16-88017668-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 88017668
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 88017668
    reference: chr 16
allele count: 186
allele frequency: 1.604554865424431e-3
allele num: 115920
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000431812
  ensembl transcript: ENST00000466197
  gene symbol: BANP
  hgvsc: ENST00000466197.1:c.165A>G
  hgvsp: ENST00000466197.1:c.165A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000172530
  ensembl transcript: ENST00000488074
  gene symbol: BANP
  hgvsc: ENST00000488074.1:n.587A>G
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000347290
  ensembl transcript: ENST00000355163
  gene symbol: BANP
  hgvsc: ENST00000355163.5:c.183A>G
  hgvsp: ENST00000355163.5:c.183A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000172530
  ensembl transcript: ENST00000472964
  gene symbol: BANP
  hgvsc: ENST00000472964.1:n.133A>G
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000390504
  ensembl transcript: ENST00000412691
  gene symbol: BANP
  hgvsc: ENST00000412691.1:c.165A>G
  hgvsp: ENST00000412691.1:c.165A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000286122
  ensembl transcript: ENST00000286122
  gene symbol: BANP
  hgvsc: ENST00000286122.7:c.163-22A>G
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000376902
  ensembl transcript: ENST00000393207
  gene symbol: BANP
  hgvsc: ENST00000393207.1:c.163-22A>G
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000411479
  ensembl transcript: ENST00000439677
  gene symbol: BANP
  hgvsc: ENST00000439677.1:c.183A>G
  hgvsp: ENST00000439677.1:c.183A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000401454
  ensembl transcript: ENST00000436274
  gene symbol: BANP
  hgvsc: ENST00000436274.1:c.165A>G
  hgvsp: ENST00000436274.1:c.165A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000432508
  ensembl transcript: ENST00000479780
  gene symbol: BANP
  hgvsc: ENST00000479780.2:c.165A>G
  hgvsp: ENST00000479780.2:c.165A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000347125
  ensembl transcript: ENST00000355022
  gene symbol: BANP
  hgvsc: ENST00000355022.4:c.165A>G
  hgvsp: ENST00000355022.4:c.165A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000435727
  ensembl transcript: ENST00000459966
  gene symbol: BANP
  hgvsc: ENST00000459966.1:c.*64A>G
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000399576
  ensembl transcript: ENST00000436970
  gene symbol: BANP
  hgvsc: ENST00000436970.1:c.165A>G
  hgvsp: ENST00000436970.1:c.165A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000436869
  ensembl transcript: ENST00000485772
  gene symbol: BANP
  hgvsc: ENST00000485772.1:c.*64A>G
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000172530
  ensembl transcript: ENST00000474563
  gene symbol: BANP
  hgvsc: ENST00000474563.2:n.596A>G
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000410089
  ensembl transcript: ENST00000456902
  gene symbol: BANP
  hgvsc: ENST00000456902.1:c.165A>G
  hgvsp: ENST00000456902.1:c.165A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000172530
  ensembl transcript: ENST00000569400
  gene symbol: BANP
  hgvsc: ENST00000569400.1:n.613A>G
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000444352
  ensembl transcript: ENST00000538234
  gene symbol: BANP
  hgvsc: ENST00000538234.1:c.165A>G
  hgvsp: ENST00000538234.1:c.165A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: c.165A>G
num of homozygotes: 3
population: European (Non-Finnish)
population: South Asian
population: Other
population: European (Finnish)
population: Latino
population: East Asian
population: African
reference allele: A
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS

16-88017671-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 88017671
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 88017671
    reference: chr 16
allele count: 2
allele frequency: 1.723840717117738e-5
allele num: 116020
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000411479
  ensembl transcript: ENST00000439677
  gene symbol: BANP
  hgvsc: ENST00000439677.1:c.186C>T
  hgvsp: ENST00000439677.1:c.186C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000376903
  ensembl transcript: ENST00000393208
  gene symbol: BANP
  hgvsc: ENST00000393208.2:c.168C>T
  hgvsp: ENST00000393208.2:c.168C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000390504
  ensembl transcript: ENST00000412691
  gene symbol: BANP
  hgvsc: ENST00000412691.1:c.168C>T
  hgvsp: ENST00000412691.1:c.168C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172530
  ensembl transcript: ENST00000488074
  gene symbol: BANP
  hgvsc: ENST00000488074.1:n.590C>T
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000347290
  ensembl transcript: ENST00000355163
  gene symbol: BANP
  hgvsc: ENST00000355163.5:c.186C>T
  hgvsp: ENST00000355163.5:c.186C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172530
  ensembl transcript: ENST00000472964
  gene symbol: BANP
  hgvsc: ENST00000472964.1:n.136C>T
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000435727
  ensembl transcript: ENST00000459966
  gene symbol: BANP
  hgvsc: ENST00000459966.1:c.*67C>T
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000444352
  ensembl transcript: ENST00000538234
  gene symbol: BANP
  hgvsc: ENST00000538234.1:c.168C>T
  hgvsp: ENST00000538234.1:c.168C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000286122
  ensembl transcript: ENST00000286122
  gene symbol: BANP
  hgvsc: ENST00000286122.7:c.163-19C>T
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000347125
  ensembl transcript: ENST00000355022
  gene symbol: BANP
  hgvsc: ENST00000355022.4:c.168C>T
  hgvsp: ENST00000355022.4:c.168C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000432508
  ensembl transcript: ENST00000479780
  gene symbol: BANP
  hgvsc: ENST00000479780.2:c.168C>T
  hgvsp: ENST00000479780.2:c.168C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000399576
  ensembl transcript: ENST00000436970
  gene symbol: BANP
  hgvsc: ENST00000436970.1:c.168C>T
  hgvsp: ENST00000436970.1:c.168C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000410089
  ensembl transcript: ENST00000456902
  gene symbol: BANP
  hgvsc: ENST00000456902.1:c.168C>T
  hgvsp: ENST00000456902.1:c.168C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000431812
  ensembl transcript: ENST00000466197
  gene symbol: BANP
  hgvsc: ENST00000466197.1:c.168C>T
  hgvsp: ENST00000466197.1:c.168C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000401454
  ensembl transcript: ENST00000436274
  gene symbol: BANP
  hgvsc: ENST00000436274.1:c.168C>T
  hgvsp: ENST00000436274.1:c.168C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172530
  ensembl transcript: ENST00000569400
  gene symbol: BANP
  hgvsc: ENST00000569400.1:n.616C>T
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000376902
  ensembl transcript: ENST00000393207
  gene symbol: BANP
  hgvsc: ENST00000393207.1:c.163-19C>T
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000436869
  ensembl transcript: ENST00000485772
  gene symbol: BANP
  hgvsc: ENST00000485772.1:c.*67C>T
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172530
  ensembl transcript: ENST00000474563
  gene symbol: BANP
  hgvsc: ENST00000474563.2:n.599C>T
  variant of: http://identifiers.org/hgnc/13450
canonical: false
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Phe56Phe
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
population: East Asian
reference allele: C
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum

16-88017674-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 88017674
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 88017674
    reference: chr 16
allele count: 1
allele frequency: 8.615936035290874e-6
allele num: 116064
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172530
  ensembl transcript: ENST00000488074
  gene symbol: BANP
  hgvsc: ENST00000488074.1:n.593G>T
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172530
  ensembl transcript: ENST00000569400
  gene symbol: BANP
  hgvsc: ENST00000569400.1:n.619G>T
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000444352
  ensembl transcript: ENST00000538234
  gene symbol: BANP
  hgvsc: ENST00000538234.1:c.171G>T
  hgvsp: ENST00000538234.1:c.171G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172530
  ensembl transcript: ENST00000472964
  gene symbol: BANP
  hgvsc: ENST00000472964.1:n.139G>T
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000431812
  ensembl transcript: ENST00000466197
  gene symbol: BANP
  hgvsc: ENST00000466197.1:c.171G>T
  hgvsp: ENST00000466197.1:c.171G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000390504
  ensembl transcript: ENST00000412691
  gene symbol: BANP
  hgvsc: ENST00000412691.1:c.171G>T
  hgvsp: ENST00000412691.1:c.171G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000347290
  ensembl transcript: ENST00000355163
  gene symbol: BANP
  hgvsc: ENST00000355163.5:c.189G>T
  hgvsp: ENST00000355163.5:c.189G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000436869
  ensembl transcript: ENST00000485772
  gene symbol: BANP
  hgvsc: ENST00000485772.1:c.*70G>T
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000410089
  ensembl transcript: ENST00000456902
  gene symbol: BANP
  hgvsc: ENST00000456902.1:c.171G>T
  hgvsp: ENST00000456902.1:c.171G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172530
  ensembl transcript: ENST00000474563
  gene symbol: BANP
  hgvsc: ENST00000474563.2:n.602G>T
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000435727
  ensembl transcript: ENST00000459966
  gene symbol: BANP
  hgvsc: ENST00000459966.1:c.*70G>T
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000347125
  ensembl transcript: ENST00000355022
  gene symbol: BANP
  hgvsc: ENST00000355022.4:c.171G>T
  hgvsp: ENST00000355022.4:c.171G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000432508
  ensembl transcript: ENST00000479780
  gene symbol: BANP
  hgvsc: ENST00000479780.2:c.171G>T
  hgvsp: ENST00000479780.2:c.171G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000401454
  ensembl transcript: ENST00000436274
  gene symbol: BANP
  hgvsc: ENST00000436274.1:c.171G>T
  hgvsp: ENST00000436274.1:c.171G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000399576
  ensembl transcript: ENST00000436970
  gene symbol: BANP
  hgvsc: ENST00000436970.1:c.171G>T
  hgvsp: ENST00000436970.1:c.171G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000376903
  ensembl transcript: ENST00000393208
  gene symbol: BANP
  hgvsc: ENST00000393208.2:c.171G>T
  hgvsp: ENST00000393208.2:c.171G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000411479
  ensembl transcript: ENST00000439677
  gene symbol: BANP
  hgvsc: ENST00000439677.1:c.189G>T
  hgvsp: ENST00000439677.1:c.189G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000376902
  ensembl transcript: ENST00000393207
  gene symbol: BANP
  hgvsc: ENST00000393207.1:c.163-16G>T
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000286122
  ensembl transcript: ENST00000286122
  gene symbol: BANP
  hgvsc: ENST00000286122.7:c.163-16G>T
  variant of: http://identifiers.org/hgnc/13450
canonical: false
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Leu57Leu
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
reference allele: G
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD

http://identifiers.org/exac.variant/16-88017695-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 88017695
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 88017695
    reference: chr 16
allele count: 1
allele frequency: 8.854572501239641e-6
allele num: 112936
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000347125
  ensembl transcript: ENST00000355022
  gene symbol: BANP
  hgvsc: ENST00000355022.4:c.192C>A
  hgvsp: ENST00000355022.4:c.192C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000390504
  ensembl transcript: ENST00000412691
  gene symbol: BANP
  hgvsc: ENST00000412691.1:c.192C>A
  hgvsp: ENST00000412691.1:c.192C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000444352
  ensembl transcript: ENST00000538234
  gene symbol: BANP
  hgvsc: ENST00000538234.1:c.192C>A
  hgvsp: ENST00000538234.1:c.192C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000410089
  ensembl transcript: ENST00000456902
  gene symbol: BANP
  hgvsc: ENST00000456902.1:c.192C>A
  hgvsp: ENST00000456902.1:c.192C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000435727
  ensembl transcript: ENST00000459966
  gene symbol: BANP
  hgvsc: ENST00000459966.1:c.*91C>A
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000432508
  ensembl transcript: ENST00000479780
  gene symbol: BANP
  hgvsc: ENST00000479780.2:c.192C>A
  hgvsp: ENST00000479780.2:c.192C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000401454
  ensembl transcript: ENST00000436274
  gene symbol: BANP
  hgvsc: ENST00000436274.1:c.192C>A
  hgvsp: ENST00000436274.1:c.192C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000399576
  ensembl transcript: ENST00000436970
  gene symbol: BANP
  hgvsc: ENST00000436970.1:c.192C>A
  hgvsp: ENST00000436970.1:c.192C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000411479
  ensembl transcript: ENST00000439677
  gene symbol: BANP
  hgvsc: ENST00000439677.1:c.210C>A
  hgvsp: ENST00000439677.1:c.210C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172530
  ensembl transcript: ENST00000474563
  gene symbol: BANP
  hgvsc: ENST00000474563.2:n.623C>A
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000286122
  ensembl transcript: ENST00000286122
  gene symbol: BANP
  hgvsc: ENST00000286122.7:c.168C>A
  hgvsp: ENST00000286122.7:c.168C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000436869
  ensembl transcript: ENST00000485772
  gene symbol: BANP
  hgvsc: ENST00000485772.1:c.*91C>A
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000431812
  ensembl transcript: ENST00000466197
  gene symbol: BANP
  hgvsc: ENST00000466197.1:c.192C>A
  hgvsp: ENST00000466197.1:c.192C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000376903
  ensembl transcript: ENST00000393208
  gene symbol: BANP
  hgvsc: ENST00000393208.2:c.192C>A
  hgvsp: ENST00000393208.2:c.192C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172530
  ensembl transcript: ENST00000472964
  gene symbol: BANP
  hgvsc: ENST00000472964.1:n.160C>A
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172530
  ensembl transcript: ENST00000569400
  gene symbol: BANP
  hgvsc: ENST00000569400.1:n.640C>A
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000376902
  ensembl transcript: ENST00000393207
  gene symbol: BANP
  hgvsc: ENST00000393207.1:c.168C>A
  hgvsp: ENST00000393207.1:c.168C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000347290
  ensembl transcript: ENST00000355163
  gene symbol: BANP
  hgvsc: ENST00000355163.5:c.210C>A
  hgvsp: ENST00000355163.5:c.210C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172530
  ensembl transcript: ENST00000488074
  gene symbol: BANP
  hgvsc: ENST00000488074.1:n.614C>A
  variant of: http://identifiers.org/hgnc/13450
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Ile56Ile
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: Other
reference allele: C
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum

16-88017698-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 88017698
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 88017698
    reference: chr 16
allele count: 1
allele frequency: 8.929847121017289e-6
allele num: 111984
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000390504
  ensembl transcript: ENST00000412691
  gene symbol: BANP
  hgvsc: ENST00000412691.1:c.195C>T
  hgvsp: ENST00000412691.1:c.195C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172530
  ensembl transcript: ENST00000569400
  gene symbol: BANP
  hgvsc: ENST00000569400.1:n.643C>T
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000435727
  ensembl transcript: ENST00000459966
  gene symbol: BANP
  hgvsc: ENST00000459966.1:c.*94C>T
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000432508
  ensembl transcript: ENST00000479780
  gene symbol: BANP
  hgvsc: ENST00000479780.2:c.195C>T
  hgvsp: ENST00000479780.2:c.195C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000444352
  ensembl transcript: ENST00000538234
  gene symbol: BANP
  hgvsc: ENST00000538234.1:c.195C>T
  hgvsp: ENST00000538234.1:c.195C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000411479
  ensembl transcript: ENST00000439677
  gene symbol: BANP
  hgvsc: ENST00000439677.1:c.213C>T
  hgvsp: ENST00000439677.1:c.213C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000347125
  ensembl transcript: ENST00000355022
  gene symbol: BANP
  hgvsc: ENST00000355022.4:c.195C>T
  hgvsp: ENST00000355022.4:c.195C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172530
  ensembl transcript: ENST00000488074
  gene symbol: BANP
  hgvsc: ENST00000488074.1:n.617C>T
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000401454
  ensembl transcript: ENST00000436274
  gene symbol: BANP
  hgvsc: ENST00000436274.1:c.195C>T
  hgvsp: ENST00000436274.1:c.195C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000286122
  ensembl transcript: ENST00000286122
  gene symbol: BANP
  hgvsc: ENST00000286122.7:c.171C>T
  hgvsp: ENST00000286122.7:c.171C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000410089
  ensembl transcript: ENST00000456902
  gene symbol: BANP
  hgvsc: ENST00000456902.1:c.195C>T
  hgvsp: ENST00000456902.1:c.195C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000399576
  ensembl transcript: ENST00000436970
  gene symbol: BANP
  hgvsc: ENST00000436970.1:c.195C>T
  hgvsp: ENST00000436970.1:c.195C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000376902
  ensembl transcript: ENST00000393207
  gene symbol: BANP
  hgvsc: ENST00000393207.1:c.171C>T
  hgvsp: ENST00000393207.1:c.171C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000376903
  ensembl transcript: ENST00000393208
  gene symbol: BANP
  hgvsc: ENST00000393208.2:c.195C>T
  hgvsp: ENST00000393208.2:c.195C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172530
  ensembl transcript: ENST00000472964
  gene symbol: BANP
  hgvsc: ENST00000472964.1:n.163C>T
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000431812
  ensembl transcript: ENST00000466197
  gene symbol: BANP
  hgvsc: ENST00000466197.1:c.195C>T
  hgvsp: ENST00000466197.1:c.195C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000436869
  ensembl transcript: ENST00000485772
  gene symbol: BANP
  hgvsc: ENST00000485772.1:c.*94C>T
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172530
  ensembl transcript: ENST00000474563
  gene symbol: BANP
  hgvsc: ENST00000474563.2:n.626C>T
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000347290
  ensembl transcript: ENST00000355163
  gene symbol: BANP
  hgvsc: ENST00000355163.5:c.213C>T
  hgvsp: ENST00000355163.5:c.213C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Cys57Cys
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: FS

16-88017714-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 88017714
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 88017714
    reference: chr 16
allele count: 1
allele frequency: 1.005388884420494e-5
allele num: 99464
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000411479
  ensembl transcript: ENST00000439677
  gene symbol: BANP
  hgvsc: ENST00000439677.1:c.229A>G
  hgvsp: ENSP00000411479.1:p.Ile77Val
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172530
  ensembl transcript: ENST00000474563
  gene symbol: BANP
  hgvsc: ENST00000474563.2:n.642A>G
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000444352
  ensembl transcript: ENST00000538234
  gene symbol: BANP
  hgvsc: ENST00000538234.1:c.211A>G
  hgvsp: ENSP00000444352.1:p.Ile71Val
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000347125
  ensembl transcript: ENST00000355022
  gene symbol: BANP
  hgvsc: ENST00000355022.4:c.211A>G
  hgvsp: ENSP00000347125.4:p.Ile71Val
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000401454
  ensembl transcript: ENST00000436274
  gene symbol: BANP
  hgvsc: ENST00000436274.1:c.211A>G
  hgvsp: ENSP00000401454.1:p.Ile71Val
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000435727
  ensembl transcript: ENST00000459966
  gene symbol: BANP
  hgvsc: ENST00000459966.1:c.*110A>G
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000376903
  ensembl transcript: ENST00000393208
  gene symbol: BANP
  hgvsc: ENST00000393208.2:c.211A>G
  hgvsp: ENSP00000376903.2:p.Ile71Val
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000432508
  ensembl transcript: ENST00000479780
  gene symbol: BANP
  hgvsc: ENST00000479780.2:c.211A>G
  hgvsp: ENSP00000432508.1:p.Ile71Val
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000410089
  ensembl transcript: ENST00000456902
  gene symbol: BANP
  hgvsc: ENST00000456902.1:c.211A>G
  hgvsp: ENSP00000410089.1:p.Ile71Val
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000431812
  ensembl transcript: ENST00000466197
  gene symbol: BANP
  hgvsc: ENST00000466197.1:c.211A>G
  hgvsp: ENSP00000431812.1:p.Ile71Val
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000399576
  ensembl transcript: ENST00000436970
  gene symbol: BANP
  hgvsc: ENST00000436970.1:c.211A>G
  hgvsp: ENSP00000399576.1:p.Ile71Val
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000376902
  ensembl transcript: ENST00000393207
  gene symbol: BANP
  hgvsc: ENST00000393207.1:c.187A>G
  hgvsp: ENSP00000376902.1:p.Ile63Val
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000390504
  ensembl transcript: ENST00000412691
  gene symbol: BANP
  hgvsc: ENST00000412691.1:c.211A>G
  hgvsp: ENSP00000390504.1:p.Ile71Val
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000436869
  ensembl transcript: ENST00000485772
  gene symbol: BANP
  hgvsc: ENST00000485772.1:c.*110A>G
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000347290
  ensembl transcript: ENST00000355163
  gene symbol: BANP
  hgvsc: ENST00000355163.5:c.229A>G
  hgvsp: ENSP00000347290.5:p.Ile77Val
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172530
  ensembl transcript: ENST00000488074
  gene symbol: BANP
  hgvsc: ENST00000488074.1:n.633A>G
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000286122
  ensembl transcript: ENST00000286122
  gene symbol: BANP
  hgvsc: ENST00000286122.7:c.187A>G
  hgvsp: ENSP00000286122.7:p.Ile63Val
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172530
  ensembl transcript: ENST00000569400
  gene symbol: BANP
  hgvsc: ENST00000569400.1:n.659A>G
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172530
  ensembl transcript: ENST00000472964
  gene symbol: BANP
  hgvsc: ENST00000472964.1:n.179A>G
  variant of: http://identifiers.org/hgnc/13450
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Ile63Val
num of homozygotes: 0
population: Latino
population: Other
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: African
reference allele: A
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ

16-88017726-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 88017726
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 88017726
    reference: chr 16
allele count: 1
allele frequency: 1.079540547542966e-5
allele num: 92632
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000376903
  ensembl transcript: ENST00000393208
  gene symbol: BANP
  hgvsc: ENST00000393208.2:c.223T>C
  hgvsp: ENST00000393208.2:c.223T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000410089
  ensembl transcript: ENST00000456902
  gene symbol: BANP
  hgvsc: ENST00000456902.1:c.223T>C
  hgvsp: ENST00000456902.1:c.223T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000436869
  ensembl transcript: ENST00000485772
  gene symbol: BANP
  hgvsc: ENST00000485772.1:c.*122T>C
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000431812
  ensembl transcript: ENST00000466197
  gene symbol: BANP
  hgvsc: ENST00000466197.1:c.223T>C
  hgvsp: ENST00000466197.1:c.223T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000444352
  ensembl transcript: ENST00000538234
  gene symbol: BANP
  hgvsc: ENST00000538234.1:c.223T>C
  hgvsp: ENST00000538234.1:c.223T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172530
  ensembl transcript: ENST00000488074
  gene symbol: BANP
  hgvsc: ENST00000488074.1:n.645T>C
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172530
  ensembl transcript: ENST00000472964
  gene symbol: BANP
  hgvsc: ENST00000472964.1:n.191T>C
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172530
  ensembl transcript: ENST00000569400
  gene symbol: BANP
  hgvsc: ENST00000569400.1:n.671T>C
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000401454
  ensembl transcript: ENST00000436274
  gene symbol: BANP
  hgvsc: ENST00000436274.1:c.223T>C
  hgvsp: ENST00000436274.1:c.223T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000411479
  ensembl transcript: ENST00000439677
  gene symbol: BANP
  hgvsc: ENST00000439677.1:c.241T>C
  hgvsp: ENST00000439677.1:c.241T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000390504
  ensembl transcript: ENST00000412691
  gene symbol: BANP
  hgvsc: ENST00000412691.1:c.223T>C
  hgvsp: ENST00000412691.1:c.223T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000376902
  ensembl transcript: ENST00000393207
  gene symbol: BANP
  hgvsc: ENST00000393207.1:c.199T>C
  hgvsp: ENST00000393207.1:c.199T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000399576
  ensembl transcript: ENST00000436970
  gene symbol: BANP
  hgvsc: ENST00000436970.1:c.223T>C
  hgvsp: ENST00000436970.1:c.223T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000435727
  ensembl transcript: ENST00000459966
  gene symbol: BANP
  hgvsc: ENST00000459966.1:c.*122T>C
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000432508
  ensembl transcript: ENST00000479780
  gene symbol: BANP
  hgvsc: ENST00000479780.2:c.223T>C
  hgvsp: ENST00000479780.2:c.223T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000347290
  ensembl transcript: ENST00000355163
  gene symbol: BANP
  hgvsc: ENST00000355163.5:c.241T>C
  hgvsp: ENST00000355163.5:c.241T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000286122
  ensembl transcript: ENST00000286122
  gene symbol: BANP
  hgvsc: ENST00000286122.7:c.199T>C
  hgvsp: ENST00000286122.7:c.199T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000347125
  ensembl transcript: ENST00000355022
  gene symbol: BANP
  hgvsc: ENST00000355022.4:c.223T>C
  hgvsp: ENST00000355022.4:c.223T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172530
  ensembl transcript: ENST00000474563
  gene symbol: BANP
  hgvsc: ENST00000474563.2:n.654T>C
  variant of: http://identifiers.org/hgnc/13450
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Leu67Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: African
population: Other
reference allele: T
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff

