20-45905258-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45905258
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 45905258
    reference: chr 20
allele count: 1
allele frequency: 8.236960890909689e-6
allele num: 121404
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000361093
  ensembl transcript: ENST00000372023
  gene symbol: ZMYND8
  hgvsc: ENST00000372023.3:c.1205C>T
  hgvsp: ENSP00000361093.3:p.Pro402Leu
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000348246
  ensembl transcript: ENST00000355972
  gene symbol: ZMYND8
  hgvsc: ENST00000355972.4:c.1220C>T
  hgvsp: ENSP00000348246.4:p.Pro407Leu
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000418495
  ensembl transcript: ENST00000467200
  gene symbol: ZMYND8
  hgvsc: ENST00000467200.2:c.999C>T
  hgvsp: ENSP00000418495.2:p.Pro334Leu
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000396725
  ensembl transcript: ENST00000446994
  gene symbol: ZMYND8
  hgvsc: ENST00000446994.2:c.1031C>T
  hgvsp: ENSP00000396725.2:p.Pro344Leu
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000420095
  ensembl transcript: ENST00000471951
  gene symbol: ZMYND8
  hgvsc: ENST00000471951.2:c.1280C>T
  hgvsp: ENSP00000420095.2:p.Pro427Leu
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000354166
  ensembl transcript: ENST00000360911
  gene symbol: ZMYND8
  hgvsc: ENST00000360911.3:c.1205C>T
  hgvsp: ENSP00000354166.3:p.Pro402Leu
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000379577
  ensembl transcript: ENST00000396281
  gene symbol: ZMYND8
  hgvsc: ENST00000396281.4:c.1220C>T
  hgvsp: ENSP00000379577.4:p.Pro407Leu
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000262975
  ensembl transcript: ENST00000262975
  gene symbol: ZMYND8
  hgvsc: ENST00000262975.4:c.1220C>T
  hgvsp: ENSP00000262975.4:p.Pro407Leu
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000392964
  ensembl transcript: ENST00000458360
  gene symbol: ZMYND8
  hgvsc: ENST00000458360.2:c.1205C>T
  hgvsp: ENSP00000392964.2:p.Pro402Leu
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000443086
  ensembl transcript: ENST00000540497
  gene symbol: ZMYND8
  hgvsc: ENST00000540497.1:c.1205C>T
  hgvsp: ENSP00000443086.1:p.Pro402Leu
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000418210
  ensembl transcript: ENST00000461685
  gene symbol: ZMYND8
  hgvsc: ENST00000461685.1:c.1280C>T
  hgvsp: ENSP00000418210.1:p.Pro427Leu
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000335537
  ensembl transcript: ENST00000352431
  gene symbol: ZMYND8
  hgvsc: ENST00000352431.2:c.1280C>T
  hgvsp: ENSP00000335537.3:p.Pro427Leu
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000312237
  ensembl transcript: ENST00000311275
  gene symbol: ZMYND8
  hgvsc: ENST00000311275.7:c.1220C>T
  hgvsp: ENSP00000312237.7:p.Pro407Leu
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101040
  ensembl transcript: ENST00000468376
  gene symbol: ZMYND8
  hgvsc: ENST00000468376.2:n.1231C>T
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000439800
  ensembl transcript: ENST00000536340
  gene symbol: ZMYND8
  hgvsc: ENST00000536340.1:c.1301C>T
  hgvsp: ENSP00000439800.1:p.Pro434Leu
  variant of: http://identifiers.org/hgnc/9397
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18148
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4321
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11689
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro427Leu
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP

20-45905263-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45905263
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 45905263
    reference: chr 20
allele count: 1
allele frequency: 8.236825198095647e-6
allele num: 121406
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000418210
  ensembl transcript: ENST00000461685
  gene symbol: ZMYND8
  hgvsc: ENST00000461685.1:c.1275A>G
  hgvsp: ENST00000461685.1:c.1275A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000418495
  ensembl transcript: ENST00000467200
  gene symbol: ZMYND8
  hgvsc: ENST00000467200.2:c.994A>G
  hgvsp: ENST00000467200.2:c.994A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000335537
  ensembl transcript: ENST00000352431
  gene symbol: ZMYND8
  hgvsc: ENST00000352431.2:c.1275A>G
  hgvsp: ENST00000352431.2:c.1275A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000396725
  ensembl transcript: ENST00000446994
  gene symbol: ZMYND8
  hgvsc: ENST00000446994.2:c.1026A>G
  hgvsp: ENST00000446994.2:c.1026A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000262975
  ensembl transcript: ENST00000262975
  gene symbol: ZMYND8
  hgvsc: ENST00000262975.4:c.1215A>G
  hgvsp: ENST00000262975.4:c.1215A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000312237
  ensembl transcript: ENST00000311275
  gene symbol: ZMYND8
  hgvsc: ENST00000311275.7:c.1215A>G
  hgvsp: ENST00000311275.7:c.1215A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000348246
  ensembl transcript: ENST00000355972
  gene symbol: ZMYND8
  hgvsc: ENST00000355972.4:c.1215A>G
  hgvsp: ENST00000355972.4:c.1215A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000443086
  ensembl transcript: ENST00000540497
  gene symbol: ZMYND8
  hgvsc: ENST00000540497.1:c.1200A>G
  hgvsp: ENST00000540497.1:c.1200A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000420095
  ensembl transcript: ENST00000471951
  gene symbol: ZMYND8
  hgvsc: ENST00000471951.2:c.1275A>G
  hgvsp: ENST00000471951.2:c.1275A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000354166
  ensembl transcript: ENST00000360911
  gene symbol: ZMYND8
  hgvsc: ENST00000360911.3:c.1200A>G
  hgvsp: ENST00000360911.3:c.1200A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000439800
  ensembl transcript: ENST00000536340
  gene symbol: ZMYND8
  hgvsc: ENST00000536340.1:c.1296A>G
  hgvsp: ENST00000536340.1:c.1296A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000361093
  ensembl transcript: ENST00000372023
  gene symbol: ZMYND8
  hgvsc: ENST00000372023.3:c.1200A>G
  hgvsp: ENST00000372023.3:c.1200A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000379577
  ensembl transcript: ENST00000396281
  gene symbol: ZMYND8
  hgvsc: ENST00000396281.4:c.1215A>G
  hgvsp: ENST00000396281.4:c.1215A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000392964
  ensembl transcript: ENST00000458360
  gene symbol: ZMYND8
  hgvsc: ENST00000458360.2:c.1200A>G
  hgvsp: ENST00000458360.2:c.1200A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101040
  ensembl transcript: ENST00000468376
  gene symbol: ZMYND8
  hgvsc: ENST00000468376.2:n.1226A>G
  variant of: http://identifiers.org/hgnc/9397
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4321
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18153
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1783
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11685
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala425Ala
num of homozygotes: 0
population: Other
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: African
reference allele: T
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD

