl transcript: ENST00000565232
  gene symbol: ACSM2B
  hgvsc: ENST00000565232.1:c.1459G>A
  hgvsp: ENSP00000454995.1:p.Ala487Thr
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000327453
  ensembl transcript: ENST00000329697
  gene symbol: ACSM2B
  hgvsc: ENST00000329697.6:c.1459G>A
  hgvsp: ENSP00000327453.6:p.Ala487Thr
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000569131
  gene symbol: ACSM2B
  hgvsc: ENST00000569131.1:n.1203G>A
  variant of: http://identifiers.org/hgnc/30931
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1561
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4786
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 495
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 849
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 962
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37278
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 652
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1119
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9187
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 875
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1034
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 773
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3300
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Ala487Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: African
population: Latino
population: South Asian
population: East Asian
reference allele: C
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum

16-20554289-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20554289
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 20554289
    reference: chr 16
allele count: 1
allele frequency: 8.241305422778968e-6
allele num: 121340
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000457377
  ensembl transcript: ENST00000565322
  gene symbol: ACSM2B
  hgvsc: ENST00000565322.1:c.1219C>T
  hgvsp: ENSP00000457377.1:p.Pro407Ser
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000569131
  gene symbol: ACSM2B
  hgvsc: ENST00000569131.1:n.1200C>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000569364
  gene symbol: ACSM2B
  hgvsc: ENST00000569364.1:n.1631C>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000456378
  ensembl transcript: ENST00000567001
  gene symbol: ACSM2B
  hgvsc: ENST00000567001.1:c.1456C>T
  hgvsp: ENSP00000456378.1:p.Pro486Ser
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000454995
  ensembl transcript: ENST00000565232
  gene symbol: ACSM2B
  hgvsc: ENST00000565232.1:c.1456C>T
  hgvsp: ENSP00000454995.1:p.Pro486Ser
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000455137
  ensembl transcript: ENST00000568098
  gene symbol: ACSM2B
  hgvsc: ENST00000568098.1:c.116+194C>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000566998
  gene symbol: ACSM2B
  hgvsc: ENST00000566998.1:n.1651C>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000327453
  ensembl transcript: ENST00000329697
  gene symbol: ACSM2B
  hgvsc: ENST00000329697.6:c.1456C>T
  hgvsp: ENSP00000327453.6:p.Pro486Ser
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000563943
  gene symbol: ACSM2B
  hgvsc: ENST00000563943.1:n.1385C>T
  variant of: http://identifiers.org/hgnc/30931
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1119
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 849
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9187
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1563
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 962
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 773
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37276
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 495
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 875
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4785
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 653
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1034
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8721
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Pro486Ser
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: QD

16-20554290-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20554290
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 20554290
    reference: chr 16
allele count: 2
allele frequency: 1.648233917357551e-5
allele num: 121342
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000327453
  ensembl transcript: ENST00000329697
  gene symbol: ACSM2B
  hgvsc: ENST00000329697.6:c.1455C>T
  hgvsp: ENST00000329697.6:c.1455C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000454995
  ensembl transcript: ENST00000565232
  gene symbol: ACSM2B
  hgvsc: ENST00000565232.1:c.1455C>T
  hgvsp: ENST00000565232.1:c.1455C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000563943
  gene symbol: ACSM2B
  hgvsc: ENST00000563943.1:n.1384C>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000569364
  gene symbol: ACSM2B
  hgvsc: ENST00000569364.1:n.1630C>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000569131
  gene symbol: ACSM2B
  hgvsc: ENST00000569131.1:n.1199C>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000456378
  ensembl transcript: ENST00000567001
  gene symbol: ACSM2B
  hgvsc: ENST00000567001.1:c.1455C>T
  hgvsp: ENST00000567001.1:c.1455C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000457377
  ensembl transcript: ENST00000565322
  gene symbol: ACSM2B
  hgvsc: ENST00000565322.1:c.1218C>T
  hgvsp: ENST00000565322.1:c.1218C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000566998
  gene symbol: ACSM2B
  hgvsc: ENST00000566998.1:n.1650C>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000455137
  ensembl transcript: ENST00000568098
  gene symbol: ACSM2B
  hgvsc: ENST00000568098.1:c.116+193C>T
  variant of: http://identifiers.org/hgnc/30931
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1035
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4786
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 773
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1563
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 875
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 651
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 962
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9186
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37277
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 848
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1120
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 495
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6649
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2557
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 2.25e1
  variant carriers: 0
hgvs: p.His485His
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: East Asian
population: Latino
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

16-20554294-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20554294
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 20554294
    reference: chr 16
allele count: 1
allele frequency: 8.240762105679534e-6
allele num: 121348
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000456378
  ensembl transcript: ENST00000567001
  gene symbol: ACSM2B
  hgvsc: ENST00000567001.1:c.1451A>G
  hgvsp: ENSP00000456378.1:p.Lys484Arg
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000457377
  ensembl transcript: ENST00000565322
  gene symbol: ACSM2B
  hgvsc: ENST00000565322.1:c.1214A>G
  hgvsp: ENSP00000457377.1:p.Lys405Arg
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000569131
  gene symbol: ACSM2B
  hgvsc: ENST00000569131.1:n.1195A>G
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000569364
  gene symbol: ACSM2B
  hgvsc: ENST00000569364.1:n.1626A>G
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000327453
  ensembl transcript: ENST00000329697
  gene symbol: ACSM2B
  hgvsc: ENST00000329697.6:c.1451A>G
  hgvsp: ENSP00000327453.6:p.Lys484Arg
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000566998
  gene symbol: ACSM2B
  hgvsc: ENST00000566998.1:n.1646A>G
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000455137
  ensembl transcript: ENST00000568098
  gene symbol: ACSM2B
  hgvsc: ENST00000568098.1:c.116+189A>G
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000454995
  ensembl transcript: ENST00000565232
  gene symbol: ACSM2B
  hgvsc: ENST00000565232.1:c.1451A>G
  hgvsp: ENSP00000454995.1:p.Lys484Arg
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000563943
  gene symbol: ACSM2B
  hgvsc: ENST00000563943.1:n.1380A>G
  variant of: http://identifiers.org/hgnc/30931
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1035
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1564
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 962
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4787
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37273
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 875
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9190
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 849
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 773
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 495
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 651
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1120
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2445
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1298
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Lys484Arg
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
reference allele: T
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum

16-20554295-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20554295
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 20554295
    reference: chr 16
allele count: 11
allele frequency: 9.066482040123304e-5
allele num: 121326
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000457377
  ensembl transcript: ENST00000565322
  gene symbol: ACSM2B
  hgvsc: ENST00000565322.1:c.1213A>G
  hgvsp: ENSP00000457377.1:p.Lys405Glu
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000327453
  ensembl transcript: ENST00000329697
  gene symbol: ACSM2B
  hgvsc: ENST00000329697.6:c.1450A>G
  hgvsp: ENSP00000327453.6:p.Lys484Glu
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000454995
  ensembl transcript: ENST00000565232
  gene symbol: ACSM2B
  hgvsc: ENST00000565232.1:c.1450A>G
  hgvsp: ENSP00000454995.1:p.Lys484Glu
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000563943
  gene symbol: ACSM2B
  hgvsc: ENST00000563943.1:n.1379A>G
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000456378
  ensembl transcript: ENST00000567001
  gene symbol: ACSM2B
  hgvsc: ENST00000567001.1:c.1450A>G
  hgvsp: ENSP00000456378.1:p.Lys484Glu
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000566998
  gene symbol: ACSM2B
  hgvsc: ENST00000566998.1:n.1645A>G
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000569131
  gene symbol: ACSM2B
  hgvsc: ENST00000569131.1:n.1194A>G
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000569364
  gene symbol: ACSM2B
  hgvsc: ENST00000569364.1:n.1625A>G
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000455137
  ensembl transcript: ENST00000568098
  gene symbol: ACSM2B
  hgvsc: ENST00000568098.1:c.116+188A>G
  variant of: http://identifiers.org/hgnc/30931
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 498
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9184
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37240
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1043
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 4792
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1126
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 652
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 776
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 880
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1564
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 849
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 969
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 34595
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 6644
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Lys484Glu
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
population: Other
population: African
reference allele: T
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: MQ

16-20554301-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20554301
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 20554301
    reference: chr 16
allele count: 1
allele frequency: 8.240354664864776e-6
allele num: 121354
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000457377
  ensembl transcript: ENST00000565322
  gene symbol: ACSM2B
  hgvsc: ENST00000565322.1:c.1207C>T
  hgvsp: ENST00000565322.1:c.1207C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000563943
  gene symbol: ACSM2B
  hgvsc: ENST00000563943.1:n.1373C>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000454995
  ensembl transcript: ENST00000565232
  gene symbol: ACSM2B
  hgvsc: ENST00000565232.1:c.1444C>T
  hgvsp: ENST00000565232.1:c.1444C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000455137
  ensembl transcript: ENST00000568098
  gene symbol: ACSM2B
  hgvsc: ENST00000568098.1:c.116+182C>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000569131
  gene symbol: ACSM2B
  hgvsc: ENST00000569131.1:n.1188C>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000327453
  ensembl transcript: ENST00000329697
  gene symbol: ACSM2B
  hgvsc: ENST00000329697.6:c.1444C>T
  hgvsp: ENST00000329697.6:c.1444C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000566998
  gene symbol: ACSM2B
  hgvsc: ENST00000566998.1:n.1639C>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000456378
  ensembl transcript: ENST00000567001
  gene symbol: ACSM2B
  hgvsc: ENST00000567001.1:c.1444C>T
  hgvsp: ENST00000567001.1:c.1444C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000569364
  gene symbol: ACSM2B
  hgvsc: ENST00000569364.1:n.1619C>T
  variant of: http://identifiers.org/hgnc/30931
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4792
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 846
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1126
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37230
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 652
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 969
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 878
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 496
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 777
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1040
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1562
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9196
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34596
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Leu482Leu
num of homozygotes: 0
population: East Asian
population: Other
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: QD

16-20554303-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20554303
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 20554303
    reference: chr 16
allele count: 1
allele frequency: 8.240354664864776e-6
allele num: 121354
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000455137
  ensembl transcript: ENST00000568098
  gene symbol: ACSM2B
  hgvsc: ENST00000568098.1:c.116+180C>A
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000454995
  ensembl transcript: ENST00000565232
  gene symbol: ACSM2B
  hgvsc: ENST00000565232.1:c.1442C>A
  hgvsp: ENSP00000454995.1:p.Ala481Glu
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000327453
  ensembl transcript: ENST00000329697
  gene symbol: ACSM2B
  hgvsc: ENST00000329697.6:c.1442C>A
  hgvsp: ENSP00000327453.6:p.Ala481Glu
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000456378
  ensembl transcript: ENST00000567001
  gene symbol: ACSM2B
  hgvsc: ENST00000567001.1:c.1442C>A
  hgvsp: ENSP00000456378.1:p.Ala481Glu
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000563943
  gene symbol: ACSM2B
  hgvsc: ENST00000563943.1:n.1371C>A
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000566998
  gene symbol: ACSM2B
  hgvsc: ENST00000566998.1:n.1637C>A
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000569131
  gene symbol: ACSM2B
  hgvsc: ENST00000569131.1:n.1186C>A
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000569364
  gene symbol: ACSM2B
  hgvsc: ENST00000569364.1:n.1617C>A
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000457377
  ensembl transcript: ENST00000565322
  gene symbol: ACSM2B
  hgvsc: ENST00000565322.1:c.1205C>A
  hgvsp: ENSP00000457377.1:p.Ala402Glu
  variant of: http://identifiers.org/hgnc/30931
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37227
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1041
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 652
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 496
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 777
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 969
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4794
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 878
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1562
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 846
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9194
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1126
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1299
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Ala481Glu
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD

16-20554305-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20554305
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 20554305
    reference: chr 16
allele count: 7
allele frequency: 5.768248265405343e-5
allele num: 121354
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000454995
  ensembl transcript: ENST00000565232
  gene symbol: ACSM2B
  hgvsc: ENST00000565232.1:c.1440T>C
  hgvsp: ENST00000565232.1:c.1440T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000327453
  ensembl transcript: ENST00000329697
  gene symbol: ACSM2B
  hgvsc: ENST00000329697.6:c.1440T>C
  hgvsp: ENST00000329697.6:c.1440T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000569131
  gene symbol: ACSM2B
  hgvsc: ENST00000569131.1:n.1184T>C
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000566998
  gene symbol: ACSM2B
  hgvsc: ENST00000566998.1:n.1635T>C
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000456378
  ensembl transcript: ENST00000567001
  gene symbol: ACSM2B
  hgvsc: ENST00000567001.1:c.1440T>C
  hgvsp: ENST00000567001.1:c.1440T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000457377
  ensembl transcript: ENST00000565322
  gene symbol: ACSM2B
  hgvsc: ENST00000565322.1:c.1203T>C
  hgvsp: ENST00000565322.1:c.1203T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000455137
  ensembl transcript: ENST00000568098
  gene symbol: ACSM2B
  hgvsc: ENST00000568098.1:c.116+178T>C
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000563943
  gene symbol: ACSM2B
  hgvsc: ENST00000563943.1:n.1369T>C
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000569364
  gene symbol: ACSM2B
  hgvsc: ENST00000569364.1:n.1615T>C
  variant of: http://identifiers.org/hgnc/30931
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 878
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1562
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9196
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1042
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 969
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37222
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4791
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 496
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 777
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1126
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 844
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 653
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3296
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Asn480Asn
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum

16-20554308-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20554308
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 20554308
    reference: chr 16
allele count: 9
allele frequency: 7.416441426593711e-5
allele num: 121352
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000569131
  gene symbol: ACSM2B
  hgvsc: ENST00000569131.1:n.1181G>A
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000569364
  gene symbol: ACSM2B
  hgvsc: ENST00000569364.1:n.1612G>A
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000327453
  ensembl transcript: ENST00000329697
  gene symbol: ACSM2B
  hgvsc: ENST00000329697.6:c.1437G>A
  hgvsp: ENST00000329697.6:c.1437G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000566998
  gene symbol: ACSM2B
  hgvsc: ENST00000566998.1:n.1632G>A
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000454995
  ensembl transcript: ENST00000565232
  gene symbol: ACSM2B
  hgvsc: ENST00000565232.1:c.1437G>A
  hgvsp: ENST00000565232.1:c.1437G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000457377
  ensembl transcript: ENST00000565322
  gene symbol: ACSM2B
  hgvsc: ENST00000565322.1:c.1200G>A
  hgvsp: ENST00000565322.1:c.1200G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000563943
  gene symbol: ACSM2B
  hgvsc: ENST00000563943.1:n.1366G>A
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000456378
  ensembl transcript: ENST00000567001
  gene symbol: ACSM2B
  hgvsc: ENST00000567001.1:c.1437G>A
  hgvsp: ENST00000567001.1:c.1437G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000455137
  ensembl transcript: ENST00000568098
  gene symbol: ACSM2B
  hgvsc: ENST00000568098.1:c.116+175G>A
  variant of: http://identifiers.org/hgnc/30931
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 779
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9191
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1562
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1046
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 4789
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 969
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37207
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 880
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 654
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 845
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1126
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6653
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Glu479Glu
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
population: African
reference allele: C
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: FS

16-20554313-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20554313
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 20554313
    reference: chr 16
allele count: 3
allele frequency: 2.472269378471478e-5
allele num: 121346
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000327453
  ensembl transcript: ENST00000329697
  gene symbol: ACSM2B
  hgvsc: ENST00000329697.6:c.1432G>A
  hgvsp: ENSP00000327453.6:p.Val478Ile
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000566998
  gene symbol: ACSM2B
  hgvsc: ENST00000566998.1:n.1627G>A
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000454995
  ensembl transcript: ENST00000565232
  gene symbol: ACSM2B
  hgvsc: ENST00000565232.1:c.1432G>A
  hgvsp: ENSP00000454995.1:p.Val478Ile
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000569131
  gene symbol: ACSM2B
  hgvsc: ENST00000569131.1:n.1176G>A
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000563943
  gene symbol: ACSM2B
  hgvsc: ENST00000563943.1:n.1361G>A
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000455137
  ensembl transcript: ENST00000568098
  gene symbol: ACSM2B
  hgvsc: ENST00000568098.1:c.116+170G>A
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000569364
  gene symbol: ACSM2B
  hgvsc: ENST00000569364.1:n.1607G>A
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000456378
  ensembl transcript: ENST00000567001
  gene symbol: ACSM2B
  hgvsc: ENST00000567001.1:c.1432G>A
  hgvsp: ENSP00000456378.1:p.Val478Ile
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000457377
  ensembl transcript: ENST00000565322
  gene symbol: ACSM2B
  hgvsc: ENST00000565322.1:c.1195G>A
  hgvsp: ENSP00000457377.1:p.Val399Ile
  variant of: http://identifiers.org/hgnc/30931
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 880
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1045
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37175
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9190
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4788
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 781
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1564
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 652
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 845
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1128
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 969
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 496
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8754
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3296
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Val478Ile
num of homozygotes: 0
population: Latino
population: Other
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD

16-20554314-CT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20554314
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 20554313
    reference: chr 16
allele count: 1
allele frequency: 8.241441263248117e-6
allele num: 121338
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000563943
  gene symbol: ACSM2B
  hgvsc: ENST00000563943.1:n.1359delA
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000455137
  ensembl transcript: ENST00000568098
  gene symbol: ACSM2B
  hgvsc: ENST00000568098.1:c.116+168delA
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000569364
  gene symbol: ACSM2B
  hgvsc: ENST00000569364.1:n.1605delA
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000457377
  ensembl transcript: ENST00000565322
  gene symbol: ACSM2B
  hgvsc: ENST00000565322.1:c.1193delA
  hgvsp: ENSP00000457377.1:p.Glu398GlyfsTer2
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000566998
  gene symbol: ACSM2B
  hgvsc: ENST00000566998.1:n.1625delA
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000456378
  ensembl transcript: ENST00000567001
  gene symbol: ACSM2B
  hgvsc: ENST00000567001.1:c.1430delA
  hgvsp: ENSP00000456378.1:p.Glu477GlyfsTer2
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000327453
  ensembl transcript: ENST00000329697
  gene symbol: ACSM2B
  hgvsc: ENST00000329697.6:c.1430delA
  hgvsp: ENSP00000327453.6:p.Glu477GlyfsTer2
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000454995
  ensembl transcript: ENST00000565232
  gene symbol: ACSM2B
  hgvsc: ENST00000565232.1:c.1430delA
  hgvsp: ENSP00000454995.1:p.Glu477GlyfsTer2
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000569131
  gene symbol: ACSM2B
  hgvsc: ENST00000569131.1:n.1174delA
  variant of: http://identifiers.org/hgnc/30931
canonical: true
consequence: frameshift
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 880
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 652
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1127
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 970
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 781
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37163
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9189
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 496
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4789
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 845
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1045
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1564
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1299
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1049
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Glu477GlyfsTer2
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: CT
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD

16-20554315-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20554315
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 20554315
    reference: chr 16
allele count: 1
allele frequency: 8.241305422778968e-6
allele num: 121340
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000563943
  gene symbol: ACSM2B
  hgvsc: ENST00000563943.1:n.1359A>G
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000327453
  ensembl transcript: ENST00000329697
  gene symbol: ACSM2B
  hgvsc: ENST00000329697.6:c.1430A>G
  hgvsp: ENSP00000327453.6:p.Glu477Gly
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000457377
  ensembl transcript: ENST00000565322
  gene symbol: ACSM2B
  hgvsc: ENST00000565322.1:c.1193A>G
  hgvsp: ENSP00000457377.1:p.Glu398Gly
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000455137
  ensembl transcript: ENST00000568098
  gene symbol: ACSM2B
  hgvsc: ENST00000568098.1:c.116+168A>G
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000454995
  ensembl transcript: ENST00000565232
  gene symbol: ACSM2B
  hgvsc: ENST00000565232.1:c.1430A>G
  hgvsp: ENSP00000454995.1:p.Glu477Gly
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000569364
  gene symbol: ACSM2B
  hgvsc: ENST00000569364.1:n.1605A>G
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000569131
  gene symbol: ACSM2B
  hgvsc: ENST00000569131.1:n.1174A>G
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000456378
  ensembl transcript: ENST00000567001
  gene symbol: ACSM2B
  hgvsc: ENST00000567001.1:c.1430A>G
  hgvsp: ENSP00000456378.1:p.Glu477Gly
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000566998
  gene symbol: ACSM2B
  hgvsc: ENST00000566998.1:n.1625A>G
  variant of: http://identifiers.org/hgnc/30931
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1127
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9191
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37158
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 496
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 880
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4787
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1564
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 653
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 844
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 781
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 970
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1045
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6649
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Glu477Gly
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: T
site quality: DP
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum

16-20554317-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20554317
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 20554317
    reference: chr 16
allele count: 222
allele frequency: 1.829539648266882e-3
allele num: 121342
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000454995
  ensembl transcript: ENST00000565232
  gene symbol: ACSM2B
  hgvsc: ENST00000565232.1:c.1428G>A
  hgvsp: ENST00000565232.1:c.1428G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000327453
  ensembl transcript: ENST00000329697
  gene symbol: ACSM2B
  hgvsc: ENST00000329697.6:c.1428G>A
  hgvsp: ENST00000329697.6:c.1428G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000563943
  gene symbol: ACSM2B
  hgvsc: ENST00000563943.1:n.1357G>A
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000569364
  gene symbol: ACSM2B
  hgvsc: ENST00000569364.1:n.1603G>A
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000456378
  ensembl transcript: ENST00000567001
  gene symbol: ACSM2B
  hgvsc: ENST00000567001.1:c.1428G>A
  hgvsp: ENST00000567001.1:c.1428G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000455137
  ensembl transcript: ENST00000568098
  gene symbol: ACSM2B
  hgvsc: ENST00000568098.1:c.116+166G>A
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000566998
  gene symbol: ACSM2B
  hgvsc: ENST00000566998.1:n.1623G>A
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000569131
  gene symbol: ACSM2B
  hgvsc: ENST00000569131.1:n.1172G>A
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000457377
  ensembl transcript: ENST00000565322
  gene symbol: ACSM2B
  hgvsc: ENST00000565322.1:c.1191G>A
  hgvsp: ENST00000565322.1:c.1191G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/30931
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 7.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 9153
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 8.25e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 884
  bin: 5.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37004
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1558
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 969
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 783
  bin: 6.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 6.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 1126
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1143
  bin: 9.75e1
  variant carriers: 103
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 8.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 4782
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 847
  bin: 5.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 9.25e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 7.75e1
  variant carriers: 20
genotype quality: GenotypeQuality
  all individuals: 1297
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3277
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Ser476Ser
num of homozygotes: 1
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
population: Latino
reference allele: C
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum

16-20554318-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20554318
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 20554318
    reference: chr 16
allele count: 2
allele frequency: 1.648261084555794e-5
allele num: 121340
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000455137
  ensembl transcript: ENST00000568098
  gene symbol: ACSM2B
  hgvsc: ENST00000568098.1:c.116+165C>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000456378
  ensembl transcript: ENST00000567001
  gene symbol: ACSM2B
  hgvsc: ENST00000567001.1:c.1427C>T
  hgvsp: ENSP00000456378.1:p.Ser476Leu
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000566998
  gene symbol: ACSM2B
  hgvsc: ENST00000566998.1:n.1622C>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000563943
  gene symbol: ACSM2B
  hgvsc: ENST00000563943.1:n.1356C>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000457377
  ensembl transcript: ENST00000565322
  gene symbol: ACSM2B
  hgvsc: ENST00000565322.1:c.1190C>T
  hgvsp: ENSP00000457377.1:p.Ser397Leu
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000454995
  ensembl transcript: ENST00000565232
  gene symbol: ACSM2B
  hgvsc: ENST00000565232.1:c.1427C>T
  hgvsp: ENSP00000454995.1:p.Ser476Leu
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000569131
  gene symbol: ACSM2B
  hgvsc: ENST00000569131.1:n.1171C>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000327453
  ensembl transcript: ENST00000329697
  gene symbol: ACSM2B
  hgvsc: ENST00000329697.6:c.1427C>T
  hgvsp: ENSP00000327453.6:p.Ser476Leu
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000569364
  gene symbol: ACSM2B
  hgvsc: ENST00000569364.1:n.1602C>T
  variant of: http://identifiers.org/hgnc/30931
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 970
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1125
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36995
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4787
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 884
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9160
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1557
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 786
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 849
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1127
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1045
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6620
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Ser476Leu
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Latino
population: Other
reference allele: G
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD

16-20554319-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20554319
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 20554319
    reference: chr 16
allele count: 1
allele frequency: 8.241033755274261e-6
allele num: 121344
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000569131
  gene symbol: ACSM2B
  hgvsc: ENST00000569131.1:n.1170T>C
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000569364
  gene symbol: ACSM2B
  hgvsc: ENST00000569364.1:n.1601T>C
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000454995
  ensembl transcript: ENST00000565232
  gene symbol: ACSM2B
  hgvsc: ENST00000565232.1:c.1426T>C
  hgvsp: ENSP00000454995.1:p.Ser476Pro
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000455137
  ensembl transcript: ENST00000568098
  gene symbol: ACSM2B
  hgvsc: ENST00000568098.1:c.116+164T>C
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000566998
  gene symbol: ACSM2B
  hgvsc: ENST00000566998.1:n.1621T>C
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000563943
  gene symbol: ACSM2B
  hgvsc: ENST00000563943.1:n.1355T>C
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000327453
  ensembl transcript: ENST00000329697
  gene symbol: ACSM2B
  hgvsc: ENST00000329697.6:c.1426T>C
  hgvsp: ENSP00000327453.6:p.Ser476Pro
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000456378
  ensembl transcript: ENST00000567001
  gene symbol: ACSM2B
  hgvsc: ENST00000567001.1:c.1426T>C
  hgvsp: ENSP00000456378.1:p.Ser476Pro
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000457377
  ensembl transcript: ENST00000565322
  gene symbol: ACSM2B
  hgvsc: ENST00000565322.1:c.1189T>C
  hgvsp: ENSP00000457377.1:p.Ser397Pro
  variant of: http://identifiers.org/hgnc/30931
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 884
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36989
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 970
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1125
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 785
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4784
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1555
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 849
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9164
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1128
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2558
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Ser476Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
population: South Asian
population: Latino
population: European (Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum

16-20554321-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20554321
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 20554321
    reference: chr 16
allele count: 2
allele frequency: 1.648396933981703e-5
allele num: 121330
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000327453
  ensembl transcript: ENST00000329697
  gene symbol: ACSM2B
  hgvsc: ENST00000329697.6:c.1424C>A
  hgvsp: ENSP00000327453.6:p.Pro475His
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000455137
  ensembl transcript: ENST00000568098
  gene symbol: ACSM2B
  hgvsc: ENST00000568098.1:c.116+162C>A
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000569364
  gene symbol: ACSM2B
  hgvsc: ENST00000569364.1:n.1599C>A
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000457377
  ensembl transcript: ENST00000565322
  gene symbol: ACSM2B
  hgvsc: ENST00000565322.1:c.1187C>A
  hgvsp: ENSP00000457377.1:p.Pro396His
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000456378
  ensembl transcript: ENST00000567001
  gene symbol: ACSM2B
  hgvsc: ENST00000567001.1:c.1424C>A
  hgvsp: ENSP00000456378.1:p.Pro475His
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000563943
  gene symbol: ACSM2B
  hgvsc: ENST00000563943.1:n.1353C>A
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000566998
  gene symbol: ACSM2B
  hgvsc: ENST00000566998.1:n.1619C>A
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000569131
  gene symbol: ACSM2B
  hgvsc: ENST00000569131.1:n.1168C>A
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000454995
  ensembl transcript: ENST00000565232
  gene symbol: ACSM2B
  hgvsc: ENST00000565232.1:c.1424C>A
  hgvsp: ENSP00000454995.1:p.Pro475His
  variant of: http://identifiers.org/hgnc/30931
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1556
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 785
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 971
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 849
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36926
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4789
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9154
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 883
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1131
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1126
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2548
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Pro475His
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: VQSLOD

http://identifiers.org/exac.variant/16-20554324-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20554324
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 20554324
    reference: chr 16
allele count: 1
allele frequency: 8.241441263248117e-6
allele num: 121338
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000456378
  ensembl transcript: ENST00000567001
  gene symbol: ACSM2B
  hgvsc: ENST00000567001.1:c.1421G>T
  hgvsp: ENSP00000456378.1:p.Gly474Val
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000455137
  ensembl transcript: ENST00000568098
  gene symbol: ACSM2B
  hgvsc: ENST00000568098.1:c.116+159G>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000569364
  gene symbol: ACSM2B
  hgvsc: ENST00000569364.1:n.1596G>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000563943
  gene symbol: ACSM2B
  hgvsc: ENST00000563943.1:n.1350G>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000566998
  gene symbol: ACSM2B
  hgvsc: ENST00000566998.1:n.1616G>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000569131
  gene symbol: ACSM2B
  hgvsc: ENST00000569131.1:n.1165G>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000327453
  ensembl transcript: ENST00000329697
  gene symbol: ACSM2B
  hgvsc: ENST00000329697.6:c.1421G>T
  hgvsp: ENSP00000327453.6:p.Gly474Val
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000454995
  ensembl transcript: ENST00000565232
  gene symbol: ACSM2B
  hgvsc: ENST00000565232.1:c.1421G>T
  hgvsp: ENSP00000454995.1:p.Gly474Val
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000457377
  ensembl transcript: ENST00000565322
  gene symbol: ACSM2B
  hgvsc: ENST00000565322.1:c.1184G>T
  hgvsp: ENSP00000457377.1:p.Gly395Val
  variant of: http://identifiers.org/hgnc/30931
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 883
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1132
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1549
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36927
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 849
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 970
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4789
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 786
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9164
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1126
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3277
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8947
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Gly474Val
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
reference allele: C
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum

16-20554325-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20554325
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 20554325
    reference: chr 16
allele count: 1
allele frequency: 8.241712957621112e-6
allele num: 121334
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000455137
  ensembl transcript: ENST00000568098
  gene symbol: ACSM2B
  hgvsc: ENST00000568098.1:c.116+158G>A
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000569131
  gene symbol: ACSM2B
  hgvsc: ENST00000569131.1:n.1164G>A
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000566998
  gene symbol: ACSM2B
  hgvsc: ENST00000566998.1:n.1615G>A
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000457377
  ensembl transcript: ENST00000565322
  gene symbol: ACSM2B
  hgvsc: ENST00000565322.1:c.1183G>A
  hgvsp: ENSP00000457377.1:p.Gly395Arg
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000456378
  ensembl transcript: ENST00000567001
  gene symbol: ACSM2B
  hgvsc: ENST00000567001.1:c.1420G>A
  hgvsp: ENSP00000456378.1:p.Gly474Arg
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000563943
  gene symbol: ACSM2B
  hgvsc: ENST00000563943.1:n.1349G>A
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000454995
  ensembl transcript: ENST00000565232
  gene symbol: ACSM2B
  hgvsc: ENST00000565232.1:c.1420G>A
  hgvsp: ENSP00000454995.1:p.Gly474Arg
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000327453
  ensembl transcript: ENST00000329697
  gene symbol: ACSM2B
  hgvsc: ENST00000329697.6:c.1420G>A
  hgvsp: ENSP00000327453.6:p.Gly474Arg
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000569364
  gene symbol: ACSM2B
  hgvsc: ENST00000569364.1:n.1595G>A
  variant of: http://identifiers.org/hgnc/30931
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9154
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1126
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36920
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1553
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1132
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 970
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4788
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 849
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 883
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 786
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3278
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2545
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34269
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Gly474Arg
num of homozygotes: 0
population: East Asian
population: South Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
reference allele: C
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP

16-20554330-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20554330
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 20554330
    reference: chr 16
allele count: 1
allele frequency: 8.241984669908513e-6
allele num: 121330
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000454995
  ensembl transcript: ENST00000565232
  gene symbol: ACSM2B
  hgvsc: ENST00000565232.1:c.1415G>A
  hgvsp: ENSP00000454995.1:p.Arg472Gln
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000569131
  gene symbol: ACSM2B
  hgvsc: ENST00000569131.1:n.1159G>A
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000569364
  gene symbol: ACSM2B
  hgvsc: ENST00000569364.1:n.1590G>A
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000456378
  ensembl transcript: ENST00000567001
  gene symbol: ACSM2B
  hgvsc: ENST00000567001.1:c.1415G>A
  hgvsp: ENSP00000456378.1:p.Arg472Gln
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000563943
  gene symbol: ACSM2B
  hgvsc: ENST00000563943.1:n.1344G>A
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000457377
  ensembl transcript: ENST00000565322
  gene symbol: ACSM2B
  hgvsc: ENST00000565322.1:c.1178G>A
  hgvsp: ENSP00000457377.1:p.Arg393Gln
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000327453
  ensembl transcript: ENST00000329697
  gene symbol: ACSM2B
  hgvsc: ENST00000329697.6:c.1415G>A
  hgvsp: ENSP00000327453.6:p.Arg472Gln
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000566998
  gene symbol: ACSM2B
  hgvsc: ENST00000566998.1:n.1610G>A
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000455137
  ensembl transcript: ENST00000568098
  gene symbol: ACSM2B
  hgvsc: ENST00000568098.1:c.116+153G>A
  variant of: http://identifiers.org/hgnc/30931
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 849
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9133
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 884
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1127
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 787
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4779
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 970
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36882
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1547
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1132
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6579
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8948
  bin: 9.75e1
  variant carriers: 0
hgvs: p.Arg472Gln
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff

16-20554331-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20554331
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 20554331
    reference: chr 16
allele count: 27
allele frequency: 2.225372543848081e-4
allele num: 121328
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000456378
  ensembl transcript: ENST00000567001
  gene symbol: ACSM2B
  hgvsc: ENST00000567001.1:c.1414C>T
  hgvsp: ENSP00000456378.1:p.Arg472Trp
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000457377
  ensembl transcript: ENST00000565322
  gene symbol: ACSM2B
  hgvsc: ENST00000565322.1:c.1177C>T
  hgvsp: ENSP00000457377.1:p.Arg393Trp
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000563943
  gene symbol: ACSM2B
  hgvsc: ENST00000563943.1:n.1343C>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000569131
  gene symbol: ACSM2B
  hgvsc: ENST00000569131.1:n.1158C>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000454995
  ensembl transcript: ENST00000565232
  gene symbol: ACSM2B
  hgvsc: ENST00000565232.1:c.1414C>T
  hgvsp: ENSP00000454995.1:p.Arg472Trp
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000455137
  ensembl transcript: ENST00000568098
  gene symbol: ACSM2B
  hgvsc: ENST00000568098.1:c.116+152C>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000569364
  gene symbol: ACSM2B
  hgvsc: ENST00000569364.1:n.1589C>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000327453
  ensembl transcript: ENST00000329697
  gene symbol: ACSM2B
  hgvsc: ENST00000329697.6:c.1414C>T
  hgvsp: ENSP00000327453.6:p.Arg472Trp
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000566998
  gene symbol: ACSM2B
  hgvsc: ENST00000566998.1:n.1609C>T
  variant of: http://identifiers.org/hgnc/30931
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 787
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 971
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9129
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 884
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1126
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1541
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 851
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1147
  bin: 9.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 36845
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4776
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2544
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1046
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Arg472Trp
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: Other
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: DP

16-20554336-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20554336
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 20554336
    reference: chr 16
allele count: 2
allele frequency: 1.648532805802836e-5
allele num: 121320
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000454995
  ensembl transcript: ENST00000565232
  gene symbol: ACSM2B
  hgvsc: ENST00000565232.1:c.1410-1G>C
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000456378
  ensembl transcript: ENST00000567001
  gene symbol: ACSM2B
  hgvsc: ENST00000567001.1:c.1410-1G>C
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000455137
  ensembl transcript: ENST00000568098
  gene symbol: ACSM2B
  hgvsc: ENST00000568098.1:c.116+147G>C
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000566998
  gene symbol: ACSM2B
  hgvsc: ENST00000566998.1:n.1605-1G>C
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000569364
  gene symbol: ACSM2B
  hgvsc: ENST00000569364.1:n.1585-1G>C
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000457377
  ensembl transcript: ENST00000565322
  gene symbol: ACSM2B
  hgvsc: ENST00000565322.1:c.1173-1G>C
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000569131
  gene symbol: ACSM2B
  hgvsc: ENST00000569131.1:n.1154-1G>C
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: true
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000327453
  ensembl transcript: ENST00000329697
  gene symbol: ACSM2B
  hgvsc: ENST00000329697.6:c.1410-1G>C
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000563943
  gene symbol: ACSM2B
  hgvsc: ENST00000563943.1:n.1339-1G>C
  variant of: http://identifiers.org/hgnc/30931
canonical: true
consequence: splice acceptor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1125
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9136
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 788
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4753
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1150
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 852
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 969
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1541
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36800
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 885
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2439
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2548
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8971
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 112
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
hgvs: c.1410-1G>C
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD

http://identifiers.org/exac.variant/16-20554339-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20554339
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 20554339
    reference: chr 16
allele count: 3
allele frequency: 2.473003050037095e-5
allele num: 121310
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000456378
  ensembl transcript: ENST00000567001
  gene symbol: ACSM2B
  hgvsc: ENST00000567001.1:c.1410-4G>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000569131
  gene symbol: ACSM2B
  hgvsc: ENST00000569131.1:n.1154-4G>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000569364
  gene symbol: ACSM2B
  hgvsc: ENST00000569364.1:n.1585-4G>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000566998
  gene symbol: ACSM2B
  hgvsc: ENST00000566998.1:n.1605-4G>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000457377
  ensembl transcript: ENST00000565322
  gene symbol: ACSM2B
  hgvsc: ENST00000565322.1:c.1173-4G>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000454995
  ensembl transcript: ENST00000565232
  gene symbol: ACSM2B
  hgvsc: ENST00000565232.1:c.1410-4G>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000563943
  gene symbol: ACSM2B
  hgvsc: ENST00000563943.1:n.1339-4G>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000327453
  ensembl transcript: ENST00000329697
  gene symbol: ACSM2B
  hgvsc: ENST00000329697.6:c.1410-4G>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000455137
  ensembl transcript: ENST00000568098
  gene symbol: ACSM2B
  hgvsc: ENST00000568098.1:c.116+144G>T
  variant of: http://identifiers.org/hgnc/30931
canonical: true
consequence: splice region
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 885
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9138
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36738
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4743
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 789
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 852
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 969
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1151
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1125
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1540
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6562
  bin: 6.75e1
  variant carriers: 0
hgvs: c.1410-4G>T
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum

16-20554341-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20554341
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 20554341
    reference: chr 16
allele count: 1
allele frequency: 8.243615319934711e-6
allele num: 121306
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000566998
  gene symbol: ACSM2B
  hgvsc: ENST00000566998.1:n.1605-6C>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000456378
  ensembl transcript: ENST00000567001
  gene symbol: ACSM2B
  hgvsc: ENST00000567001.1:c.1410-6C>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000569131
  gene symbol: ACSM2B
  hgvsc: ENST00000569131.1:n.1154-6C>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000454995
  ensembl transcript: ENST00000565232
  gene symbol: ACSM2B
  hgvsc: ENST00000565232.1:c.1410-6C>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000455137
  ensembl transcript: ENST00000568098
  gene symbol: ACSM2B
  hgvsc: ENST00000568098.1:c.116+142C>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000457377
  ensembl transcript: ENST00000565322
  gene symbol: ACSM2B
  hgvsc: ENST00000565322.1:c.1173-6C>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000327453
  ensembl transcript: ENST00000329697
  gene symbol: ACSM2B
  hgvsc: ENST00000329697.6:c.1410-6C>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000569364
  gene symbol: ACSM2B
  hgvsc: ENST00000569364.1:n.1585-6C>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000563943
  gene symbol: ACSM2B
  hgvsc: ENST00000563943.1:n.1339-6C>T
  variant of: http://identifiers.org/hgnc/30931
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1126
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 885
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36704
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1540
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4738
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 789
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 969
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1152
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 852
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9109
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 5.75e1
  variant carriers: 0
hgvs: c.1410-6C>T
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
reference allele: G
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/16-20554356-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20554356
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 20554356
    reference: chr 16
allele count: 1
allele frequency: 8.246062505153789e-6
allele num: 121270
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000457377
  ensembl transcript: ENST00000565322
  gene symbol: ACSM2B
  hgvsc: ENST00000565322.1:c.1173-21G>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000456378
  ensembl transcript: ENST00000567001
  gene symbol: ACSM2B
  hgvsc: ENST00000567001.1:c.1410-21G>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000569364
  gene symbol: ACSM2B
  hgvsc: ENST00000569364.1:n.1585-21G>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000569131
  gene symbol: ACSM2B
  hgvsc: ENST00000569131.1:n.1154-21G>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000566998
  gene symbol: ACSM2B
  hgvsc: ENST00000566998.1:n.1605-21G>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000454995
  ensembl transcript: ENST00000565232
  gene symbol: ACSM2B
  hgvsc: ENST00000565232.1:c.1410-21G>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000327453
  ensembl transcript: ENST00000329697
  gene symbol: ACSM2B
  hgvsc: ENST00000329697.6:c.1410-21G>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000563943
  gene symbol: ACSM2B
  hgvsc: ENST00000563943.1:n.1339-21G>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000455137
  ensembl transcript: ENST00000568098
  gene symbol: ACSM2B
  hgvsc: ENST00000568098.1:c.116+127G>T
  variant of: http://identifiers.org/hgnc/30931
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1153
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1122
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1541
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36370
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4702
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 789
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9010
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 972
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 885
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 852
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 222
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3274
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2535
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: South Asian
population: East Asian
population: Other
reference allele: C
site quality: MQ
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP

16-20554360-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20554360
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 20554360
    reference: chr 16
allele count: 2
allele frequency: 1.649430121892886e-5
allele num: 121254
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000566998
  gene symbol: ACSM2B
  hgvsc: ENST00000566998.1:n.1605-25C>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000569131
  gene symbol: ACSM2B
  hgvsc: ENST00000569131.1:n.1154-25C>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000563943
  gene symbol: ACSM2B
  hgvsc: ENST00000563943.1:n.1339-25C>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000456378
  ensembl transcript: ENST00000567001
  gene symbol: ACSM2B
  hgvsc: ENST00000567001.1:c.1410-25C>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000454995
  ensembl transcript: ENST00000565232
  gene symbol: ACSM2B
  hgvsc: ENST00000565232.1:c.1410-25C>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000457377
  ensembl transcript: ENST00000565322
  gene symbol: ACSM2B
  hgvsc: ENST00000565322.1:c.1173-25C>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000569364
  gene symbol: ACSM2B
  hgvsc: ENST00000569364.1:n.1585-25C>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000327453
  ensembl transcript: ENST00000329697
  gene symbol: ACSM2B
  hgvsc: ENST00000329697.6:c.1410-25C>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000455137
  ensembl transcript: ENST00000568098
  gene symbol: ACSM2B
  hgvsc: ENST00000568098.1:c.116+123C>T
  variant of: http://identifiers.org/hgnc/30931
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8973
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 744
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 885
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4693
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 852
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1543
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 36288
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 789
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 972
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1122
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1153
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33104
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6513
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 252
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: South Asian
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum

16-20554360-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20554360
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 20554360
    reference: chr 16
allele count: 1
allele frequency: 8.24715060946443e-6
allele num: 121254
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000563943
  gene symbol: ACSM2B
  hgvsc: ENST00000563943.1:n.1339-25C>G
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000457377
  ensembl transcript: ENST00000565322
  gene symbol: ACSM2B
  hgvsc: ENST00000565322.1:c.1173-25C>G
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000456378
  ensembl transcript: ENST00000567001
  gene symbol: ACSM2B
  hgvsc: ENST00000567001.1:c.1410-25C>G
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000454995
  ensembl transcript: ENST00000565232
  gene symbol: ACSM2B
  hgvsc: ENST00000565232.1:c.1410-25C>G
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000327453
  ensembl transcript: ENST00000329697
  gene symbol: ACSM2B
  hgvsc: ENST00000329697.6:c.1410-25C>G
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000569131
  gene symbol: ACSM2B
  hgvsc: ENST00000569131.1:n.1154-25C>G
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000569364
  gene symbol: ACSM2B
  hgvsc: ENST00000569364.1:n.1585-25C>G
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000455137
  ensembl transcript: ENST00000568098
  gene symbol: ACSM2B
  hgvsc: ENST00000568098.1:c.116+123C>G
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000566998
  gene symbol: ACSM2B
  hgvsc: ENST00000566998.1:n.1605-25C>G
  variant of: http://identifiers.org/hgnc/30931
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1122
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1543
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 789
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4693
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8973
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 744
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36288
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 885
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 852
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1153
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 972
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6513
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8983
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
population: African
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: ReadPosRankSum

16-20554361-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20554361
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 20554361
    reference: chr 16
allele count: 1
allele frequency: 8.246742536698004e-6
allele num: 121260
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000327453
  ensembl transcript: ENST00000329697
  gene symbol: ACSM2B
  hgvsc: ENST00000329697.6:c.1410-26T>C
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000455137
  ensembl transcript: ENST00000568098
  gene symbol: ACSM2B
  hgvsc: ENST00000568098.1:c.116+122T>C
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000454995
  ensembl transcript: ENST00000565232
  gene symbol: ACSM2B
  hgvsc: ENST00000565232.1:c.1410-26T>C
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000569131
  gene symbol: ACSM2B
  hgvsc: ENST00000569131.1:n.1154-26T>C
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000457377
  ensembl transcript: ENST00000565322
  gene symbol: ACSM2B
  hgvsc: ENST00000565322.1:c.1173-26T>C
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000566998
  gene symbol: ACSM2B
  hgvsc: ENST00000566998.1:n.1605-26T>C
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000569364
  gene symbol: ACSM2B
  hgvsc: ENST00000569364.1:n.1585-26T>C
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000456378
  ensembl transcript: ENST00000567001
  gene symbol: ACSM2B
  hgvsc: ENST00000567001.1:c.1410-26T>C
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000563943
  gene symbol: ACSM2B
  hgvsc: ENST00000563943.1:n.1339-26T>C
  variant of: http://identifiers.org/hgnc/30931
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8935
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1540
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 772
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 884
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 852
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4684
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 971
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36298
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1122
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 789
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1158
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 263
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 154
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 198
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 156
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6518
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: A
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum

16-20554361-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20554361
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 20554361
    reference: chr 16
allele count: 5
allele frequency: 4.123371268349002e-5
allele num: 121260
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000454995
  ensembl transcript: ENST00000565232
  gene symbol: ACSM2B
  hgvsc: ENST00000565232.1:c.1410-26T>A
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000569364
  gene symbol: ACSM2B
  hgvsc: ENST00000569364.1:n.1585-26T>A
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000327453
  ensembl transcript: ENST00000329697
  gene symbol: ACSM2B
  hgvsc: ENST00000329697.6:c.1410-26T>A
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000566998
  gene symbol: ACSM2B
  hgvsc: ENST00000566998.1:n.1605-26T>A
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000569131
  gene symbol: ACSM2B
  hgvsc: ENST00000569131.1:n.1154-26T>A
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000457377
  ensembl transcript: ENST00000565322
  gene symbol: ACSM2B
  hgvsc: ENST00000565322.1:c.1173-26T>A
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000456378
  ensembl transcript: ENST00000567001
  gene symbol: ACSM2B
  hgvsc: ENST00000567001.1:c.1410-26T>A
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000563943
  gene symbol: ACSM2B
  hgvsc: ENST00000563943.1:n.1339-26T>A
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000455137
  ensembl transcript: ENST00000568098
  gene symbol: ACSM2B
  hgvsc: ENST00000568098.1:c.116+122T>A
  variant of: http://identifiers.org/hgnc/30931
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1122
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 772
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 36298
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 971
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1540
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 789
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 884
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4684
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8935
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 852
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1158
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 154
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1303
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1045
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8982
  bin: 9.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 6518
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: Other
reference allele: A
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQ

http://identifiers.org/exac.variant/16-20554365-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20554365
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 20554365
    reference: chr 16
allele count: 1
allele frequency: 8.248511143738554e-6
allele num: 121234
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000327453
  ensembl transcript: ENST00000329697
  gene symbol: ACSM2B
  hgvsc: ENST00000329697.6:c.1410-30G>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000563943
  gene symbol: ACSM2B
  hgvsc: ENST00000563943.1:n.1339-30G>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000569131
  gene symbol: ACSM2B
  hgvsc: ENST00000569131.1:n.1154-30G>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000569364
  gene symbol: ACSM2B
  hgvsc: ENST00000569364.1:n.1585-30G>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000566998
  gene symbol: ACSM2B
  hgvsc: ENST00000566998.1:n.1605-30G>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000456378
  ensembl transcript: ENST00000567001
  gene symbol: ACSM2B
  hgvsc: ENST00000567001.1:c.1410-30G>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000457377
  ensembl transcript: ENST00000565322
  gene symbol: ACSM2B
  hgvsc: ENST00000565322.1:c.1173-30G>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000455137
  ensembl transcript: ENST00000568098
  gene symbol: ACSM2B
  hgvsc: ENST00000568098.1:c.116+118G>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000454995
  ensembl transcript: ENST00000565232
  gene symbol: ACSM2B
  hgvsc: ENST00000565232.1:c.1410-30G>T
  variant of: http://identifiers.org/hgnc/30931
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 774
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 884
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8888
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4685
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 852
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1159
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 789
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1122
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 971
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36336
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1542
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 225
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 192
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3283
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 257
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
reference allele: C
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD

16-20554366-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20554366
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 20554366
    reference: chr 16
allele count: 2
allele frequency: 1.649511744523621e-5
allele num: 121248
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000454995
  ensembl transcript: ENST00000565232
  gene symbol: ACSM2B
  hgvsc: ENST00000565232.1:c.1410-31A>C
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000563943
  gene symbol: ACSM2B
  hgvsc: ENST00000563943.1:n.1339-31A>C
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000457377
  ensembl transcript: ENST00000565322
  gene symbol: ACSM2B
  hgvsc: ENST00000565322.1:c.1173-31A>C
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000455137
  ensembl transcript: ENST00000568098
  gene symbol: ACSM2B
  hgvsc: ENST00000568098.1:c.116+117A>C
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000327453
  ensembl transcript: ENST00000329697
  gene symbol: ACSM2B
  hgvsc: ENST00000329697.6:c.1410-31A>C
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000456378
  ensembl transcript: ENST00000567001
  gene symbol: ACSM2B
  hgvsc: ENST00000567001.1:c.1410-31A>C
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000569131
  gene symbol: ACSM2B
  hgvsc: ENST00000569131.1:n.1154-31A>C
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000569364
  gene symbol: ACSM2B
  hgvsc: ENST00000569364.1:n.1585-31A>C
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000566998
  gene symbol: ACSM2B
  hgvsc: ENST00000566998.1:n.1605-31A>C
  variant of: http://identifiers.org/hgnc/30931
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 971
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1542
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8883
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 852
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36351
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 788
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4679
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 767
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 884
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1121
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1161
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 190
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 245
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3289
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 236
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 181
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum

16-20554367-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20554367
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 20554367
    reference: chr 16
allele count: 3
allele frequency: 2.474512521033356e-5
allele num: 121236
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000456378
  ensembl transcript: ENST00000567001
  gene symbol: ACSM2B
  hgvsc: ENST00000567001.1:c.1410-32C>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000569131
  gene symbol: ACSM2B
  hgvsc: ENST00000569131.1:n.1154-32C>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000566998
  gene symbol: ACSM2B
  hgvsc: ENST00000566998.1:n.1605-32C>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000327453
  ensembl transcript: ENST00000329697
  gene symbol: ACSM2B
  hgvsc: ENST00000329697.6:c.1410-32C>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000563943
  gene symbol: ACSM2B
  hgvsc: ENST00000563943.1:n.1339-32C>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000454995
  ensembl transcript: ENST00000565232
  gene symbol: ACSM2B
  hgvsc: ENST00000565232.1:c.1410-32C>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000457377
  ensembl transcript: ENST00000565322
  gene symbol: ACSM2B
  hgvsc: ENST00000565322.1:c.1173-32C>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000455137
  ensembl transcript: ENST00000568098
  gene symbol: ACSM2B
  hgvsc: ENST00000568098.1:c.116+116C>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000569364
  gene symbol: ACSM2B
  hgvsc: ENST00000569364.1:n.1585-32C>T
  variant of: http://identifiers.org/hgnc/30931
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1121
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1161
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1544
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36338
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 851
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8884
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4692
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 972
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 788
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 884
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 150
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3295
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 241
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 225
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
population: South Asian
population: East Asian
population: Latino
reference allele: G
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: DP

http://identifiers.org/exac.variant/16-20554370-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20554370
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 20554370
    reference: chr 16
allele count: 148
allele frequency: 1.221081812481436e-3
allele num: 121204
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000569131
  gene symbol: ACSM2B
  hgvsc: ENST00000569131.1:n.1154-35G>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000457377
  ensembl transcript: ENST00000565322
  gene symbol: ACSM2B
  hgvsc: ENST00000565322.1:c.1173-35G>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000566998
  gene symbol: ACSM2B
  hgvsc: ENST00000566998.1:n.1605-35G>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000569364
  gene symbol: ACSM2B
  hgvsc: ENST00000569364.1:n.1585-35G>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000455137
  ensembl transcript: ENST00000568098
  gene symbol: ACSM2B
  hgvsc: ENST00000568098.1:c.116+113G>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000327453
  ensembl transcript: ENST00000329697
  gene symbol: ACSM2B
  hgvsc: ENST00000329697.6:c.1410-35G>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000456378
  ensembl transcript: ENST00000567001
  gene symbol: ACSM2B
  hgvsc: ENST00000567001.1:c.1410-35G>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000454995
  ensembl transcript: ENST00000565232
  gene symbol: ACSM2B
  hgvsc: ENST00000565232.1:c.1410-35G>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000563943
  gene symbol: ACSM2B
  hgvsc: ENST00000563943.1:n.1339-35G>T
  variant of: http://identifiers.org/hgnc/30931
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1221
  bin: 9.75e1
  variant carriers: 61
genotype depth: GenotypeDepth
  all individuals: 849
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1122
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8887
  bin: 2.75e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 883
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 7.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 8.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 4697
  bin: 3.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 1542
  bin: 3.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 746
  bin: 1.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 970
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 9.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 36262
  bin: 2.25e1
  variant carriers: 10
genotype quality: GenotypeQuality
  all individuals: 2446
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1048
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 184
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32945
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 1
population: Other
population: East Asian
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum

16-20554370-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20554370
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 20554370
    reference: chr 16
allele count: 1
allele frequency: 8.250552787036732e-6
allele num: 121204
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000569131
  gene symbol: ACSM2B
  hgvsc: ENST00000569131.1:n.1154-35G>A
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000327453
  ensembl transcript: ENST00000329697
  gene symbol: ACSM2B
  hgvsc: ENST00000329697.6:c.1410-35G>A
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000566998
  gene symbol: ACSM2B
  hgvsc: ENST00000566998.1:n.1605-35G>A
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000569364
  gene symbol: ACSM2B
  hgvsc: ENST00000569364.1:n.1585-35G>A
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000563943
  gene symbol: ACSM2B
  hgvsc: ENST00000563943.1:n.1339-35G>A
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000454995
  ensembl transcript: ENST00000565232
  gene symbol: ACSM2B
  hgvsc: ENST00000565232.1:c.1410-35G>A
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000456378
  ensembl transcript: ENST00000567001
  gene symbol: ACSM2B
  hgvsc: ENST00000567001.1:c.1410-35G>A
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000457377
  ensembl transcript: ENST00000565322
  gene symbol: ACSM2B
  hgvsc: ENST00000565322.1:c.1173-35G>A
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000455137
  ensembl transcript: ENST00000568098
  gene symbol: ACSM2B
  hgvsc: ENST00000568098.1:c.116+113G>A
  variant of: http://identifiers.org/hgnc/30931
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1122
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8887
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36262
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1542
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 883
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 849
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4697
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1221
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 746
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 970
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9120
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 165
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2446
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 184
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum

16-20554373-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20554373
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 20554373
    reference: chr 16
allele count: 7
allele frequency: 5.776149453741294e-5
allele num: 121188
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000569364
  gene symbol: ACSM2B
  hgvsc: ENST00000569364.1:n.1585-38G>A
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000569131
  gene symbol: ACSM2B
  hgvsc: ENST00000569131.1:n.1154-38G>A
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000327453
  ensembl transcript: ENST00000329697
  gene symbol: ACSM2B
  hgvsc: ENST00000329697.6:c.1410-38G>A
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000454995
  ensembl transcript: ENST00000565232
  gene symbol: ACSM2B
  hgvsc: ENST00000565232.1:c.1410-38G>A
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000563943
  gene symbol: ACSM2B
  hgvsc: ENST00000563943.1:n.1339-38G>A
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000455137
  ensembl transcript: ENST00000568098
  gene symbol: ACSM2B
  hgvsc: ENST00000568098.1:c.116+110G>A
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000457377
  ensembl transcript: ENST00000565322
  gene symbol: ACSM2B
  hgvsc: ENST00000565322.1:c.1173-38G>A
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000566998
  gene symbol: ACSM2B
  hgvsc: ENST00000566998.1:n.1605-38G>A
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000456378
  ensembl transcript: ENST00000567001
  gene symbol: ACSM2B
  hgvsc: ENST00000567001.1:c.1410-38G>A
  variant of: http://identifiers.org/hgnc/30931
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8917
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 850
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4714
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 682
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1226
  bin: 9.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 36278
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1542
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 883
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 968
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1122
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 193
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1312
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2553
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3327
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33023
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: African
reference allele: C
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ

16-20554374-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20554374
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 20554374
    reference: chr 16
allele count: 1
allele frequency: 8.251642076773278e-6
allele num: 121188
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000327453
  ensembl transcript: ENST00000329697
  gene symbol: ACSM2B
  hgvsc: ENST00000329697.6:c.1410-39C>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000569364
  gene symbol: ACSM2B
  hgvsc: ENST00000569364.1:n.1585-39C>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000456378
  ensembl transcript: ENST00000567001
  gene symbol: ACSM2B
  hgvsc: ENST00000567001.1:c.1410-39C>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000563943
  gene symbol: ACSM2B
  hgvsc: ENST00000563943.1:n.1339-39C>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000454995
  ensembl transcript: ENST00000565232
  gene symbol: ACSM2B
  hgvsc: ENST00000565232.1:c.1410-39C>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000455137
  ensembl transcript: ENST00000568098
  gene symbol: ACSM2B
  hgvsc: ENST00000568098.1:c.116+109C>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000566998
  gene symbol: ACSM2B
  hgvsc: ENST00000566998.1:n.1605-39C>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000457377
  ensembl transcript: ENST00000565322
  gene symbol: ACSM2B
  hgvsc: ENST00000565322.1:c.1173-39C>T
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000569131
  gene symbol: ACSM2B
  hgvsc: ENST00000569131.1:n.1154-39C>T
  variant of: http://identifiers.org/hgnc/30931
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 793
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 883
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36280
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 849
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1227
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1540
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4727
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1123
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8940
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 968
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 190
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33040
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6558
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 126
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: DP

16-20554380-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20554380
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 20554380
    reference: chr 16
allele count: 3
allele frequency: 2.476514388548598e-5
allele num: 121138
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000456378
  ensembl transcript: ENST00000567001
  gene symbol: ACSM2B
  hgvsc: ENST00000567001.1:c.1410-45G>C
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000563943
  gene symbol: ACSM2B
  hgvsc: ENST00000563943.1:n.1339-45G>C
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000454995
  ensembl transcript: ENST00000565232
  gene symbol: ACSM2B
  hgvsc: ENST00000565232.1:c.1410-45G>C
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000569364
  gene symbol: ACSM2B
  hgvsc: ENST00000569364.1:n.1585-45G>C
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000457377
  ensembl transcript: ENST00000565322
  gene symbol: ACSM2B
  hgvsc: ENST00000565322.1:c.1173-45G>C
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000327453
  ensembl transcript: ENST00000329697
  gene symbol: ACSM2B
  hgvsc: ENST00000329697.6:c.1410-45G>C
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000569131
  gene symbol: ACSM2B
  hgvsc: ENST00000569131.1:n.1154-45G>C
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000566998
  gene symbol: ACSM2B
  hgvsc: ENST00000566998.1:n.1605-45G>C
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000455137
  ensembl transcript: ENST00000568098
  gene symbol: ACSM2B
  hgvsc: ENST00000568098.1:c.116+103G>C
  variant of: http://identifiers.org/hgnc/30931
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 850
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4757
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1229
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8994
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36361
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1124
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1540
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 968
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 885
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2588
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 144
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33127
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Other
population: European (Finnish)
population: East Asian
population: African
population: Latino
reference allele: C
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff

16-20554381-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20554381
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 20554381
    reference: chr 16
allele count: 1
allele frequency: 8.25559316436886e-6
allele num: 121130
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000456378
  ensembl transcript: ENST00000567001
  gene symbol: ACSM2B
  hgvsc: ENST00000567001.1:c.1410-46A>G
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000455137
  ensembl transcript: ENST00000568098
  gene symbol: ACSM2B
  hgvsc: ENST00000568098.1:c.116+102A>G
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000457377
  ensembl transcript: ENST00000565322
  gene symbol: ACSM2B
  hgvsc: ENST00000565322.1:c.1173-46A>G
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000327453
  ensembl transcript: ENST00000329697
  gene symbol: ACSM2B
  hgvsc: ENST00000329697.6:c.1410-46A>G
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000566998
  gene symbol: ACSM2B
  hgvsc: ENST00000566998.1:n.1605-46A>G
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000569131
  gene symbol: ACSM2B
  hgvsc: ENST00000569131.1:n.1154-46A>G
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000569364
  gene symbol: ACSM2B
  hgvsc: ENST00000569364.1:n.1585-46A>G
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl protein: ENSP00000454995
  ensembl transcript: ENST00000565232
  gene symbol: ACSM2B
  hgvsc: ENST00000565232.1:c.1410-46A>G
  variant of: http://identifiers.org/hgnc/30931
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000066813
  ensembl transcript: ENST00000563943
  gene symbol: ACSM2B
  hgvsc: ENST00000563943.1:n.1339-46A>G
  variant of: http://identifiers.org/hgnc/30931
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 885
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1124
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1541
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9012
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 969
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4756
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 849
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36363
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1230
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33176
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1319
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 105
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
reference allele: T

GenotypeQuality
all individuals: 556
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 143
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 191
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 345
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 681
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 513
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 324
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 74
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 96
bin: 9.25e1
variant carriers: 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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66630
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.637070305752289e-5
allele num: 11578
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16322
num of homozygotes: 0

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

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

DP
type: SiteQuality
SIO_000300: 6.302945e6

MQRankSum
type: SiteQuality
SIO_000300: 1.2e-2

QD
type: SiteQuality
SIO_000300: 9.66e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.73e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.59e-1

FS
type: SiteQuality
SIO_000300: 6.639e0

VQSLOD
type: SiteQuality
SIO_000300: -1.274e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -2.193e0

MQ
type: SiteQuality
SIO_000300: 5.426e1

GenotypeQuality
all individuals: 334
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 643
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 147
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 74
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 499
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 330
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 183
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1510
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 96
bin: 9.25e1
variant carriers: 0

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16288
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.00228173411793e-5
allele num: 66616
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.79e-1

FS
type: SiteQuality
SIO_000300: 3.573e0

QD
type: SiteQuality
SIO_000300: 8.73e0

MQ
type: SiteQuality
SIO_000300: 5.74e1

VQSLOD
type: SiteQuality
SIO_000300: -1.569e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

DP
type: SiteQuality
SIO_000300: 6.302857e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.45e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.241e0