16-88017735-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 88017735
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 88017735
    reference: chr 16
allele count: 1
allele frequency: 1.136751165169944e-5
allele num: 87970
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000376902
  ensembl transcript: ENST00000393207
  gene symbol: BANP
  hgvsc: ENST00000393207.1:c.208C>T
  hgvsp: ENST00000393207.1:c.208C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000431812
  ensembl transcript: ENST00000466197
  gene symbol: BANP
  hgvsc: ENST00000466197.1:c.232C>T
  hgvsp: ENST00000466197.1:c.232C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000347125
  ensembl transcript: ENST00000355022
  gene symbol: BANP
  hgvsc: ENST00000355022.4:c.232C>T
  hgvsp: ENST00000355022.4:c.232C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000347290
  ensembl transcript: ENST00000355163
  gene symbol: BANP
  hgvsc: ENST00000355163.5:c.250C>T
  hgvsp: ENST00000355163.5:c.250C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000435727
  ensembl transcript: ENST00000459966
  gene symbol: BANP
  hgvsc: ENST00000459966.1:c.*131C>T
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000444352
  ensembl transcript: ENST00000538234
  gene symbol: BANP
  hgvsc: ENST00000538234.1:c.232C>T
  hgvsp: ENST00000538234.1:c.232C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000399576
  ensembl transcript: ENST00000436970
  gene symbol: BANP
  hgvsc: ENST00000436970.1:c.232C>T
  hgvsp: ENST00000436970.1:c.232C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000286122
  ensembl transcript: ENST00000286122
  gene symbol: BANP
  hgvsc: ENST00000286122.7:c.208C>T
  hgvsp: ENST00000286122.7:c.208C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000436869
  ensembl transcript: ENST00000485772
  gene symbol: BANP
  hgvsc: ENST00000485772.1:c.*131C>T
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172530
  ensembl transcript: ENST00000488074
  gene symbol: BANP
  hgvsc: ENST00000488074.1:n.654C>T
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000410089
  ensembl transcript: ENST00000456902
  gene symbol: BANP
  hgvsc: ENST00000456902.1:c.232C>T
  hgvsp: ENST00000456902.1:c.232C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000390504
  ensembl transcript: ENST00000412691
  gene symbol: BANP
  hgvsc: ENST00000412691.1:c.232C>T
  hgvsp: ENST00000412691.1:c.232C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000376903
  ensembl transcript: ENST00000393208
  gene symbol: BANP
  hgvsc: ENST00000393208.2:c.232C>T
  hgvsp: ENST00000393208.2:c.232C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000411479
  ensembl transcript: ENST00000439677
  gene symbol: BANP
  hgvsc: ENST00000439677.1:c.250C>T
  hgvsp: ENST00000439677.1:c.250C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000432508
  ensembl transcript: ENST00000479780
  gene symbol: BANP
  hgvsc: ENST00000479780.2:c.232C>T
  hgvsp: ENST00000479780.2:c.232C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000401454
  ensembl transcript: ENST00000436274
  gene symbol: BANP
  hgvsc: ENST00000436274.1:c.232C>T
  hgvsp: ENST00000436274.1:c.232C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172530
  ensembl transcript: ENST00000472964
  gene symbol: BANP
  hgvsc: ENST00000472964.1:n.200C>T
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172530
  ensembl transcript: ENST00000569400
  gene symbol: BANP
  hgvsc: ENST00000569400.1:n.680C>T
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172530
  ensembl transcript: ENST00000474563
  gene symbol: BANP
  hgvsc: ENST00000474563.2:n.663C>T
  variant of: http://identifiers.org/hgnc/13450
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Leu70Leu
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: C
site quality: DP
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum

16-88017744-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 88017744
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 88017744
    reference: chr 16
allele count: 1
allele frequency: 1.168551930447789e-5
allele num: 85576
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000347290
  ensembl transcript: ENST00000355163
  gene symbol: BANP
  hgvsc: ENST00000355163.5:c.259A>G
  hgvsp: ENSP00000347290.5:p.Thr87Ala
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000435727
  ensembl transcript: ENST00000459966
  gene symbol: BANP
  hgvsc: ENST00000459966.1:c.*140A>G
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000376902
  ensembl transcript: ENST00000393207
  gene symbol: BANP
  hgvsc: ENST00000393207.1:c.217A>G
  hgvsp: ENSP00000376902.1:p.Thr73Ala
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172530
  ensembl transcript: ENST00000569400
  gene symbol: BANP
  hgvsc: ENST00000569400.1:n.689A>G
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000401454
  ensembl transcript: ENST00000436274
  gene symbol: BANP
  hgvsc: ENST00000436274.1:c.241A>G
  hgvsp: ENSP00000401454.1:p.Thr81Ala
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172530
  ensembl transcript: ENST00000474563
  gene symbol: BANP
  hgvsc: ENST00000474563.2:n.672A>G
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000376903
  ensembl transcript: ENST00000393208
  gene symbol: BANP
  hgvsc: ENST00000393208.2:c.241A>G
  hgvsp: ENSP00000376903.2:p.Thr81Ala
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000436869
  ensembl transcript: ENST00000485772
  gene symbol: BANP
  hgvsc: ENST00000485772.1:c.*140A>G
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000431812
  ensembl transcript: ENST00000466197
  gene symbol: BANP
  hgvsc: ENST00000466197.1:c.241A>G
  hgvsp: ENSP00000431812.1:p.Thr81Ala
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000286122
  ensembl transcript: ENST00000286122
  gene symbol: BANP
  hgvsc: ENST00000286122.7:c.217A>G
  hgvsp: ENSP00000286122.7:p.Thr73Ala
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000432508
  ensembl transcript: ENST00000479780
  gene symbol: BANP
  hgvsc: ENST00000479780.2:c.241A>G
  hgvsp: ENSP00000432508.1:p.Thr81Ala
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000390504
  ensembl transcript: ENST00000412691
  gene symbol: BANP
  hgvsc: ENST00000412691.1:c.241A>G
  hgvsp: ENSP00000390504.1:p.Thr81Ala
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000410089
  ensembl transcript: ENST00000456902
  gene symbol: BANP
  hgvsc: ENST00000456902.1:c.241A>G
  hgvsp: ENSP00000410089.1:p.Thr81Ala
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000411479
  ensembl transcript: ENST00000439677
  gene symbol: BANP
  hgvsc: ENST00000439677.1:c.259A>G
  hgvsp: ENSP00000411479.1:p.Thr87Ala
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000444352
  ensembl transcript: ENST00000538234
  gene symbol: BANP
  hgvsc: ENST00000538234.1:c.241A>G
  hgvsp: ENSP00000444352.1:p.Thr81Ala
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000399576
  ensembl transcript: ENST00000436970
  gene symbol: BANP
  hgvsc: ENST00000436970.1:c.241A>G
  hgvsp: ENSP00000399576.1:p.Thr81Ala
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172530
  ensembl transcript: ENST00000472964
  gene symbol: BANP
  hgvsc: ENST00000472964.1:n.209A>G
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172530
  ensembl transcript: ENST00000488074
  gene symbol: BANP
  hgvsc: ENST00000488074.1:n.663A>G
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000347125
  ensembl transcript: ENST00000355022
  gene symbol: BANP
  hgvsc: ENST00000355022.4:c.241A>G
  hgvsp: ENSP00000347125.4:p.Thr81Ala
  variant of: http://identifiers.org/hgnc/13450
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Thr73Ala
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: A
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff

16-88017746-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 88017746
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 88017746
    reference: chr 16
allele count: 5
allele frequency: 5.953373181244493e-5
allele num: 83986
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000432508
  ensembl transcript: ENST00000479780
  gene symbol: BANP
  hgvsc: ENST00000479780.2:c.243T>C
  hgvsp: ENST00000479780.2:c.243T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000376903
  ensembl transcript: ENST00000393208
  gene symbol: BANP
  hgvsc: ENST00000393208.2:c.243T>C
  hgvsp: ENST00000393208.2:c.243T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000435727
  ensembl transcript: ENST00000459966
  gene symbol: BANP
  hgvsc: ENST00000459966.1:c.*142T>C
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000411479
  ensembl transcript: ENST00000439677
  gene symbol: BANP
  hgvsc: ENST00000439677.1:c.261T>C
  hgvsp: ENST00000439677.1:c.261T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000410089
  ensembl transcript: ENST00000456902
  gene symbol: BANP
  hgvsc: ENST00000456902.1:c.243T>C
  hgvsp: ENST00000456902.1:c.243T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000347125
  ensembl transcript: ENST00000355022
  gene symbol: BANP
  hgvsc: ENST00000355022.4:c.243T>C
  hgvsp: ENST00000355022.4:c.243T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000286122
  ensembl transcript: ENST00000286122
  gene symbol: BANP
  hgvsc: ENST00000286122.7:c.219T>C
  hgvsp: ENST00000286122.7:c.219T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000444352
  ensembl transcript: ENST00000538234
  gene symbol: BANP
  hgvsc: ENST00000538234.1:c.243T>C
  hgvsp: ENST00000538234.1:c.243T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172530
  ensembl transcript: ENST00000474563
  gene symbol: BANP
  hgvsc: ENST00000474563.2:n.674T>C
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172530
  ensembl transcript: ENST00000488074
  gene symbol: BANP
  hgvsc: ENST00000488074.1:n.665T>C
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000347290
  ensembl transcript: ENST00000355163
  gene symbol: BANP
  hgvsc: ENST00000355163.5:c.261T>C
  hgvsp: ENST00000355163.5:c.261T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000436869
  ensembl transcript: ENST00000485772
  gene symbol: BANP
  hgvsc: ENST00000485772.1:c.*142T>C
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000431812
  ensembl transcript: ENST00000466197
  gene symbol: BANP
  hgvsc: ENST00000466197.1:c.243T>C
  hgvsp: ENST00000466197.1:c.243T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000390504
  ensembl transcript: ENST00000412691
  gene symbol: BANP
  hgvsc: ENST00000412691.1:c.243T>C
  hgvsp: ENST00000412691.1:c.243T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000401454
  ensembl transcript: ENST00000436274
  gene symbol: BANP
  hgvsc: ENST00000436274.1:c.243T>C
  hgvsp: ENST00000436274.1:c.243T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172530
  ensembl transcript: ENST00000472964
  gene symbol: BANP
  hgvsc: ENST00000472964.1:n.211T>C
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000376902
  ensembl transcript: ENST00000393207
  gene symbol: BANP
  hgvsc: ENST00000393207.1:c.219T>C
  hgvsp: ENST00000393207.1:c.219T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000399576
  ensembl transcript: ENST00000436970
  gene symbol: BANP
  hgvsc: ENST00000436970.1:c.243T>C
  hgvsp: ENST00000436970.1:c.243T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172530
  ensembl transcript: ENST00000569400
  gene symbol: BANP
  hgvsc: ENST00000569400.1:n.691T>C
  variant of: http://identifiers.org/hgnc/13450
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Thr73Thr
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
population: Other
reference allele: T
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum

16-88017755-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 88017755
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 88017755
    reference: chr 16
allele count: 0
allele frequency: 0.0e0
allele num: 81662
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000432508
  ensembl transcript: ENST00000479780
  gene symbol: BANP
  hgvsc: ENST00000479780.2:c.252C>T
  hgvsp: ENST00000479780.2:c.252C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000435727
  ensembl transcript: ENST00000459966
  gene symbol: BANP
  hgvsc: ENST00000459966.1:c.*151C>T
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000376903
  ensembl transcript: ENST00000393208
  gene symbol: BANP
  hgvsc: ENST00000393208.2:c.252C>T
  hgvsp: ENST00000393208.2:c.252C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000444352
  ensembl transcript: ENST00000538234
  gene symbol: BANP
  hgvsc: ENST00000538234.1:c.252C>T
  hgvsp: ENST00000538234.1:c.252C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172530
  ensembl transcript: ENST00000474563
  gene symbol: BANP
  hgvsc: ENST00000474563.2:n.683C>T
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000347125
  ensembl transcript: ENST00000355022
  gene symbol: BANP
  hgvsc: ENST00000355022.4:c.252C>T
  hgvsp: ENST00000355022.4:c.252C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000431812
  ensembl transcript: ENST00000466197
  gene symbol: BANP
  hgvsc: ENST00000466197.1:c.252C>T
  hgvsp: ENST00000466197.1:c.252C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000411479
  ensembl transcript: ENST00000439677
  gene symbol: BANP
  hgvsc: ENST00000439677.1:c.270C>T
  hgvsp: ENST00000439677.1:c.270C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000390504
  ensembl transcript: ENST00000412691
  gene symbol: BANP
  hgvsc: ENST00000412691.1:c.252C>T
  hgvsp: ENST00000412691.1:c.252C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000376902
  ensembl transcript: ENST00000393207
  gene symbol: BANP
  hgvsc: ENST00000393207.1:c.228C>T
  hgvsp: ENST00000393207.1:c.228C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000286122
  ensembl transcript: ENST00000286122
  gene symbol: BANP
  hgvsc: ENST00000286122.7:c.228C>T
  hgvsp: ENST00000286122.7:c.228C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000410089
  ensembl transcript: ENST00000456902
  gene symbol: BANP
  hgvsc: ENST00000456902.1:c.252C>T
  hgvsp: ENST00000456902.1:c.252C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000401454
  ensembl transcript: ENST00000436274
  gene symbol: BANP
  hgvsc: ENST00000436274.1:c.252C>T
  hgvsp: ENST00000436274.1:c.252C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172530
  ensembl transcript: ENST00000569400
  gene symbol: BANP
  hgvsc: ENST00000569400.1:n.700C>T
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172530
  ensembl transcript: ENST00000488074
  gene symbol: BANP
  hgvsc: ENST00000488074.1:n.674C>T
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000347290
  ensembl transcript: ENST00000355163
  gene symbol: BANP
  hgvsc: ENST00000355163.5:c.270C>T
  hgvsp: ENST00000355163.5:c.270C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172530
  ensembl transcript: ENST00000472964
  gene symbol: BANP
  hgvsc: ENST00000472964.1:n.220C>T
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000399576
  ensembl transcript: ENST00000436970
  gene symbol: BANP
  hgvsc: ENST00000436970.1:c.252C>T
  hgvsp: ENST00000436970.1:c.252C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000436869
  ensembl transcript: ENST00000485772
  gene symbol: BANP
  hgvsc: ENST00000485772.1:c.*151C>T
  variant of: http://identifiers.org/hgnc/13450
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Ser76Ser
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ

16-88017758-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 88017758
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 88017758
    reference: chr 16
allele count: 8
allele frequency: 9.869476177551876e-5
allele num: 81058
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172530
  ensembl transcript: ENST00000488074
  gene symbol: BANP
  hgvsc: ENST00000488074.1:n.677A>G
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000376903
  ensembl transcript: ENST00000393208
  gene symbol: BANP
  hgvsc: ENST00000393208.2:c.255A>G
  hgvsp: ENST00000393208.2:c.255A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000411479
  ensembl transcript: ENST00000439677
  gene symbol: BANP
  hgvsc: ENST00000439677.1:c.273A>G
  hgvsp: ENST00000439677.1:c.273A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000390504
  ensembl transcript: ENST00000412691
  gene symbol: BANP
  hgvsc: ENST00000412691.1:c.255A>G
  hgvsp: ENST00000412691.1:c.255A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172530
  ensembl transcript: ENST00000569400
  gene symbol: BANP
  hgvsc: ENST00000569400.1:n.703A>G
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000436869
  ensembl transcript: ENST00000485772
  gene symbol: BANP
  hgvsc: ENST00000485772.1:c.*154A>G
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000444352
  ensembl transcript: ENST00000538234
  gene symbol: BANP
  hgvsc: ENST00000538234.1:c.255A>G
  hgvsp: ENST00000538234.1:c.255A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000286122
  ensembl transcript: ENST00000286122
  gene symbol: BANP
  hgvsc: ENST00000286122.7:c.231A>G
  hgvsp: ENST00000286122.7:c.231A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000435727
  ensembl transcript: ENST00000459966
  gene symbol: BANP
  hgvsc: ENST00000459966.1:c.*154A>G
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000401454
  ensembl transcript: ENST00000436274
  gene symbol: BANP
  hgvsc: ENST00000436274.1:c.255A>G
  hgvsp: ENST00000436274.1:c.255A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000376902
  ensembl transcript: ENST00000393207
  gene symbol: BANP
  hgvsc: ENST00000393207.1:c.231A>G
  hgvsp: ENST00000393207.1:c.231A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172530
  ensembl transcript: ENST00000474563
  gene symbol: BANP
  hgvsc: ENST00000474563.2:n.686A>G
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000431812
  ensembl transcript: ENST00000466197
  gene symbol: BANP
  hgvsc: ENST00000466197.1:c.255A>G
  hgvsp: ENST00000466197.1:c.255A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000432508
  ensembl transcript: ENST00000479780
  gene symbol: BANP
  hgvsc: ENST00000479780.2:c.255A>G
  hgvsp: ENST00000479780.2:c.255A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172530
  ensembl transcript: ENST00000472964
  gene symbol: BANP
  hgvsc: ENST00000472964.1:n.223A>G
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000399576
  ensembl transcript: ENST00000436970
  gene symbol: BANP
  hgvsc: ENST00000436970.1:c.255A>G
  hgvsp: ENST00000436970.1:c.255A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000347290
  ensembl transcript: ENST00000355163
  gene symbol: BANP
  hgvsc: ENST00000355163.5:c.273A>G
  hgvsp: ENST00000355163.5:c.273A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000410089
  ensembl transcript: ENST00000456902
  gene symbol: BANP
  hgvsc: ENST00000456902.1:c.255A>G
  hgvsp: ENST00000456902.1:c.255A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000347125
  ensembl transcript: ENST00000355022
  gene symbol: BANP
  hgvsc: ENST00000355022.4:c.255A>G
  hgvsp: ENST00000355022.4:c.255A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Leu77Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: African
population: Latino
population: Other
population: South Asian
reference allele: A
site quality: QD
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD

http://identifiers.org/exac.variant/16-88017763-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 88017763
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 88017763
    reference: chr 16
allele count: 1
allele frequency: 1.238390092879257e-5
allele num: 80750
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000444352
  ensembl transcript: ENST00000538234
  gene symbol: BANP
  hgvsc: ENST00000538234.1:c.260A>C
  hgvsp: ENSP00000444352.1:p.Glu87Ala
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000432508
  ensembl transcript: ENST00000479780
  gene symbol: BANP
  hgvsc: ENST00000479780.2:c.260A>C
  hgvsp: ENSP00000432508.1:p.Glu87Ala
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000410089
  ensembl transcript: ENST00000456902
  gene symbol: BANP
  hgvsc: ENST00000456902.1:c.260A>C
  hgvsp: ENSP00000410089.1:p.Glu87Ala
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000286122
  ensembl transcript: ENST00000286122
  gene symbol: BANP
  hgvsc: ENST00000286122.7:c.236A>C
  hgvsp: ENSP00000286122.7:p.Glu79Ala
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000431812
  ensembl transcript: ENST00000466197
  gene symbol: BANP
  hgvsc: ENST00000466197.1:c.260A>C
  hgvsp: ENSP00000431812.1:p.Glu87Ala
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000347125
  ensembl transcript: ENST00000355022
  gene symbol: BANP
  hgvsc: ENST00000355022.4:c.260A>C
  hgvsp: ENSP00000347125.4:p.Glu87Ala
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000376903
  ensembl transcript: ENST00000393208
  gene symbol: BANP
  hgvsc: ENST00000393208.2:c.260A>C
  hgvsp: ENSP00000376903.2:p.Glu87Ala
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000401454
  ensembl transcript: ENST00000436274
  gene symbol: BANP
  hgvsc: ENST00000436274.1:c.260A>C
  hgvsp: ENSP00000401454.1:p.Glu87Ala
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000390504
  ensembl transcript: ENST00000412691
  gene symbol: BANP
  hgvsc: ENST00000412691.1:c.260A>C
  hgvsp: ENSP00000390504.1:p.Glu87Ala
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000399576
  ensembl transcript: ENST00000436970
  gene symbol: BANP
  hgvsc: ENST00000436970.1:c.260A>C
  hgvsp: ENSP00000399576.1:p.Glu87Ala
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000411479
  ensembl transcript: ENST00000439677
  gene symbol: BANP
  hgvsc: ENST00000439677.1:c.278A>C
  hgvsp: ENSP00000411479.1:p.Glu93Ala
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000436869
  ensembl transcript: ENST00000485772
  gene symbol: BANP
  hgvsc: ENST00000485772.1:c.*159A>C
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000376902
  ensembl transcript: ENST00000393207
  gene symbol: BANP
  hgvsc: ENST00000393207.1:c.236A>C
  hgvsp: ENSP00000376902.1:p.Glu79Ala
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000435727
  ensembl transcript: ENST00000459966
  gene symbol: BANP
  hgvsc: ENST00000459966.1:c.*159A>C
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000347290
  ensembl transcript: ENST00000355163
  gene symbol: BANP
  hgvsc: ENST00000355163.5:c.278A>C
  hgvsp: ENSP00000347290.5:p.Glu93Ala
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172530
  ensembl transcript: ENST00000472964
  gene symbol: BANP
  hgvsc: ENST00000472964.1:n.228A>C
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172530
  ensembl transcript: ENST00000569400
  gene symbol: BANP
  hgvsc: ENST00000569400.1:n.708A>C
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172530
  ensembl transcript: ENST00000474563
  gene symbol: BANP
  hgvsc: ENST00000474563.2:n.691A>C
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172530
  ensembl transcript: ENST00000488074
  gene symbol: BANP
  hgvsc: ENST00000488074.1:n.682A>C
  variant of: http://identifiers.org/hgnc/13450
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Glu79Ala
num of homozygotes: 0
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Latino
reference allele: A
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum

16-88017773-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 88017773
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 88017773
    reference: chr 16
allele count: 1
allele frequency: 1.248501797842589e-5
allele num: 80096
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000410089
  ensembl transcript: ENST00000456902
  gene symbol: BANP
  hgvsc: ENST00000456902.1:c.270T>C
  hgvsp: ENST00000456902.1:c.270T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172530
  ensembl transcript: ENST00000472964
  gene symbol: BANP
  hgvsc: ENST00000472964.1:n.238T>C
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000411479
  ensembl transcript: ENST00000439677
  gene symbol: BANP
  hgvsc: ENST00000439677.1:c.288T>C
  hgvsp: ENST00000439677.1:c.288T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000399576
  ensembl transcript: ENST00000436970
  gene symbol: BANP
  hgvsc: ENST00000436970.1:c.270T>C
  hgvsp: ENST00000436970.1:c.270T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000432508
  ensembl transcript: ENST00000479780
  gene symbol: BANP
  hgvsc: ENST00000479780.2:c.270T>C
  hgvsp: ENST00000479780.2:c.270T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000444352
  ensembl transcript: ENST00000538234
  gene symbol: BANP
  hgvsc: ENST00000538234.1:c.270T>C
  hgvsp: ENST00000538234.1:c.270T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172530
  ensembl transcript: ENST00000569400
  gene symbol: BANP
  hgvsc: ENST00000569400.1:n.718T>C
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000376902
  ensembl transcript: ENST00000393207
  gene symbol: BANP
  hgvsc: ENST00000393207.1:c.246T>C
  hgvsp: ENST00000393207.1:c.246T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000390504
  ensembl transcript: ENST00000412691
  gene symbol: BANP
  hgvsc: ENST00000412691.1:c.270T>C
  hgvsp: ENST00000412691.1:c.270T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000431812
  ensembl transcript: ENST00000466197
  gene symbol: BANP
  hgvsc: ENST00000466197.1:c.270T>C
  hgvsp: ENST00000466197.1:c.270T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000286122
  ensembl transcript: ENST00000286122
  gene symbol: BANP
  hgvsc: ENST00000286122.7:c.246T>C
  hgvsp: ENST00000286122.7:c.246T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000401454
  ensembl transcript: ENST00000436274
  gene symbol: BANP
  hgvsc: ENST00000436274.1:c.270T>C
  hgvsp: ENST00000436274.1:c.270T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000347290
  ensembl transcript: ENST00000355163
  gene symbol: BANP
  hgvsc: ENST00000355163.5:c.288T>C
  hgvsp: ENST00000355163.5:c.288T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172530
  ensembl transcript: ENST00000488074
  gene symbol: BANP
  hgvsc: ENST00000488074.1:n.692T>C
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172530
  ensembl transcript: ENST00000474563
  gene symbol: BANP
  hgvsc: ENST00000474563.2:n.701T>C
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000347125
  ensembl transcript: ENST00000355022
  gene symbol: BANP
  hgvsc: ENST00000355022.4:c.270T>C
  hgvsp: ENST00000355022.4:c.270T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000436869
  ensembl transcript: ENST00000485772
  gene symbol: BANP
  hgvsc: ENST00000485772.1:c.*169T>C
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000435727
  ensembl transcript: ENST00000459966
  gene symbol: BANP
  hgvsc: ENST00000459966.1:c.*169T>C
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000376903
  ensembl transcript: ENST00000393208
  gene symbol: BANP
  hgvsc: ENST00000393208.2:c.270T>C
  hgvsp: ENST00000393208.2:c.270T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Asp82Asp
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
population: Latino
reference allele: T
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum

16-88017774-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 88017774
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 88017774
    reference: chr 16
allele count: 0
allele frequency: 0.0e0
allele num: 79998
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000431812
  ensembl transcript: ENST00000466197
  gene symbol: BANP
  hgvsc: ENST00000466197.1:c.271C>G
  hgvsp: ENSP00000431812.1:p.Leu91Val
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000286122
  ensembl transcript: ENST00000286122
  gene symbol: BANP
  hgvsc: ENST00000286122.7:c.247C>G
  hgvsp: ENSP00000286122.7:p.Leu83Val
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000410089
  ensembl transcript: ENST00000456902
  gene symbol: BANP
  hgvsc: ENST00000456902.1:c.271C>G
  hgvsp: ENSP00000410089.1:p.Leu91Val
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172530
  ensembl transcript: ENST00000488074
  gene symbol: BANP
  hgvsc: ENST00000488074.1:n.693C>G
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000444352
  ensembl transcript: ENST00000538234
  gene symbol: BANP
  hgvsc: ENST00000538234.1:c.271C>G
  hgvsp: ENSP00000444352.1:p.Leu91Val
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000432508
  ensembl transcript: ENST00000479780
  gene symbol: BANP
  hgvsc: ENST00000479780.2:c.271C>G
  hgvsp: ENSP00000432508.1:p.Leu91Val
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172530
  ensembl transcript: ENST00000569400
  gene symbol: BANP
  hgvsc: ENST00000569400.1:n.719C>G
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000435727
  ensembl transcript: ENST00000459966
  gene symbol: BANP
  hgvsc: ENST00000459966.1:c.*170C>G
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000376902
  ensembl transcript: ENST00000393207
  gene symbol: BANP
  hgvsc: ENST00000393207.1:c.247C>G
  hgvsp: ENSP00000376902.1:p.Leu83Val
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000401454
  ensembl transcript: ENST00000436274
  gene symbol: BANP
  hgvsc: ENST00000436274.1:c.271C>G
  hgvsp: ENSP00000401454.1:p.Leu91Val
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000411479
  ensembl transcript: ENST00000439677
  gene symbol: BANP
  hgvsc: ENST00000439677.1:c.289C>G
  hgvsp: ENSP00000411479.1:p.Leu97Val
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000390504
  ensembl transcript: ENST00000412691
  gene symbol: BANP
  hgvsc: ENST00000412691.1:c.271C>G
  hgvsp: ENSP00000390504.1:p.Leu91Val
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000347125
  ensembl transcript: ENST00000355022
  gene symbol: BANP
  hgvsc: ENST00000355022.4:c.271C>G
  hgvsp: ENSP00000347125.4:p.Leu91Val
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000399576
  ensembl transcript: ENST00000436970
  gene symbol: BANP
  hgvsc: ENST00000436970.1:c.271C>G
  hgvsp: ENSP00000399576.1:p.Leu91Val
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172530
  ensembl transcript: ENST00000474563
  gene symbol: BANP
  hgvsc: ENST00000474563.2:n.702C>G
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000376903
  ensembl transcript: ENST00000393208
  gene symbol: BANP
  hgvsc: ENST00000393208.2:c.271C>G
  hgvsp: ENSP00000376903.2:p.Leu91Val
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000436869
  ensembl transcript: ENST00000485772
  gene symbol: BANP
  hgvsc: ENST00000485772.1:c.*170C>G
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172530
  ensembl transcript: ENST00000472964
  gene symbol: BANP
  hgvsc: ENST00000472964.1:n.239C>G
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000347290
  ensembl transcript: ENST00000355163
  gene symbol: BANP
  hgvsc: ENST00000355163.5:c.289C>G
  hgvsp: ENSP00000347290.5:p.Leu97Val
  variant of: http://identifiers.org/hgnc/13450
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Leu83Val
num of homozygotes: 0
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: African
population: Latino
reference allele: C
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: QD