20-45905266-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45905266
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 45905266
    reference: chr 20
allele count: 3
allele frequency: 2.471047559428694e-5
allele num: 121406
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000443086
  ensembl transcript: ENST00000540497
  gene symbol: ZMYND8
  hgvsc: ENST00000540497.1:c.1197G>A
  hgvsp: ENST00000540497.1:c.1197G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000439800
  ensembl transcript: ENST00000536340
  gene symbol: ZMYND8
  hgvsc: ENST00000536340.1:c.1293G>A
  hgvsp: ENST00000536340.1:c.1293G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000335537
  ensembl transcript: ENST00000352431
  gene symbol: ZMYND8
  hgvsc: ENST00000352431.2:c.1272G>A
  hgvsp: ENST00000352431.2:c.1272G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000420095
  ensembl transcript: ENST00000471951
  gene symbol: ZMYND8
  hgvsc: ENST00000471951.2:c.1272G>A
  hgvsp: ENST00000471951.2:c.1272G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000396725
  ensembl transcript: ENST00000446994
  gene symbol: ZMYND8
  hgvsc: ENST00000446994.2:c.1023G>A
  hgvsp: ENST00000446994.2:c.1023G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000348246
  ensembl transcript: ENST00000355972
  gene symbol: ZMYND8
  hgvsc: ENST00000355972.4:c.1212G>A
  hgvsp: ENST00000355972.4:c.1212G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000418495
  ensembl transcript: ENST00000467200
  gene symbol: ZMYND8
  hgvsc: ENST00000467200.2:c.991G>A
  hgvsp: ENST00000467200.2:c.991G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000418210
  ensembl transcript: ENST00000461685
  gene symbol: ZMYND8
  hgvsc: ENST00000461685.1:c.1272G>A
  hgvsp: ENST00000461685.1:c.1272G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000312237
  ensembl transcript: ENST00000311275
  gene symbol: ZMYND8
  hgvsc: ENST00000311275.7:c.1212G>A
  hgvsp: ENST00000311275.7:c.1212G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000262975
  ensembl transcript: ENST00000262975
  gene symbol: ZMYND8
  hgvsc: ENST00000262975.4:c.1212G>A
  hgvsp: ENST00000262975.4:c.1212G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000361093
  ensembl transcript: ENST00000372023
  gene symbol: ZMYND8
  hgvsc: ENST00000372023.3:c.1197G>A
  hgvsp: ENST00000372023.3:c.1197G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000354166
  ensembl transcript: ENST00000360911
  gene symbol: ZMYND8
  hgvsc: ENST00000360911.3:c.1197G>A
  hgvsp: ENST00000360911.3:c.1197G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000392964
  ensembl transcript: ENST00000458360
  gene symbol: ZMYND8
  hgvsc: ENST00000458360.2:c.1197G>A
  hgvsp: ENST00000458360.2:c.1197G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101040
  ensembl transcript: ENST00000468376
  gene symbol: ZMYND8
  hgvsc: ENST00000468376.2:n.1223G>A
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000379577
  ensembl transcript: ENST00000396281
  gene symbol: ZMYND8
  hgvsc: ENST00000396281.4:c.1212G>A
  hgvsp: ENST00000396281.4:c.1212G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr424Thr
num of homozygotes: 0
population: Other
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
population: African
reference allele: C
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum

20-45905267-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45905267
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 45905267
    reference: chr 20
allele count: 2
allele frequency: 1.647337901950448e-5
allele num: 121408
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000335537
  ensembl transcript: ENST00000352431
  gene symbol: ZMYND8
  hgvsc: ENST00000352431.2:c.1271C>T
  hgvsp: ENSP00000335537.3:p.Thr424Met
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000418495
  ensembl transcript: ENST00000467200
  gene symbol: ZMYND8
  hgvsc: ENST00000467200.2:c.990C>T
  hgvsp: ENSP00000418495.2:p.Thr331Met
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000396725
  ensembl transcript: ENST00000446994
  gene symbol: ZMYND8
  hgvsc: ENST00000446994.2:c.1022C>T
  hgvsp: ENSP00000396725.2:p.Thr341Met
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000443086
  ensembl transcript: ENST00000540497
  gene symbol: ZMYND8
  hgvsc: ENST00000540497.1:c.1196C>T
  hgvsp: ENSP00000443086.1:p.Thr399Met
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000354166
  ensembl transcript: ENST00000360911
  gene symbol: ZMYND8
  hgvsc: ENST00000360911.3:c.1196C>T
  hgvsp: ENSP00000354166.3:p.Thr399Met
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000418210
  ensembl transcript: ENST00000461685
  gene symbol: ZMYND8
  hgvsc: ENST00000461685.1:c.1271C>T
  hgvsp: ENSP00000418210.1:p.Thr424Met
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101040
  ensembl transcript: ENST00000468376
  gene symbol: ZMYND8
  hgvsc: ENST00000468376.2:n.1222C>T
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000439800
  ensembl transcript: ENST00000536340
  gene symbol: ZMYND8
  hgvsc: ENST00000536340.1:c.1292C>T
  hgvsp: ENSP00000439800.1:p.Thr431Met
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000420095
  ensembl transcript: ENST00000471951
  gene symbol: ZMYND8
  hgvsc: ENST00000471951.2:c.1271C>T
  hgvsp: ENSP00000420095.2:p.Thr424Met
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000262975
  ensembl transcript: ENST00000262975
  gene symbol: ZMYND8
  hgvsc: ENST00000262975.4:c.1211C>T
  hgvsp: ENSP00000262975.4:p.Thr404Met
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000361093
  ensembl transcript: ENST00000372023
  gene symbol: ZMYND8
  hgvsc: ENST00000372023.3:c.1196C>T
  hgvsp: ENSP00000361093.3:p.Thr399Met
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000348246
  ensembl transcript: ENST00000355972
  gene symbol: ZMYND8
  hgvsc: ENST00000355972.4:c.1211C>T
  hgvsp: ENSP00000348246.4:p.Thr404Met
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000312237
  ensembl transcript: ENST00000311275
  gene symbol: ZMYND8
  hgvsc: ENST00000311275.7:c.1211C>T
  hgvsp: ENSP00000312237.7:p.Thr404Met
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000379577
  ensembl transcript: ENST00000396281
  gene symbol: ZMYND8
  hgvsc: ENST00000396281.4:c.1211C>T
  hgvsp: ENSP00000379577.4:p.Thr404Met
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000392964
  ensembl transcript: ENST00000458360
  gene symbol: ZMYND8
  hgvsc: ENST00000458360.2:c.1196C>T
  hgvsp: ENSP00000392964.2:p.Thr399Met
  variant of: http://identifiers.org/hgnc/9397
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4320
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18153
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1784
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11688
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr424Met
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
population: African
population: Other
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/20-45905293-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45905293
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 45905293
    reference: chr 20
allele count: 402
allele frequency: 3.311258278145695e-3
allele num: 121404
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000262975
  ensembl transcript: ENST00000262975
  gene symbol: ZMYND8
  hgvsc: ENST00000262975.4:c.1185G>T
  hgvsp: ENSP00000262975.4:p.Glu395Asp
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000348246
  ensembl transcript: ENST00000355972
  gene symbol: ZMYND8
  hgvsc: ENST00000355972.4:c.1185G>T
  hgvsp: ENSP00000348246.4:p.Glu395Asp
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000379577
  ensembl transcript: ENST00000396281
  gene symbol: ZMYND8
  hgvsc: ENST00000396281.4:c.1185G>T
  hgvsp: ENSP00000379577.4:p.Glu395Asp
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000439800
  ensembl transcript: ENST00000536340
  gene symbol: ZMYND8
  hgvsc: ENST00000536340.1:c.1266G>T
  hgvsp: ENSP00000439800.1:p.Glu422Asp
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000335537
  ensembl transcript: ENST00000352431
  gene symbol: ZMYND8
  hgvsc: ENST00000352431.2:c.1245G>T
  hgvsp: ENSP00000335537.3:p.Glu415Asp
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000420095
  ensembl transcript: ENST00000471951
  gene symbol: ZMYND8
  hgvsc: ENST00000471951.2:c.1245G>T
  hgvsp: ENSP00000420095.2:p.Glu415Asp
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000392964
  ensembl transcript: ENST00000458360
  gene symbol: ZMYND8
  hgvsc: ENST00000458360.2:c.1170G>T
  hgvsp: ENSP00000392964.2:p.Glu390Asp
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000396725
  ensembl transcript: ENST00000446994
  gene symbol: ZMYND8
  hgvsc: ENST00000446994.2:c.996G>T
  hgvsp: ENSP00000396725.2:p.Glu332Asp
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000361093
  ensembl transcript: ENST00000372023
  gene symbol: ZMYND8
  hgvsc: ENST00000372023.3:c.1170G>T
  hgvsp: ENSP00000361093.3:p.Glu390Asp
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000312237
  ensembl transcript: ENST00000311275
  gene symbol: ZMYND8
  hgvsc: ENST00000311275.7:c.1185G>T
  hgvsp: ENSP00000312237.7:p.Glu395Asp
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000418210
  ensembl transcript: ENST00000461685
  gene symbol: ZMYND8
  hgvsc: ENST00000461685.1:c.1245G>T
  hgvsp: ENSP00000418210.1:p.Glu415Asp
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000443086
  ensembl transcript: ENST00000540497
  gene symbol: ZMYND8
  hgvsc: ENST00000540497.1:c.1170G>T
  hgvsp: ENSP00000443086.1:p.Glu390Asp
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101040
  ensembl transcript: ENST00000468376
  gene symbol: ZMYND8
  hgvsc: ENST00000468376.2:n.1196G>T
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000418495
  ensembl transcript: ENST00000467200
  gene symbol: ZMYND8
  hgvsc: ENST00000467200.2:c.964G>T
  hgvsp: ENSP00000418495.2:p.Glu322Asp
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000354166
  ensembl transcript: ENST00000360911
  gene symbol: ZMYND8
  hgvsc: ENST00000360911.3:c.1170G>T
  hgvsp: ENSP00000354166.3:p.Glu390Asp
  variant of: http://identifiers.org/hgnc/9397
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 6.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 22803
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4261
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18078
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Glu415Asp
num of homozygotes: 16
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
reference allele: C
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: DP