MQRankSum
type: SiteQuality
SIO_000300: 1.66e0

GenotypeQuality
all individuals: 1100
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 74
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 96
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 386
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 145
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 174
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 434
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 54932
bin: 9.75e1
variant carriers: 1

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

East Asian
type: Population
allele count: 1
allele frequency: 1.155802126675913e-4
allele num: 8652
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16276
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66596
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

FS
type: SiteQuality
SIO_000300: 2.1037e1

DP
type: SiteQuality
SIO_000300: 6.300426e6

ClippingRankSum
type: SiteQuality
SIO_000300: 2.14e-1

MQ
type: SiteQuality
SIO_000300: 5.606e1

VQSLOD
type: SiteQuality
SIO_000300: -4.672e0

MQRankSum
type: SiteQuality
SIO_000300: 3.22e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.54e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.72e-1

QD
type: SiteQuality
SIO_000300: 9.359999999999999e0

GenotypeQuality
all individuals: 745
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 118
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 639
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 680
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 74
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 95
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 168
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 361
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 131
bin: 7.25e1
variant carriers: 0

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

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.173601679219657e-5
allele num: 16198
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66558
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 4.607e0

VQSLOD
type: SiteQuality
SIO_000300: -1.639e0

MQRankSum
type: SiteQuality
SIO_000300: 3.23e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 2.69e-1

QD
type: SiteQuality
SIO_000300: 5.75e0

MQ
type: SiteQuality
SIO_000300: 5.07e1

DP
type: SiteQuality
SIO_000300: 6.299334e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.19e0

GenotypeQuality
all individuals: 403
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 352
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 706
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 467
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 674
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 108
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 171
bin: 7.75e1
variant carriers: 0

South Asian
type: Population
allele count: 65
allele frequency: 4.012841091492777e-3
allele num: 16198
num of homozygotes: 0

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

East Asian
type: Population
allele count: 2
allele frequency: 2.311604253351826e-4
allele num: 8652
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.506805275966709e-5
allele num: 66566
num of homozygotes: 0

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

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

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

VQSLOD
type: SiteQuality
SIO_000300: -6.733e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.17e-1

FS
type: SiteQuality
SIO_000300: 8.637e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.38e0

DP
type: SiteQuality
SIO_000300: 6.299287e6

MQRankSum
type: SiteQuality
SIO_000300: 4.03e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.95e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

QD
type: SiteQuality
SIO_000300: 1.071e1

MQ
type: SiteQuality
SIO_000300: 5.354e1

GenotypeQuality
all individuals: 124
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 671
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 338
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 352
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 95
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 400
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 678
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 172
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 144
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 54932
bin: 9.75e1
variant carriers: 9

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

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

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: 1.155802126675913e-4
allele num: 8652
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 8
allele frequency: 1.201923076923077e-4
allele num: 66560
num of homozygotes: 0

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

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

DP
type: SiteQuality
SIO_000300: 6.299298e6

FS
type: SiteQuality
SIO_000300: 8.536e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.01e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.49e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.455e0

MQRankSum
type: SiteQuality
SIO_000300: -1.25e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.4e-1

QD
type: SiteQuality
SIO_000300: 1.325e1

MQ
type: SiteQuality
SIO_000300: 5.43e1

GenotypeQuality
all individuals: 346
bin: 8.75e1
variant carriers: 6

GenotypeQuality
all individuals: 887
bin: 7.5e0
variant carriers: 2

GenotypeQuality
all individuals: 539
bin: 5.75e1
variant carriers: 7

GenotypeQuality
all individuals: 3366
bin: 5.25e1
variant carriers: 6

GenotypeQuality
all individuals: 889
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6130
bin: 4.75e1
variant carriers: 7

GenotypeQuality
all individuals: 7182
bin: 3.25e1
variant carriers: 4

GenotypeQuality
all individuals: 779
bin: 8.25e1
variant carriers: 13

GenotypeQuality
all individuals: 1542
bin: 1.75e1
variant carriers: 3

GenotypeQuality
all individuals: 7518
bin: 3.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1109
bin: 2.5e0
variant carriers: 1

GenotypeQuality
all individuals: 442
bin: 9.25e1
variant carriers: 10

GenotypeQuality
all individuals: 948
bin: 7.25e1
variant carriers: 13

GenotypeQuality
all individuals: 3482
bin: 9.75e1
variant carriers: 260

African
type: Population
allele count: 311
allele frequency: 3.972917731221257e-2
allele num: 7828
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 20
allele frequency: 3.616244168806278e-4
allele num: 55306
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5318
num of homozygotes: 0

Latino
type: Population
allele count: 12
allele frequency: 1.346196993493381e-3
allele num: 8914
num of homozygotes: 0

East Asian
type: Population
allele count: 7
allele frequency: 1.067724222086638e-3
allele num: 6556
num of homozygotes: 0

South Asian
type: Population
allele count: 6
allele frequency: 4.616094783812894e-4
allele num: 12998
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 732
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.645e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-2

FS
type: SiteQuality
SIO_000300: 1.354e0

MQRankSum
type: SiteQuality
SIO_000300: -1.444e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.62e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.157e0

MQ
type: SiteQuality
SIO_000300: 3.938e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.6e-1

QD
type: SiteQuality
SIO_000300: 4.57e0

DP
type: SiteQuality
SIO_000300: 1.108886e6

GenotypeQuality
all individuals: 1013
bin: 7.25e1
variant carriers: 13

GenotypeQuality
all individuals: 1217
bin: 7.75e1
variant carriers: 10

GenotypeQuality
all individuals: 363
bin: 8.75e1
variant carriers: 6

GenotypeQuality
all individuals: 3715
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1017
bin: 1.75e1
variant carriers: 3

GenotypeQuality
all individuals: 7378
bin: 3.75e1
variant carriers: 2

GenotypeQuality
all individuals: 2869
bin: 6.75e1
variant carriers: 12

GenotypeQuality
all individuals: 3490
bin: 9.75e1
variant carriers: 256

GenotypeQuality
all individuals: 924
bin: 2.5e0
variant carriers: 1

GenotypeQuality
all individuals: 732
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1821
bin: 5.25e1
variant carriers: 8

GenotypeQuality
all individuals: 455
bin: 9.25e1
variant carriers: 9

GenotypeQuality
all individuals: 10843
bin: 6.25e1
variant carriers: 9

GenotypeQuality
all individuals: 800
bin: 7.5e0
variant carriers: 2

Latino
type: Population
allele count: 12
allele frequency: 1.333926189417519e-3
allele num: 8996
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 18
allele frequency: 3.231829933927033e-4
allele num: 55696
num of homozygotes: 0

South Asian
type: Population
allele count: 6
allele frequency: 4.551661356395084e-4
allele num: 13182
num of homozygotes: 0

East Asian
type: Population
allele count: 6
allele frequency: 9.082652134423251e-4
allele num: 6606
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5344
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 734
num of homozygotes: 0

African
type: Population
allele count: 311
allele frequency: 3.948704926358557e-2
allele num: 7876
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.687e0

MQ
type: SiteQuality
SIO_000300: 3.931e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.92e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.1e-3

DP
type: SiteQuality
SIO_000300: 1.131569e6

VQSLOD
type: SiteQuality
SIO_000300: -2.055e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.29e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.12e-1

QD
type: SiteQuality
SIO_000300: 4.24e0

GenotypeQuality
all individuals: 576
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2010
bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3548
bin: 9.75e1
variant carriers: 2

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2198
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1811
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3153
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 706
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 284
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30244
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 105
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6519
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4956
bin: 6.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5692
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8796
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14016
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.369612831485662e-5
allele num: 59354
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9784
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7506
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 808
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.330147e6

QD
type: SiteQuality
SIO_000300: 1.31e1

VQSLOD
type: SiteQuality
SIO_000300: 4.64e0

MQRankSum
type: SiteQuality
SIO_000300: 5.72e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.37e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.34e-1

MQ
type: SiteQuality
SIO_000300: 4.523e1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.01e-1

GenotypeQuality
all individuals: 32215
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1499
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 382
bin: 4.75e1
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GenotypeQuality
all individuals: 639
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2007
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 800
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 129
bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 92
bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3602
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1874
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2280
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 670
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9024
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5868
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61154
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.561475409836066e-4
allele num: 7808
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 820
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10190
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14340
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.758e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.5e-3

DP
type: SiteQuality
SIO_000300: 1.386282e6

MQ
type: SiteQuality
SIO_000300: 4.333e1

MQRankSum
type: SiteQuality
SIO_000300: -4.0e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.964e0

QD
type: SiteQuality
SIO_000300: 1.074e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.99e-1

GenotypeQuality
all individuals: 92
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 129
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 382
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1524
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 58
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variant carriers: 0

GenotypeQuality
all individuals: 5528
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variant carriers: 0

GenotypeQuality
all individuals: 1032
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variant carriers: 0

GenotypeQuality
all individuals: 2007
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variant carriers: 0

GenotypeQuality
all individuals: 646
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variant carriers: 0

GenotypeQuality
all individuals: 330
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32215
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variant carriers: 0

GenotypeQuality
all individuals: 670
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 800
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1874
bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61154
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10190
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14340
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.280737704918033e-4
allele num: 7808
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 820
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9024
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5868
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.758e0

QD
type: SiteQuality
SIO_000300: 1.074e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.5e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.99e-1

MQRankSum
type: SiteQuality
SIO_000300: -4.0e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.0e0

MQ
type: SiteQuality
SIO_000300: 4.333e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.964e0

DP
type: SiteQuality
SIO_000300: 1.386282e6

GenotypeQuality
all individuals: 99
bin: 2.5e0
variant carriers: 1

GenotypeQuality
all individuals: 52
bin: 1.25e1
variant carriers: 3

GenotypeQuality
all individuals: 6041
bin: 6.75e1
variant carriers: 2

GenotypeQuality
all individuals: 2549
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 750
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variant carriers: 0

GenotypeQuality
all individuals: 182
bin: 4.75e1
variant carriers: 3

GenotypeQuality
all individuals: 36714
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variant carriers: 0

GenotypeQuality
all individuals: 792
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variant carriers: 2

GenotypeQuality
all individuals: 217
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variant carriers: 10

GenotypeQuality
all individuals: 3631
bin: 9.75e1
variant carriers: 16

GenotypeQuality
all individuals: 675
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variant carriers: 4

GenotypeQuality
all individuals: 381
bin: 3.75e1
variant carriers: 3

GenotypeQuality
all individuals: 274
bin: 5.75e1
variant carriers: 3

GenotypeQuality
all individuals: 880
bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 12
allele frequency: 8.064516129032258e-4
allele num: 14880
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 848
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 9.228497600590623e-5
allele num: 10836
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 33
allele frequency: 5.185906905113618e-4
allele num: 63634
num of homozygotes: 1

African
type: Population
allele count: 9
allele frequency: 9.572431397574984e-4
allele num: 9402
num of homozygotes: 1

East Asian
type: Population
allele count: 2
allele frequency: 2.416042522348393e-4
allele num: 8278
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6120
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.75e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 5.53e-1

VQSLOD
type: SiteQuality
SIO_000300: -9.099e0

MQ
type: SiteQuality
SIO_000300: 4.565e1

DP
type: SiteQuality
SIO_000300: 1.458647e6

MQRankSum
type: SiteQuality
SIO_000300: -3.526e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.58e-1

FS
type: SiteQuality
SIO_000300: 3.7319e1

QD
type: SiteQuality
SIO_000300: 9.1e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.13e-1

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

GenotypeQuality
all individuals: 340
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 878
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
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variant carriers: 0

GenotypeQuality
all individuals: 2086
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variant carriers: 0

GenotypeQuality
all individuals: 2371
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 431
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GenotypeQuality
all individuals: 36243
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variant carriers: 0

GenotypeQuality
all individuals: 27
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variant carriers: 0

GenotypeQuality
all individuals: 506
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variant carriers: 0

GenotypeQuality
all individuals: 1042
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variant carriers: 0

GenotypeQuality
all individuals: 2320
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6444
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2981
bin: 7.75e1
variant carriers: 0

South Asian
type: Population
allele count: 3
allele frequency: 1.953379346269045e-4
allele num: 15358
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9682
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11110
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64800
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8460
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6262
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 4.111e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.47e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.17e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.861e0

MQRankSum
type: SiteQuality
SIO_000300: -3.71e-1

DP
type: SiteQuality
SIO_000300: 1.495885e6

FS
type: SiteQuality
SIO_000300: 8.957000000000001e0

QD
type: SiteQuality
SIO_000300: 1.106e1

VQSLOD
type: SiteQuality
SIO_000300: -2.48e0

GenotypeQuality
all individuals: 382
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2429
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3057
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 69
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GenotypeQuality
all individuals: 465
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GenotypeQuality
all individuals: 1063
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variant carriers: 0

GenotypeQuality
all individuals: 29
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GenotypeQuality
all individuals: 905
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GenotypeQuality
all individuals: 320
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GenotypeQuality
all individuals: 6536
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variant carriers: 0

GenotypeQuality
all individuals: 2150
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variant carriers: 0