16-88017776-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 88017776
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 88017776
    reference: chr 16
allele count: 1
allele frequency: 1.251282564628744e-5
allele num: 79918
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000432508
  ensembl transcript: ENST00000479780
  gene symbol: BANP
  hgvsc: ENST00000479780.2:c.273G>T
  hgvsp: ENST00000479780.2:c.273G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000444352
  ensembl transcript: ENST00000538234
  gene symbol: BANP
  hgvsc: ENST00000538234.1:c.273G>T
  hgvsp: ENST00000538234.1:c.273G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000436869
  ensembl transcript: ENST00000485772
  gene symbol: BANP
  hgvsc: ENST00000485772.1:c.*172G>T
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000401454
  ensembl transcript: ENST00000436274
  gene symbol: BANP
  hgvsc: ENST00000436274.1:c.273G>T
  hgvsp: ENST00000436274.1:c.273G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000435727
  ensembl transcript: ENST00000459966
  gene symbol: BANP
  hgvsc: ENST00000459966.1:c.*172G>T
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172530
  ensembl transcript: ENST00000474563
  gene symbol: BANP
  hgvsc: ENST00000474563.2:n.704G>T
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172530
  ensembl transcript: ENST00000569400
  gene symbol: BANP
  hgvsc: ENST00000569400.1:n.721G>T
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000411479
  ensembl transcript: ENST00000439677
  gene symbol: BANP
  hgvsc: ENST00000439677.1:c.291G>T
  hgvsp: ENST00000439677.1:c.291G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000390504
  ensembl transcript: ENST00000412691
  gene symbol: BANP
  hgvsc: ENST00000412691.1:c.273G>T
  hgvsp: ENST00000412691.1:c.273G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000376903
  ensembl transcript: ENST00000393208
  gene symbol: BANP
  hgvsc: ENST00000393208.2:c.273G>T
  hgvsp: ENST00000393208.2:c.273G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000410089
  ensembl transcript: ENST00000456902
  gene symbol: BANP
  hgvsc: ENST00000456902.1:c.273G>T
  hgvsp: ENST00000456902.1:c.273G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000431812
  ensembl transcript: ENST00000466197
  gene symbol: BANP
  hgvsc: ENST00000466197.1:c.273G>T
  hgvsp: ENST00000466197.1:c.273G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000347125
  ensembl transcript: ENST00000355022
  gene symbol: BANP
  hgvsc: ENST00000355022.4:c.273G>T
  hgvsp: ENST00000355022.4:c.273G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000347290
  ensembl transcript: ENST00000355163
  gene symbol: BANP
  hgvsc: ENST00000355163.5:c.291G>T
  hgvsp: ENST00000355163.5:c.291G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000376902
  ensembl transcript: ENST00000393207
  gene symbol: BANP
  hgvsc: ENST00000393207.1:c.249G>T
  hgvsp: ENST00000393207.1:c.249G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172530
  ensembl transcript: ENST00000472964
  gene symbol: BANP
  hgvsc: ENST00000472964.1:n.241G>T
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000286122
  ensembl transcript: ENST00000286122
  gene symbol: BANP
  hgvsc: ENST00000286122.7:c.249G>T
  hgvsp: ENST00000286122.7:c.249G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172530
  ensembl transcript: ENST00000488074
  gene symbol: BANP
  hgvsc: ENST00000488074.1:n.695G>T
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000399576
  ensembl transcript: ENST00000436970
  gene symbol: BANP
  hgvsc: ENST00000436970.1:c.273G>T
  hgvsp: ENST00000436970.1:c.273G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Leu83Leu
num of homozygotes: 0
population: Other
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
reference allele: G
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff

16-88017781-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 88017781
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 88017781
    reference: chr 16
allele count: 6
allele frequency: 7.526342197691921e-5
allele num: 79720
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000347290
  ensembl transcript: ENST00000355163
  gene symbol: BANP
  hgvsc: ENST00000355163.5:c.296C>T
  hgvsp: ENSP00000347290.5:p.Thr99Met
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000401454
  ensembl transcript: ENST00000436274
  gene symbol: BANP
  hgvsc: ENST00000436274.1:c.278C>T
  hgvsp: ENSP00000401454.1:p.Thr93Met
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000444352
  ensembl transcript: ENST00000538234
  gene symbol: BANP
  hgvsc: ENST00000538234.1:c.278C>T
  hgvsp: ENSP00000444352.1:p.Thr93Met
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000410089
  ensembl transcript: ENST00000456902
  gene symbol: BANP
  hgvsc: ENST00000456902.1:c.278C>T
  hgvsp: ENSP00000410089.1:p.Thr93Met
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000432508
  ensembl transcript: ENST00000479780
  gene symbol: BANP
  hgvsc: ENST00000479780.2:c.278C>T
  hgvsp: ENSP00000432508.1:p.Thr93Met
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000411479
  ensembl transcript: ENST00000439677
  gene symbol: BANP
  hgvsc: ENST00000439677.1:c.296C>T
  hgvsp: ENSP00000411479.1:p.Thr99Met
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172530
  ensembl transcript: ENST00000474563
  gene symbol: BANP
  hgvsc: ENST00000474563.2:n.709C>T
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000347125
  ensembl transcript: ENST00000355022
  gene symbol: BANP
  hgvsc: ENST00000355022.4:c.278C>T
  hgvsp: ENSP00000347125.4:p.Thr93Met
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000399576
  ensembl transcript: ENST00000436970
  gene symbol: BANP
  hgvsc: ENST00000436970.1:c.278C>T
  hgvsp: ENSP00000399576.1:p.Thr93Met
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000431812
  ensembl transcript: ENST00000466197
  gene symbol: BANP
  hgvsc: ENST00000466197.1:c.278C>T
  hgvsp: ENSP00000431812.1:p.Thr93Met
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000390504
  ensembl transcript: ENST00000412691
  gene symbol: BANP
  hgvsc: ENST00000412691.1:c.278C>T
  hgvsp: ENSP00000390504.1:p.Thr93Met
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000435727
  ensembl transcript: ENST00000459966
  gene symbol: BANP
  hgvsc: ENST00000459966.1:c.*177C>T
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000286122
  ensembl transcript: ENST00000286122
  gene symbol: BANP
  hgvsc: ENST00000286122.7:c.254C>T
  hgvsp: ENSP00000286122.7:p.Thr85Met
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000376902
  ensembl transcript: ENST00000393207
  gene symbol: BANP
  hgvsc: ENST00000393207.1:c.254C>T
  hgvsp: ENSP00000376902.1:p.Thr85Met
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172530
  ensembl transcript: ENST00000472964
  gene symbol: BANP
  hgvsc: ENST00000472964.1:n.246C>T
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000376903
  ensembl transcript: ENST00000393208
  gene symbol: BANP
  hgvsc: ENST00000393208.2:c.278C>T
  hgvsp: ENSP00000376903.2:p.Thr93Met
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172530
  ensembl transcript: ENST00000569400
  gene symbol: BANP
  hgvsc: ENST00000569400.1:n.726C>T
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000436869
  ensembl transcript: ENST00000485772
  gene symbol: BANP
  hgvsc: ENST00000485772.1:c.*177C>T
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172530
  ensembl transcript: ENST00000488074
  gene symbol: BANP
  hgvsc: ENST00000488074.1:n.700C>T
  variant of: http://identifiers.org/hgnc/13450
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Thr85Met
num of homozygotes: 0
population: Latino
population: South Asian
population: Other
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: QD
site quality: ClippingRankSum

16-88017782-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 88017782
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 88017782
    reference: chr 16
allele count: 34
allele frequency: 4.27243025885901e-4
allele num: 79580
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000432508
  ensembl transcript: ENST00000479780
  gene symbol: BANP
  hgvsc: ENST00000479780.2:c.279G>A
  hgvsp: ENST00000479780.2:c.279G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000410089
  ensembl transcript: ENST00000456902
  gene symbol: BANP
  hgvsc: ENST00000456902.1:c.279G>A
  hgvsp: ENST00000456902.1:c.279G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000376903
  ensembl transcript: ENST00000393208
  gene symbol: BANP
  hgvsc: ENST00000393208.2:c.279G>A
  hgvsp: ENST00000393208.2:c.279G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172530
  ensembl transcript: ENST00000569400
  gene symbol: BANP
  hgvsc: ENST00000569400.1:n.727G>A
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000436869
  ensembl transcript: ENST00000485772
  gene symbol: BANP
  hgvsc: ENST00000485772.1:c.*178G>A
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000376902
  ensembl transcript: ENST00000393207
  gene symbol: BANP
  hgvsc: ENST00000393207.1:c.255G>A
  hgvsp: ENST00000393207.1:c.255G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172530
  ensembl transcript: ENST00000472964
  gene symbol: BANP
  hgvsc: ENST00000472964.1:n.247G>A
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000399576
  ensembl transcript: ENST00000436970
  gene symbol: BANP
  hgvsc: ENST00000436970.1:c.279G>A
  hgvsp: ENST00000436970.1:c.279G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000401454
  ensembl transcript: ENST00000436274
  gene symbol: BANP
  hgvsc: ENST00000436274.1:c.279G>A
  hgvsp: ENST00000436274.1:c.279G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000390504
  ensembl transcript: ENST00000412691
  gene symbol: BANP
  hgvsc: ENST00000412691.1:c.279G>A
  hgvsp: ENST00000412691.1:c.279G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000411479
  ensembl transcript: ENST00000439677
  gene symbol: BANP
  hgvsc: ENST00000439677.1:c.297G>A
  hgvsp: ENST00000439677.1:c.297G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000444352
  ensembl transcript: ENST00000538234
  gene symbol: BANP
  hgvsc: ENST00000538234.1:c.279G>A
  hgvsp: ENST00000538234.1:c.279G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000286122
  ensembl transcript: ENST00000286122
  gene symbol: BANP
  hgvsc: ENST00000286122.7:c.255G>A
  hgvsp: ENST00000286122.7:c.255G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000431812
  ensembl transcript: ENST00000466197
  gene symbol: BANP
  hgvsc: ENST00000466197.1:c.279G>A
  hgvsp: ENST00000466197.1:c.279G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000347125
  ensembl transcript: ENST00000355022
  gene symbol: BANP
  hgvsc: ENST00000355022.4:c.279G>A
  hgvsp: ENST00000355022.4:c.279G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000347290
  ensembl transcript: ENST00000355163
  gene symbol: BANP
  hgvsc: ENST00000355163.5:c.297G>A
  hgvsp: ENST00000355163.5:c.297G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172530
  ensembl transcript: ENST00000488074
  gene symbol: BANP
  hgvsc: ENST00000488074.1:n.701G>A
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000435727
  ensembl transcript: ENST00000459966
  gene symbol: BANP
  hgvsc: ENST00000459966.1:c.*178G>A
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172530
  ensembl transcript: ENST00000474563
  gene symbol: BANP
  hgvsc: ENST00000474563.2:n.710G>A
  variant of: http://identifiers.org/hgnc/13450
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Thr85Thr
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: MQ
site quality: FS

16-88017782-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 88017782
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 88017782
    reference: chr 16
allele count: 12
allele frequency: 1.507916561950239e-4
allele num: 79580
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000347125
  ensembl transcript: ENST00000355022
  gene symbol: BANP
  hgvsc: ENST00000355022.4:c.279G>C
  hgvsp: ENST00000355022.4:c.279G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000435727
  ensembl transcript: ENST00000459966
  gene symbol: BANP
  hgvsc: ENST00000459966.1:c.*178G>C
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000347290
  ensembl transcript: ENST00000355163
  gene symbol: BANP
  hgvsc: ENST00000355163.5:c.297G>C
  hgvsp: ENST00000355163.5:c.297G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000376903
  ensembl transcript: ENST00000393208
  gene symbol: BANP
  hgvsc: ENST00000393208.2:c.279G>C
  hgvsp: ENST00000393208.2:c.279G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000376902
  ensembl transcript: ENST00000393207
  gene symbol: BANP
  hgvsc: ENST00000393207.1:c.255G>C
  hgvsp: ENST00000393207.1:c.255G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000444352
  ensembl transcript: ENST00000538234
  gene symbol: BANP
  hgvsc: ENST00000538234.1:c.279G>C
  hgvsp: ENST00000538234.1:c.279G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000432508
  ensembl transcript: ENST00000479780
  gene symbol: BANP
  hgvsc: ENST00000479780.2:c.279G>C
  hgvsp: ENST00000479780.2:c.279G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172530
  ensembl transcript: ENST00000569400
  gene symbol: BANP
  hgvsc: ENST00000569400.1:n.727G>C
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000436869
  ensembl transcript: ENST00000485772
  gene symbol: BANP
  hgvsc: ENST00000485772.1:c.*178G>C
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172530
  ensembl transcript: ENST00000472964
  gene symbol: BANP
  hgvsc: ENST00000472964.1:n.247G>C
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000410089
  ensembl transcript: ENST00000456902
  gene symbol: BANP
  hgvsc: ENST00000456902.1:c.279G>C
  hgvsp: ENST00000456902.1:c.279G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000286122
  ensembl transcript: ENST00000286122
  gene symbol: BANP
  hgvsc: ENST00000286122.7:c.255G>C
  hgvsp: ENST00000286122.7:c.255G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000390504
  ensembl transcript: ENST00000412691
  gene symbol: BANP
  hgvsc: ENST00000412691.1:c.279G>C
  hgvsp: ENST00000412691.1:c.279G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172530
  ensembl transcript: ENST00000488074
  gene symbol: BANP
  hgvsc: ENST00000488074.1:n.701G>C
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000411479
  ensembl transcript: ENST00000439677
  gene symbol: BANP
  hgvsc: ENST00000439677.1:c.297G>C
  hgvsp: ENST00000439677.1:c.297G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000399576
  ensembl transcript: ENST00000436970
  gene symbol: BANP
  hgvsc: ENST00000436970.1:c.279G>C
  hgvsp: ENST00000436970.1:c.279G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172530
  ensembl transcript: ENST00000474563
  gene symbol: BANP
  hgvsc: ENST00000474563.2:n.710G>C
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000401454
  ensembl transcript: ENST00000436274
  gene symbol: BANP
  hgvsc: ENST00000436274.1:c.279G>C
  hgvsp: ENST00000436274.1:c.279G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000431812
  ensembl transcript: ENST00000466197
  gene symbol: BANP
  hgvsc: ENST00000466197.1:c.279G>C
  hgvsp: ENST00000466197.1:c.279G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Thr85Thr
num of homozygotes: 0
population: Latino
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: G
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP

http://identifiers.org/exac.variant/16-88017786-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 88017786
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 88017786
    reference: chr 16
allele count: 1
allele frequency: 1.244121525790639e-5
allele num: 80378
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000411479
  ensembl transcript: ENST00000439677
  gene symbol: BANP
  hgvsc: ENST00000439677.1:c.301A>C
  hgvsp: ENSP00000411479.1:p.Lys101Gln
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000436869
  ensembl transcript: ENST00000485772
  gene symbol: BANP
  hgvsc: ENST00000485772.1:c.*182A>C
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000347290
  ensembl transcript: ENST00000355163
  gene symbol: BANP
  hgvsc: ENST00000355163.5:c.301A>C
  hgvsp: ENSP00000347290.5:p.Lys101Gln
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000286122
  ensembl transcript: ENST00000286122
  gene symbol: BANP
  hgvsc: ENST00000286122.7:c.259A>C
  hgvsp: ENSP00000286122.7:p.Lys87Gln
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000399576
  ensembl transcript: ENST00000436970
  gene symbol: BANP
  hgvsc: ENST00000436970.1:c.283A>C
  hgvsp: ENSP00000399576.1:p.Lys95Gln
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000401454
  ensembl transcript: ENST00000436274
  gene symbol: BANP
  hgvsc: ENST00000436274.1:c.283A>C
  hgvsp: ENSP00000401454.1:p.Lys95Gln
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000432508
  ensembl transcript: ENST00000479780
  gene symbol: BANP
  hgvsc: ENST00000479780.2:c.283A>C
  hgvsp: ENSP00000432508.1:p.Lys95Gln
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172530
  ensembl transcript: ENST00000472964
  gene symbol: BANP
  hgvsc: ENST00000472964.1:n.251A>C
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000435727
  ensembl transcript: ENST00000459966
  gene symbol: BANP
  hgvsc: ENST00000459966.1:c.*182A>C
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000390504
  ensembl transcript: ENST00000412691
  gene symbol: BANP
  hgvsc: ENST00000412691.1:c.283A>C
  hgvsp: ENSP00000390504.1:p.Lys95Gln
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000410089
  ensembl transcript: ENST00000456902
  gene symbol: BANP
  hgvsc: ENST00000456902.1:c.283A>C
  hgvsp: ENSP00000410089.1:p.Lys95Gln
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000431812
  ensembl transcript: ENST00000466197
  gene symbol: BANP
  hgvsc: ENST00000466197.1:c.283A>C
  hgvsp: ENSP00000431812.1:p.Lys95Gln
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000347125
  ensembl transcript: ENST00000355022
  gene symbol: BANP
  hgvsc: ENST00000355022.4:c.283A>C
  hgvsp: ENSP00000347125.4:p.Lys95Gln
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000376903
  ensembl transcript: ENST00000393208
  gene symbol: BANP
  hgvsc: ENST00000393208.2:c.283A>C
  hgvsp: ENSP00000376903.2:p.Lys95Gln
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000444352
  ensembl transcript: ENST00000538234
  gene symbol: BANP
  hgvsc: ENST00000538234.1:c.283A>C
  hgvsp: ENSP00000444352.1:p.Lys95Gln
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172530
  ensembl transcript: ENST00000488074
  gene symbol: BANP
  hgvsc: ENST00000488074.1:n.705A>C
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172530
  ensembl transcript: ENST00000474563
  gene symbol: BANP
  hgvsc: ENST00000474563.2:n.714A>C
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172530
  ensembl transcript: ENST00000569400
  gene symbol: BANP
  hgvsc: ENST00000569400.1:n.731A>C
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000376902
  ensembl transcript: ENST00000393207
  gene symbol: BANP
  hgvsc: ENST00000393207.1:c.259A>C
  hgvsp: ENSP00000376902.1:p.Lys87Gln
  variant of: http://identifiers.org/hgnc/13450
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Lys87Gln
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: South Asian
reference allele: A
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum

16-88017787-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 88017787
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 88017787
    reference: chr 16
allele count: 1
allele frequency: 1.244555071561917e-5
allele num: 80350
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000347125
  ensembl transcript: ENST00000355022
  gene symbol: BANP
  hgvsc: ENST00000355022.4:c.284A>G
  hgvsp: ENSP00000347125.4:p.Lys95Arg
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000444352
  ensembl transcript: ENST00000538234
  gene symbol: BANP
  hgvsc: ENST00000538234.1:c.284A>G
  hgvsp: ENSP00000444352.1:p.Lys95Arg
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000376902
  ensembl transcript: ENST00000393207
  gene symbol: BANP
  hgvsc: ENST00000393207.1:c.260A>G
  hgvsp: ENSP00000376902.1:p.Lys87Arg
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172530
  ensembl transcript: ENST00000569400
  gene symbol: BANP
  hgvsc: ENST00000569400.1:n.732A>G
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000411479
  ensembl transcript: ENST00000439677
  gene symbol: BANP
  hgvsc: ENST00000439677.1:c.302A>G
  hgvsp: ENSP00000411479.1:p.Lys101Arg
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000376903
  ensembl transcript: ENST00000393208
  gene symbol: BANP
  hgvsc: ENST00000393208.2:c.284A>G
  hgvsp: ENSP00000376903.2:p.Lys95Arg
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000399576
  ensembl transcript: ENST00000436970
  gene symbol: BANP
  hgvsc: ENST00000436970.1:c.284A>G
  hgvsp: ENSP00000399576.1:p.Lys95Arg
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000432508
  ensembl transcript: ENST00000479780
  gene symbol: BANP
  hgvsc: ENST00000479780.2:c.284A>G
  hgvsp: ENSP00000432508.1:p.Lys95Arg
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000436869
  ensembl transcript: ENST00000485772
  gene symbol: BANP
  hgvsc: ENST00000485772.1:c.*183A>G
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000286122
  ensembl transcript: ENST00000286122
  gene symbol: BANP
  hgvsc: ENST00000286122.7:c.260A>G
  hgvsp: ENSP00000286122.7:p.Lys87Arg
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000401454
  ensembl transcript: ENST00000436274
  gene symbol: BANP
  hgvsc: ENST00000436274.1:c.284A>G
  hgvsp: ENSP00000401454.1:p.Lys95Arg
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172530
  ensembl transcript: ENST00000472964
  gene symbol: BANP
  hgvsc: ENST00000472964.1:n.252A>G
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000431812
  ensembl transcript: ENST00000466197
  gene symbol: BANP
  hgvsc: ENST00000466197.1:c.284A>G
  hgvsp: ENSP00000431812.1:p.Lys95Arg
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172530
  ensembl transcript: ENST00000474563
  gene symbol: BANP
  hgvsc: ENST00000474563.2:n.715A>G
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000410089
  ensembl transcript: ENST00000456902
  gene symbol: BANP
  hgvsc: ENST00000456902.1:c.284A>G
  hgvsp: ENSP00000410089.1:p.Lys95Arg
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000390504
  ensembl transcript: ENST00000412691
  gene symbol: BANP
  hgvsc: ENST00000412691.1:c.284A>G
  hgvsp: ENSP00000390504.1:p.Lys95Arg
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000435727
  ensembl transcript: ENST00000459966
  gene symbol: BANP
  hgvsc: ENST00000459966.1:c.*183A>G
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172530
  ensembl transcript: ENST00000488074
  gene symbol: BANP
  hgvsc: ENST00000488074.1:n.706A>G
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000347290
  ensembl transcript: ENST00000355163
  gene symbol: BANP
  hgvsc: ENST00000355163.5:c.302A>G
  hgvsp: ENSP00000347290.5:p.Lys101Arg
  variant of: http://identifiers.org/hgnc/13450
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Lys87Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: African
population: Latino
population: South Asian
population: East Asian
reference allele: A
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/16-88017790-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 88017790
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 88017790
    reference: chr 16
allele count: 1
allele frequency: 1.238881042642286e-5
allele num: 80718
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000444352
  ensembl transcript: ENST00000538234
  gene symbol: BANP
  hgvsc: ENST00000538234.1:c.287A>C
  hgvsp: ENSP00000444352.1:p.Gln96Pro
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000410089
  ensembl transcript: ENST00000456902
  gene symbol: BANP
  hgvsc: ENST00000456902.1:c.287A>C
  hgvsp: ENSP00000410089.1:p.Gln96Pro
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000376902
  ensembl transcript: ENST00000393207
  gene symbol: BANP
  hgvsc: ENST00000393207.1:c.263A>C
  hgvsp: ENSP00000376902.1:p.Gln88Pro
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000390504
  ensembl transcript: ENST00000412691
  gene symbol: BANP
  hgvsc: ENST00000412691.1:c.287A>C
  hgvsp: ENSP00000390504.1:p.Gln96Pro
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172530
  ensembl transcript: ENST00000488074
  gene symbol: BANP
  hgvsc: ENST00000488074.1:n.709A>C
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000376903
  ensembl transcript: ENST00000393208
  gene symbol: BANP
  hgvsc: ENST00000393208.2:c.287A>C
  hgvsp: ENSP00000376903.2:p.Gln96Pro
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000286122
  ensembl transcript: ENST00000286122
  gene symbol: BANP
  hgvsc: ENST00000286122.7:c.263A>C
  hgvsp: ENSP00000286122.7:p.Gln88Pro
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000432508
  ensembl transcript: ENST00000479780
  gene symbol: BANP
  hgvsc: ENST00000479780.2:c.287A>C
  hgvsp: ENSP00000432508.1:p.Gln96Pro
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000347290
  ensembl transcript: ENST00000355163
  gene symbol: BANP
  hgvsc: ENST00000355163.5:c.305A>C
  hgvsp: ENSP00000347290.5:p.Gln102Pro
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172530
  ensembl transcript: ENST00000569400
  gene symbol: BANP
  hgvsc: ENST00000569400.1:n.735A>C
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000399576
  ensembl transcript: ENST00000436970
  gene symbol: BANP
  hgvsc: ENST00000436970.1:c.287A>C
  hgvsp: ENSP00000399576.1:p.Gln96Pro
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000411479
  ensembl transcript: ENST00000439677
  gene symbol: BANP
  hgvsc: ENST00000439677.1:c.305A>C
  hgvsp: ENSP00000411479.1:p.Gln102Pro
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000431812
  ensembl transcript: ENST00000466197
  gene symbol: BANP
  hgvsc: ENST00000466197.1:c.287A>C
  hgvsp: ENSP00000431812.1:p.Gln96Pro
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000436869
  ensembl transcript: ENST00000485772
  gene symbol: BANP
  hgvsc: ENST00000485772.1:c.*186A>C
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000435727
  ensembl transcript: ENST00000459966
  gene symbol: BANP
  hgvsc: ENST00000459966.1:c.*186A>C
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172530
  ensembl transcript: ENST00000474563
  gene symbol: BANP
  hgvsc: ENST00000474563.2:n.718A>C
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000347125
  ensembl transcript: ENST00000355022
  gene symbol: BANP
  hgvsc: ENST00000355022.4:c.287A>C
  hgvsp: ENSP00000347125.4:p.Gln96Pro
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172530
  ensembl transcript: ENST00000472964
  gene symbol: BANP
  hgvsc: ENST00000472964.1:n.255A>C
  variant of: http://identifiers.org/hgnc/13450
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln88Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
population: Latino
population: European (Finnish)
population: East Asian
reference allele: A
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: QD