20-45905306-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45905306
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 45905306
    reference: chr 20
allele count: 3
allele frequency: 2.471088267272907e-5
allele num: 121404
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000396725
  ensembl transcript: ENST00000446994
  gene symbol: ZMYND8
  hgvsc: ENST00000446994.2:c.983T>C
  hgvsp: ENSP00000396725.2:p.Ile328Thr
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000335537
  ensembl transcript: ENST00000352431
  gene symbol: ZMYND8
  hgvsc: ENST00000352431.2:c.1232T>C
  hgvsp: ENSP00000335537.3:p.Ile411Thr
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000312237
  ensembl transcript: ENST00000311275
  gene symbol: ZMYND8
  hgvsc: ENST00000311275.7:c.1172T>C
  hgvsp: ENSP00000312237.7:p.Ile391Thr
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000418210
  ensembl transcript: ENST00000461685
  gene symbol: ZMYND8
  hgvsc: ENST00000461685.1:c.1232T>C
  hgvsp: ENSP00000418210.1:p.Ile411Thr
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000379577
  ensembl transcript: ENST00000396281
  gene symbol: ZMYND8
  hgvsc: ENST00000396281.4:c.1172T>C
  hgvsp: ENSP00000379577.4:p.Ile391Thr
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000439800
  ensembl transcript: ENST00000536340
  gene symbol: ZMYND8
  hgvsc: ENST00000536340.1:c.1253T>C
  hgvsp: ENSP00000439800.1:p.Ile418Thr
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000354166
  ensembl transcript: ENST00000360911
  gene symbol: ZMYND8
  hgvsc: ENST00000360911.3:c.1157T>C
  hgvsp: ENSP00000354166.3:p.Ile386Thr
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000443086
  ensembl transcript: ENST00000540497
  gene symbol: ZMYND8
  hgvsc: ENST00000540497.1:c.1157T>C
  hgvsp: ENSP00000443086.1:p.Ile386Thr
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000262975
  ensembl transcript: ENST00000262975
  gene symbol: ZMYND8
  hgvsc: ENST00000262975.4:c.1172T>C
  hgvsp: ENSP00000262975.4:p.Ile391Thr
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000348246
  ensembl transcript: ENST00000355972
  gene symbol: ZMYND8
  hgvsc: ENST00000355972.4:c.1172T>C
  hgvsp: ENSP00000348246.4:p.Ile391Thr
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000361093
  ensembl transcript: ENST00000372023
  gene symbol: ZMYND8
  hgvsc: ENST00000372023.3:c.1157T>C
  hgvsp: ENSP00000361093.3:p.Ile386Thr
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000418495
  ensembl transcript: ENST00000467200
  gene symbol: ZMYND8
  hgvsc: ENST00000467200.2:c.951T>C
  hgvsp: ENSP00000418495.2:p.Ile318Thr
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000392964
  ensembl transcript: ENST00000458360
  gene symbol: ZMYND8
  hgvsc: ENST00000458360.2:c.1157T>C
  hgvsp: ENSP00000392964.2:p.Ile386Thr
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101040
  ensembl transcript: ENST00000468376
  gene symbol: ZMYND8
  hgvsc: ENST00000468376.2:n.1183T>C
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000420095
  ensembl transcript: ENST00000471951
  gene symbol: ZMYND8
  hgvsc: ENST00000471951.2:c.1232T>C
  hgvsp: ENSP00000420095.2:p.Ile411Thr
  variant of: http://identifiers.org/hgnc/9397
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11671
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4313
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 841
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1803
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile411Thr
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
population: Other
reference allele: A
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum

20-45905311-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45905311
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 45905311
    reference: chr 20
allele count: 1
allele frequency: 8.236689509752241e-6
allele num: 121408
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000443086
  ensembl transcript: ENST00000540497
  gene symbol: ZMYND8
  hgvsc: ENST00000540497.1:c.1152C>G
  hgvsp: ENST00000540497.1:c.1152C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000354166
  ensembl transcript: ENST00000360911
  gene symbol: ZMYND8
  hgvsc: ENST00000360911.3:c.1152C>G
  hgvsp: ENST00000360911.3:c.1152C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000379577
  ensembl transcript: ENST00000396281
  gene symbol: ZMYND8
  hgvsc: ENST00000396281.4:c.1167C>G
  hgvsp: ENST00000396281.4:c.1167C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000262975
  ensembl transcript: ENST00000262975
  gene symbol: ZMYND8
  hgvsc: ENST00000262975.4:c.1167C>G
  hgvsp: ENST00000262975.4:c.1167C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000312237
  ensembl transcript: ENST00000311275
  gene symbol: ZMYND8
  hgvsc: ENST00000311275.7:c.1167C>G
  hgvsp: ENST00000311275.7:c.1167C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000392964
  ensembl transcript: ENST00000458360
  gene symbol: ZMYND8
  hgvsc: ENST00000458360.2:c.1152C>G
  hgvsp: ENST00000458360.2:c.1152C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000361093
  ensembl transcript: ENST00000372023
  gene symbol: ZMYND8
  hgvsc: ENST00000372023.3:c.1152C>G
  hgvsp: ENST00000372023.3:c.1152C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000420095
  ensembl transcript: ENST00000471951
  gene symbol: ZMYND8
  hgvsc: ENST00000471951.2:c.1227C>G
  hgvsp: ENST00000471951.2:c.1227C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000396725
  ensembl transcript: ENST00000446994
  gene symbol: ZMYND8
  hgvsc: ENST00000446994.2:c.978C>G
  hgvsp: ENST00000446994.2:c.978C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000439800
  ensembl transcript: ENST00000536340
  gene symbol: ZMYND8
  hgvsc: ENST00000536340.1:c.1248C>G
  hgvsp: ENST00000536340.1:c.1248C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000348246
  ensembl transcript: ENST00000355972
  gene symbol: ZMYND8
  hgvsc: ENST00000355972.4:c.1167C>G
  hgvsp: ENST00000355972.4:c.1167C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000418210
  ensembl transcript: ENST00000461685
  gene symbol: ZMYND8
  hgvsc: ENST00000461685.1:c.1227C>G
  hgvsp: ENST00000461685.1:c.1227C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000418495
  ensembl transcript: ENST00000467200
  gene symbol: ZMYND8
  hgvsc: ENST00000467200.2:c.946C>G
  hgvsp: ENST00000467200.2:c.946C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000335537
  ensembl transcript: ENST00000352431
  gene symbol: ZMYND8
  hgvsc: ENST00000352431.2:c.1227C>G
  hgvsp: ENST00000352431.2:c.1227C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101040
  ensembl transcript: ENST00000468376
  gene symbol: ZMYND8
  hgvsc: ENST00000468376.2:n.1178C>G
  variant of: http://identifiers.org/hgnc/9397
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11674
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala409Ala
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: DP

20-45905319-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45905319
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 45905319
    reference: chr 20
allele count: 1
allele frequency: 8.236825198095647e-6
allele num: 121406
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101040
  ensembl transcript: ENST00000468376
  gene symbol: ZMYND8
  hgvsc: ENST00000468376.2:n.1170G>A
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000361093
  ensembl transcript: ENST00000372023
  gene symbol: ZMYND8
  hgvsc: ENST00000372023.3:c.1144G>A
  hgvsp: ENSP00000361093.3:p.Gly382Ser
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000354166
  ensembl transcript: ENST00000360911
  gene symbol: ZMYND8
  hgvsc: ENST00000360911.3:c.1144G>A
  hgvsp: ENSP00000354166.3:p.Gly382Ser
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000418210
  ensembl transcript: ENST00000461685
  gene symbol: ZMYND8
  hgvsc: ENST00000461685.1:c.1219G>A
  hgvsp: ENSP00000418210.1:p.Gly407Ser
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000262975
  ensembl transcript: ENST00000262975
  gene symbol: ZMYND8
  hgvsc: ENST00000262975.4:c.1159G>A
  hgvsp: ENSP00000262975.4:p.Gly387Ser
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000379577
  ensembl transcript: ENST00000396281
  gene symbol: ZMYND8
  hgvsc: ENST00000396281.4:c.1159G>A
  hgvsp: ENSP00000379577.4:p.Gly387Ser
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000335537
  ensembl transcript: ENST00000352431
  gene symbol: ZMYND8
  hgvsc: ENST00000352431.2:c.1219G>A
  hgvsp: ENSP00000335537.3:p.Gly407Ser
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000312237
  ensembl transcript: ENST00000311275
  gene symbol: ZMYND8
  hgvsc: ENST00000311275.7:c.1159G>A
  hgvsp: ENSP00000312237.7:p.Gly387Ser
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000348246
  ensembl transcript: ENST00000355972
  gene symbol: ZMYND8
  hgvsc: ENST00000355972.4:c.1159G>A
  hgvsp: ENSP00000348246.4:p.Gly387Ser
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000443086
  ensembl transcript: ENST00000540497
  gene symbol: ZMYND8
  hgvsc: ENST00000540497.1:c.1144G>A
  hgvsp: ENSP00000443086.1:p.Gly382Ser
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000418495
  ensembl transcript: ENST00000467200
  gene symbol: ZMYND8
  hgvsc: ENST00000467200.2:c.938G>A
  hgvsp: ENSP00000418495.2:p.Gly314Ser
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000396725
  ensembl transcript: ENST00000446994
  gene symbol: ZMYND8
  hgvsc: ENST00000446994.2:c.970G>A
  hgvsp: ENSP00000396725.2:p.Gly324Ser
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000439800
  ensembl transcript: ENST00000536340
  gene symbol: ZMYND8
  hgvsc: ENST00000536340.1:c.1240G>A
  hgvsp: ENSP00000439800.1:p.Gly414Ser
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000392964
  ensembl transcript: ENST00000458360
  gene symbol: ZMYND8
  hgvsc: ENST00000458360.2:c.1144G>A
  hgvsp: ENSP00000392964.2:p.Gly382Ser
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000420095
  ensembl transcript: ENST00000471951
  gene symbol: ZMYND8
  hgvsc: ENST00000471951.2:c.1219G>A
  hgvsp: ENSP00000420095.2:p.Gly407Ser
  variant of: http://identifiers.org/hgnc/9397
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 842
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22924
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4316
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly407Ser
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
population: African
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD

20-45905320-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45905320
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 45905320
    reference: chr 20
allele count: 2
allele frequency: 1.647283629295292e-5
allele num: 121412
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000418495
  ensembl transcript: ENST00000467200
  gene symbol: ZMYND8
  hgvsc: ENST00000467200.2:c.937C>T
  hgvsp: ENST00000467200.2:c.937C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000379577
  ensembl transcript: ENST00000396281
  gene symbol: ZMYND8
  hgvsc: ENST00000396281.4:c.1158C>T
  hgvsp: ENST00000396281.4:c.1158C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000420095
  ensembl transcript: ENST00000471951
  gene symbol: ZMYND8
  hgvsc: ENST00000471951.2:c.1218C>T
  hgvsp: ENST00000471951.2:c.1218C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000262975
  ensembl transcript: ENST00000262975
  gene symbol: ZMYND8
  hgvsc: ENST00000262975.4:c.1158C>T
  hgvsp: ENST00000262975.4:c.1158C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101040
  ensembl transcript: ENST00000468376
  gene symbol: ZMYND8
  hgvsc: ENST00000468376.2:n.1169C>T
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000418210
  ensembl transcript: ENST00000461685
  gene symbol: ZMYND8
  hgvsc: ENST00000461685.1:c.1218C>T
  hgvsp: ENST00000461685.1:c.1218C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000392964
  ensembl transcript: ENST00000458360
  gene symbol: ZMYND8
  hgvsc: ENST00000458360.2:c.1143C>T
  hgvsp: ENST00000458360.2:c.1143C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000335537
  ensembl transcript: ENST00000352431
  gene symbol: ZMYND8
  hgvsc: ENST00000352431.2:c.1218C>T
  hgvsp: ENST00000352431.2:c.1218C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000439800
  ensembl transcript: ENST00000536340
  gene symbol: ZMYND8
  hgvsc: ENST00000536340.1:c.1239C>T
  hgvsp: ENST00000536340.1:c.1239C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000361093
  ensembl transcript: ENST00000372023
  gene symbol: ZMYND8
  hgvsc: ENST00000372023.3:c.1143C>T
  hgvsp: ENST00000372023.3:c.1143C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000312237
  ensembl transcript: ENST00000311275
  gene symbol: ZMYND8
  hgvsc: ENST00000311275.7:c.1158C>T
  hgvsp: ENST00000311275.7:c.1158C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000396725
  ensembl transcript: ENST00000446994
  gene symbol: ZMYND8
  hgvsc: ENST00000446994.2:c.969C>T
  hgvsp: ENST00000446994.2:c.969C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000348246
  ensembl transcript: ENST00000355972
  gene symbol: ZMYND8
  hgvsc: ENST00000355972.4:c.1158C>T
  hgvsp: ENST00000355972.4:c.1158C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000443086
  ensembl transcript: ENST00000540497
  gene symbol: ZMYND8
  hgvsc: ENST00000540497.1:c.1143C>T
  hgvsp: ENST00000540497.1:c.1143C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000354166
  ensembl transcript: ENST00000360911
  gene symbol: ZMYND8
  hgvsc: ENST00000360911.3:c.1143C>T
  hgvsp: ENST00000360911.3:c.1143C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11673
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4316
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22925
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1808
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18072
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala406Ala
num of homozygotes: 0
population: Other
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: MQ
site quality: MQRankSum