GenotypeQuality
all individuals: 36314
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2064
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3816
bin: 9.75e1
variant carriers: 2

East Asian
type: Population
allele count: 2
allele frequency: 2.357934449422306e-4
allele num: 8482
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6308
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15474
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9740
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65064
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11162
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.503834e6

VQSLOD
type: SiteQuality
SIO_000300: -2.868e0

MQ
type: SiteQuality
SIO_000300: 4.103e1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.12e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.92e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.45e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.803e0

FS
type: SiteQuality
SIO_000300: 1.0508e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

QD
type: SiteQuality
SIO_000300: 1.436e1

GenotypeQuality
all individuals: 29
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 257
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 320
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3057
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 382
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variant carriers: 0

GenotypeQuality
all individuals: 245
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GenotypeQuality
all individuals: 2150
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 465
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GenotypeQuality
all individuals: 1063
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GenotypeQuality
all individuals: 2429
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variant carriers: 0

GenotypeQuality
all individuals: 69
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GenotypeQuality
all individuals: 36314
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 905
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 148
bin: 4.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11162
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6308
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.073896471166851e-5
allele num: 65064
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15474
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8482
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9740
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.45e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -2.868e0

MQRankSum
type: SiteQuality
SIO_000300: 2.92e-1

FS
type: SiteQuality
SIO_000300: 1.0508e1

MQ
type: SiteQuality
SIO_000300: 4.103e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.803e0

QD
type: SiteQuality
SIO_000300: 1.436e1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.12e-1

DP
type: SiteQuality
SIO_000300: 1.503834e6

GenotypeQuality
all individuals: 169
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 309
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
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GenotypeQuality
all individuals: 6687
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GenotypeQuality
all individuals: 1105
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GenotypeQuality
all individuals: 945
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GenotypeQuality
all individuals: 3844
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GenotypeQuality
all individuals: 14
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GenotypeQuality
all individuals: 372
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GenotypeQuality
all individuals: 292
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GenotypeQuality
all individuals: 36807
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GenotypeQuality
all individuals: 2234
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GenotypeQuality
all individuals: 219
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2500
bin: 7.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15684
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11240
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6344
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.527043948324833e-5
allele num: 65486
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9844
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 868
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8562
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.517027e6

VQSLOD
type: SiteQuality
SIO_000300: -2.772e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.28e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.43e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 3.914e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 8.97e-1

QD
type: SiteQuality
SIO_000300: 1.182e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.56e0

GenotypeQuality
all individuals: 8
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variant carriers: 0

GenotypeQuality
all individuals: 234
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GenotypeQuality
all individuals: 973
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GenotypeQuality
all individuals: 2307
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GenotypeQuality
all individuals: 30
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GenotypeQuality
all individuals: 109
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 145
bin: 5.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8590
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6388
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9918
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.299609424215698e-5
allele num: 15874
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65826
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11324
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.5e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 5.6e-2

VQSLOD
type: SiteQuality
SIO_000300: -2.485e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.062e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.81e-1

FS
type: SiteQuality
SIO_000300: 3.746e0

DP
type: SiteQuality
SIO_000300: 1.528761e6

QD
type: SiteQuality
SIO_000300: 3.082e1

MQ
type: SiteQuality
SIO_000300: 3.796e1

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.25e1
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 880
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9972
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15994
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66044
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6428
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11364
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.160631383472609e-4
allele num: 8616
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.05e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -1.39e-1

DP
type: SiteQuality
SIO_000300: 1.534636e6

MQ
type: SiteQuality
SIO_000300: 3.878e1

QD
type: SiteQuality
SIO_000300: 9.51e0

VQSLOD
type: SiteQuality
SIO_000300: -3.894e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.93e0

FS
type: SiteQuality
SIO_000300: 3.911e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.46e0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 23

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6468
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66194
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10022
num of homozygotes: 0

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

South Asian
type: Population
allele count: 26
allele frequency: 1.611303916707982e-3
allele num: 16136
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 884
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.42e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 3.987e1

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -2.537e0

BaseQRankSum
type: SiteQuality
SIO_000300: -8.500000000000001e-2

DP
type: SiteQuality
SIO_000300: 1.542496e6

MQRankSum
type: SiteQuality
SIO_000300: 7.0e-1

QD
type: SiteQuality
SIO_000300: 1.251e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 1.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66238
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16170
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10046
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6478
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 886
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.750700280112045e-4
allele num: 11424
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.588e0

DP
type: SiteQuality
SIO_000300: 1.544548e6

VQSLOD
type: SiteQuality
SIO_000300: -2.357e0

MQRankSum
type: SiteQuality
SIO_000300: 1.07e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.73e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.37e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

FS
type: SiteQuality
SIO_000300: 1.948e0

QD
type: SiteQuality
SIO_000300: 9.949999999999999e0

MQ
type: SiteQuality
SIO_000300: 4.199e1

GenotypeQuality
all individuals: 1055
bin: 8.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 319
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GenotypeQuality
all individuals: 80
bin: 5.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11500
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.502900598154438e-5
allele num: 66538
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6546
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10196
num of homozygotes: 0

South Asian
type: Population
allele count: 7
allele frequency: 4.25273390036452e-4
allele num: 16460
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 896
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BaseQRankSum
type: SiteQuality
SIO_000300: -1.804e0

MQ
type: SiteQuality
SIO_000300: 4.114e1

VQSLOD
type: SiteQuality
SIO_000300: -2.492e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.8e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.8e-2

QD
type: SiteQuality
SIO_000300: 9.609999999999999e0

MQRankSum
type: SiteQuality
SIO_000300: 6.51e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.75e-1

DP
type: SiteQuality
SIO_000300: 1.561259e6

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 3

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 150
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GenotypeQuality
all individuals: 2500
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variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11510
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16476
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6552
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.003995313767311e-5
allele num: 66578
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.155802126675913e-4
allele num: 8652
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
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VQSLOD
type: SiteQuality
SIO_000300: -1.978e0

FS
type: SiteQuality
SIO_000300: 7.63e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.16e0

DP
type: SiteQuality
SIO_000300: 1.56267e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.85e-1

MQ
type: SiteQuality
SIO_000300: 3.921e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.99e-1

QD
type: SiteQuality
SIO_000300: 1.038e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.46e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1064
bin: 8.75e1
variant carriers: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
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East Asian
type: Population
allele count: 1
allele frequency: 1.155802126675913e-4
allele num: 8652
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66628
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -1.064e0

FS
type: SiteQuality
SIO_000300: 1.105e0

MQRankSum
type: SiteQuality
SIO_000300: 7.68e-1

ReadPosRankSum
type: SiteQuality
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QD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.565644e6

MQ
type: SiteQuality
SIO_000300: 4.136e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.906e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 1.8e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 25
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 4.75e1
variant carriers: 0

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

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

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10274
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South Asian
type: Population
allele count: 0
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allele num: 16486
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 7.68e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

BaseQRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 4.136e1

FS
type: SiteQuality
SIO_000300: 1.105e0

ReadPosRankSum
type: SiteQuality
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QD
type: SiteQuality
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VQSLOD
type: SiteQuality
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DP
type: SiteQuality
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ClippingRankSum
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SIO_000300: -1.064e0

GenotypeQuality
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variant carriers: 14

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 10

GenotypeQuality
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GenotypeQuality
all individuals: 13
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 9655
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variant carriers: 6040

GenotypeQuality
all individuals: 37
bin: 4.25e1
variant carriers: 6

South Asian
type: Population
allele count: 1224
allele frequency: 7.424481378139026e-2
allele num: 16486
num of homozygotes: 64

Latino
type: Population
allele count: 963
allele frequency: 8.35792397153272e-2
allele num: 11522
num of homozygotes: 40

East Asian
type: Population
allele count: 1467
allele frequency: 1.699884125144843e-1
allele num: 8630
num of homozygotes: 138

African
type: Population
allele count: 1208
allele frequency: 1.17601246105919e-1
allele num: 10272
num of homozygotes: 109

European (Non-Finnish)
type: Population
allele count: 1496
allele frequency: 2.24496533509409e-2
allele num: 66638
num of homozygotes: 10

Other
type: Population
allele count: 56
allele frequency: 6.222222222222222e-2
allele num: 900
num of homozygotes: 3

European (Finnish)
type: Population
allele count: 122
allele frequency: 1.854103343465046e-2
allele num: 6580
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.74e-1

QD
type: SiteQuality
SIO_000300: 1.261e1

MQ
type: SiteQuality
SIO_000300: 4.031e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.11e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.88e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.33e0

DP
type: SiteQuality
SIO_000300: 1.808934e6

MQRankSum
type: SiteQuality
SIO_000300: 6.95e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.569999999999999e-2

FS
type: SiteQuality
SIO_000300: 6.39e-1

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

GenotypeQuality
all individuals: 6621
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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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GenotypeQuality
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GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 96
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1041
bin: 8.75e1
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: 10326
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: 6594
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.49947518368571e-5
allele num: 66690
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.788535e6

MQ
type: SiteQuality
SIO_000300: 4.063e1

QD
type: SiteQuality
SIO_000300: 1.157e1

MQRankSum
type: SiteQuality
SIO_000300: 1.9e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.69e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.69e-1

FS
type: SiteQuality
SIO_000300: 9.645e0

VQSLOD
type: SiteQuality
SIO_000300: -3.117e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.6e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

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

GenotypeQuality
all individuals: 13
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 3.75e1
variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10334
num of homozygotes: 0

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

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

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

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

MQRankSum
type: SiteQuality
SIO_000300: 8.699999999999999e-2

DP
type: SiteQuality
SIO_000300: 1.78958e6

FS
type: SiteQuality
SIO_000300: 1.964e0

VQSLOD
type: SiteQuality
SIO_000300: -2.206e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.01e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 3.46e0

MQ
type: SiteQuality
SIO_000300: 4.16e1

QD
type: SiteQuality
SIO_000300: 1.195e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.53e-1

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

GenotypeQuality
all individuals: 10
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 6
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variant carriers: 0

GenotypeQuality
all individuals: 1292
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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
all individuals: 2433
bin: 8.25e1
variant carriers: 0

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

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

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

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10340
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: -2.582e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.8e-1

QD
type: SiteQuality
SIO_000300: 1.126e1

FS
type: SiteQuality
SIO_000300: 6.784e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.6e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 9.419999999999999e-1

MQRankSum
type: SiteQuality
SIO_000300: 8.1e-2

MQ
type: SiteQuality
SIO_000300: 4.167e1

DP
type: SiteQuality
SIO_000300: 1.789767e6

GenotypeQuality
all individuals: 3291
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 3
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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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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 2437
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variant carriers: 0

GenotypeQuality
all individuals: 6640
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 2.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 3
allele frequency: 1.816860465116279e-4
allele num: 16512
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66714
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.647526807333103e-5
allele num: 11564
num of homozygotes: 0

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

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

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

DP
type: SiteQuality
SIO_000300: 1.790674e6

ClippingRankSum
type: SiteQuality
SIO_000300: -3.29e-1

FS
type: SiteQuality
SIO_000300: 5.612e0

MQRankSum
type: SiteQuality
SIO_000300: 9.99e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 9.13e-1

QD
type: SiteQuality
SIO_000300: 1.148e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.48e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.867e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

MQ
type: SiteQuality
SIO_000300: 3.989e1

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

GenotypeQuality
all individuals: 2436
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1049
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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: 4
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 9
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variant carriers: 0

GenotypeQuality
all individuals: 34629
bin: 6.25e1
variant carriers: 0

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

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

East Asian
type: Population
allele count: 8
allele frequency: 9.244280101687081e-4
allele num: 8654
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.997691777331455e-5
allele num: 66718
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.66183574879227e-5
allele num: 10350
num of homozygotes: 0

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: -8.19e-1

FS
type: SiteQuality
SIO_000300: 3.434e0

BaseQRankSum
type: SiteQuality
SIO_000300: 8.75e-1

MQ
type: SiteQuality
SIO_000300: 4.072e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.03e-1

VQSLOD
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: 7.27e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

DP
type: SiteQuality
SIO_000300: 1.791636e6

QD
type: SiteQuality
SIO_000300: 1.091e1

GenotypeQuality
all individuals: 5
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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
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 4
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variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498845888665727e-5
allele num: 66718
num of homozygotes: 0

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

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

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

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

DP
type: SiteQuality
SIO_000300: 1.791636e6

ClippingRankSum
type: SiteQuality
SIO_000300: -8.19e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.03e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.27e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 8.75e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.714e0

MQ
type: SiteQuality
SIO_000300: 4.072e1

FS
type: SiteQuality
SIO_000300: 3.434e0

QD
type: SiteQuality
SIO_000300: 1.091e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

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

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

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10362
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 2.092e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.696e0

ReadPosRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: -2.315e0

MQ
type: SiteQuality
SIO_000300: 4.3e1

DP
type: SiteQuality
SIO_000300: 1.792231e6

QD
type: SiteQuality
SIO_000300: 9.98e0

MQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -3.096e0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8720
bin: 9.75e1
variant carriers: 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: 11568
num of homozygotes: 0