16-88017794-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 88017794
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 88017794
    reference: chr 16
allele count: 1
allele frequency: 1.236950175646925e-5
allele num: 80844
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000286122
  ensembl transcript: ENST00000286122
  gene symbol: BANP
  hgvsc: ENST00000286122.7:c.267C>G
  hgvsp: ENSP00000286122.7:p.His89Gln
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000432508
  ensembl transcript: ENST00000479780
  gene symbol: BANP
  hgvsc: ENST00000479780.2:c.291C>G
  hgvsp: ENSP00000432508.1:p.His97Gln
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000347125
  ensembl transcript: ENST00000355022
  gene symbol: BANP
  hgvsc: ENST00000355022.4:c.291C>G
  hgvsp: ENSP00000347125.4:p.His97Gln
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000399576
  ensembl transcript: ENST00000436970
  gene symbol: BANP
  hgvsc: ENST00000436970.1:c.291C>G
  hgvsp: ENSP00000399576.1:p.His97Gln
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000376902
  ensembl transcript: ENST00000393207
  gene symbol: BANP
  hgvsc: ENST00000393207.1:c.267C>G
  hgvsp: ENSP00000376902.1:p.His89Gln
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172530
  ensembl transcript: ENST00000488074
  gene symbol: BANP
  hgvsc: ENST00000488074.1:n.713C>G
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000376903
  ensembl transcript: ENST00000393208
  gene symbol: BANP
  hgvsc: ENST00000393208.2:c.291C>G
  hgvsp: ENSP00000376903.2:p.His97Gln
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172530
  ensembl transcript: ENST00000472964
  gene symbol: BANP
  hgvsc: ENST00000472964.1:n.259C>G
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000435727
  ensembl transcript: ENST00000459966
  gene symbol: BANP
  hgvsc: ENST00000459966.1:c.*190C>G
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000390504
  ensembl transcript: ENST00000412691
  gene symbol: BANP
  hgvsc: ENST00000412691.1:c.291C>G
  hgvsp: ENSP00000390504.1:p.His97Gln
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172530
  ensembl transcript: ENST00000474563
  gene symbol: BANP
  hgvsc: ENST00000474563.2:n.722C>G
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000436869
  ensembl transcript: ENST00000485772
  gene symbol: BANP
  hgvsc: ENST00000485772.1:c.*190C>G
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000411479
  ensembl transcript: ENST00000439677
  gene symbol: BANP
  hgvsc: ENST00000439677.1:c.309C>G
  hgvsp: ENSP00000411479.1:p.His103Gln
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000431812
  ensembl transcript: ENST00000466197
  gene symbol: BANP
  hgvsc: ENST00000466197.1:c.291C>G
  hgvsp: ENSP00000431812.1:p.His97Gln
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172530
  ensembl transcript: ENST00000569400
  gene symbol: BANP
  hgvsc: ENST00000569400.1:n.739C>G
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000444352
  ensembl transcript: ENST00000538234
  gene symbol: BANP
  hgvsc: ENST00000538234.1:c.291C>G
  hgvsp: ENSP00000444352.1:p.His97Gln
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000347290
  ensembl transcript: ENST00000355163
  gene symbol: BANP
  hgvsc: ENST00000355163.5:c.309C>G
  hgvsp: ENSP00000347290.5:p.His103Gln
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000410089
  ensembl transcript: ENST00000456902
  gene symbol: BANP
  hgvsc: ENST00000456902.1:c.291C>G
  hgvsp: ENSP00000410089.1:p.His97Gln
  variant of: http://identifiers.org/hgnc/13450
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12074
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His89Gln
num of homozygotes: 0
population: African
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
reference allele: C
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD

16-88017794-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 88017794
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 88017794
    reference: chr 16
allele count: 1
allele frequency: 1.236950175646925e-5
allele num: 80844
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000410089
  ensembl transcript: ENST00000456902
  gene symbol: BANP
  hgvsc: ENST00000456902.1:c.291C>T
  hgvsp: ENST00000456902.1:c.291C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000286122
  ensembl transcript: ENST00000286122
  gene symbol: BANP
  hgvsc: ENST00000286122.7:c.267C>T
  hgvsp: ENST00000286122.7:c.267C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000435727
  ensembl transcript: ENST00000459966
  gene symbol: BANP
  hgvsc: ENST00000459966.1:c.*190C>T
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172530
  ensembl transcript: ENST00000488074
  gene symbol: BANP
  hgvsc: ENST00000488074.1:n.713C>T
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000444352
  ensembl transcript: ENST00000538234
  gene symbol: BANP
  hgvsc: ENST00000538234.1:c.291C>T
  hgvsp: ENST00000538234.1:c.291C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000347125
  ensembl transcript: ENST00000355022
  gene symbol: BANP
  hgvsc: ENST00000355022.4:c.291C>T
  hgvsp: ENST00000355022.4:c.291C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000376903
  ensembl transcript: ENST00000393208
  gene symbol: BANP
  hgvsc: ENST00000393208.2:c.291C>T
  hgvsp: ENST00000393208.2:c.291C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000376902
  ensembl transcript: ENST00000393207
  gene symbol: BANP
  hgvsc: ENST00000393207.1:c.267C>T
  hgvsp: ENST00000393207.1:c.267C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000431812
  ensembl transcript: ENST00000466197
  gene symbol: BANP
  hgvsc: ENST00000466197.1:c.291C>T
  hgvsp: ENST00000466197.1:c.291C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000347290
  ensembl transcript: ENST00000355163
  gene symbol: BANP
  hgvsc: ENST00000355163.5:c.309C>T
  hgvsp: ENST00000355163.5:c.309C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000411479
  ensembl transcript: ENST00000439677
  gene symbol: BANP
  hgvsc: ENST00000439677.1:c.309C>T
  hgvsp: ENST00000439677.1:c.309C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172530
  ensembl transcript: ENST00000474563
  gene symbol: BANP
  hgvsc: ENST00000474563.2:n.722C>T
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000399576
  ensembl transcript: ENST00000436970
  gene symbol: BANP
  hgvsc: ENST00000436970.1:c.291C>T
  hgvsp: ENST00000436970.1:c.291C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000390504
  ensembl transcript: ENST00000412691
  gene symbol: BANP
  hgvsc: ENST00000412691.1:c.291C>T
  hgvsp: ENST00000412691.1:c.291C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172530
  ensembl transcript: ENST00000472964
  gene symbol: BANP
  hgvsc: ENST00000472964.1:n.259C>T
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172530
  ensembl transcript: ENST00000569400
  gene symbol: BANP
  hgvsc: ENST00000569400.1:n.739C>T
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000436869
  ensembl transcript: ENST00000485772
  gene symbol: BANP
  hgvsc: ENST00000485772.1:c.*190C>T
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000432508
  ensembl transcript: ENST00000479780
  gene symbol: BANP
  hgvsc: ENST00000479780.2:c.291C>T
  hgvsp: ENST00000479780.2:c.291C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18420
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His89His
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Latino
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD

16-88017796-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 88017796
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 88017796
    reference: chr 16
allele count: 0
allele frequency: 0.0e0
allele num: 81018
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172530
  ensembl transcript: ENST00000569400
  gene symbol: BANP
  hgvsc: ENST00000569400.1:n.741G>A
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000435727
  ensembl transcript: ENST00000459966
  gene symbol: BANP
  hgvsc: ENST00000459966.1:c.*192G>A
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000376902
  ensembl transcript: ENST00000393207
  gene symbol: BANP
  hgvsc: ENST00000393207.1:c.269G>A
  hgvsp: ENSP00000376902.1:p.Ser90Asn
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000347290
  ensembl transcript: ENST00000355163
  gene symbol: BANP
  hgvsc: ENST00000355163.5:c.311G>A
  hgvsp: ENSP00000347290.5:p.Ser104Asn
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000444352
  ensembl transcript: ENST00000538234
  gene symbol: BANP
  hgvsc: ENST00000538234.1:c.293G>A
  hgvsp: ENSP00000444352.1:p.Ser98Asn
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000399576
  ensembl transcript: ENST00000436970
  gene symbol: BANP
  hgvsc: ENST00000436970.1:c.293G>A
  hgvsp: ENSP00000399576.1:p.Ser98Asn
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000432508
  ensembl transcript: ENST00000479780
  gene symbol: BANP
  hgvsc: ENST00000479780.2:c.293G>A
  hgvsp: ENSP00000432508.1:p.Ser98Asn
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000390504
  ensembl transcript: ENST00000412691
  gene symbol: BANP
  hgvsc: ENST00000412691.1:c.293G>A
  hgvsp: ENSP00000390504.1:p.Ser98Asn
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000410089
  ensembl transcript: ENST00000456902
  gene symbol: BANP
  hgvsc: ENST00000456902.1:c.293G>A
  hgvsp: ENSP00000410089.1:p.Ser98Asn
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000431812
  ensembl transcript: ENST00000466197
  gene symbol: BANP
  hgvsc: ENST00000466197.1:c.293G>A
  hgvsp: ENSP00000431812.1:p.Ser98Asn
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000347125
  ensembl transcript: ENST00000355022
  gene symbol: BANP
  hgvsc: ENST00000355022.4:c.293G>A
  hgvsp: ENSP00000347125.4:p.Ser98Asn
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000286122
  ensembl transcript: ENST00000286122
  gene symbol: BANP
  hgvsc: ENST00000286122.7:c.269G>A
  hgvsp: ENSP00000286122.7:p.Ser90Asn
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000436869
  ensembl transcript: ENST00000485772
  gene symbol: BANP
  hgvsc: ENST00000485772.1:c.*192G>A
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172530
  ensembl transcript: ENST00000474563
  gene symbol: BANP
  hgvsc: ENST00000474563.2:n.724G>A
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000411479
  ensembl transcript: ENST00000439677
  gene symbol: BANP
  hgvsc: ENST00000439677.1:c.311G>A
  hgvsp: ENSP00000411479.1:p.Ser104Asn
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172530
  ensembl transcript: ENST00000472964
  gene symbol: BANP
  hgvsc: ENST00000472964.1:n.261G>A
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172530
  ensembl transcript: ENST00000488074
  gene symbol: BANP
  hgvsc: ENST00000488074.1:n.715G>A
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000376903
  ensembl transcript: ENST00000393208
  gene symbol: BANP
  hgvsc: ENST00000393208.2:c.293G>A
  hgvsp: ENSP00000376903.2:p.Ser98Asn
  variant of: http://identifiers.org/hgnc/13450
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 3096
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4893
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser90Asn
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: Other
population: East Asian
reference allele: G
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum

16-88017797-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 88017797
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 88017797
    reference: chr 16
allele count: 6
allele frequency: 7.396632066865555e-5
allele num: 81118
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000436869
  ensembl transcript: ENST00000485772
  gene symbol: BANP
  hgvsc: ENST00000485772.1:c.*193C>T
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172530
  ensembl transcript: ENST00000472964
  gene symbol: BANP
  hgvsc: ENST00000472964.1:n.262C>T
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172530
  ensembl transcript: ENST00000474563
  gene symbol: BANP
  hgvsc: ENST00000474563.2:n.725C>T
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000376902
  ensembl transcript: ENST00000393207
  gene symbol: BANP
  hgvsc: ENST00000393207.1:c.270C>T
  hgvsp: ENST00000393207.1:c.270C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000444352
  ensembl transcript: ENST00000538234
  gene symbol: BANP
  hgvsc: ENST00000538234.1:c.294C>T
  hgvsp: ENST00000538234.1:c.294C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172530
  ensembl transcript: ENST00000488074
  gene symbol: BANP
  hgvsc: ENST00000488074.1:n.716C>T
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000410089
  ensembl transcript: ENST00000456902
  gene symbol: BANP
  hgvsc: ENST00000456902.1:c.294C>T
  hgvsp: ENST00000456902.1:c.294C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000432508
  ensembl transcript: ENST00000479780
  gene symbol: BANP
  hgvsc: ENST00000479780.2:c.294C>T
  hgvsp: ENST00000479780.2:c.294C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000376903
  ensembl transcript: ENST00000393208
  gene symbol: BANP
  hgvsc: ENST00000393208.2:c.294C>T
  hgvsp: ENST00000393208.2:c.294C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000286122
  ensembl transcript: ENST00000286122
  gene symbol: BANP
  hgvsc: ENST00000286122.7:c.270C>T
  hgvsp: ENST00000286122.7:c.270C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000431812
  ensembl transcript: ENST00000466197
  gene symbol: BANP
  hgvsc: ENST00000466197.1:c.294C>T
  hgvsp: ENST00000466197.1:c.294C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000411479
  ensembl transcript: ENST00000439677
  gene symbol: BANP
  hgvsc: ENST00000439677.1:c.312C>T
  hgvsp: ENST00000439677.1:c.312C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000390504
  ensembl transcript: ENST00000412691
  gene symbol: BANP
  hgvsc: ENST00000412691.1:c.294C>T
  hgvsp: ENST00000412691.1:c.294C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000347290
  ensembl transcript: ENST00000355163
  gene symbol: BANP
  hgvsc: ENST00000355163.5:c.312C>T
  hgvsp: ENST00000355163.5:c.312C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172530
  ensembl transcript: ENST00000569400
  gene symbol: BANP
  hgvsc: ENST00000569400.1:n.742C>T
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000399576
  ensembl transcript: ENST00000436970
  gene symbol: BANP
  hgvsc: ENST00000436970.1:c.294C>T
  hgvsp: ENST00000436970.1:c.294C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000347125
  ensembl transcript: ENST00000355022
  gene symbol: BANP
  hgvsc: ENST00000355022.4:c.294C>T
  hgvsp: ENST00000355022.4:c.294C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000435727
  ensembl transcript: ENST00000459966
  gene symbol: BANP
  hgvsc: ENST00000459966.1:c.*193C>T
  variant of: http://identifiers.org/hgnc/13450
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16819
  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Ser90Ser
num of homozygotes: 0
population: South Asian
population: Other
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum

16-88017800-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 88017800
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 88017800
    reference: chr 16
allele count: 0
allele frequency: 0.0e0
allele num: 81698
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000435727
  ensembl transcript: ENST00000459966
  gene symbol: BANP
  hgvsc: ENST00000459966.1:c.*196C>T
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000390504
  ensembl transcript: ENST00000412691
  gene symbol: BANP
  hgvsc: ENST00000412691.1:c.297C>T
  hgvsp: ENST00000412691.1:c.297C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172530
  ensembl transcript: ENST00000488074
  gene symbol: BANP
  hgvsc: ENST00000488074.1:n.719C>T
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172530
  ensembl transcript: ENST00000472964
  gene symbol: BANP
  hgvsc: ENST00000472964.1:n.265C>T
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000347290
  ensembl transcript: ENST00000355163
  gene symbol: BANP
  hgvsc: ENST00000355163.5:c.315C>T
  hgvsp: ENST00000355163.5:c.315C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000431812
  ensembl transcript: ENST00000466197
  gene symbol: BANP
  hgvsc: ENST00000466197.1:c.297C>T
  hgvsp: ENST00000466197.1:c.297C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172530
  ensembl transcript: ENST00000569400
  gene symbol: BANP
  hgvsc: ENST00000569400.1:n.745C>T
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000286122
  ensembl transcript: ENST00000286122
  gene symbol: BANP
  hgvsc: ENST00000286122.7:c.273C>T
  hgvsp: ENST00000286122.7:c.273C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000444352
  ensembl transcript: ENST00000538234
  gene symbol: BANP
  hgvsc: ENST00000538234.1:c.297C>T
  hgvsp: ENST00000538234.1:c.297C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000376902
  ensembl transcript: ENST00000393207
  gene symbol: BANP
  hgvsc: ENST00000393207.1:c.273C>T
  hgvsp: ENST00000393207.1:c.273C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000399576
  ensembl transcript: ENST00000436970
  gene symbol: BANP
  hgvsc: ENST00000436970.1:c.297C>T
  hgvsp: ENST00000436970.1:c.297C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000436869
  ensembl transcript: ENST00000485772
  gene symbol: BANP
  hgvsc: ENST00000485772.1:c.*196C>T
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000411479
  ensembl transcript: ENST00000439677
  gene symbol: BANP
  hgvsc: ENST00000439677.1:c.315C>T
  hgvsp: ENST00000439677.1:c.315C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000376903
  ensembl transcript: ENST00000393208
  gene symbol: BANP
  hgvsc: ENST00000393208.2:c.297C>T
  hgvsp: ENST00000393208.2:c.297C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000432508
  ensembl transcript: ENST00000479780
  gene symbol: BANP
  hgvsc: ENST00000479780.2:c.297C>T
  hgvsp: ENST00000479780.2:c.297C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000410089
  ensembl transcript: ENST00000456902
  gene symbol: BANP
  hgvsc: ENST00000456902.1:c.297C>T
  hgvsp: ENST00000456902.1:c.297C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172530
  ensembl transcript: ENST00000474563
  gene symbol: BANP
  hgvsc: ENST00000474563.2:n.728C>T
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000347125
  ensembl transcript: ENST00000355022
  gene symbol: BANP
  hgvsc: ENST00000355022.4:c.297C>T
  hgvsp: ENST00000355022.4:c.297C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 18177
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro91Pro
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD

http://identifiers.org/exac.variant/16-88017801-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 88017801
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 88017801
    reference: chr 16
allele count: 11
allele frequency: 1.339862116007698e-4
allele num: 82098
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000411479
  ensembl transcript: ENST00000439677
  gene symbol: BANP
  hgvsc: ENST00000439677.1:c.316A>C
  hgvsp: ENSP00000411479.1:p.Ile106Leu
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000435727
  ensembl transcript: ENST00000459966
  gene symbol: BANP
  hgvsc: ENST00000459966.1:c.*197A>C
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000347125
  ensembl transcript: ENST00000355022
  gene symbol: BANP
  hgvsc: ENST00000355022.4:c.298A>C
  hgvsp: ENSP00000347125.4:p.Ile100Leu
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000399576
  ensembl transcript: ENST00000436970
  gene symbol: BANP
  hgvsc: ENST00000436970.1:c.298A>C
  hgvsp: ENSP00000399576.1:p.Ile100Leu
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000347290
  ensembl transcript: ENST00000355163
  gene symbol: BANP
  hgvsc: ENST00000355163.5:c.316A>C
  hgvsp: ENSP00000347290.5:p.Ile106Leu
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172530
  ensembl transcript: ENST00000488074
  gene symbol: BANP
  hgvsc: ENST00000488074.1:n.720A>C
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172530
  ensembl transcript: ENST00000472964
  gene symbol: BANP
  hgvsc: ENST00000472964.1:n.266A>C
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000431812
  ensembl transcript: ENST00000466197
  gene symbol: BANP
  hgvsc: ENST00000466197.1:c.298A>C
  hgvsp: ENSP00000431812.1:p.Ile100Leu
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000432508
  ensembl transcript: ENST00000479780
  gene symbol: BANP
  hgvsc: ENST00000479780.2:c.298A>C
  hgvsp: ENSP00000432508.1:p.Ile100Leu
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000390504
  ensembl transcript: ENST00000412691
  gene symbol: BANP
  hgvsc: ENST00000412691.1:c.298A>C
  hgvsp: ENSP00000390504.1:p.Ile100Leu
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172530
  ensembl transcript: ENST00000474563
  gene symbol: BANP
  hgvsc: ENST00000474563.2:n.729A>C
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000286122
  ensembl transcript: ENST00000286122
  gene symbol: BANP
  hgvsc: ENST00000286122.7:c.274A>C
  hgvsp: ENSP00000286122.7:p.Ile92Leu
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172530
  ensembl transcript: ENST00000569400
  gene symbol: BANP
  hgvsc: ENST00000569400.1:n.746A>C
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000410089
  ensembl transcript: ENST00000456902
  gene symbol: BANP
  hgvsc: ENST00000456902.1:c.298A>C
  hgvsp: ENSP00000410089.1:p.Ile100Leu
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000436869
  ensembl transcript: ENST00000485772
  gene symbol: BANP
  hgvsc: ENST00000485772.1:c.*197A>C
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000376903
  ensembl transcript: ENST00000393208
  gene symbol: BANP
  hgvsc: ENST00000393208.2:c.298A>C
  hgvsp: ENSP00000376903.2:p.Ile100Leu
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000444352
  ensembl transcript: ENST00000538234
  gene symbol: BANP
  hgvsc: ENST00000538234.1:c.298A>C
  hgvsp: ENSP00000444352.1:p.Ile100Leu
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000376902
  ensembl transcript: ENST00000393207
  gene symbol: BANP
  hgvsc: ENST00000393207.1:c.274A>C
  hgvsp: ENSP00000376902.1:p.Ile92Leu
  variant of: http://identifiers.org/hgnc/13450
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1327
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile92Leu
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
population: African
population: Latino
population: European (Non-Finnish)
reference allele: A
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: MQ

16-88017809-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 88017809
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 88017809
    reference: chr 16
allele count: 58438
allele frequency: 5.965130759651308e-1
allele num: 97966
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000432508
  ensembl transcript: ENST00000479780
  gene symbol: BANP
  hgvsc: ENST00000479780.2:c.306C>T
  hgvsp: ENST00000479780.2:c.306C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000376902
  ensembl transcript: ENST00000393207
  gene symbol: BANP
  hgvsc: ENST00000393207.1:c.282C>T
  hgvsp: ENST00000393207.1:c.282C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000376903
  ensembl transcript: ENST00000393208
  gene symbol: BANP
  hgvsc: ENST00000393208.2:c.306C>T
  hgvsp: ENST00000393208.2:c.306C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000410089
  ensembl transcript: ENST00000456902
  gene symbol: BANP
  hgvsc: ENST00000456902.1:c.306C>T
  hgvsp: ENST00000456902.1:c.306C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000286122
  ensembl transcript: ENST00000286122
  gene symbol: BANP
  hgvsc: ENST00000286122.7:c.282C>T
  hgvsp: ENST00000286122.7:c.282C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000399576
  ensembl transcript: ENST00000436970
  gene symbol: BANP
  hgvsc: ENST00000436970.1:c.306C>T
  hgvsp: ENST00000436970.1:c.306C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000444352
  ensembl transcript: ENST00000538234
  gene symbol: BANP
  hgvsc: ENST00000538234.1:c.306C>T
  hgvsp: ENST00000538234.1:c.306C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000390504
  ensembl transcript: ENST00000412691
  gene symbol: BANP
  hgvsc: ENST00000412691.1:c.306C>T
  hgvsp: ENST00000412691.1:c.306C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000435727
  ensembl transcript: ENST00000459966
  gene symbol: BANP
  hgvsc: ENST00000459966.1:c.*205C>T
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000431812
  ensembl transcript: ENST00000466197
  gene symbol: BANP
  hgvsc: ENST00000466197.1:c.306C>T
  hgvsp: ENST00000466197.1:c.306C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000436869
  ensembl transcript: ENST00000485772
  gene symbol: BANP
  hgvsc: ENST00000485772.1:c.*205C>T
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000411479
  ensembl transcript: ENST00000439677
  gene symbol: BANP
  hgvsc: ENST00000439677.1:c.324C>T
  hgvsp: ENST00000439677.1:c.324C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000347290
  ensembl transcript: ENST00000355163
  gene symbol: BANP
  hgvsc: ENST00000355163.5:c.324C>T
  hgvsp: ENST00000355163.5:c.324C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000347125
  ensembl transcript: ENST00000355022
  gene symbol: BANP
  hgvsc: ENST00000355022.4:c.306C>T
  hgvsp: ENST00000355022.4:c.306C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172530
  ensembl transcript: ENST00000569400
  gene symbol: BANP
  hgvsc: ENST00000569400.1:n.754C>T
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172530
  ensembl transcript: ENST00000474563
  gene symbol: BANP
  hgvsc: ENST00000474563.2:n.737C>T
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172530
  ensembl transcript: ENST00000488074
  gene symbol: BANP
  hgvsc: ENST00000488074.1:n.728C>T
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172530
  ensembl transcript: ENST00000472964
  gene symbol: BANP
  hgvsc: ENST00000472964.1:n.274C>T
  variant of: http://identifiers.org/hgnc/13450
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 8.75e1
  variant carriers: 223
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 7.25e1
  variant carriers: 261
genotype quality: GenotypeQuality
hgvs: p.Val94Val
num of homozygotes: 16989
population: East Asian
population: African
population: Other
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: QD

http://identifiers.org/exac.variant/16-88017812-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 88017812
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 88017812
    reference: chr 16
allele count: 1
allele frequency: 1.332232021528869e-5
allele num: 75062
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000286122
  ensembl transcript: ENST00000286122
  gene symbol: BANP
  hgvsc: ENST00000286122.7:c.285C>A
  hgvsp: ENST00000286122.7:c.285C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000347290
  ensembl transcript: ENST00000355163
  gene symbol: BANP
  hgvsc: ENST00000355163.5:c.327C>A
  hgvsp: ENST00000355163.5:c.327C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000411479
  ensembl transcript: ENST00000439677
  gene symbol: BANP
  hgvsc: ENST00000439677.1:c.327C>A
  hgvsp: ENST00000439677.1:c.327C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000436869
  ensembl transcript: ENST00000485772
  gene symbol: BANP
  hgvsc: ENST00000485772.1:c.*208C>A
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000390504
  ensembl transcript: ENST00000412691
  gene symbol: BANP
  hgvsc: ENST00000412691.1:c.309C>A
  hgvsp: ENST00000412691.1:c.309C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172530
  ensembl transcript: ENST00000474563
  gene symbol: BANP
  hgvsc: ENST00000474563.2:n.740C>A
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000399576
  ensembl transcript: ENST00000436970
  gene symbol: BANP
  hgvsc: ENST00000436970.1:c.309C>A
  hgvsp: ENST00000436970.1:c.309C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172530
  ensembl transcript: ENST00000569400
  gene symbol: BANP
  hgvsc: ENST00000569400.1:n.757C>A
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172530
  ensembl transcript: ENST00000488074
  gene symbol: BANP
  hgvsc: ENST00000488074.1:n.731C>A
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000347125
  ensembl transcript: ENST00000355022
  gene symbol: BANP
  hgvsc: ENST00000355022.4:c.309C>A
  hgvsp: ENST00000355022.4:c.309C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000431812
  ensembl transcript: ENST00000466197
  gene symbol: BANP
  hgvsc: ENST00000466197.1:c.309C>A
  hgvsp: ENST00000466197.1:c.309C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000432508
  ensembl transcript: ENST00000479780
  gene symbol: BANP
  hgvsc: ENST00000479780.2:c.309C>A
  hgvsp: ENST00000479780.2:c.309C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000376903
  ensembl transcript: ENST00000393208
  gene symbol: BANP
  hgvsc: ENST00000393208.2:c.309C>A
  hgvsp: ENST00000393208.2:c.309C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000444352
  ensembl transcript: ENST00000538234
  gene symbol: BANP
  hgvsc: ENST00000538234.1:c.309C>A
  hgvsp: ENST00000538234.1:c.309C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000435727
  ensembl transcript: ENST00000459966
  gene symbol: BANP
  hgvsc: ENST00000459966.1:c.*208C>A
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000410089
  ensembl transcript: ENST00000456902
  gene symbol: BANP
  hgvsc: ENST00000456902.1:c.309C>A
  hgvsp: ENST00000456902.1:c.309C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172530
  ensembl transcript: ENST00000472964
  gene symbol: BANP
  hgvsc: ENST00000472964.1:n.277C>A
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000376902
  ensembl transcript: ENST00000393207
  gene symbol: BANP
  hgvsc: ENST00000393207.1:c.285C>A
  hgvsp: ENST00000393207.1:c.285C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1375
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro95Pro
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: C
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: DP