20-45905320-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45905320
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 45905320
    reference: chr 20
allele count: 3
allele frequency: 2.470925443942938e-5
allele num: 121412
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000443086
  ensembl transcript: ENST00000540497
  gene symbol: ZMYND8
  hgvsc: ENST00000540497.1:c.1143C>A
  hgvsp: ENST00000540497.1:c.1143C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000354166
  ensembl transcript: ENST00000360911
  gene symbol: ZMYND8
  hgvsc: ENST00000360911.3:c.1143C>A
  hgvsp: ENST00000360911.3:c.1143C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101040
  ensembl transcript: ENST00000468376
  gene symbol: ZMYND8
  hgvsc: ENST00000468376.2:n.1169C>A
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000418495
  ensembl transcript: ENST00000467200
  gene symbol: ZMYND8
  hgvsc: ENST00000467200.2:c.937C>A
  hgvsp: ENST00000467200.2:c.937C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000348246
  ensembl transcript: ENST00000355972
  gene symbol: ZMYND8
  hgvsc: ENST00000355972.4:c.1158C>A
  hgvsp: ENST00000355972.4:c.1158C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000262975
  ensembl transcript: ENST00000262975
  gene symbol: ZMYND8
  hgvsc: ENST00000262975.4:c.1158C>A
  hgvsp: ENST00000262975.4:c.1158C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000418210
  ensembl transcript: ENST00000461685
  gene symbol: ZMYND8
  hgvsc: ENST00000461685.1:c.1218C>A
  hgvsp: ENST00000461685.1:c.1218C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000379577
  ensembl transcript: ENST00000396281
  gene symbol: ZMYND8
  hgvsc: ENST00000396281.4:c.1158C>A
  hgvsp: ENST00000396281.4:c.1158C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000392964
  ensembl transcript: ENST00000458360
  gene symbol: ZMYND8
  hgvsc: ENST00000458360.2:c.1143C>A
  hgvsp: ENST00000458360.2:c.1143C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000361093
  ensembl transcript: ENST00000372023
  gene symbol: ZMYND8
  hgvsc: ENST00000372023.3:c.1143C>A
  hgvsp: ENST00000372023.3:c.1143C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000420095
  ensembl transcript: ENST00000471951
  gene symbol: ZMYND8
  hgvsc: ENST00000471951.2:c.1218C>A
  hgvsp: ENST00000471951.2:c.1218C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000396725
  ensembl transcript: ENST00000446994
  gene symbol: ZMYND8
  hgvsc: ENST00000446994.2:c.969C>A
  hgvsp: ENST00000446994.2:c.969C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000439800
  ensembl transcript: ENST00000536340
  gene symbol: ZMYND8
  hgvsc: ENST00000536340.1:c.1239C>A
  hgvsp: ENST00000536340.1:c.1239C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000312237
  ensembl transcript: ENST00000311275
  gene symbol: ZMYND8
  hgvsc: ENST00000311275.7:c.1158C>A
  hgvsp: ENST00000311275.7:c.1158C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000335537
  ensembl transcript: ENST00000352431
  gene symbol: ZMYND8
  hgvsc: ENST00000352431.2:c.1218C>A
  hgvsp: ENST00000352431.2:c.1218C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 22925
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11673
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1808
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala406Ala
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: African
population: Other
population: Latino
population: East Asian
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: DP

20-45905322-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45905322
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 45905322
    reference: chr 20
allele count: 5
allele frequency: 4.118276912939626e-5
allele num: 121410
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000348246
  ensembl transcript: ENST00000355972
  gene symbol: ZMYND8
  hgvsc: ENST00000355972.4:c.1156G>A
  hgvsp: ENSP00000348246.4:p.Ala386Thr
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000443086
  ensembl transcript: ENST00000540497
  gene symbol: ZMYND8
  hgvsc: ENST00000540497.1:c.1141G>A
  hgvsp: ENSP00000443086.1:p.Ala381Thr
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000262975
  ensembl transcript: ENST00000262975
  gene symbol: ZMYND8
  hgvsc: ENST00000262975.4:c.1156G>A
  hgvsp: ENSP00000262975.4:p.Ala386Thr
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101040
  ensembl transcript: ENST00000468376
  gene symbol: ZMYND8
  hgvsc: ENST00000468376.2:n.1167G>A
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000312237
  ensembl transcript: ENST00000311275
  gene symbol: ZMYND8
  hgvsc: ENST00000311275.7:c.1156G>A
  hgvsp: ENSP00000312237.7:p.Ala386Thr
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000418210
  ensembl transcript: ENST00000461685
  gene symbol: ZMYND8
  hgvsc: ENST00000461685.1:c.1216G>A
  hgvsp: ENSP00000418210.1:p.Ala406Thr
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000396725
  ensembl transcript: ENST00000446994
  gene symbol: ZMYND8
  hgvsc: ENST00000446994.2:c.967G>A
  hgvsp: ENSP00000396725.2:p.Ala323Thr
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000418495
  ensembl transcript: ENST00000467200
  gene symbol: ZMYND8
  hgvsc: ENST00000467200.2:c.935G>A
  hgvsp: ENSP00000418495.2:p.Ala313Thr
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000354166
  ensembl transcript: ENST00000360911
  gene symbol: ZMYND8
  hgvsc: ENST00000360911.3:c.1141G>A
  hgvsp: ENSP00000354166.3:p.Ala381Thr
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000361093
  ensembl transcript: ENST00000372023
  gene symbol: ZMYND8
  hgvsc: ENST00000372023.3:c.1141G>A
  hgvsp: ENSP00000361093.3:p.Ala381Thr
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000420095
  ensembl transcript: ENST00000471951
  gene symbol: ZMYND8
  hgvsc: ENST00000471951.2:c.1216G>A
  hgvsp: ENSP00000420095.2:p.Ala406Thr
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000379577
  ensembl transcript: ENST00000396281
  gene symbol: ZMYND8
  hgvsc: ENST00000396281.4:c.1156G>A
  hgvsp: ENSP00000379577.4:p.Ala386Thr
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000439800
  ensembl transcript: ENST00000536340
  gene symbol: ZMYND8
  hgvsc: ENST00000536340.1:c.1237G>A
  hgvsp: ENSP00000439800.1:p.Ala413Thr
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000335537
  ensembl transcript: ENST00000352431
  gene symbol: ZMYND8
  hgvsc: ENST00000352431.2:c.1216G>A
  hgvsp: ENSP00000335537.3:p.Ala406Thr
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000392964
  ensembl transcript: ENST00000458360
  gene symbol: ZMYND8
  hgvsc: ENST00000458360.2:c.1141G>A
  hgvsp: ENSP00000392964.2:p.Ala381Thr
  variant of: http://identifiers.org/hgnc/9397
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22924
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 842
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11678
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18071
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala406Thr
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: QD