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

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

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

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

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

MQ
type: SiteQuality
SIO_000300: 4.136e1

DP
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-3

MQRankSum
type: SiteQuality
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QD
type: SiteQuality
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FS
type: SiteQuality
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VQSLOD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2558
bin: 7.25e1
variant carriers: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10362
num of homozygotes: 0

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

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

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

MQRankSum
type: SiteQuality
SIO_000300: -7.85e-1

QD
type: SiteQuality
SIO_000300: 9.529999999999999e0

BaseQRankSum
type: SiteQuality
SIO_000300: -6.054e0

FS
type: SiteQuality
SIO_000300: 6.042e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.429e0

VQSLOD
type: SiteQuality
SIO_000300: -2.063e0

MQ
type: SiteQuality
SIO_000300: 4.001e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

DP
type: SiteQuality
SIO_000300: 1.792441e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.5e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

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

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

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

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

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: 1.498800959232614e-5
allele num: 66720
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 4.43e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.01e0

FS
type: SiteQuality
SIO_000300: 8.539e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.93e-1

MQ
type: SiteQuality
SIO_000300: 4.206e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.62e0

VQSLOD
type: SiteQuality
SIO_000300: -2.952e0

DP
type: SiteQuality
SIO_000300: 1.792546e6

QD
type: SiteQuality
SIO_000300: 6.58e0

GenotypeQuality
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variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10364
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: 2
allele frequency: 2.997512064986062e-5
allele num: 66722
num of homozygotes: 0

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

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

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

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

VQSLOD
type: SiteQuality
SIO_000300: -2.305e0

MQRankSum
type: SiteQuality
SIO_000300: 8.999999999999999e-3

DP
type: SiteQuality
SIO_000300: 1.792603e6

MQ
type: SiteQuality
SIO_000300: 4.286e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.17e0

QD
type: SiteQuality
SIO_000300: 7.84e0

FS
type: SiteQuality
SIO_000300: 2.722e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.957e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.26e0

GenotypeQuality
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variant carriers: 1

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

GenotypeQuality
all individuals: 2
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variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66726
num of homozygotes: 0

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

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

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

MQRankSum
type: SiteQuality
SIO_000300: 1.09e0

DP
type: SiteQuality
SIO_000300: 1.792727e6

QD
type: SiteQuality
SIO_000300: 1.414e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

MQ
type: SiteQuality
SIO_000300: 4.533e1

FS
type: SiteQuality
SIO_000300: 1.9376e1

VQSLOD
type: SiteQuality
SIO_000300: -3.853e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.900000000000001e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 3.53e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.17e-1

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

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

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

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

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

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

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

African
type: Population
allele count: 9
allele frequency: 8.699014111734003e-4
allele num: 10346
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.790000000000001e-2

DP
type: SiteQuality
SIO_000300: 1.794909e6

FS
type: SiteQuality
SIO_000300: 2.4092e1

VQSLOD
type: SiteQuality
SIO_000300: -2.37e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.3e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.06e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.76e0

MQRankSum
type: SiteQuality
SIO_000300: -3.179e0

QD
type: SiteQuality
SIO_000300: 1.01e0

MQ
type: SiteQuality
SIO_000300: 4.342e1

GenotypeQuality
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variant carriers: 0

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

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.498666187093487e-5
allele num: 66726
num of homozygotes: 0

African
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allele frequency: 0.0e0
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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11572
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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
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BaseQRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.794171e6

ReadPosRankSum
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VQSLOD
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InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-3

FS
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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MQRankSum
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MQ
type: SiteQuality
SIO_000300: 4.749e1

QD
type: SiteQuality
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GenotypeQuality
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variant carriers: 0

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

South Asian
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allele num: 16512
num of homozygotes: 0

African
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allele frequency: 0.0e0
allele num: 10368
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 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: 11574
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.498711108446736e-5
allele num: 66724
num of homozygotes: 0

Other
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num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 7.113e0

BaseQRankSum
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MQ
type: SiteQuality
SIO_000300: 4.018e1

ReadPosRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.794261e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.19e-2

VQSLOD
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MQRankSum
type: SiteQuality
SIO_000300: 3.9e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 1.35e0

QD
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele num: 16512
num of homozygotes: 0

Latino
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East Asian
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African
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allele frequency: 6.751543209876543e-4
allele num: 10368
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European (Finnish)
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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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European (Non-Finnish)
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allele count: 0
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allele num: 66724
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FS
type: SiteQuality
SIO_000300: 1.753e0

InbreedingCoeff
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MQRankSum
type: SiteQuality
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VQSLOD
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QD
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DP
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MQ
type: SiteQuality
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ClippingRankSum
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BaseQRankSum
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 8
allele frequency: 1.199004825994425e-4
allele num: 66722
num of homozygotes: 0

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

Latino
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allele count: 1
allele frequency: 8.640055296353897e-5
allele num: 11574
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10368
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 4.018e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.06e-1

InbreedingCoeff
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SIO_000300: 2.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.28e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.64e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.085e0

DP
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SIO_000300: 1.795046e6

VQSLOD
type: SiteQuality
SIO_000300: -2.419e0

QD
type: SiteQuality
SIO_000300: 1.189e1

FS
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10368
num of homozygotes: 0

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

South Asian
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allele count: 3
allele frequency: 1.816860465116279e-4
allele num: 16512
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66716
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.25e-1

InbreedingCoeff
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SIO_000300: 1.5e-3

MQRankSum
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ClippingRankSum
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DP
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FS
type: SiteQuality
SIO_000300: 1.7051e1

MQ
type: SiteQuality
SIO_000300: 3.968e1

VQSLOD
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BaseQRankSum
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SIO_000300: -3.348e0

QD
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SIO_000300: 9.65e0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 5.25e1
variant carriers: 0

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

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

African
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allele count: 1
allele frequency: 9.645061728395061e-5
allele num: 10368
num of homozygotes: 0

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

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

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

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

FS
type: SiteQuality
SIO_000300: 7.18e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.6e-3

MQRankSum
type: SiteQuality
SIO_000300: 2.48e0

MQ
type: SiteQuality
SIO_000300: 3.958e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.71e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.71e-1

DP
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SIO_000300: 1.794688e6

BaseQRankSum
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SIO_000300: -1.64e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.67e-1

QD
type: SiteQuality
SIO_000300: 3.058e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10366
num of homozygotes: 0

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

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

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

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

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

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

DP
type: SiteQuality
SIO_000300: 1.794659e6

QD
type: SiteQuality
SIO_000300: 1.175e1

MQ
type: SiteQuality
SIO_000300: 3.985e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.398e0

FS
type: SiteQuality
SIO_000300: 1.395e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.7e-3

MQRankSum
type: SiteQuality
SIO_000300: 2.71e0

VQSLOD
type: SiteQuality
SIO_000300: -4.273e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.63e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.45e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 221

GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

African
type: Population
allele count: 3
allele frequency: 2.892402622445044e-4
allele num: 10372
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.511944360447536e-4
allele num: 6614
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 192
allele frequency: 2.877956650777948e-3
allele num: 66714
num of homozygotes: 1

East Asian
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allele count: 3
allele frequency: 3.467406380027739e-4
allele num: 8652
num of homozygotes: 0

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

South Asian
type: Population
allele count: 5
allele frequency: 3.028834504482675e-4
allele num: 16508
num of homozygotes: 0

Latino
type: Population
allele count: 18
allele frequency: 1.555209953343701e-3
allele num: 11574
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.19e0

VQSLOD
type: SiteQuality
SIO_000300: -1.912e0

MQ
type: SiteQuality
SIO_000300: 3.928e1

QD
type: SiteQuality
SIO_000300: 1.19e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.98e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.5e-3

DP
type: SiteQuality
SIO_000300: 1.811441e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.06e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.610000000000001e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 1
allele frequency: 9.641342074816814e-5
allele num: 10372
num of homozygotes: 0

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

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

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
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MQRankSum
type: SiteQuality
SIO_000300: 1.07e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.5e-3

FS
type: SiteQuality
SIO_000300: 2.355e1

ReadPosRankSum
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ClippingRankSum
type: SiteQuality
SIO_000300: -9.56e-1

MQ
type: SiteQuality
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DP
type: SiteQuality
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VQSLOD
type: SiteQuality
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BaseQRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498980693128672e-5
allele num: 66712
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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Other
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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 count: 0
allele frequency: 0.0e0
allele num: 11574
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
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QD
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ClippingRankSum
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VQSLOD
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BaseQRankSum
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DP
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MQ
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FS
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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MQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 2

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10372
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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South Asian
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East Asian
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allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 2
allele frequency: 2.998141152485459e-5
allele num: 66708
num of homozygotes: 0

InbreedingCoeff
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MQRankSum
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ReadPosRankSum
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MQ
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BaseQRankSum
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QD
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ClippingRankSum
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FS
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DP
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

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

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

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

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

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

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

European (Finnish)
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East Asian
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Other
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European (Non-Finnish)
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South Asian
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African
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FS
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BaseQRankSum
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MQRankSum
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ClippingRankSum
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QD
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VQSLOD
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InbreedingCoeff
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MQ
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DP
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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Latino
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allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
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African
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European (Non-Finnish)
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allele frequency: 1.499745043342632e-5
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European (Finnish)
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Other
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QD
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InbreedingCoeff
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MQRankSum
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FS
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MQ
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BaseQRankSum
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ClippingRankSum
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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European (Finnish)
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Latino
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African
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East Asian
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Other
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ReadPosRankSum
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FS
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VQSLOD
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BaseQRankSum
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InbreedingCoeff
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DP
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MQRankSum
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QD
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ClippingRankSum
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Finnish)
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allele num: 6614
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Latino
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South Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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African
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Other
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VQSLOD
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DP
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FS
type: SiteQuality
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ClippingRankSum
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InbreedingCoeff
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MQ
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MQRankSum
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BaseQRankSum
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ReadPosRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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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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num of homozygotes: 0

Other
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num of homozygotes: 0

East Asian
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Latino
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European (Non-Finnish)
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European (Finnish)
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QD
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ClippingRankSum
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MQRankSum
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FS
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VQSLOD
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BaseQRankSum
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DP
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MQ
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InbreedingCoeff
type: SiteQuality
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele num: 66674
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European (Finnish)
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African
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Other
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South Asian
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East Asian
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Latino
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QD
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FS
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ReadPosRankSum
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BaseQRankSum
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MQRankSum
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VQSLOD
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InbreedingCoeff
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MQ
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ClippingRankSum
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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East Asian
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African
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South Asian
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Latino
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European (Non-Finnish)
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European (Finnish)
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DP
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VQSLOD
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FS
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ReadPosRankSum
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ClippingRankSum
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MQ
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InbreedingCoeff
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QD
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MQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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South Asian
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East Asian
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European (Finnish)
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European (Non-Finnish)
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Latino
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Other
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BaseQRankSum
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FS
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InbreedingCoeff
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MQRankSum
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DP
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QD
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ReadPosRankSum
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MQ
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VQSLOD
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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Latino
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allele frequency: 2.591121091725686e-4
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European (Finnish)
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European (Non-Finnish)
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East Asian
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South Asian
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African
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DP
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FS
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ClippingRankSum
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VQSLOD
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MQRankSum
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InbreedingCoeff
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QD
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BaseQRankSum
type: SiteQuality
SIO_000300: 9.22e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.1e-2

MQ
type: SiteQuality
SIO_000300: 4.078e1

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

GenotypeQuality
all individuals: 2471
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2552
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 134
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 214
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 9073
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1314
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 149
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 177
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 168
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1058
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3337
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10314
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16452
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499925003749813e-5
allele num: 66670
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 3.15e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.95e0

VQSLOD
type: SiteQuality
SIO_000300: -2.377e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.6e-3

MQRankSum
type: SiteQuality
SIO_000300: 1.39e0

FS
type: SiteQuality
SIO_000300: 6.01e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.4e-2

MQ
type: SiteQuality
SIO_000300: 4.174e1

QD
type: SiteQuality
SIO_000300: 1.627e1

DP
type: SiteQuality
SIO_000300: 1.815883e6

GenotypeQuality
all individuals: 108
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 46
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 178
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2502
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1319
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 96
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9079
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 1070
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3385
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 139
bin: 3.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 6593
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.999220202747286e-5
allele num: 66684
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.072382803011902e-5
allele num: 16468
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

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: 10234
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: 1.817337e6

VQSLOD
type: SiteQuality
SIO_000300: -3.132e0

MQRankSum
type: SiteQuality
SIO_000300: 1.35e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.04e-1

MQ
type: SiteQuality
SIO_000300: 4.12e1

BaseQRankSum
type: SiteQuality
SIO_000300: 9.07e-1

QD
type: SiteQuality
SIO_000300: 1.497e1

FS
type: SiteQuality
SIO_000300: 7.957e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.620000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

GenotypeQuality
all individuals: 26
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 98
bin: 4.25e1
variant carriers: 0