16-88017813-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 88017813
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 88017813
    reference: chr 16
allele count: 3
allele frequency: 4.011124184404749e-5
allele num: 74792
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172530
  ensembl transcript: ENST00000472964
  gene symbol: BANP
  hgvsc: ENST00000472964.1:n.278A>G
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172530
  ensembl transcript: ENST00000474563
  gene symbol: BANP
  hgvsc: ENST00000474563.2:n.741A>G
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000411479
  ensembl transcript: ENST00000439677
  gene symbol: BANP
  hgvsc: ENST00000439677.1:c.328A>G
  hgvsp: ENSP00000411479.1:p.Met110Val
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172530
  ensembl transcript: ENST00000569400
  gene symbol: BANP
  hgvsc: ENST00000569400.1:n.758A>G
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000390504
  ensembl transcript: ENST00000412691
  gene symbol: BANP
  hgvsc: ENST00000412691.1:c.310A>G
  hgvsp: ENSP00000390504.1:p.Met104Val
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000399576
  ensembl transcript: ENST00000436970
  gene symbol: BANP
  hgvsc: ENST00000436970.1:c.310A>G
  hgvsp: ENSP00000399576.1:p.Met104Val
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000286122
  ensembl transcript: ENST00000286122
  gene symbol: BANP
  hgvsc: ENST00000286122.7:c.286A>G
  hgvsp: ENSP00000286122.7:p.Met96Val
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000347290
  ensembl transcript: ENST00000355163
  gene symbol: BANP
  hgvsc: ENST00000355163.5:c.328A>G
  hgvsp: ENSP00000347290.5:p.Met110Val
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000376903
  ensembl transcript: ENST00000393208
  gene symbol: BANP
  hgvsc: ENST00000393208.2:c.310A>G
  hgvsp: ENSP00000376903.2:p.Met104Val
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000410089
  ensembl transcript: ENST00000456902
  gene symbol: BANP
  hgvsc: ENST00000456902.1:c.310A>G
  hgvsp: ENSP00000410089.1:p.Met104Val
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000431812
  ensembl transcript: ENST00000466197
  gene symbol: BANP
  hgvsc: ENST00000466197.1:c.310A>G
  hgvsp: ENSP00000431812.1:p.Met104Val
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172530
  ensembl transcript: ENST00000488074
  gene symbol: BANP
  hgvsc: ENST00000488074.1:n.732A>G
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000347125
  ensembl transcript: ENST00000355022
  gene symbol: BANP
  hgvsc: ENST00000355022.4:c.310A>G
  hgvsp: ENSP00000347125.4:p.Met104Val
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000435727
  ensembl transcript: ENST00000459966
  gene symbol: BANP
  hgvsc: ENST00000459966.1:c.*209A>G
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000432508
  ensembl transcript: ENST00000479780
  gene symbol: BANP
  hgvsc: ENST00000479780.2:c.310A>G
  hgvsp: ENSP00000432508.1:p.Met104Val
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000444352
  ensembl transcript: ENST00000538234
  gene symbol: BANP
  hgvsc: ENST00000538234.1:c.310A>G
  hgvsp: ENSP00000444352.1:p.Met104Val
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000436869
  ensembl transcript: ENST00000485772
  gene symbol: BANP
  hgvsc: ENST00000485772.1:c.*209A>G
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000376902
  ensembl transcript: ENST00000393207
  gene symbol: BANP
  hgvsc: ENST00000393207.1:c.286A>G
  hgvsp: ENSP00000376902.1:p.Met96Val
  variant of: http://identifiers.org/hgnc/13450
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3313
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1442
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Met96Val
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
reference allele: A
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum

16-88017814-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 88017814
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 88017814
    reference: chr 16
allele count: 0
allele frequency: 0.0e0
allele num: 74482
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000444352
  ensembl transcript: ENST00000538234
  gene symbol: BANP
  hgvsc: ENST00000538234.1:c.311T>C
  hgvsp: ENSP00000444352.1:p.Met104Thr
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000347290
  ensembl transcript: ENST00000355163
  gene symbol: BANP
  hgvsc: ENST00000355163.5:c.329T>C
  hgvsp: ENSP00000347290.5:p.Met110Thr
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000286122
  ensembl transcript: ENST00000286122
  gene symbol: BANP
  hgvsc: ENST00000286122.7:c.287T>C
  hgvsp: ENSP00000286122.7:p.Met96Thr
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000435727
  ensembl transcript: ENST00000459966
  gene symbol: BANP
  hgvsc: ENST00000459966.1:c.*210T>C
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000436869
  ensembl transcript: ENST00000485772
  gene symbol: BANP
  hgvsc: ENST00000485772.1:c.*210T>C
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172530
  ensembl transcript: ENST00000569400
  gene symbol: BANP
  hgvsc: ENST00000569400.1:n.759T>C
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000431812
  ensembl transcript: ENST00000466197
  gene symbol: BANP
  hgvsc: ENST00000466197.1:c.311T>C
  hgvsp: ENSP00000431812.1:p.Met104Thr
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172530
  ensembl transcript: ENST00000474563
  gene symbol: BANP
  hgvsc: ENST00000474563.2:n.742T>C
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000376902
  ensembl transcript: ENST00000393207
  gene symbol: BANP
  hgvsc: ENST00000393207.1:c.287T>C
  hgvsp: ENSP00000376902.1:p.Met96Thr
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000410089
  ensembl transcript: ENST00000456902
  gene symbol: BANP
  hgvsc: ENST00000456902.1:c.311T>C
  hgvsp: ENSP00000410089.1:p.Met104Thr
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000399576
  ensembl transcript: ENST00000436970
  gene symbol: BANP
  hgvsc: ENST00000436970.1:c.311T>C
  hgvsp: ENSP00000399576.1:p.Met104Thr
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000432508
  ensembl transcript: ENST00000479780
  gene symbol: BANP
  hgvsc: ENST00000479780.2:c.311T>C
  hgvsp: ENSP00000432508.1:p.Met104Thr
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000411479
  ensembl transcript: ENST00000439677
  gene symbol: BANP
  hgvsc: ENST00000439677.1:c.329T>C
  hgvsp: ENSP00000411479.1:p.Met110Thr
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000347125
  ensembl transcript: ENST00000355022
  gene symbol: BANP
  hgvsc: ENST00000355022.4:c.311T>C
  hgvsp: ENSP00000347125.4:p.Met104Thr
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172530
  ensembl transcript: ENST00000488074
  gene symbol: BANP
  hgvsc: ENST00000488074.1:n.733T>C
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172530
  ensembl transcript: ENST00000472964
  gene symbol: BANP
  hgvsc: ENST00000472964.1:n.279T>C
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000390504
  ensembl transcript: ENST00000412691
  gene symbol: BANP
  hgvsc: ENST00000412691.1:c.311T>C
  hgvsp: ENSP00000390504.1:p.Met104Thr
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000376903
  ensembl transcript: ENST00000393208
  gene symbol: BANP
  hgvsc: ENST00000393208.2:c.311T>C
  hgvsp: ENSP00000376903.2:p.Met104Thr
  variant of: http://identifiers.org/hgnc/13450
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21771
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Met96Thr
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: T
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ

16-88017821-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 88017821
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 88017821
    reference: chr 16
allele count: 5
allele frequency: 7.016165244723844e-5
allele num: 71264
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000432508
  ensembl transcript: ENST00000479780
  gene symbol: BANP
  hgvsc: ENST00000479780.2:c.318C>T
  hgvsp: ENST00000479780.2:c.318C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000390504
  ensembl transcript: ENST00000412691
  gene symbol: BANP
  hgvsc: ENST00000412691.1:c.318C>T
  hgvsp: ENST00000412691.1:c.318C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000376902
  ensembl transcript: ENST00000393207
  gene symbol: BANP
  hgvsc: ENST00000393207.1:c.294C>T
  hgvsp: ENST00000393207.1:c.294C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000399576
  ensembl transcript: ENST00000436970
  gene symbol: BANP
  hgvsc: ENST00000436970.1:c.318C>T
  hgvsp: ENST00000436970.1:c.318C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000376903
  ensembl transcript: ENST00000393208
  gene symbol: BANP
  hgvsc: ENST00000393208.2:c.318C>T
  hgvsp: ENST00000393208.2:c.318C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000435727
  ensembl transcript: ENST00000459966
  gene symbol: BANP
  hgvsc: ENST00000459966.1:c.*217C>T
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000411479
  ensembl transcript: ENST00000439677
  gene symbol: BANP
  hgvsc: ENST00000439677.1:c.336C>T
  hgvsp: ENST00000439677.1:c.336C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000286122
  ensembl transcript: ENST00000286122
  gene symbol: BANP
  hgvsc: ENST00000286122.7:c.294C>T
  hgvsp: ENST00000286122.7:c.294C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172530
  ensembl transcript: ENST00000472964
  gene symbol: BANP
  hgvsc: ENST00000472964.1:n.286C>T
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000431812
  ensembl transcript: ENST00000466197
  gene symbol: BANP
  hgvsc: ENST00000466197.1:c.318C>T
  hgvsp: ENST00000466197.1:c.318C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000444352
  ensembl transcript: ENST00000538234
  gene symbol: BANP
  hgvsc: ENST00000538234.1:c.318C>T
  hgvsp: ENST00000538234.1:c.318C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172530
  ensembl transcript: ENST00000488074
  gene symbol: BANP
  hgvsc: ENST00000488074.1:n.740C>T
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000410089
  ensembl transcript: ENST00000456902
  gene symbol: BANP
  hgvsc: ENST00000456902.1:c.318C>T
  hgvsp: ENST00000456902.1:c.318C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000347125
  ensembl transcript: ENST00000355022
  gene symbol: BANP
  hgvsc: ENST00000355022.4:c.318C>T
  hgvsp: ENST00000355022.4:c.318C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172530
  ensembl transcript: ENST00000569400
  gene symbol: BANP
  hgvsc: ENST00000569400.1:n.766C>T
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000347290
  ensembl transcript: ENST00000355163
  gene symbol: BANP
  hgvsc: ENST00000355163.5:c.336C>T
  hgvsp: ENST00000355163.5:c.336C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172530
  ensembl transcript: ENST00000474563
  gene symbol: BANP
  hgvsc: ENST00000474563.2:n.749C>T
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000436869
  ensembl transcript: ENST00000485772
  gene symbol: BANP
  hgvsc: ENST00000485772.1:c.*217C>T
  variant of: http://identifiers.org/hgnc/13450
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22913
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala98Ala
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: African
population: East Asian
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: DP
site quality: QD
site quality: ClippingRankSum

16-88017833-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 88017833
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 88017833
    reference: chr 16
allele count: 5
allele frequency: 7.916653472244213e-5
allele num: 63158
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000431812
  ensembl transcript: ENST00000466197
  gene symbol: BANP
  hgvsc: ENST00000466197.1:c.330C>T
  hgvsp: ENST00000466197.1:c.330C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000347125
  ensembl transcript: ENST00000355022
  gene symbol: BANP
  hgvsc: ENST00000355022.4:c.330C>T
  hgvsp: ENST00000355022.4:c.330C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000410089
  ensembl transcript: ENST00000456902
  gene symbol: BANP
  hgvsc: ENST00000456902.1:c.330C>T
  hgvsp: ENST00000456902.1:c.330C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000444352
  ensembl transcript: ENST00000538234
  gene symbol: BANP
  hgvsc: ENST00000538234.1:c.330C>T
  hgvsp: ENST00000538234.1:c.330C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000376903
  ensembl transcript: ENST00000393208
  gene symbol: BANP
  hgvsc: ENST00000393208.2:c.330C>T
  hgvsp: ENST00000393208.2:c.330C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000411479
  ensembl transcript: ENST00000439677
  gene symbol: BANP
  hgvsc: ENST00000439677.1:c.348C>T
  hgvsp: ENST00000439677.1:c.348C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000376902
  ensembl transcript: ENST00000393207
  gene symbol: BANP
  hgvsc: ENST00000393207.1:c.306C>T
  hgvsp: ENST00000393207.1:c.306C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000286122
  ensembl transcript: ENST00000286122
  gene symbol: BANP
  hgvsc: ENST00000286122.7:c.306C>T
  hgvsp: ENST00000286122.7:c.306C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000390504
  ensembl transcript: ENST00000412691
  gene symbol: BANP
  hgvsc: ENST00000412691.1:c.330C>T
  hgvsp: ENST00000412691.1:c.330C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172530
  ensembl transcript: ENST00000488074
  gene symbol: BANP
  hgvsc: ENST00000488074.1:n.752C>T
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000399576
  ensembl transcript: ENST00000436970
  gene symbol: BANP
  hgvsc: ENST00000436970.1:c.330C>T
  hgvsp: ENST00000436970.1:c.330C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000432508
  ensembl transcript: ENST00000479780
  gene symbol: BANP
  hgvsc: ENST00000479780.2:c.330C>T
  hgvsp: ENST00000479780.2:c.330C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172530
  ensembl transcript: ENST00000569400
  gene symbol: BANP
  hgvsc: ENST00000569400.1:n.778C>T
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172530
  ensembl transcript: ENST00000472964
  gene symbol: BANP
  hgvsc: ENST00000472964.1:n.298C>T
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000436869
  ensembl transcript: ENST00000485772
  gene symbol: BANP
  hgvsc: ENST00000485772.1:c.*229C>T
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172530
  ensembl transcript: ENST00000474563
  gene symbol: BANP
  hgvsc: ENST00000474563.2:n.761C>T
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000347290
  ensembl transcript: ENST00000355163
  gene symbol: BANP
  hgvsc: ENST00000355163.5:c.348C>T
  hgvsp: ENST00000355163.5:c.348C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000435727
  ensembl transcript: ENST00000459966
  gene symbol: BANP
  hgvsc: ENST00000459966.1:c.*229C>T
  variant of: http://identifiers.org/hgnc/13450
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2195
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu102Leu
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum

16-88017841-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 88017841
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 88017841
    reference: chr 16
allele count: 1
allele frequency: 1.760811381884773e-5
allele num: 56792
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000431812
  ensembl transcript: ENST00000466197
  gene symbol: BANP
  hgvsc: ENST00000466197.1:c.338C>T
  hgvsp: ENSP00000431812.1:p.Thr113Ile
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000376903
  ensembl transcript: ENST00000393208
  gene symbol: BANP
  hgvsc: ENST00000393208.2:c.338C>T
  hgvsp: ENSP00000376903.2:p.Thr113Ile
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000347290
  ensembl transcript: ENST00000355163
  gene symbol: BANP
  hgvsc: ENST00000355163.5:c.356C>T
  hgvsp: ENSP00000347290.5:p.Thr119Ile
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000411479
  ensembl transcript: ENST00000439677
  gene symbol: BANP
  hgvsc: ENST00000439677.1:c.356C>T
  hgvsp: ENSP00000411479.1:p.Thr119Ile
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000436869
  ensembl transcript: ENST00000485772
  gene symbol: BANP
  hgvsc: ENST00000485772.1:c.*237C>T
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172530
  ensembl transcript: ENST00000569400
  gene symbol: BANP
  hgvsc: ENST00000569400.1:n.786C>T
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000435727
  ensembl transcript: ENST00000459966
  gene symbol: BANP
  hgvsc: ENST00000459966.1:c.*237C>T
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000410089
  ensembl transcript: ENST00000456902
  gene symbol: BANP
  hgvsc: ENST00000456902.1:c.338C>T
  hgvsp: ENSP00000410089.1:p.Thr113Ile
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000376902
  ensembl transcript: ENST00000393207
  gene symbol: BANP
  hgvsc: ENST00000393207.1:c.314C>T
  hgvsp: ENSP00000376902.1:p.Thr105Ile
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000399576
  ensembl transcript: ENST00000436970
  gene symbol: BANP
  hgvsc: ENST00000436970.1:c.338C>T
  hgvsp: ENSP00000399576.1:p.Thr113Ile
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000432508
  ensembl transcript: ENST00000479780
  gene symbol: BANP
  hgvsc: ENST00000479780.2:c.338C>T
  hgvsp: ENSP00000432508.1:p.Thr113Ile
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000347125
  ensembl transcript: ENST00000355022
  gene symbol: BANP
  hgvsc: ENST00000355022.4:c.338C>T
  hgvsp: ENSP00000347125.4:p.Thr113Ile
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000390504
  ensembl transcript: ENST00000412691
  gene symbol: BANP
  hgvsc: ENST00000412691.1:c.338C>T
  hgvsp: ENSP00000390504.1:p.Thr113Ile
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000286122
  ensembl transcript: ENST00000286122
  gene symbol: BANP
  hgvsc: ENST00000286122.7:c.314C>T
  hgvsp: ENSP00000286122.7:p.Thr105Ile
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000444352
  ensembl transcript: ENST00000538234
  gene symbol: BANP
  hgvsc: ENST00000538234.1:c.338C>T
  hgvsp: ENSP00000444352.1:p.Thr113Ile
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172530
  ensembl transcript: ENST00000472964
  gene symbol: BANP
  hgvsc: ENST00000472964.1:n.306C>T
  variant of: http://identifiers.org/hgnc/13450
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4302
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6564
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16232
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1259
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr105Ile
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum

16-88017847-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 88017847
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 88017847
    reference: chr 16
allele count: 2
allele frequency: 3.759115855950681e-5
allele num: 53204
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000376903
  ensembl transcript: ENST00000393208
  gene symbol: BANP
  hgvsc: ENST00000393208.2:c.344C>T
  hgvsp: ENSP00000376903.2:p.Thr115Met
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000390504
  ensembl transcript: ENST00000412691
  gene symbol: BANP
  hgvsc: ENST00000412691.1:c.344C>T
  hgvsp: ENSP00000390504.1:p.Thr115Met
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000431812
  ensembl transcript: ENST00000466197
  gene symbol: BANP
  hgvsc: ENST00000466197.1:c.344C>T
  hgvsp: ENSP00000431812.1:p.Thr115Met
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000399576
  ensembl transcript: ENST00000436970
  gene symbol: BANP
  hgvsc: ENST00000436970.1:c.344C>T
  hgvsp: ENSP00000399576.1:p.Thr115Met
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000444352
  ensembl transcript: ENST00000538234
  gene symbol: BANP
  hgvsc: ENST00000538234.1:c.344C>T
  hgvsp: ENSP00000444352.1:p.Thr115Met
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172530
  ensembl transcript: ENST00000569400
  gene symbol: BANP
  hgvsc: ENST00000569400.1:n.792C>T
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172530
  ensembl transcript: ENST00000472964
  gene symbol: BANP
  hgvsc: ENST00000472964.1:n.312C>T
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000286122
  ensembl transcript: ENST00000286122
  gene symbol: BANP
  hgvsc: ENST00000286122.7:c.320C>T
  hgvsp: ENSP00000286122.7:p.Thr107Met
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000411479
  ensembl transcript: ENST00000439677
  gene symbol: BANP
  hgvsc: ENST00000439677.1:c.362C>T
  hgvsp: ENSP00000411479.1:p.Thr121Met
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000347125
  ensembl transcript: ENST00000355022
  gene symbol: BANP
  hgvsc: ENST00000355022.4:c.344C>T
  hgvsp: ENSP00000347125.4:p.Thr115Met
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000432508
  ensembl transcript: ENST00000479780
  gene symbol: BANP
  hgvsc: ENST00000479780.2:c.344C>T
  hgvsp: ENSP00000432508.1:p.Thr115Met
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000347290
  ensembl transcript: ENST00000355163
  gene symbol: BANP
  hgvsc: ENST00000355163.5:c.362C>T
  hgvsp: ENSP00000347290.5:p.Thr121Met
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000410089
  ensembl transcript: ENST00000456902
  gene symbol: BANP
  hgvsc: ENST00000456902.1:c.344C>T
  hgvsp: ENSP00000410089.1:p.Thr115Met
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000376902
  ensembl transcript: ENST00000393207
  gene symbol: BANP
  hgvsc: ENST00000393207.1:c.320C>T
  hgvsp: ENSP00000376902.1:p.Thr107Met
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000436869
  ensembl transcript: ENST00000485772
  gene symbol: BANP
  hgvsc: ENST00000485772.1:c.*243C>T
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000435727
  ensembl transcript: ENST00000459966
  gene symbol: BANP
  hgvsc: ENST00000459966.1:c.*243C>T
  variant of: http://identifiers.org/hgnc/13450
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2966
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 969
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4000
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15553
  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Thr107Met
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
population: European (Finnish)
population: East Asian
reference allele: C
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD

16-88017848-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 88017848
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 88017848
    reference: chr 16
allele count: 2
allele frequency: 4.223329673114283e-5
allele num: 47356
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000347125
  ensembl transcript: ENST00000355022
  gene symbol: BANP
  hgvsc: ENST00000355022.4:c.345G>A
  hgvsp: ENST00000355022.4:c.345G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000286122
  ensembl transcript: ENST00000286122
  gene symbol: BANP
  hgvsc: ENST00000286122.7:c.321G>A
  hgvsp: ENST00000286122.7:c.321G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172530
  ensembl transcript: ENST00000569400
  gene symbol: BANP
  hgvsc: ENST00000569400.1:n.793G>A
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000431812
  ensembl transcript: ENST00000466197
  gene symbol: BANP
  hgvsc: ENST00000466197.1:c.345G>A
  hgvsp: ENST00000466197.1:c.345G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000399576
  ensembl transcript: ENST00000436970
  gene symbol: BANP
  hgvsc: ENST00000436970.1:c.345G>A
  hgvsp: ENST00000436970.1:c.345G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000376902
  ensembl transcript: ENST00000393207
  gene symbol: BANP
  hgvsc: ENST00000393207.1:c.321G>A
  hgvsp: ENST00000393207.1:c.321G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000436869
  ensembl transcript: ENST00000485772
  gene symbol: BANP
  hgvsc: ENST00000485772.1:c.*244G>A
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000347290
  ensembl transcript: ENST00000355163
  gene symbol: BANP
  hgvsc: ENST00000355163.5:c.363G>A
  hgvsp: ENST00000355163.5:c.363G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000435727
  ensembl transcript: ENST00000459966
  gene symbol: BANP
  hgvsc: ENST00000459966.1:c.*244G>A
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000410089
  ensembl transcript: ENST00000456902
  gene symbol: BANP
  hgvsc: ENST00000456902.1:c.345G>A
  hgvsp: ENST00000456902.1:c.345G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000444352
  ensembl transcript: ENST00000538234
  gene symbol: BANP
  hgvsc: ENST00000538234.1:c.345G>A
  hgvsp: ENST00000538234.1:c.345G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000411479
  ensembl transcript: ENST00000439677
  gene symbol: BANP
  hgvsc: ENST00000439677.1:c.363G>A
  hgvsp: ENST00000439677.1:c.363G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000376903
  ensembl transcript: ENST00000393208
  gene symbol: BANP
  hgvsc: ENST00000393208.2:c.345G>A
  hgvsp: ENST00000393208.2:c.345G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000432508
  ensembl transcript: ENST00000479780
  gene symbol: BANP
  hgvsc: ENST00000479780.2:c.345G>A
  hgvsp: ENST00000479780.2:c.345G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000390504
  ensembl transcript: ENST00000412691
  gene symbol: BANP
  hgvsc: ENST00000412691.1:c.345G>A
  hgvsp: ENST00000412691.1:c.345G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172530
  ensembl transcript: ENST00000472964
  gene symbol: BANP
  hgvsc: ENST00000472964.1:n.313G>A
  variant of: http://identifiers.org/hgnc/13450
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2025
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24107
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11975
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr107Thr
num of homozygotes: 0
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
reference allele: G
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS

16-88017875-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 88017875
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 88017875
    reference: chr 16
allele count: 0
allele frequency: 0.0e0
allele num: 27184
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000432508
  ensembl transcript: ENST00000479780
  gene symbol: BANP
  hgvsc: ENST00000479780.2:c.362+10G>C
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000376903
  ensembl transcript: ENST00000393208
  gene symbol: BANP
  hgvsc: ENST00000393208.2:c.362+10G>C
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000286122
  ensembl transcript: ENST00000286122
  gene symbol: BANP
  hgvsc: ENST00000286122.7:c.338+10G>C
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000376902
  ensembl transcript: ENST00000393207
  gene symbol: BANP
  hgvsc: ENST00000393207.1:c.338+10G>C
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000431812
  ensembl transcript: ENST00000466197
  gene symbol: BANP
  hgvsc: ENST00000466197.1:c.362+10G>C
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000436869
  ensembl transcript: ENST00000485772
  gene symbol: BANP
  hgvsc: ENST00000485772.1:c.*261+10G>C
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000411479
  ensembl transcript: ENST00000439677
  gene symbol: BANP
  hgvsc: ENST00000439677.1:c.380+10G>C
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000444352
  ensembl transcript: ENST00000538234
  gene symbol: BANP
  hgvsc: ENST00000538234.1:c.362+10G>C
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000347290
  ensembl transcript: ENST00000355163
  gene symbol: BANP
  hgvsc: ENST00000355163.5:c.380+10G>C
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000347125
  ensembl transcript: ENST00000355022
  gene symbol: BANP
  hgvsc: ENST00000355022.4:c.362+10G>C
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000435727
  ensembl transcript: ENST00000459966
  gene symbol: BANP
  hgvsc: ENST00000459966.1:c.*261+10G>C
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000399576
  ensembl transcript: ENST00000436970
  gene symbol: BANP
  hgvsc: ENST00000436970.1:c.362+10G>C
  variant of: http://identifiers.org/hgnc/13450
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29464
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2900
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5791
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14909
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1661
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum

http://identifiers.org/exac.variant/16-88017876-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 88017876
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 88017876
    reference: chr 16
allele count: 2
allele frequency: 7.579777154551656e-5
allele num: 26386
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000347125
  ensembl transcript: ENST00000355022
  gene symbol: BANP
  hgvsc: ENST00000355022.4:c.362+11A>C
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000376903
  ensembl transcript: ENST00000393208
  gene symbol: BANP
  hgvsc: ENST00000393208.2:c.362+11A>C
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000376902
  ensembl transcript: ENST00000393207
  gene symbol: BANP
  hgvsc: ENST00000393207.1:c.338+11A>C
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000432508
  ensembl transcript: ENST00000479780
  gene symbol: BANP
  hgvsc: ENST00000479780.2:c.362+11A>C
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000411479
  ensembl transcript: ENST00000439677
  gene symbol: BANP
  hgvsc: ENST00000439677.1:c.380+11A>C
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000436869
  ensembl transcript: ENST00000485772
  gene symbol: BANP
  hgvsc: ENST00000485772.1:c.*261+11A>C
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000435727
  ensembl transcript: ENST00000459966
  gene symbol: BANP
  hgvsc: ENST00000459966.1:c.*261+11A>C
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000431812
  ensembl transcript: ENST00000466197
  gene symbol: BANP
  hgvsc: ENST00000466197.1:c.362+11A>C
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000444352
  ensembl transcript: ENST00000538234
  gene symbol: BANP
  hgvsc: ENST00000538234.1:c.362+11A>C
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000286122
  ensembl transcript: ENST00000286122
  gene symbol: BANP
  hgvsc: ENST00000286122.7:c.338+11A>C
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000347290
  ensembl transcript: ENST00000355163
  gene symbol: BANP
  hgvsc: ENST00000355163.5:c.380+11A>C
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000399576
  ensembl transcript: ENST00000436970
  gene symbol: BANP
  hgvsc: ENST00000436970.1:c.362+11A>C
  variant of: http://identifiers.org/hgnc/13450
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5501
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1647
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14444
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 30097
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1740
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2871
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: Other
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
population: South Asian
reference allele: A
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum

16-88017882-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 88017882
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 88017882
    reference: chr 16
allele count: 1
allele frequency: 4.545867806164197e-5
allele num: 21998
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000411479
  ensembl transcript: ENST00000439677
  gene symbol: BANP
  hgvsc: ENST00000439677.1:c.380+17G>A
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000286122
  ensembl transcript: ENST00000286122
  gene symbol: BANP
  hgvsc: ENST00000286122.7:c.338+17G>A
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000376902
  ensembl transcript: ENST00000393207
  gene symbol: BANP
  hgvsc: ENST00000393207.1:c.338+17G>A
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000436869
  ensembl transcript: ENST00000485772
  gene symbol: BANP
  hgvsc: ENST00000485772.1:c.*261+17G>A
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000435727
  ensembl transcript: ENST00000459966
  gene symbol: BANP
  hgvsc: ENST00000459966.1:c.*261+17G>A
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000444352
  ensembl transcript: ENST00000538234
  gene symbol: BANP
  hgvsc: ENST00000538234.1:c.362+17G>A
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000432508
  ensembl transcript: ENST00000479780
  gene symbol: BANP
  hgvsc: ENST00000479780.2:c.362+17G>A
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000347290
  ensembl transcript: ENST00000355163
  gene symbol: BANP
  hgvsc: ENST00000355163.5:c.380+17G>A
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000376903
  ensembl transcript: ENST00000393208
  gene symbol: BANP
  hgvsc: ENST00000393208.2:c.362+17G>A
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000399576
  ensembl transcript: ENST00000436970
  gene symbol: BANP
  hgvsc: ENST00000436970.1:c.362+17G>A
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000347125
  ensembl transcript: ENST00000355022
  gene symbol: BANP
  hgvsc: ENST00000355022.4:c.362+17G>A
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000431812
  ensembl transcript: ENST00000466197
  gene symbol: BANP
  hgvsc: ENST00000466197.1:c.362+17G>A
  variant of: http://identifiers.org/hgnc/13450
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11645
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33419
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3969
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2527
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1482
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1531
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: G
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD

16-88017886-CG-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 88017886
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 88017885
    reference: chr 16
allele count: 0
allele frequency: 0.0e0
allele num: 20100
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000444352
  ensembl transcript: ENST00000538234
  gene symbol: BANP
  hgvsc: ENST00000538234.1:c.362+25delG
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000432508
  ensembl transcript: ENST00000479780
  gene symbol: BANP
  hgvsc: ENST00000479780.2:c.362+25delG
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000411479
  ensembl transcript: ENST00000439677
  gene symbol: BANP
  hgvsc: ENST00000439677.1:c.380+25delG
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000399576
  ensembl transcript: ENST00000436970
  gene symbol: BANP
  hgvsc: ENST00000436970.1:c.362+25delG
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000436869
  ensembl transcript: ENST00000485772
  gene symbol: BANP
  hgvsc: ENST00000485772.1:c.*261+25delG
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000435727
  ensembl transcript: ENST00000459966
  gene symbol: BANP
  hgvsc: ENST00000459966.1:c.*261+25delG
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000347290
  ensembl transcript: ENST00000355163
  gene symbol: BANP
  hgvsc: ENST00000355163.5:c.380+25delG
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000431812
  ensembl transcript: ENST00000466197
  gene symbol: BANP
  hgvsc: ENST00000466197.1:c.362+25delG
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000347125
  ensembl transcript: ENST00000355022
  gene symbol: BANP
  hgvsc: ENST00000355022.4:c.362+25delG
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000286122
  ensembl transcript: ENST00000286122
  gene symbol: BANP
  hgvsc: ENST00000286122.7:c.338+25delG
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000376902
  ensembl transcript: ENST00000393207
  gene symbol: BANP
  hgvsc: ENST00000393207.1:c.338+25delG
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000376903
  ensembl transcript: ENST00000393208
  gene symbol: BANP
  hgvsc: ENST00000393208.2:c.362+25delG
  variant of: http://identifiers.org/hgnc/13450
canonical: true
consequence: intron
filter: AC_Adj0
genotype depth: GenotypeDepth
  all individuals: 2273
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1276
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34544
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3530
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10139
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1398
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: CG
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: DP
site quality: BaseQRankSum

16-88017886-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 88017886
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 88017886
    reference: chr 16
allele count: 2
allele frequency: 9.950248756218905e-5
allele num: 20100
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000376902
  ensembl transcript: ENST00000393207
  gene symbol: BANP
  hgvsc: ENST00000393207.1:c.338+21C>T
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000432508
  ensembl transcript: ENST00000479780
  gene symbol: BANP
  hgvsc: ENST00000479780.2:c.362+21C>T
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000347125
  ensembl transcript: ENST00000355022
  gene symbol: BANP
  hgvsc: ENST00000355022.4:c.362+21C>T
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000431812
  ensembl transcript: ENST00000466197
  gene symbol: BANP
  hgvsc: ENST00000466197.1:c.362+21C>T
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000411479
  ensembl transcript: ENST00000439677
  gene symbol: BANP
  hgvsc: ENST00000439677.1:c.380+21C>T
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000436869
  ensembl transcript: ENST00000485772
  gene symbol: BANP
  hgvsc: ENST00000485772.1:c.*261+21C>T
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000347290
  ensembl transcript: ENST00000355163
  gene symbol: BANP
  hgvsc: ENST00000355163.5:c.380+21C>T
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000286122
  ensembl transcript: ENST00000286122
  gene symbol: BANP
  hgvsc: ENST00000286122.7:c.338+21C>T
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000444352
  ensembl transcript: ENST00000538234
  gene symbol: BANP
  hgvsc: ENST00000538234.1:c.362+21C>T
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000435727
  ensembl transcript: ENST00000459966
  gene symbol: BANP
  hgvsc: ENST00000459966.1:c.*261+21C>T
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000376903
  ensembl transcript: ENST00000393208
  gene symbol: BANP
  hgvsc: ENST00000393208.2:c.362+21C>T
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000399576
  ensembl transcript: ENST00000436970
  gene symbol: BANP
  hgvsc: ENST00000436970.1:c.362+21C>T
  variant of: http://identifiers.org/hgnc/13450
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 34544
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1276
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2273
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10139
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3530
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1398
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: FS
site quality: ReadPosRankSum

16-88017887-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 88017887
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 88017887
    reference: chr 16
allele count: 3
allele frequency: 1.598806224685568e-4
allele num: 18764
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000376903
  ensembl transcript: ENST00000393208
  gene symbol: BANP
  hgvsc: ENST00000393208.2:c.362+22G>A
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000432508
  ensembl transcript: ENST00000479780
  gene symbol: BANP
  hgvsc: ENST00000479780.2:c.362+22G>A
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000436869
  ensembl transcript: ENST00000485772
  gene symbol: BANP
  hgvsc: ENST00000485772.1:c.*261+22G>A
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000435727
  ensembl transcript: ENST00000459966
  gene symbol: BANP
  hgvsc: ENST00000459966.1:c.*261+22G>A
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000444352
  ensembl transcript: ENST00000538234
  gene symbol: BANP
  hgvsc: ENST00000538234.1:c.362+22G>A
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000347290
  ensembl transcript: ENST00000355163
  gene symbol: BANP
  hgvsc: ENST00000355163.5:c.380+22G>A
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000411479
  ensembl transcript: ENST00000439677
  gene symbol: BANP
  hgvsc: ENST00000439677.1:c.380+22G>A
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000431812
  ensembl transcript: ENST00000466197
  gene symbol: BANP
  hgvsc: ENST00000466197.1:c.362+22G>A
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000399576
  ensembl transcript: ENST00000436970
  gene symbol: BANP
  hgvsc: ENST00000436970.1:c.362+22G>A
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000376902
  ensembl transcript: ENST00000393207
  gene symbol: BANP
  hgvsc: ENST00000393207.1:c.338+22G>A
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000347125
  ensembl transcript: ENST00000355022
  gene symbol: BANP
  hgvsc: ENST00000355022.4:c.362+22G>A
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000286122
  ensembl transcript: ENST00000286122
  gene symbol: BANP
  hgvsc: ENST00000286122.7:c.338+22G>A
  variant of: http://identifiers.org/hgnc/13450
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3308
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 736
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9208
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2023
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34878
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1256
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1108
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: African
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum

16-88017891-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 88017891
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 88017891
    reference: chr 16
allele count: 1
allele frequency: 5.448997384481256e-5
allele num: 18352
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000436869
  ensembl transcript: ENST00000485772
  gene symbol: BANP
  hgvsc: ENST00000485772.1:c.*261+26C>T
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000347290
  ensembl transcript: ENST00000355163
  gene symbol: BANP
  hgvsc: ENST00000355163.5:c.380+26C>T
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000399576
  ensembl transcript: ENST00000436970
  gene symbol: BANP
  hgvsc: ENST00000436970.1:c.362+26C>T
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000444352
  ensembl transcript: ENST00000538234
  gene symbol: BANP
  hgvsc: ENST00000538234.1:c.362+26C>T
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000435727
  ensembl transcript: ENST00000459966
  gene symbol: BANP
  hgvsc: ENST00000459966.1:c.*261+26C>T
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000376902
  ensembl transcript: ENST00000393207
  gene symbol: BANP
  hgvsc: ENST00000393207.1:c.338+26C>T
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000432508
  ensembl transcript: ENST00000479780
  gene symbol: BANP
  hgvsc: ENST00000479780.2:c.362+26C>T
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000411479
  ensembl transcript: ENST00000439677
  gene symbol: BANP
  hgvsc: ENST00000439677.1:c.380+26C>T
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000347125
  ensembl transcript: ENST00000355022
  gene symbol: BANP
  hgvsc: ENST00000355022.4:c.362+26C>T
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000286122
  ensembl transcript: ENST00000286122
  gene symbol: BANP
  hgvsc: ENST00000286122.7:c.338+26C>T
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000431812
  ensembl transcript: ENST00000466197
  gene symbol: BANP
  hgvsc: ENST00000466197.1:c.362+26C>T
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000376903
  ensembl transcript: ENST00000393208
  gene symbol: BANP
  hgvsc: ENST00000393208.2:c.362+26C>T
  variant of: http://identifiers.org/hgnc/13450
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1185
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 951
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 884
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8311
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35433
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3237
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
population: European (Finnish)
reference allele: C
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum

16-88017897-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 88017897
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 88017897
    reference: chr 16
allele count: 2
allele frequency: 1.182592242194891e-4
allele num: 16912
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000435727
  ensembl transcript: ENST00000459966
  gene symbol: BANP
  hgvsc: ENST00000459966.1:c.*261+32G>T
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000347125
  ensembl transcript: ENST00000355022
  gene symbol: BANP
  hgvsc: ENST00000355022.4:c.362+32G>T
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000286122
  ensembl transcript: ENST00000286122
  gene symbol: BANP
  hgvsc: ENST00000286122.7:c.338+32G>T
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000431812
  ensembl transcript: ENST00000466197
  gene symbol: BANP
  hgvsc: ENST00000466197.1:c.362+32G>T
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000411479
  ensembl transcript: ENST00000439677
  gene symbol: BANP
  hgvsc: ENST00000439677.1:c.380+32G>T
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000376902
  ensembl transcript: ENST00000393207
  gene symbol: BANP
  hgvsc: ENST00000393207.1:c.338+32G>T
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000444352
  ensembl transcript: ENST00000538234
  gene symbol: BANP
  hgvsc: ENST00000538234.1:c.362+32G>T
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000399576
  ensembl transcript: ENST00000436970
  gene symbol: BANP
  hgvsc: ENST00000436970.1:c.362+32G>T
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000432508
  ensembl transcript: ENST00000479780
  gene symbol: BANP
  hgvsc: ENST00000479780.2:c.362+32G>T
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000376903
  ensembl transcript: ENST00000393208
  gene symbol: BANP
  hgvsc: ENST00000393208.2:c.362+32G>T
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000436869
  ensembl transcript: ENST00000485772
  gene symbol: BANP
  hgvsc: ENST00000485772.1:c.*261+32G>T
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000347290
  ensembl transcript: ENST00000355163
  gene symbol: BANP
  hgvsc: ENST00000355163.5:c.380+32G>T
  variant of: http://identifiers.org/hgnc/13450
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1318
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 883
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6931
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 34832
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1337
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3263
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Other
population: European (Finnish)
reference allele: G
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum

16-88017914-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 88017914
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 88017914
    reference: chr 16
allele count: 0
allele frequency: 0.0e0
allele num: 12328
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000399576
  ensembl transcript: ENST00000436970
  gene symbol: BANP
  hgvsc: ENST00000436970.1:c.362+49C>T
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000347290
  ensembl transcript: ENST00000355163
  gene symbol: BANP
  hgvsc: ENST00000355163.5:c.380+49C>T
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000286122
  ensembl transcript: ENST00000286122
  gene symbol: BANP
  hgvsc: ENST00000286122.7:c.338+49C>T
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000347125
  ensembl transcript: ENST00000355022
  gene symbol: BANP
  hgvsc: ENST00000355022.4:c.362+49C>T
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000435727
  ensembl transcript: ENST00000459966
  gene symbol: BANP
  hgvsc: ENST00000459966.1:c.*261+49C>T
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000436869
  ensembl transcript: ENST00000485772
  gene symbol: BANP
  hgvsc: ENST00000485772.1:c.*261+49C>T
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000411479
  ensembl transcript: ENST00000439677
  gene symbol: BANP
  hgvsc: ENST00000439677.1:c.380+49C>T
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000432508
  ensembl transcript: ENST00000479780
  gene symbol: BANP
  hgvsc: ENST00000479780.2:c.362+49C>T
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000376903
  ensembl transcript: ENST00000393208
  gene symbol: BANP
  hgvsc: ENST00000393208.2:c.362+49C>T
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000444352
  ensembl transcript: ENST00000538234
  gene symbol: BANP
  hgvsc: ENST00000538234.1:c.362+49C>T
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000431812
  ensembl transcript: ENST00000466197
  gene symbol: BANP
  hgvsc: ENST00000466197.1:c.362+49C>T
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000376902
  ensembl transcript: ENST00000393207
  gene symbol: BANP
  hgvsc: ENST00000393207.1:c.338+49C>T
  variant of: http://identifiers.org/hgnc/13450
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 1555
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32660
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5736
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2659
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: Other
reference allele: C
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD

16-88017915-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 88017915
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 88017915
    reference: chr 16
allele count: 27
allele frequency: 2.155172413793103e-3
allele num: 12528
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000432508
  ensembl transcript: ENST00000479780
  gene symbol: BANP
  hgvsc: ENST00000479780.2:c.362+50G>A
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000444352
  ensembl transcript: ENST00000538234
  gene symbol: BANP
  hgvsc: ENST00000538234.1:c.362+50G>A
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000399576
  ensembl transcript: ENST00000436970
  gene symbol: BANP
  hgvsc: ENST00000436970.1:c.362+50G>A
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000431812
  ensembl transcript: ENST00000466197
  gene symbol: BANP
  hgvsc: ENST00000466197.1:c.362+50G>A
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000286122
  ensembl transcript: ENST00000286122
  gene symbol: BANP
  hgvsc: ENST00000286122.7:c.338+50G>A
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000411479
  ensembl transcript: ENST00000439677
  gene symbol: BANP
  hgvsc: ENST00000439677.1:c.380+50G>A
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000347290
  ensembl transcript: ENST00000355163
  gene symbol: BANP
  hgvsc: ENST00000355163.5:c.380+50G>A
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000347125
  ensembl transcript: ENST00000355022
  gene symbol: BANP
  hgvsc: ENST00000355022.4:c.362+50G>A
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000376902
  ensembl transcript: ENST00000393207
  gene symbol: BANP
  hgvsc: ENST00000393207.1:c.338+50G>A
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000436869
  ensembl transcript: ENST00000485772
  gene symbol: BANP
  hgvsc: ENST00000485772.1:c.*261+50G>A
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000376903
  ensembl transcript: ENST00000393208
  gene symbol: BANP
  hgvsc: ENST00000393208.2:c.362+50G>A
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000435727
  ensembl transcript: ENST00000459966
  gene symbol: BANP
  hgvsc: ENST00000459966.1:c.*261+50G>A
  variant of: http://identifiers.org/hgnc/13450
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 32740
  bin: 2.5e0
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5762
  bin: 7.5e0
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 723
  bin: 2.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1506
  bin: 1.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 2.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2674
  bin: 1.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: Other
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP

16-88017916-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 88017916
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 88017916
    reference: chr 16
allele count: 1
allele frequency: 8.067118425298483e-5
allele num: 12396
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000444352
  ensembl transcript: ENST00000538234
  gene symbol: BANP
  hgvsc: ENST00000538234.1:c.362+51C>T
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000347125
  ensembl transcript: ENST00000355022
  gene symbol: BANP
  hgvsc: ENST00000355022.4:c.362+51C>T
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000347290
  ensembl transcript: ENST00000355163
  gene symbol: BANP
  hgvsc: ENST00000355163.5:c.380+51C>T
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000436869
  ensembl transcript: ENST00000485772
  gene symbol: BANP
  hgvsc: ENST00000485772.1:c.*261+51C>T
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000411479
  ensembl transcript: ENST00000439677
  gene symbol: BANP
  hgvsc: ENST00000439677.1:c.380+51C>T
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000376903
  ensembl transcript: ENST00000393208
  gene symbol: BANP
  hgvsc: ENST00000393208.2:c.362+51C>T
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000399576
  ensembl transcript: ENST00000436970
  gene symbol: BANP
  hgvsc: ENST00000436970.1:c.362+51C>T
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000376902
  ensembl transcript: ENST00000393207
  gene symbol: BANP
  hgvsc: ENST00000393207.1:c.338+51C>T
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000432508
  ensembl transcript: ENST00000479780
  gene symbol: BANP
  hgvsc: ENST00000479780.2:c.362+51C>T
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000286122
  ensembl transcript: ENST00000286122
  gene symbol: BANP
  hgvsc: ENST00000286122.7:c.338+51C>T
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000435727
  ensembl transcript: ENST00000459966
  gene symbol: BANP
  hgvsc: ENST00000459966.1:c.*261+51C>T
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000431812
  ensembl transcript: ENST00000466197
  gene symbol: BANP
  hgvsc: ENST00000466197.1:c.362+51C>T
  variant of: http://identifiers.org/hgnc/13450
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 32810
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1482
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 735
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5766
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2668
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: QD
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD

16-88037040-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 88037040
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 88037040
    reference: chr 16
allele count: 1
allele frequency: 9.291953168556031e-5
allele num: 10762
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000431812
  ensembl transcript: ENST00000466197
  gene symbol: BANP
  hgvsc: ENST00000466197.1:c.363-48A>G
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000347125
  ensembl transcript: ENST00000355022
  gene symbol: BANP
  hgvsc: ENST00000355022.4:c.363-2656A>G
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000432508
  ensembl transcript: ENST00000479780
  gene symbol: BANP
  hgvsc: ENST00000479780.2:c.363-2656A>G
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000444352
  ensembl transcript: ENST00000538234
  gene symbol: BANP
  hgvsc: ENST00000538234.1:c.363-861A>G
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000347290
  ensembl transcript: ENST00000355163
  gene symbol: BANP
  hgvsc: ENST00000355163.5:c.381-2656A>G
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000435727
  ensembl transcript: ENST00000459966
  gene symbol: BANP
  hgvsc: ENST00000459966.1:c.*262-2656A>G
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000399576
  ensembl transcript: ENST00000436970
  gene symbol: BANP
  hgvsc: ENST00000436970.1:c.363-861A>G
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000411479
  ensembl transcript: ENST00000439677
  gene symbol: BANP
  hgvsc: ENST00000439677.1:c.381-2656A>G
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000436869
  ensembl transcript: ENST00000485772
  gene symbol: BANP
  hgvsc: ENST00000485772.1:c.*262-377A>G
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000376903
  ensembl transcript: ENST00000393208
  gene symbol: BANP
  hgvsc: ENST00000393208.2:c.363-2656A>G
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000286122
  ensembl transcript: ENST00000286122
  gene symbol: BANP
  hgvsc: ENST00000286122.7:c.339-861A>G
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000376902
  ensembl transcript: ENST00000393207
  gene symbol: BANP
  hgvsc: ENST00000393207.1:c.339-861A>G
  variant of: http://identifiers.org/hgnc/13450
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1077
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2490
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 891
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1004
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: A
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD

16-88037053-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 88037053
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 88037053
    reference: chr 16
allele count: 8
allele frequency: 7.434944237918215e-4
allele num: 10760
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000347290
  ensembl transcript: ENST00000355163
  gene symbol: BANP
  hgvsc: ENST00000355163.5:c.381-2643G>A
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000431812
  ensembl transcript: ENST00000466197
  gene symbol: BANP
  hgvsc: ENST00000466197.1:c.363-35G>A
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000376903
  ensembl transcript: ENST00000393208
  gene symbol: BANP
  hgvsc: ENST00000393208.2:c.363-2643G>A
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000286122
  ensembl transcript: ENST00000286122
  gene symbol: BANP
  hgvsc: ENST00000286122.7:c.339-848G>A
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000399576
  ensembl transcript: ENST00000436970
  gene symbol: BANP
  hgvsc: ENST00000436970.1:c.363-848G>A
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000432508
  ensembl transcript: ENST00000479780
  gene symbol: BANP
  hgvsc: ENST00000479780.2:c.363-2643G>A
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000347125
  ensembl transcript: ENST00000355022
  gene symbol: BANP
  hgvsc: ENST00000355022.4:c.363-2643G>A
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000376902
  ensembl transcript: ENST00000393207
  gene symbol: BANP
  hgvsc: ENST00000393207.1:c.339-848G>A
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000444352
  ensembl transcript: ENST00000538234
  gene symbol: BANP
  hgvsc: ENST00000538234.1:c.363-848G>A
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000435727
  ensembl transcript: ENST00000459966
  gene symbol: BANP
  hgvsc: ENST00000459966.1:c.*262-2643G>A
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000436869
  ensembl transcript: ENST00000485772
  gene symbol: BANP
  hgvsc: ENST00000485772.1:c.*262-364G>A
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000411479
  ensembl transcript: ENST00000439677
  gene symbol: BANP
  hgvsc: ENST00000439677.1:c.381-2643G>A
  variant of: http://identifiers.org/hgnc/13450
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 906
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 575
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2354
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 741
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1078
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1006
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 6.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: South Asian
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
reference allele: G
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS

16-88037090-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 88037090
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 88037090
    reference: chr 16
allele count: 2
allele frequency: 1.857700167193015e-4
allele num: 10766
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000347290
  ensembl transcript: ENST00000355163
  gene symbol: BANP
  hgvsc: ENST00000355163.5:c.381-2606T>G
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000399576
  ensembl transcript: ENST00000436970
  gene symbol: BANP
  hgvsc: ENST00000436970.1:c.363-811T>G
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000411479
  ensembl transcript: ENST00000439677
  gene symbol: BANP
  hgvsc: ENST00000439677.1:c.381-2606T>G
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000376903
  ensembl transcript: ENST00000393208
  gene symbol: BANP
  hgvsc: ENST00000393208.2:c.363-2606T>G
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000431812
  ensembl transcript: ENST00000466197
  gene symbol: BANP
  hgvsc: ENST00000466197.1:c.365T>G
  hgvsp: ENSP00000431812.1:p.Leu122Arg
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000347125
  ensembl transcript: ENST00000355022
  gene symbol: BANP
  hgvsc: ENST00000355022.4:c.363-2606T>G
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000435727
  ensembl transcript: ENST00000459966
  gene symbol: BANP
  hgvsc: ENST00000459966.1:c.*262-2606T>G
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000286122
  ensembl transcript: ENST00000286122
  gene symbol: BANP
  hgvsc: ENST00000286122.7:c.339-811T>G
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000436869
  ensembl transcript: ENST00000485772
  gene symbol: BANP
  hgvsc: ENST00000485772.1:c.*262-327T>G
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000376902
  ensembl transcript: ENST00000393207
  gene symbol: BANP
  hgvsc: ENST00000393207.1:c.339-811T>G
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000432508
  ensembl transcript: ENST00000479780
  gene symbol: BANP
  hgvsc: ENST00000479780.2:c.363-2606T>G
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000444352
  ensembl transcript: ENST00000538234
  gene symbol: BANP
  hgvsc: ENST00000538234.1:c.363-811T>G
  variant of: http://identifiers.org/hgnc/13450
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 740
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2242
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 585
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1079
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 910
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu122Arg
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: T
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/16-88037118-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 88037118
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 88037118
    reference: chr 16
allele count: 1
allele frequency: 9.288500835965076e-5
allele num: 10766
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000431812
  ensembl transcript: ENST00000466197
  gene symbol: BANP
  hgvsc: ENST00000466197.1:c.*6C>A
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000436869
  ensembl transcript: ENST00000485772
  gene symbol: BANP
  hgvsc: ENST00000485772.1:c.*262-299C>A
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000347290
  ensembl transcript: ENST00000355163
  gene symbol: BANP
  hgvsc: ENST00000355163.5:c.381-2578C>A
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000347125
  ensembl transcript: ENST00000355022
  gene symbol: BANP
  hgvsc: ENST00000355022.4:c.363-2578C>A
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000444352
  ensembl transcript: ENST00000538234
  gene symbol: BANP
  hgvsc: ENST00000538234.1:c.363-783C>A
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000376902
  ensembl transcript: ENST00000393207
  gene symbol: BANP
  hgvsc: ENST00000393207.1:c.339-783C>A
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000286122
  ensembl transcript: ENST00000286122
  gene symbol: BANP
  hgvsc: ENST00000286122.7:c.339-783C>A
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000399576
  ensembl transcript: ENST00000436970
  gene symbol: BANP
  hgvsc: ENST00000436970.1:c.363-783C>A
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000376903
  ensembl transcript: ENST00000393208
  gene symbol: BANP
  hgvsc: ENST00000393208.2:c.363-2578C>A
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000435727
  ensembl transcript: ENST00000459966
  gene symbol: BANP
  hgvsc: ENST00000459966.1:c.*262-2578C>A
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000411479
  ensembl transcript: ENST00000439677
  gene symbol: BANP
  hgvsc: ENST00000439677.1:c.381-2578C>A
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000432508
  ensembl transcript: ENST00000479780
  gene symbol: BANP
  hgvsc: ENST00000479780.2:c.363-2578C>A
  variant of: http://identifiers.org/hgnc/13450
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 911
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1007
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2297
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 740
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1079
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: European (Finnish)
population: African
reference allele: C
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD

16-88037128-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 88037128
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 88037128
    reference: chr 16
allele count: 2
allele frequency: 1.858390633711206e-4
allele num: 10762
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000347290
  ensembl transcript: ENST00000355163
  gene symbol: BANP
  hgvsc: ENST00000355163.5:c.381-2568A>G
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000411479
  ensembl transcript: ENST00000439677
  gene symbol: BANP
  hgvsc: ENST00000439677.1:c.381-2568A>G
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000436869
  ensembl transcript: ENST00000485772
  gene symbol: BANP
  hgvsc: ENST00000485772.1:c.*262-289A>G
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000431812
  ensembl transcript: ENST00000466197
  gene symbol: BANP
  hgvsc: ENST00000466197.1:c.*16A>G
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000444352
  ensembl transcript: ENST00000538234
  gene symbol: BANP
  hgvsc: ENST00000538234.1:c.363-773A>G
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000286122
  ensembl transcript: ENST00000286122
  gene symbol: BANP
  hgvsc: ENST00000286122.7:c.339-773A>G
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000347125
  ensembl transcript: ENST00000355022
  gene symbol: BANP
  hgvsc: ENST00000355022.4:c.363-2568A>G
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000432508
  ensembl transcript: ENST00000479780
  gene symbol: BANP
  hgvsc: ENST00000479780.2:c.363-2568A>G
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000435727
  ensembl transcript: ENST00000459966
  gene symbol: BANP
  hgvsc: ENST00000459966.1:c.*262-2568A>G
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000399576
  ensembl transcript: ENST00000436970
  gene symbol: BANP
  hgvsc: ENST00000436970.1:c.363-773A>G
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000376903
  ensembl transcript: ENST00000393208
  gene symbol: BANP
  hgvsc: ENST00000393208.2:c.363-2568A>G
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000376902
  ensembl transcript: ENST00000393207
  gene symbol: BANP
  hgvsc: ENST00000393207.1:c.339-773A>G
  variant of: http://identifiers.org/hgnc/13450
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 911
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 740
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1079
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2316
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1007
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 1
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
reference allele: A
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: FS
site quality: VQSLOD

16-88037862-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 88037862
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 88037862
    reference: chr 16
allele count: 1
allele frequency: 5.659309564233164e-5
allele num: 17670
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000435727
  ensembl transcript: ENST00000459966
  gene symbol: BANP
  hgvsc: ENST00000459966.1:c.*262-1834T>C
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000444352
  ensembl transcript: ENST00000538234
  gene symbol: BANP
  hgvsc: ENST00000538234.1:c.363-39T>C
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000432508
  ensembl transcript: ENST00000479780
  gene symbol: BANP
  hgvsc: ENST00000479780.2:c.363-1834T>C
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000347125
  ensembl transcript: ENST00000355022
  gene symbol: BANP
  hgvsc: ENST00000355022.4:c.363-1834T>C
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000431812
  ensembl transcript: ENST00000466197
  gene symbol: BANP
  hgvsc: ENST00000466197.1:c.*58-39T>C
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000376902
  ensembl transcript: ENST00000393207
  gene symbol: BANP
  hgvsc: ENST00000393207.1:c.339-39T>C
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000286122
  ensembl transcript: ENST00000286122
  gene symbol: BANP
  hgvsc: ENST00000286122.7:c.339-39T>C
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000411479
  ensembl transcript: ENST00000439677
  gene symbol: BANP
  hgvsc: ENST00000439677.1:c.381-1834T>C
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000399576
  ensembl transcript: ENST00000436970
  gene symbol: BANP
  hgvsc: ENST00000436970.1:c.363-39T>C
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000376903
  ensembl transcript: ENST00000393208
  gene symbol: BANP
  hgvsc: ENST00000393208.2:c.363-1834T>C
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000347290
  ensembl transcript: ENST00000355163
  gene symbol: BANP
  hgvsc: ENST00000355163.5:c.381-1834T>C
  variant of: http://identifiers.org/hgnc/13450
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1660
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3572
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1360
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1541
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 177
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: African
population: Other
population: Latino
reference allele: T
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum

16-88037867-CCTT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 88037867
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 88037864
    reference: chr 16
allele count: 1
allele frequency: 5.659950192438306e-5
allele num: 17668
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000286122
  ensembl transcript: ENST00000286122
  gene symbol: BANP
  hgvsc: ENST00000286122.7:c.339-30_339-28delCTT
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000376902
  ensembl transcript: ENST00000393207
  gene symbol: BANP
  hgvsc: ENST00000393207.1:c.339-30_339-28delCTT
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000432508
  ensembl transcript: ENST00000479780
  gene symbol: BANP
  hgvsc: ENST00000479780.2:c.363-1825_363-1823delCTT
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000444352
  ensembl transcript: ENST00000538234
  gene symbol: BANP
  hgvsc: ENST00000538234.1:c.363-30_363-28delCTT
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000347125
  ensembl transcript: ENST00000355022
  gene symbol: BANP
  hgvsc: ENST00000355022.4:c.363-1825_363-1823delCTT
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000435727
  ensembl transcript: ENST00000459966
  gene symbol: BANP
  hgvsc: ENST00000459966.1:c.*262-1825_*262-1823delCTT
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000411479
  ensembl transcript: ENST00000439677
  gene symbol: BANP
  hgvsc: ENST00000439677.1:c.381-1825_381-1823delCTT
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000399576
  ensembl transcript: ENST00000436970
  gene symbol: BANP
  hgvsc: ENST00000436970.1:c.363-30_363-28delCTT
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000431812
  ensembl transcript: ENST00000466197
  gene symbol: BANP
  hgvsc: ENST00000466197.1:c.*58-30_*58-28delCTT
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000347290
  ensembl transcript: ENST00000355163
  gene symbol: BANP
  hgvsc: ENST00000355163.5:c.381-1825_381-1823delCTT
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000376903
  ensembl transcript: ENST00000393208
  gene symbol: BANP
  hgvsc: ENST00000393208.2:c.363-1825_363-1823delCTT
  variant of: http://identifiers.org/hgnc/13450
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1363
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1735
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1491
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3592
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1130
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: CCTT
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: QD

16-88037892-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 88037892
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 88037892
    reference: chr 16
allele count: 1
allele frequency: 5.614823133071308e-5
allele num: 17810
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000347125
  ensembl transcript: ENST00000355022
  gene symbol: BANP
  hgvsc: ENST00000355022.4:c.363-1804G>C
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000286122
  ensembl transcript: ENST00000286122
  gene symbol: BANP
  hgvsc: ENST00000286122.7:c.339-9G>C
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000376902
  ensembl transcript: ENST00000393207
  gene symbol: BANP
  hgvsc: ENST00000393207.1:c.339-9G>C
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000444352
  ensembl transcript: ENST00000538234
  gene symbol: BANP
  hgvsc: ENST00000538234.1:c.363-9G>C
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000411479
  ensembl transcript: ENST00000439677
  gene symbol: BANP
  hgvsc: ENST00000439677.1:c.381-1804G>C
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000432508
  ensembl transcript: ENST00000479780
  gene symbol: BANP
  hgvsc: ENST00000479780.2:c.363-1804G>C
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000399576
  ensembl transcript: ENST00000436970
  gene symbol: BANP
  hgvsc: ENST00000436970.1:c.363-9G>C
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000435727
  ensembl transcript: ENST00000459966
  gene symbol: BANP
  hgvsc: ENST00000459966.1:c.*262-1804G>C
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000431812
  ensembl transcript: ENST00000466197
  gene symbol: BANP
  hgvsc: ENST00000466197.1:c.*58-9G>C
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000347290
  ensembl transcript: ENST00000355163
  gene symbol: BANP
  hgvsc: ENST00000355163.5:c.381-1804G>C
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000376903
  ensembl transcript: ENST00000393208
  gene symbol: BANP
  hgvsc: ENST00000393208.2:c.363-1804G>C
  variant of: http://identifiers.org/hgnc/13450
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3672
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1271
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1381
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2006
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: Other
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum

16-88037902-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 88037902
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 88037902
    reference: chr 16
allele count: 1
allele frequency: 5.597850425436632e-5
allele num: 17864
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000286122
  ensembl transcript: ENST00000286122
  gene symbol: BANP
  hgvsc: ENST00000286122.7:c.340G>A
  hgvsp: ENSP00000286122.7:p.Val114Ile
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000431812
  ensembl transcript: ENST00000466197
  gene symbol: BANP
  hgvsc: ENST00000466197.1:c.*59G>A
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000376903
  ensembl transcript: ENST00000393208
  gene symbol: BANP
  hgvsc: ENST00000393208.2:c.363-1794G>A
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000347125
  ensembl transcript: ENST00000355022
  gene symbol: BANP
  hgvsc: ENST00000355022.4:c.363-1794G>A
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000347290
  ensembl transcript: ENST00000355163
  gene symbol: BANP
  hgvsc: ENST00000355163.5:c.381-1794G>A
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000376902
  ensembl transcript: ENST00000393207
  gene symbol: BANP
  hgvsc: ENST00000393207.1:c.340G>A
  hgvsp: ENSP00000376902.1:p.Val114Ile
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000435727
  ensembl transcript: ENST00000459966
  gene symbol: BANP
  hgvsc: ENST00000459966.1:c.*262-1794G>A
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000444352
  ensembl transcript: ENST00000538234
  gene symbol: BANP
  hgvsc: ENST00000538234.1:c.364G>A
  hgvsp: ENSP00000444352.1:p.Val122Ile
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000411479
  ensembl transcript: ENST00000439677
  gene symbol: BANP
  hgvsc: ENST00000439677.1:c.381-1794G>A
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000399576
  ensembl transcript: ENST00000436970
  gene symbol: BANP
  hgvsc: ENST00000436970.1:c.364G>A
  hgvsp: ENSP00000399576.1:p.Val122Ile
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000432508
  ensembl transcript: ENST00000479780
  gene symbol: BANP
  hgvsc: ENST00000479780.2:c.363-1794G>A
  variant of: http://identifiers.org/hgnc/13450
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2060
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1391
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3698
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1327
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val114Ile
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
population: African
population: Other
reference allele: G
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS

16-88037903-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 88037903
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 88037903
    reference: chr 16
allele count: 1
allele frequency: 5.597223777006605e-5
allele num: 17866
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000432508
  ensembl transcript: ENST00000479780
  gene symbol: BANP
  hgvsc: ENST00000479780.2:c.363-1793T>C
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000347125
  ensembl transcript: ENST00000355022
  gene symbol: BANP
  hgvsc: ENST00000355022.4:c.363-1793T>C
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000376903
  ensembl transcript: ENST00000393208
  gene symbol: BANP
  hgvsc: ENST00000393208.2:c.363-1793T>C
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000347290
  ensembl transcript: ENST00000355163
  gene symbol: BANP
  hgvsc: ENST00000355163.5:c.381-1793T>C
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000444352
  ensembl transcript: ENST00000538234
  gene symbol: BANP
  hgvsc: ENST00000538234.1:c.365T>C
  hgvsp: ENSP00000444352.1:p.Val122Ala
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000399576
  ensembl transcript: ENST00000436970
  gene symbol: BANP
  hgvsc: ENST00000436970.1:c.365T>C
  hgvsp: ENSP00000399576.1:p.Val122Ala
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000376902
  ensembl transcript: ENST00000393207
  gene symbol: BANP
  hgvsc: ENST00000393207.1:c.341T>C
  hgvsp: ENSP00000376902.1:p.Val114Ala
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000435727
  ensembl transcript: ENST00000459966
  gene symbol: BANP
  hgvsc: ENST00000459966.1:c.*262-1793T>C
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000431812
  ensembl transcript: ENST00000466197
  gene symbol: BANP
  hgvsc: ENST00000466197.1:c.*60T>C
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000411479
  ensembl transcript: ENST00000439677
  gene symbol: BANP
  hgvsc: ENST00000439677.1:c.381-1793T>C
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000286122
  ensembl transcript: ENST00000286122
  gene symbol: BANP
  hgvsc: ENST00000286122.7:c.341T>C
  hgvsp: ENSP00000286122.7:p.Val114Ala
  variant of: http://identifiers.org/hgnc/13450
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2063
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1315
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1387
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3704
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val114Ala
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: African
population: East Asian
reference allele: T
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: DP

16-88037913-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 88037913
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 88037913
    reference: chr 16
allele count: 1
allele frequency: 5.589714924538849e-5
allele num: 17890
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000347290
  ensembl transcript: ENST00000355163
  gene symbol: BANP
  hgvsc: ENST00000355163.5:c.381-1783G>A
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000376903
  ensembl transcript: ENST00000393208
  gene symbol: BANP
  hgvsc: ENST00000393208.2:c.363-1783G>A
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000432508
  ensembl transcript: ENST00000479780
  gene symbol: BANP
  hgvsc: ENST00000479780.2:c.363-1783G>A
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000444352
  ensembl transcript: ENST00000538234
  gene symbol: BANP
  hgvsc: ENST00000538234.1:c.375G>A
  hgvsp: ENST00000538234.1:c.375G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000376902
  ensembl transcript: ENST00000393207
  gene symbol: BANP
  hgvsc: ENST00000393207.1:c.351G>A
  hgvsp: ENST00000393207.1:c.351G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000347125
  ensembl transcript: ENST00000355022
  gene symbol: BANP
  hgvsc: ENST00000355022.4:c.363-1783G>A
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000431812
  ensembl transcript: ENST00000466197
  gene symbol: BANP
  hgvsc: ENST00000466197.1:c.*70G>A
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000435727
  ensembl transcript: ENST00000459966
  gene symbol: BANP
  hgvsc: ENST00000459966.1:c.*262-1783G>A
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000286122
  ensembl transcript: ENST00000286122
  gene symbol: BANP
  hgvsc: ENST00000286122.7:c.351G>A
  hgvsp: ENST00000286122.7:c.351G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000411479
  ensembl transcript: ENST00000439677
  gene symbol: BANP
  hgvsc: ENST00000439677.1:c.381-1783G>A
  variant of: http://identifiers.org/hgnc/13450
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1357
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1399
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2043
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3727
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Gln117Gln
num of homozygotes: 0
population: South Asian
population: Other
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
reference allele: G
site quality: DP
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff

16-88037939-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 88037939
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 88037939
    reference: chr 16
allele count: 1
allele frequency: 5.665722379603399e-5
allele num: 17650
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000376902
  ensembl transcript: ENST00000393207
  gene symbol: BANP
  hgvsc: ENST00000393207.1:c.377G>A
  hgvsp: ENSP00000376902.1:p.Arg126Gln
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000431812
  ensembl transcript: ENST00000466197
  gene symbol: BANP
  hgvsc: ENST00000466197.1:c.*96G>A
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000432508
  ensembl transcript: ENST00000479780
  gene symbol: BANP
  hgvsc: ENST00000479780.2:c.363-1757G>A
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000376903
  ensembl transcript: ENST00000393208
  gene symbol: BANP
  hgvsc: ENST00000393208.2:c.363-1757G>A
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000435727
  ensembl transcript: ENST00000459966
  gene symbol: BANP
  hgvsc: ENST00000459966.1:c.*262-1757G>A
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000444352
  ensembl transcript: ENST00000538234
  gene symbol: BANP
  hgvsc: ENST00000538234.1:c.401G>A
  hgvsp: ENSP00000444352.1:p.Arg134Gln
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000286122
  ensembl transcript: ENST00000286122
  gene symbol: BANP
  hgvsc: ENST00000286122.7:c.377G>A
  hgvsp: ENSP00000286122.7:p.Arg126Gln
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000347290
  ensembl transcript: ENST00000355163
  gene symbol: BANP
  hgvsc: ENST00000355163.5:c.381-1757G>A
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000347125
  ensembl transcript: ENST00000355022
  gene symbol: BANP
  hgvsc: ENST00000355022.4:c.363-1757G>A
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000411479
  ensembl transcript: ENST00000439677
  gene symbol: BANP
  hgvsc: ENST00000439677.1:c.381-1757G>A
  variant of: http://identifiers.org/hgnc/13450
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1353
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1389
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1872
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3700
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 737
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5033
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Arg126Gln
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: VQSLOD

16-88037947-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 88037947
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 88037947
    reference: chr 16
allele count: 1
allele frequency: 5.744485294117647e-5
allele num: 17408
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000431812
  ensembl transcript: ENST00000466197
  gene symbol: BANP
  hgvsc: ENST00000466197.1:c.*104G>A
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000347290
  ensembl transcript: ENST00000355163
  gene symbol: BANP
  hgvsc: ENST00000355163.5:c.381-1749G>A
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000432508
  ensembl transcript: ENST00000479780
  gene symbol: BANP
  hgvsc: ENST00000479780.2:c.363-1749G>A
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000435727
  ensembl transcript: ENST00000459966
  gene symbol: BANP
  hgvsc: ENST00000459966.1:c.*262-1749G>A
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000286122
  ensembl transcript: ENST00000286122
  gene symbol: BANP
  hgvsc: ENST00000286122.7:c.385G>A
  hgvsp: ENSP00000286122.7:p.Ala129Thr
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000444352
  ensembl transcript: ENST00000538234
  gene symbol: BANP
  hgvsc: ENST00000538234.1:c.409G>A
  hgvsp: ENSP00000444352.1:p.Ala137Thr
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000347125
  ensembl transcript: ENST00000355022
  gene symbol: BANP
  hgvsc: ENST00000355022.4:c.363-1749G>A
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000376902
  ensembl transcript: ENST00000393207
  gene symbol: BANP
  hgvsc: ENST00000393207.1:c.385G>A
  hgvsp: ENSP00000376902.1:p.Ala129Thr
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000411479
  ensembl transcript: ENST00000439677
  gene symbol: BANP
  hgvsc: ENST00000439677.1:c.381-1749G>A
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000376903
  ensembl transcript: ENST00000393208
  gene symbol: BANP
  hgvsc: ENST00000393208.2:c.363-1749G>A
  variant of: http://identifiers.org/hgnc/13450
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1866
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1363
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 660
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3615
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1296
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 158
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Ala129Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
population: East Asian
population: South Asian
population: Latino
reference allele: G
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: QD

http://identifiers.org/exac.variant/16-88037971-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 88037971
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 88037971
    reference: chr 16
allele count: 2
allele frequency: 1.216841080554879e-4
allele num: 16436
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000431812
  ensembl transcript: ENST00000466197
  gene symbol: BANP
  hgvsc: ENST00000466197.1:c.*128C>A
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000347290
  ensembl transcript: ENST00000355163
  gene symbol: BANP
  hgvsc: ENST00000355163.5:c.381-1725C>A
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000376902
  ensembl transcript: ENST00000393207
  gene symbol: BANP
  hgvsc: ENST00000393207.1:c.409C>A
  hgvsp: ENSP00000376902.1:p.Pro137Thr
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000376903
  ensembl transcript: ENST00000393208
  gene symbol: BANP
  hgvsc: ENST00000393208.2:c.363-1725C>A
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000444352
  ensembl transcript: ENST00000538234
  gene symbol: BANP
  hgvsc: ENST00000538234.1:c.433C>A
  hgvsp: ENSP00000444352.1:p.Pro145Thr
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000435727
  ensembl transcript: ENST00000459966
  gene symbol: BANP
  hgvsc: ENST00000459966.1:c.*262-1725C>A
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000347125
  ensembl transcript: ENST00000355022
  gene symbol: BANP
  hgvsc: ENST00000355022.4:c.363-1725C>A
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000286122
  ensembl transcript: ENST00000286122
  gene symbol: BANP
  hgvsc: ENST00000286122.7:c.409C>A
  hgvsp: ENSP00000286122.7:p.Pro137Thr
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000411479
  ensembl transcript: ENST00000439677
  gene symbol: BANP
  hgvsc: ENST00000439677.1:c.381-1725C>A
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000432508
  ensembl transcript: ENST00000479780
  gene symbol: BANP
  hgvsc: ENST00000479780.2:c.363-1725C>A
  variant of: http://identifiers.org/hgnc/13450
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1015
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1813
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1558
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 781
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 992
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2998
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 870
  bin: 9.75e1
  variant carriers: 2
hgvs: p.Pro137Thr
num of homozygotes: 0
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum

16-88037990-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 88037990
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 88037990
    reference: chr 16
allele count: 1
allele frequency: 6.836204539239814e-5
allele num: 14628
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000431812
  ensembl transcript: ENST00000466197
  gene symbol: BANP
  hgvsc: ENST00000466197.1:c.*147C>T
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000347125
  ensembl transcript: ENST00000355022
  gene symbol: BANP
  hgvsc: ENST00000355022.4:c.363-1706C>T
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000376903
  ensembl transcript: ENST00000393208
  gene symbol: BANP
  hgvsc: ENST00000393208.2:c.363-1706C>T
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000286122
  ensembl transcript: ENST00000286122
  gene symbol: BANP
  hgvsc: ENST00000286122.7:c.428C>T
  hgvsp: ENSP00000286122.7:p.Pro143Leu
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000444352
  ensembl transcript: ENST00000538234
  gene symbol: BANP
  hgvsc: ENST00000538234.1:c.452C>T
  hgvsp: ENSP00000444352.1:p.Pro151Leu
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000411479
  ensembl transcript: ENST00000439677
  gene symbol: BANP
  hgvsc: ENST00000439677.1:c.381-1706C>T
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000347290
  ensembl transcript: ENST00000355163
  gene symbol: BANP
  hgvsc: ENST00000355163.5:c.381-1706C>T
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000432508
  ensembl transcript: ENST00000479780
  gene symbol: BANP
  hgvsc: ENST00000479780.2:c.363-1706C>T
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000376902
  ensembl transcript: ENST00000393207
  gene symbol: BANP
  hgvsc: ENST00000393207.1:c.428C>T
  hgvsp: ENSP00000376902.1:p.Pro143Leu
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000435727
  ensembl transcript: ENST00000459966
  gene symbol: BANP
  hgvsc: ENST00000459966.1:c.*262-1706C>T
  variant of: http://identifiers.org/hgnc/13450
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1779
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1687
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1795
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1461
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1627
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 153
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 867
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Pro143Leu
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
reference allele: C
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: VQSLOD

http://identifiers.org/exac.variant/16-88038036-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 88038036
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 88038036
    reference: chr 16
allele count: 8
allele frequency: 9.995002498750624e-4
allele num: 8004
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000347290
  ensembl transcript: ENST00000355163
  gene symbol: BANP
  hgvsc: ENST00000355163.5:c.381-1660A>C
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000376903
  ensembl transcript: ENST00000393208
  gene symbol: BANP
  hgvsc: ENST00000393208.2:c.363-1660A>C
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000411479
  ensembl transcript: ENST00000439677
  gene symbol: BANP
  hgvsc: ENST00000439677.1:c.381-1660A>C
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000444352
  ensembl transcript: ENST00000538234
  gene symbol: BANP
  hgvsc: ENST00000538234.1:c.479+19A>C
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000347125
  ensembl transcript: ENST00000355022
  gene symbol: BANP
  hgvsc: ENST00000355022.4:c.363-1660A>C
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000376902
  ensembl transcript: ENST00000393207
  gene symbol: BANP
  hgvsc: ENST00000393207.1:c.455+19A>C
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000435727
  ensembl transcript: ENST00000459966
  gene symbol: BANP
  hgvsc: ENST00000459966.1:c.*262-1660A>C
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000432508
  ensembl transcript: ENST00000479780
  gene symbol: BANP
  hgvsc: ENST00000479780.2:c.363-1660A>C
  variant of: http://identifiers.org/hgnc/13450
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172530
  ensembl protein: ENSP00000286122
  ensembl transcript: ENST00000286122
  gene symbol: BANP
  hgvsc: ENST00000286122.7:c.455+19A>C
  variant of: http://identifiers.org/hgnc/13450
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 1398
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 5.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 3474
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2870
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3031
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 997
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 283
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 615
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 238
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
reference allele: A

Annotation
canonical: false
consequence: synonymous_variant
consequence: splice_region_variant
ensembl gene: ENSG00000172530
ensembl protein: ENSP00000376903
ensembl transcript: ENST00000393208
gene symbol: BANP
hgvsc: ENST00000393208.2:c.165A>G
hgvsp: ENST00000393208.2:c.165A>G(p.%3D)
variant of: http://identifiers.org/hgnc/13450

GenotypeDepth
all individuals: 55
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2719
bin: 7.5e0
variant carriers: 1

GenotypeDepth
all individuals: 208
bin: 4.75e1
variant carriers: 11

GenotypeDepth
all individuals: 7581
bin: 2.75e1
variant carriers: 33

GenotypeDepth
all individuals: 66
bin: 8.75e1
variant carriers: 2

GenotypeDepth
all individuals: 569
bin: 1.75e1
variant carriers: 10

GenotypeDepth
all individuals: 135
bin: 5.75e1
variant carriers: 5

GenotypeDepth
all individuals: 292
bin: 4.25e1
variant carriers: 17

GenotypeDepth
all individuals: 85
bin: 8.25e1
variant carriers: 1

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

GenotypeDepth
all individuals: 1765
bin: 3.25e1
variant carriers: 34

GenotypeDepth
all individuals: 44581
bin: 2.25e1
variant carriers: 22

GenotypeDepth
all individuals: 378
bin: 3.75e1
variant carriers: 26

GenotypeDepth
all individuals: 687
bin: 9.75e1
variant carriers: 3

GenotypeDepth
all individuals: 951
bin: 1.25e1
variant carriers: 5

GenotypeDepth
all individuals: 87
bin: 7.75e1
variant carriers: 2

GenotypeDepth
all individuals: 95
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 120
bin: 6.75e1
variant carriers: 3

GenotypeDepth
all individuals: 146
bin: 6.25e1
variant carriers: 5

GenotypeDepth
all individuals: 166
bin: 5.25e1
variant carriers: 5

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

GenotypeQuality
all individuals: 203
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 1.75e1
variant carriers: 1

GenotypeQuality
all individuals: 277
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 136
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 199
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 796
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2369
bin: 9.75e1
variant carriers: 178

GenotypeQuality
all individuals: 3244
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 609
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 559
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 239
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 47339
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3185
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 753
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 453
bin: 8.25e1
variant carriers: 2

GenotypeQuality
all individuals: 228
bin: 9.25e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 61
allele frequency: 9.584262954466895e-4
allele num: 63646
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15668
num of homozygotes: 0

Other
type: Population
allele count: 6
allele frequency: 6.880733944954129e-3
allele num: 872
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 111
allele frequency: 1.79902755267423e-2
allele num: 6170
num of homozygotes: 3

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11228
num of homozygotes: 0

East Asian
type: Population
allele count: 8
allele frequency: 9.416195856873823e-4
allele num: 8496
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9840
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 3.739e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.459e0

DP
type: SiteQuality
SIO_000300: 1.439157e6

MQRankSum
type: SiteQuality
SIO_000300: -2.14e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.87e-2

QD
type: SiteQuality
SIO_000300: 1.027e1

VQSLOD
type: SiteQuality
SIO_000300: -1.721e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.11e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.01e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

GenotypeDepth
all individuals: 197
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2656
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 130
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 44543
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 939
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 161
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 141
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 55
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1807
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 529
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 359
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 118
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 95
bin: 7.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 7757
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 281
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 686
bin: 9.75e1
variant carriers: 2

GenotypeDepth
all individuals: 84
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 85
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 64
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 93
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 321
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3195
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 143
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 786
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 745
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 47875
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3205
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 451
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 224
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2194
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 238
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 24
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 275
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 200
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 206
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 501
bin: 5.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15692
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 2.032520325203252e-4
allele num: 9840
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63716
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11232
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6164
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8504
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.249e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.29e0

MQ
type: SiteQuality
SIO_000300: 4.049e1

DP
type: SiteQuality
SIO_000300: 1.439863e6

MQRankSum
type: SiteQuality
SIO_000300: -1.755e0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 2.96e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

VQSLOD
type: SiteQuality
SIO_000300: -3.136e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.16e-1

GenotypeDepth
all individuals: 55
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 551
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 44251
bin: 2.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 356
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 141
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 278
bin: 4.25e1
variant carriers: 1

GenotypeDepth
all individuals: 1012
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 161
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1821
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 684
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 84
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2633
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 95
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 197
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7968
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 85
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 131
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 64
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 119
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2195
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 283
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 292
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3271
bin: 2.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 447
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 206
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 409
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 147
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 93
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 198
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 783
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 47909
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3218
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 744
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 224
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 234
bin: 3.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6174
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.914244963451596e-5
allele num: 11218
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63756
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9828
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8504
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15710
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.440967e6

FS
type: SiteQuality
SIO_000300: 2.497e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.03e-1

MQ
type: SiteQuality
SIO_000300: 3.853e1

MQRankSum
type: SiteQuality
SIO_000300: 4.1e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -3.475e0

QD
type: SiteQuality
SIO_000300: 1.087e1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.57e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.716e0

GenotypeDepth
all individuals: 945
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 119
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 49
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 283
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 85
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 84
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8701
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 165
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1905
bin: 3.25e1
variant carriers: 1

GenotypeDepth
all individuals: 3254
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 95
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 141
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 684
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 55
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 392
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 39215
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 207
bin: 4.75e1
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GenotypeDepth
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South Asian
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MQ
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InbreedingCoeff
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MQRankSum
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GenotypeDepth
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European (Finnish)
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African
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South Asian
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East Asian
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European (Non-Finnish)
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MQ
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FS
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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South Asian
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European (Non-Finnish)
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East Asian
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African
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DP
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FS
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MQRankSum
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MQ
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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Latino
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East Asian
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South Asian
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African
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QD
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European (Non-Finnish)
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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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African
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European (Finnish)
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Latino
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European (Non-Finnish)
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South Asian
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Other
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FS
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ReadPosRankSum
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DP
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MQRankSum
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QD
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BaseQRankSum
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VQSLOD
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MQ
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ClippingRankSum
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InbreedingCoeff
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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allele num: 7776
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East Asian
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European (Non-Finnish)
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European (Finnish)
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African
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South Asian
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Other
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VQSLOD
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MQ
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InbreedingCoeff
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BaseQRankSum
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DP
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QD
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MQRankSum
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FS
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ReadPosRankSum
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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Latino
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East Asian
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Other
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African
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European (Non-Finnish)
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European (Finnish)
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VQSLOD
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ReadPosRankSum
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QD
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DP
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InbreedingCoeff
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ClippingRankSum
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FS
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BaseQRankSum
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MQRankSum
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MQ
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

European (Non-Finnish)
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East Asian
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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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South Asian
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QD
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DP
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FS
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BaseQRankSum
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ClippingRankSum
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ReadPosRankSum
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MQRankSum
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InbreedingCoeff
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MQ
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VQSLOD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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South Asian
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Other
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European (Non-Finnish)
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East Asian
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European (Finnish)
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Latino
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FS
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ReadPosRankSum
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MQRankSum
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DP
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MQ
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InbreedingCoeff
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VQSLOD
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ClippingRankSum
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QD
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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African
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ReadPosRankSum
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MQ
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DP
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InbreedingCoeff
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VQSLOD
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QD
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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European (Non-Finnish)
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South Asian
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European (Finnish)
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African
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DP
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MQ
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MQRankSum
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VQSLOD
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FS
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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South Asian
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African
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European (Non-Finnish)
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European (Finnish)
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Latino
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BaseQRankSum
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DP
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FS
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ReadPosRankSum
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MQ
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MQRankSum
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VQSLOD
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InbreedingCoeff
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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African
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European (Finnish)
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East Asian
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European (Non-Finnish)
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VQSLOD
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ReadPosRankSum
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MQRankSum
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MQ
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FS
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DP
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QD
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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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VQSLOD
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InbreedingCoeff
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DP
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MQ
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VQSLOD
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DP
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GenotypeQuality
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QD
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MQ
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FS
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African
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DP
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MQ
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VQSLOD
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QD
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FS
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DP
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InbreedingCoeff
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East Asian
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African
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European (Finnish)
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Latino
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European (Non-Finnish)
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QD
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MQ
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MQRankSum
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VQSLOD
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DP
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InbreedingCoeff
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Latino
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African
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European (Non-Finnish)
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variant carriers: 24150

GenotypeQuality
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variant carriers: 991

GenotypeQuality
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variant carriers: 3000

GenotypeQuality
all individuals: 781
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variant carriers: 722

GenotypeQuality
all individuals: 632
bin: 9.25e1
variant carriers: 613

East Asian
type: Population
allele count: 3649
allele frequency: 5.431676094075618e-1
allele num: 6718
num of homozygotes: 889

African
type: Population
allele count: 6369
allele frequency: 7.426539179104478e-1
allele num: 8576
num of homozygotes: 2322

Other
type: Population
allele count: 440
allele frequency: 5.866666666666667e-1
allele num: 750
num of homozygotes: 122

European (Finnish)
type: Population
allele count: 2882
allele frequency: 5.675462780622292e-1
allele num: 5078
num of homozygotes: 757

South Asian
type: Population
allele count: 5125
allele frequency: 3.64301961899346e-1
allele num: 14068
num of homozygotes: 871

Latino
type: Population
allele count: 5551
allele frequency: 6.133701657458563e-1
allele num: 9050
num of homozygotes: 1579

European (Non-Finnish)
type: Population
allele count: 34422
allele frequency: 6.40695380262815e-1
allele num: 53726
num of homozygotes: 10449

FS
type: SiteQuality
SIO_000300: 1.29e0

MQRankSum
type: SiteQuality
SIO_000300: -7.37e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.2e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.38e0

VQSLOD
type: SiteQuality
SIO_000300: 2.02e0

MQ
type: SiteQuality
SIO_000300: 4.73e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.99e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.67e-1

DP
type: SiteQuality
SIO_000300: 1.487563e6

QD
type: SiteQuality
SIO_000300: 1.843e1

GenotypeDepth
all individuals: 44
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 50
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variant carriers: 0

GenotypeDepth
all individuals: 83
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
all individuals: 82
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variant carriers: 0

GenotypeDepth
all individuals: 79
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variant carriers: 0

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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variant carriers: 1

GenotypeDepth
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
all individuals: 856
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variant carriers: 2

GenotypeQuality
all individuals: 109
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6668
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6346
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.494512073438436e-5
allele num: 40088
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 578
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5012
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12624
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3746
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.077e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.22e-1

MQRankSum
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SIO_000300: 1.92e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.6e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -1.92e0

VQSLOD
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SIO_000300: -2.49e0

MQ
type: SiteQuality
SIO_000300: 5.182e1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.840000000000001e-1

QD
type: SiteQuality
SIO_000300: 9.5e0

DP
type: SiteQuality
SIO_000300: 9.26682e5

GenotypeDepth
all individuals: 6126
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
all individuals: 44
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variant carriers: 0

GenotypeDepth
all individuals: 21651
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variant carriers: 2

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
all individuals: 82
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

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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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 3

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 408
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GenotypeQuality
all individuals: 13881
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variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 580
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3732
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 3.178639542275906e-4
allele num: 6292
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 39952
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6654
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5004
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.950389569088885e-5
allele num: 12578
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.598e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.3e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.52e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 9.21262e5

ClippingRankSum
type: SiteQuality
SIO_000300: -9.56e-1

QD
type: SiteQuality
SIO_000300: 1.175e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.22e0

MQ
type: SiteQuality
SIO_000300: 4.729e1

MQRankSum
type: SiteQuality
SIO_000300: 7.05e-1

GenotypeDepth
all individuals: 94
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6088
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variant carriers: 0

GenotypeDepth
all individuals: 2316
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 83
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variant carriers: 0

GenotypeDepth
all individuals: 491
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 72
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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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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 206
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GenotypeQuality
all individuals: 404
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variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12542
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3704
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6616
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4984
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 39784
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6272
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 580
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.808e0

VQSLOD
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SIO_000300: -1.837e0

ClippingRankSum
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SIO_000300: -3.61e-1

InbreedingCoeff
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SIO_000300: -5.4e-3

QD
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SIO_000300: 7.06e0

BaseQRankSum
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SIO_000300: -1.881e0

DP
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SIO_000300: 9.18172e5

MQRankSum
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SIO_000300: -1.307e0

ReadPosRankSum
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SIO_000300: 3.61e-1

MQ
type: SiteQuality
SIO_000300: 4.859e1

GenotypeDepth
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bin: 4.75e1
variant carriers: 0

GenotypeDepth
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 5

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 67
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GenotypeQuality
all individuals: 418
bin: 4.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5994
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3480
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 1.318217769575534e-4
allele num: 37930
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 562
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6384
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4700
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12214
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 8.29e-1

InbreedingCoeff
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SIO_000300: -6.6e-3

BaseQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.344e1

FS
type: SiteQuality
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DP
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QD
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ClippingRankSum
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 5

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1508
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GenotypeQuality
all individuals: 327
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variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 510
num of homozygotes: 0

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

African
type: Population
allele count: 2
allele frequency: 3.428179636612959e-4
allele num: 5834
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East Asian
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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allele frequency: 1.956181533646322e-4
allele num: 5112
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 6.005645306588193e-5
allele num: 33302
num of homozygotes: 0

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

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

East Asian
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South Asian
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African
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European (Non-Finnish)
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allele frequency: 3.371771528761211e-5
allele num: 29658
num of homozygotes: 0

Other
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VQSLOD
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SIO_000300: -1.685e0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 4982
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 27624
num of homozygotes: 0

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

Latino
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allele count: 1
allele frequency: 2.465483234714004e-4
allele num: 4056
num of homozygotes: 0

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

East Asian
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allele frequency: 3.142677561282213e-4
allele num: 3182
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MQRankSum
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SIO_000300: -1.408e0

ReadPosRankSum
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FS
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DP
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MQ
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VQSLOD
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InbreedingCoeff
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BaseQRankSum
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SIO_000300: 2.13e0

ClippingRankSum
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SIO_000300: -1.64e-1

QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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allele frequency: 0.0e0
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South Asian
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East Asian
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European (Non-Finnish)
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allele num: 24248
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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Latino
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African
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BaseQRankSum
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SIO_000300: -9.61e-1

QD
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ReadPosRankSum
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ClippingRankSum
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InbreedingCoeff
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DP
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MQRankSum
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MQ
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VQSLOD
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FS
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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Latino
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European (Non-Finnish)
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East Asian
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European (Finnish)
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Other
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South Asian
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InbreedingCoeff
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QD
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MQRankSum
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ReadPosRankSum
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MQ
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DP
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FS
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BaseQRankSum
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VQSLOD
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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European (Non-Finnish)
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East Asian
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African
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European (Finnish)
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South Asian
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ReadPosRankSum
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DP
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InbreedingCoeff
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MQ
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BaseQRankSum
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QD
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FS
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MQRankSum
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VQSLOD
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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East Asian
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African
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Latino
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European (Non-Finnish)
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South Asian
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Other
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FS
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ReadPosRankSum
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DP
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InbreedingCoeff
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SIO_000300: -6.73e-2

BaseQRankSum
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SIO_000300: -6.29e-1

MQRankSum
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SIO_000300: 1.03e0

MQ
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SIO_000300: 4.292e1

QD
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SIO_000300: 1.45e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.1e-1

VQSLOD
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SIO_000300: -1.161e0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 734
num of homozygotes: 0

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

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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

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

MQRankSum
type: SiteQuality
SIO_000300: -7.27e-1

QD
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ReadPosRankSum
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ClippingRankSum
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InbreedingCoeff
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VQSLOD
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FS
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SIO_000300: 0.0e0

MQ
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DP
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SIO_000300: 4.15209e5

BaseQRankSum
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SIO_000300: 1.54e0

GenotypeDepth
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variant carriers: 0

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

Latino
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allele frequency: 0.0e0
allele num: 734
num of homozygotes: 0

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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

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

European (Non-Finnish)
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allele frequency: 2.435460301997078e-4
allele num: 8212
num of homozygotes: 0

BaseQRankSum
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SIO_000300: 1.54e0

MQRankSum
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SIO_000300: -7.27e-1

DP
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InbreedingCoeff
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VQSLOD
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ClippingRankSum
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QD
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MQ
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FS
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SIO_000300: 0.0e0

ReadPosRankSum
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SIO_000300: 5.5e-1

GenotypeDepth
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variant carriers: 0

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

South Asian
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allele frequency: 1.285347043701799e-4
allele num: 7780
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele frequency: 1.348072256672958e-4
allele num: 7418
num of homozygotes: 0

African
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allele frequency: 5.720823798627002e-4
allele num: 1748
num of homozygotes: 0

FS
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SIO_000300: 7.365e0

BaseQRankSum
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InbreedingCoeff
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SIO_000300: -7.69e-2

MQRankSum
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ClippingRankSum
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QD
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MQ
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VQSLOD
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DP
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ReadPosRankSum
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GenotypeDepth
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variant carriers: 1

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

South Asian
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allele count: 1
allele frequency: 1.295336787564767e-4
allele num: 7720
num of homozygotes: 0

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

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

African
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num of homozygotes: 0

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

European (Finnish)
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allele frequency: 0.0e0
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QD
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MQRankSum
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DP
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FS
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BaseQRankSum
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MQ
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ClippingRankSum
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InbreedingCoeff
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VQSLOD
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele count: 0
allele frequency: 0.0e0
allele num: 1608
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 466
num of homozygotes: 0

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

European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 6454
num of homozygotes: 0

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

European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 4712
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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South Asian
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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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FS
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MQ
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BaseQRankSum
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ClippingRankSum
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InbreedingCoeff
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DP
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ReadPosRankSum
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MQRankSum
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VQSLOD
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

Latino
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allele count: 3
allele frequency: 8.152173913043478e-3
allele num: 368
num of homozygotes: 0

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

Other
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South Asian
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East Asian
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African
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allele frequency: 1.673640167364017e-2
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European (Non-Finnish)
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allele frequency: 0.0e0
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InbreedingCoeff
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ReadPosRankSum
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QD
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MQ
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MQRankSum
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FS
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VQSLOD
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ClippingRankSum
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BaseQRankSum
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SIO_000300: -1.191e0

DP
type: SiteQuality
SIO_000300: 2.74753e5

GenotypeDepth
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bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 52
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12366
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 605
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 107
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 4.25e1
variant carriers: 1

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 82
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 110
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1440
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 42
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.661129568106312e-3
allele num: 602
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 128
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5118
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4700
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 366
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.025e1

DP
type: SiteQuality
SIO_000300: 2.74578e5

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.59e0

MQ
type: SiteQuality
SIO_000300: 4.906e1

MQRankSum
type: SiteQuality
SIO_000300: -3.76e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.72e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.64e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.669999999999999e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.1e0

GenotypeDepth
all individuals: 191
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 742
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 454
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 92
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.332977872567315e-4
allele num: 7502
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 134
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 190
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2724
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 118
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.97e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.97e-2

DP
type: SiteQuality
SIO_000300: 2.18684e5

ClippingRankSum
type: SiteQuality
SIO_000300: 6.57e-1

QD
type: SiteQuality
SIO_000300: 1.062e1

ReadPosRankSum
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SIO_000300: -3.28e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.218e0

VQSLOD
type: SiteQuality
SIO_000300: -1.1e-3

GenotypeDepth
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bin: 9.75e1
variant carriers: 0

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

GenotypeQuality
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bin: 1.75e1
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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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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GenotypeQuality
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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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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 273
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variant carriers: 0

GenotypeQuality
all individuals: 2427
bin: 9.75e1
variant carriers: 8

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 92
num of homozygotes: 0

South Asian
type: Population
allele count: 8
allele frequency: 1.066382298053852e-3
allele num: 7502
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 118
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2722
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 190
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 134
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.75e-1

DP
type: SiteQuality
SIO_000300: 2.19103e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.350000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.67e-2

MQRankSum
type: SiteQuality
SIO_000300: 6.73e-1

MQ
type: SiteQuality
SIO_000300: 5.963e1

QD
type: SiteQuality
SIO_000300: 1.307e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.71e0

VQSLOD
type: SiteQuality
SIO_000300: 3.62e-1

FS
type: SiteQuality
SIO_000300: 6.78e-1

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

GenotypeDepth
all individuals: 1006
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variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 362
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2014
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variant carriers: 0

GenotypeQuality
all individuals: 452
bin: 8.25e1
variant carriers: 0

South Asian
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allele count: 2
allele frequency: 2.664535038635758e-4
allele num: 7506
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 190
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 132
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2726
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 92
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 118
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.19583e5

VQSLOD
type: SiteQuality
SIO_000300: -9.257e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.64e-1

QD
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SIO_000300: 7.67e0

MQ
type: SiteQuality
SIO_000300: 5.93e1

MQRankSum
type: SiteQuality
SIO_000300: 8.1e-2

FS
type: SiteQuality
SIO_000300: 6.58e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.22e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 5.02e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.13e0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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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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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 132
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.332267519317879e-4
allele num: 7506
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2726
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 118
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 92
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 190
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.198e0

DP
type: SiteQuality
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BaseQRankSum
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InbreedingCoeff
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SIO_000300: -3.44e-2

VQSLOD
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ClippingRankSum
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MQ
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SIO_000300: 5.891e1

MQRankSum
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SIO_000300: 1.36e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.15e-1

QD
type: SiteQuality
SIO_000300: 1.016e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 6.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 190
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2724
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 92
num of homozygotes: 0

South Asian
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allele count: 2
allele frequency: 2.664535038635758e-4
allele num: 7506
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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 132
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 118
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.978e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.33e-2

DP
type: SiteQuality
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QD
type: SiteQuality
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FS
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VQSLOD
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 1750
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6222
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 452
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.30718954248366e-4
allele num: 7650
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 1088
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 216
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 292
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 7.22e-1

DP
type: SiteQuality
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QD
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FS
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MQRankSum
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BaseQRankSum
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InbreedingCoeff
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ClippingRankSum
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MQ
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 1752
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 288
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 1
allele frequency: 2.183406113537118e-3
allele num: 458
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6212
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.72e-2

MQRankSum
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VQSLOD
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BaseQRankSum
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SIO_000300: 1.58e-1

DP
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SIO_000300: 2.68758e5

ReadPosRankSum
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SIO_000300: 2.63e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.723e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.78e-1

QD
type: SiteQuality
SIO_000300: 1.584e1

GenotypeQuality
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bin: 5.25e1
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.584786053882726e-4
allele num: 6310
num of homozygotes: 0

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

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

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

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

East Asian
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allele frequency: 0.0e0
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MQRankSum
type: SiteQuality
SIO_000300: -8.4e-1

InbreedingCoeff
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SIO_000300: -1.13e-2

ClippingRankSum
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SIO_000300: -6.5e-1

QD
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SIO_000300: 1.019e1

BaseQRankSum
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SIO_000300: 6.67e-1

DP
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SIO_000300: 2.7257e5

MQ
type: SiteQuality
SIO_000300: 5.898e1

VQSLOD
type: SiteQuality
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FS
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SIO_000300: 3.78e0

ReadPosRankSum
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SIO_000300: 1.22e0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6332
num of homozygotes: 0

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

South Asian
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allele count: 1
allele frequency: 1.305483028720627e-4
allele num: 7660
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 302
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 1758
num of homozygotes: 0

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

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

DP
type: SiteQuality
SIO_000300: 2.74012e5

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.75e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.46e-1

VQSLOD
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BaseQRankSum
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SIO_000300: 5.1e-1

QD
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SIO_000300: 4.92e0

MQRankSum
type: SiteQuality
SIO_000300: 1.49e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.33e-2

FS
type: SiteQuality
SIO_000300: 3.401e0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 15
bin: 5.25e1
variant carriers: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 302
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.305483028720627e-4
allele num: 7660
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6334
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 220
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 1758
num of homozygotes: 0

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

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.173e1

MQRankSum
type: SiteQuality
SIO_000300: -1.281e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.11e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.77e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.34e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.51e0

VQSLOD
type: SiteQuality
SIO_000300: -7.2e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.74019e5

GenotypeQuality
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variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7662
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 216
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1116
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.574307304785894e-4
allele num: 6352
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 304
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 484
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 1756
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.74506e5

FS
type: SiteQuality
SIO_000300: 5.899e0

QD
type: SiteQuality
SIO_000300: 1.048e1

ClippingRankSum
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VQSLOD
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BaseQRankSum
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MQRankSum
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SIO_000300: -3.44e-1

MQ
type: SiteQuality
SIO_000300: 5.922e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.72e-1

InbreedingCoeff
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SIO_000300: -1.23e-2

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 1736
num of homozygotes: 0

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

South Asian
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allele frequency: 1.310615989515072e-4
allele num: 7630
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 1100
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6182
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
allele num: 486
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Other
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num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.38e-1

FS
type: SiteQuality
SIO_000300: 6.385e0

ClippingRankSum
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BaseQRankSum
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InbreedingCoeff
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DP
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MQRankSum
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MQ
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QD
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VQSLOD
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SIO_000300: -1.06e-1

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6044
num of homozygotes: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 1722
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 216
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
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South Asian
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allele frequency: 1.322401481089659e-4
allele num: 7562
num of homozygotes: 0

Latino
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MQ
type: SiteQuality
SIO_000300: 5.924e1

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

South Asian
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allele frequency: 2.824060999717594e-4
allele num: 7082
num of homozygotes: 0

European (Non-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 frequency: 0.0e0
allele num: 288
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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 486
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 1692
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 3.07e-1

BaseQRankSum
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MQ
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QD
type: SiteQuality
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MQRankSum
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InbreedingCoeff
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ClippingRankSum
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SIO_000300: 3.86e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.48077e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.02e-1

GenotypeQuality
all individuals: 154
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1632
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 126
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 304
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 249
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2913
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 538
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 53
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 233
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 214
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 272
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2546
bin: 6.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 174
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 948
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5090
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1666
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.666666666666667e-4
allele num: 6000
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 478
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 272
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.72e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -4.87e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.14e-1

QD
type: SiteQuality
SIO_000300: 9.75e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.87e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 2.12511e5

VQSLOD
type: SiteQuality
SIO_000300: 2.83e-1

GenotypeQuality
all individuals: 177
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 105
bin: 8.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 692
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 327
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 593
bin: 1.25e1
variant carriers: 1

GenotypeQuality
all individuals: 2215
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 4.25e1
variant carriers: 1

GenotypeQuality
all individuals: 53
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 610
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 211
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 103
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 130
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 181
bin: 7.25e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.138731952291275e-4
allele num: 3186
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1926
num of homozygotes: 0