http://identifiers.org/exac.variant/20-45905322-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45905322
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 45905322
    reference: chr 20
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000348246
  ensembl transcript: ENST00000355972
  gene symbol: ZMYND8
  hgvsc: ENST00000355972.4:c.1156G>T
  hgvsp: ENSP00000348246.4:p.Ala386Ser
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000379577
  ensembl transcript: ENST00000396281
  gene symbol: ZMYND8
  hgvsc: ENST00000396281.4:c.1156G>T
  hgvsp: ENSP00000379577.4:p.Ala386Ser
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000420095
  ensembl transcript: ENST00000471951
  gene symbol: ZMYND8
  hgvsc: ENST00000471951.2:c.1216G>T
  hgvsp: ENSP00000420095.2:p.Ala406Ser
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000354166
  ensembl transcript: ENST00000360911
  gene symbol: ZMYND8
  hgvsc: ENST00000360911.3:c.1141G>T
  hgvsp: ENSP00000354166.3:p.Ala381Ser
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000443086
  ensembl transcript: ENST00000540497
  gene symbol: ZMYND8
  hgvsc: ENST00000540497.1:c.1141G>T
  hgvsp: ENSP00000443086.1:p.Ala381Ser
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000312237
  ensembl transcript: ENST00000311275
  gene symbol: ZMYND8
  hgvsc: ENST00000311275.7:c.1156G>T
  hgvsp: ENSP00000312237.7:p.Ala386Ser
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000439800
  ensembl transcript: ENST00000536340
  gene symbol: ZMYND8
  hgvsc: ENST00000536340.1:c.1237G>T
  hgvsp: ENSP00000439800.1:p.Ala413Ser
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000262975
  ensembl transcript: ENST00000262975
  gene symbol: ZMYND8
  hgvsc: ENST00000262975.4:c.1156G>T
  hgvsp: ENSP00000262975.4:p.Ala386Ser
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000418495
  ensembl transcript: ENST00000467200
  gene symbol: ZMYND8
  hgvsc: ENST00000467200.2:c.935G>T
  hgvsp: ENSP00000418495.2:p.Ala313Ser
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000335537
  ensembl transcript: ENST00000352431
  gene symbol: ZMYND8
  hgvsc: ENST00000352431.2:c.1216G>T
  hgvsp: ENSP00000335537.3:p.Ala406Ser
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000396725
  ensembl transcript: ENST00000446994
  gene symbol: ZMYND8
  hgvsc: ENST00000446994.2:c.967G>T
  hgvsp: ENSP00000396725.2:p.Ala323Ser
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000392964
  ensembl transcript: ENST00000458360
  gene symbol: ZMYND8
  hgvsc: ENST00000458360.2:c.1141G>T
  hgvsp: ENSP00000392964.2:p.Ala381Ser
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000418210
  ensembl transcript: ENST00000461685
  gene symbol: ZMYND8
  hgvsc: ENST00000461685.1:c.1216G>T
  hgvsp: ENSP00000418210.1:p.Ala406Ser
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101040
  ensembl transcript: ENST00000468376
  gene symbol: ZMYND8
  hgvsc: ENST00000468376.2:n.1167G>T
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000361093
  ensembl transcript: ENST00000372023
  gene symbol: ZMYND8
  hgvsc: ENST00000372023.3:c.1141G>T
  hgvsp: ENSP00000361093.3:p.Ala381Ser
  variant of: http://identifiers.org/hgnc/9397
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18071
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 842
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala406Ser
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
population: European (Finnish)
population: Latino
population: African
reference allele: C
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: DP

20-45905323-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45905323
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 45905323
    reference: chr 20
allele count: 1
allele frequency: 8.236689509752241e-6
allele num: 121408
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000418210
  ensembl transcript: ENST00000461685
  gene symbol: ZMYND8
  hgvsc: ENST00000461685.1:c.1215C>T
  hgvsp: ENST00000461685.1:c.1215C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000312237
  ensembl transcript: ENST00000311275
  gene symbol: ZMYND8
  hgvsc: ENST00000311275.7:c.1155C>T
  hgvsp: ENST00000311275.7:c.1155C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000418495
  ensembl transcript: ENST00000467200
  gene symbol: ZMYND8
  hgvsc: ENST00000467200.2:c.934C>T
  hgvsp: ENST00000467200.2:c.934C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000335537
  ensembl transcript: ENST00000352431
  gene symbol: ZMYND8
  hgvsc: ENST00000352431.2:c.1215C>T
  hgvsp: ENST00000352431.2:c.1215C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101040
  ensembl transcript: ENST00000468376
  gene symbol: ZMYND8
  hgvsc: ENST00000468376.2:n.1166C>T
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000348246
  ensembl transcript: ENST00000355972
  gene symbol: ZMYND8
  hgvsc: ENST00000355972.4:c.1155C>T
  hgvsp: ENST00000355972.4:c.1155C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000361093
  ensembl transcript: ENST00000372023
  gene symbol: ZMYND8
  hgvsc: ENST00000372023.3:c.1140C>T
  hgvsp: ENST00000372023.3:c.1140C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000354166
  ensembl transcript: ENST00000360911
  gene symbol: ZMYND8
  hgvsc: ENST00000360911.3:c.1140C>T
  hgvsp: ENST00000360911.3:c.1140C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000379577
  ensembl transcript: ENST00000396281
  gene symbol: ZMYND8
  hgvsc: ENST00000396281.4:c.1155C>T
  hgvsp: ENST00000396281.4:c.1155C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000443086
  ensembl transcript: ENST00000540497
  gene symbol: ZMYND8
  hgvsc: ENST00000540497.1:c.1140C>T
  hgvsp: ENST00000540497.1:c.1140C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000396725
  ensembl transcript: ENST00000446994
  gene symbol: ZMYND8
  hgvsc: ENST00000446994.2:c.966C>T
  hgvsp: ENST00000446994.2:c.966C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000439800
  ensembl transcript: ENST00000536340
  gene symbol: ZMYND8
  hgvsc: ENST00000536340.1:c.1236C>T
  hgvsp: ENST00000536340.1:c.1236C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000392964
  ensembl transcript: ENST00000458360
  gene symbol: ZMYND8
  hgvsc: ENST00000458360.2:c.1140C>T
  hgvsp: ENST00000458360.2:c.1140C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000420095
  ensembl transcript: ENST00000471951
  gene symbol: ZMYND8
  hgvsc: ENST00000471951.2:c.1215C>T
  hgvsp: ENST00000471951.2:c.1215C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000262975
  ensembl transcript: ENST00000262975
  gene symbol: ZMYND8
  hgvsc: ENST00000262975.4:c.1155C>T
  hgvsp: ENST00000262975.4:c.1155C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22927
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 842
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11678
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser405Ser
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD

20-45905329-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45905329
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 45905329
    reference: chr 20
allele count: 1
allele frequency: 8.236689509752241e-6
allele num: 121408
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000312237
  ensembl transcript: ENST00000311275
  gene symbol: ZMYND8
  hgvsc: ENST00000311275.7:c.1149C>T
  hgvsp: ENST00000311275.7:c.1149C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101040
  ensembl transcript: ENST00000468376
  gene symbol: ZMYND8
  hgvsc: ENST00000468376.2:n.1160C>T
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000379577
  ensembl transcript: ENST00000396281
  gene symbol: ZMYND8
  hgvsc: ENST00000396281.4:c.1149C>T
  hgvsp: ENST00000396281.4:c.1149C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000262975
  ensembl transcript: ENST00000262975
  gene symbol: ZMYND8
  hgvsc: ENST00000262975.4:c.1149C>T
  hgvsp: ENST00000262975.4:c.1149C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000418210
  ensembl transcript: ENST00000461685
  gene symbol: ZMYND8
  hgvsc: ENST00000461685.1:c.1209C>T
  hgvsp: ENST00000461685.1:c.1209C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000354166
  ensembl transcript: ENST00000360911
  gene symbol: ZMYND8
  hgvsc: ENST00000360911.3:c.1134C>T
  hgvsp: ENST00000360911.3:c.1134C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000361093
  ensembl transcript: ENST00000372023
  gene symbol: ZMYND8
  hgvsc: ENST00000372023.3:c.1134C>T
  hgvsp: ENST00000372023.3:c.1134C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000348246
  ensembl transcript: ENST00000355972
  gene symbol: ZMYND8
  hgvsc: ENST00000355972.4:c.1149C>T
  hgvsp: ENST00000355972.4:c.1149C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000420095
  ensembl transcript: ENST00000471951
  gene symbol: ZMYND8
  hgvsc: ENST00000471951.2:c.1209C>T
  hgvsp: ENST00000471951.2:c.1209C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000439800
  ensembl transcript: ENST00000536340
  gene symbol: ZMYND8
  hgvsc: ENST00000536340.1:c.1230C>T
  hgvsp: ENST00000536340.1:c.1230C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000335537
  ensembl transcript: ENST00000352431
  gene symbol: ZMYND8
  hgvsc: ENST00000352431.2:c.1209C>T
  hgvsp: ENST00000352431.2:c.1209C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000392964
  ensembl transcript: ENST00000458360
  gene symbol: ZMYND8
  hgvsc: ENST00000458360.2:c.1134C>T
  hgvsp: ENST00000458360.2:c.1134C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000443086
  ensembl transcript: ENST00000540497
  gene symbol: ZMYND8
  hgvsc: ENST00000540497.1:c.1134C>T
  hgvsp: ENST00000540497.1:c.1134C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000418495
  ensembl transcript: ENST00000467200
  gene symbol: ZMYND8
  hgvsc: ENST00000467200.2:c.928C>T
  hgvsp: ENST00000467200.2:c.928C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000396725
  ensembl transcript: ENST00000446994
  gene symbol: ZMYND8
  hgvsc: ENST00000446994.2:c.960C>T
  hgvsp: ENST00000446994.2:c.960C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1808
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn403Asn
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: ReadPosRankSum

20-45905330-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45905330
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 45905330
    reference: chr 20
allele count: 1
allele frequency: 8.236825198095647e-6
allele num: 121406
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000361093
  ensembl transcript: ENST00000372023
  gene symbol: ZMYND8
  hgvsc: ENST00000372023.3:c.1133A>G
  hgvsp: ENSP00000361093.3:p.Asn378Ser
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000396725
  ensembl transcript: ENST00000446994
  gene symbol: ZMYND8
  hgvsc: ENST00000446994.2:c.959A>G
  hgvsp: ENSP00000396725.2:p.Asn320Ser
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000443086
  ensembl transcript: ENST00000540497
  gene symbol: ZMYND8
  hgvsc: ENST00000540497.1:c.1133A>G
  hgvsp: ENSP00000443086.1:p.Asn378Ser
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000392964
  ensembl transcript: ENST00000458360
  gene symbol: ZMYND8
  hgvsc: ENST00000458360.2:c.1133A>G
  hgvsp: ENSP00000392964.2:p.Asn378Ser
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000418495
  ensembl transcript: ENST00000467200
  gene symbol: ZMYND8
  hgvsc: ENST00000467200.2:c.927A>G
  hgvsp: ENSP00000418495.2:p.Asn310Ser
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000312237
  ensembl transcript: ENST00000311275
  gene symbol: ZMYND8
  hgvsc: ENST00000311275.7:c.1148A>G
  hgvsp: ENSP00000312237.7:p.Asn383Ser
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000348246
  ensembl transcript: ENST00000355972
  gene symbol: ZMYND8
  hgvsc: ENST00000355972.4:c.1148A>G
  hgvsp: ENSP00000348246.4:p.Asn383Ser
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101040
  ensembl transcript: ENST00000468376
  gene symbol: ZMYND8
  hgvsc: ENST00000468376.2:n.1159A>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000439800
  ensembl transcript: ENST00000536340
  gene symbol: ZMYND8
  hgvsc: ENST00000536340.1:c.1229A>G
  hgvsp: ENSP00000439800.1:p.Asn410Ser
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000335537
  ensembl transcript: ENST00000352431
  gene symbol: ZMYND8
  hgvsc: ENST00000352431.2:c.1208A>G
  hgvsp: ENSP00000335537.3:p.Asn403Ser
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000418210
  ensembl transcript: ENST00000461685
  gene symbol: ZMYND8
  hgvsc: ENST00000461685.1:c.1208A>G
  hgvsp: ENSP00000418210.1:p.Asn403Ser
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000420095
  ensembl transcript: ENST00000471951
  gene symbol: ZMYND8
  hgvsc: ENST00000471951.2:c.1208A>G
  hgvsp: ENSP00000420095.2:p.Asn403Ser
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000354166
  ensembl transcript: ENST00000360911
  gene symbol: ZMYND8
  hgvsc: ENST00000360911.3:c.1133A>G
  hgvsp: ENSP00000354166.3:p.Asn378Ser
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000262975
  ensembl transcript: ENST00000262975
  gene symbol: ZMYND8
  hgvsc: ENST00000262975.4:c.1148A>G
  hgvsp: ENSP00000262975.4:p.Asn383Ser
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000379577
  ensembl transcript: ENST00000396281
  gene symbol: ZMYND8
  hgvsc: ENST00000396281.4:c.1148A>G
  hgvsp: ENSP00000379577.4:p.Asn383Ser
  variant of: http://identifiers.org/hgnc/9397
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18065
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1808
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11681
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn403Ser
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: African
population: East Asian
reference allele: T
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum

20-45905332-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45905332
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 45905332
    reference: chr 20
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000262975
  ensembl transcript: ENST00000262975
  gene symbol: ZMYND8
  hgvsc: ENST00000262975.4:c.1146C>T
  hgvsp: ENST00000262975.4:c.1146C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000418495
  ensembl transcript: ENST00000467200
  gene symbol: ZMYND8
  hgvsc: ENST00000467200.2:c.925C>T
  hgvsp: ENST00000467200.2:c.925C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000348246
  ensembl transcript: ENST00000355972
  gene symbol: ZMYND8
  hgvsc: ENST00000355972.4:c.1146C>T
  hgvsp: ENST00000355972.4:c.1146C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000361093
  ensembl transcript: ENST00000372023
  gene symbol: ZMYND8
  hgvsc: ENST00000372023.3:c.1131C>T
  hgvsp: ENST00000372023.3:c.1131C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000354166
  ensembl transcript: ENST00000360911
  gene symbol: ZMYND8
  hgvsc: ENST00000360911.3:c.1131C>T
  hgvsp: ENST00000360911.3:c.1131C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000418210
  ensembl transcript: ENST00000461685
  gene symbol: ZMYND8
  hgvsc: ENST00000461685.1:c.1206C>T
  hgvsp: ENST00000461685.1:c.1206C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000392964
  ensembl transcript: ENST00000458360
  gene symbol: ZMYND8
  hgvsc: ENST00000458360.2:c.1131C>T
  hgvsp: ENST00000458360.2:c.1131C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000443086
  ensembl transcript: ENST00000540497
  gene symbol: ZMYND8
  hgvsc: ENST00000540497.1:c.1131C>T
  hgvsp: ENST00000540497.1:c.1131C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000379577
  ensembl transcript: ENST00000396281
  gene symbol: ZMYND8
  hgvsc: ENST00000396281.4:c.1146C>T
  hgvsp: ENST00000396281.4:c.1146C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000439800
  ensembl transcript: ENST00000536340
  gene symbol: ZMYND8
  hgvsc: ENST00000536340.1:c.1227C>T
  hgvsp: ENST00000536340.1:c.1227C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000312237
  ensembl transcript: ENST00000311275
  gene symbol: ZMYND8
  hgvsc: ENST00000311275.7:c.1146C>T
  hgvsp: ENST00000311275.7:c.1146C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000396725
  ensembl transcript: ENST00000446994
  gene symbol: ZMYND8
  hgvsc: ENST00000446994.2:c.957C>T
  hgvsp: ENST00000446994.2:c.957C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101040
  ensembl transcript: ENST00000468376
  gene symbol: ZMYND8
  hgvsc: ENST00000468376.2:n.1157C>T
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000420095
  ensembl transcript: ENST00000471951
  gene symbol: ZMYND8
  hgvsc: ENST00000471951.2:c.1206C>T
  hgvsp: ENST00000471951.2:c.1206C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000335537
  ensembl transcript: ENST00000352431
  gene symbol: ZMYND8
  hgvsc: ENST00000352431.2:c.1206C>T
  hgvsp: ENST00000352431.2:c.1206C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 842
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22931
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr402Thr
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
population: Other
reference allele: G
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: DP

20-45905341-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45905341
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 45905341
    reference: chr 20
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000354166
  ensembl transcript: ENST00000360911
  gene symbol: ZMYND8
  hgvsc: ENST00000360911.3:c.1122C>T
  hgvsp: ENST00000360911.3:c.1122C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000443086
  ensembl transcript: ENST00000540497
  gene symbol: ZMYND8
  hgvsc: ENST00000540497.1:c.1122C>T
  hgvsp: ENST00000540497.1:c.1122C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000348246
  ensembl transcript: ENST00000355972
  gene symbol: ZMYND8
  hgvsc: ENST00000355972.4:c.1137C>T
  hgvsp: ENST00000355972.4:c.1137C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000361093
  ensembl transcript: ENST00000372023
  gene symbol: ZMYND8
  hgvsc: ENST00000372023.3:c.1122C>T
  hgvsp: ENST00000372023.3:c.1122C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000262975
  ensembl transcript: ENST00000262975
  gene symbol: ZMYND8
  hgvsc: ENST00000262975.4:c.1137C>T
  hgvsp: ENST00000262975.4:c.1137C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000335537
  ensembl transcript: ENST00000352431
  gene symbol: ZMYND8
  hgvsc: ENST00000352431.2:c.1197C>T
  hgvsp: ENST00000352431.2:c.1197C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000418210
  ensembl transcript: ENST00000461685
  gene symbol: ZMYND8
  hgvsc: ENST00000461685.1:c.1197C>T
  hgvsp: ENST00000461685.1:c.1197C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000420095
  ensembl transcript: ENST00000471951
  gene symbol: ZMYND8
  hgvsc: ENST00000471951.2:c.1197C>T
  hgvsp: ENST00000471951.2:c.1197C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000392964
  ensembl transcript: ENST00000458360
  gene symbol: ZMYND8
  hgvsc: ENST00000458360.2:c.1122C>T
  hgvsp: ENST00000458360.2:c.1122C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000439800
  ensembl transcript: ENST00000536340
  gene symbol: ZMYND8
  hgvsc: ENST00000536340.1:c.1218C>T
  hgvsp: ENST00000536340.1:c.1218C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000418495
  ensembl transcript: ENST00000467200
  gene symbol: ZMYND8
  hgvsc: ENST00000467200.2:c.916C>T
  hgvsp: ENST00000467200.2:c.916C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000379577
  ensembl transcript: ENST00000396281
  gene symbol: ZMYND8
  hgvsc: ENST00000396281.4:c.1137C>T
  hgvsp: ENST00000396281.4:c.1137C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000312237
  ensembl transcript: ENST00000311275
  gene symbol: ZMYND8
  hgvsc: ENST00000311275.7:c.1137C>T
  hgvsp: ENST00000311275.7:c.1137C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101040
  ensembl transcript: ENST00000468376
  gene symbol: ZMYND8
  hgvsc: ENST00000468376.2:n.1148C>T
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000396725
  ensembl transcript: ENST00000446994
  gene symbol: ZMYND8
  hgvsc: ENST00000446994.2:c.948C>T
  hgvsp: ENST00000446994.2:c.948C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 841
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11690
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18044
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu399Leu
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Latino
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum

20-45905354-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45905354
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 45905354
    reference: chr 20
allele count: 1
allele frequency: 8.236418146476461e-6
allele num: 121412
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000418210
  ensembl transcript: ENST00000461685
  gene symbol: ZMYND8
  hgvsc: ENST00000461685.1:c.1184A>G
  hgvsp: ENSP00000418210.1:p.Tyr395Cys
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000420095
  ensembl transcript: ENST00000471951
  gene symbol: ZMYND8
  hgvsc: ENST00000471951.2:c.1184A>G
  hgvsp: ENSP00000420095.2:p.Tyr395Cys
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000335537
  ensembl transcript: ENST00000352431
  gene symbol: ZMYND8
  hgvsc: ENST00000352431.2:c.1184A>G
  hgvsp: ENSP00000335537.3:p.Tyr395Cys
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000443086
  ensembl transcript: ENST00000540497
  gene symbol: ZMYND8
  hgvsc: ENST00000540497.1:c.1109A>G
  hgvsp: ENSP00000443086.1:p.Tyr370Cys
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000396725
  ensembl transcript: ENST00000446994
  gene symbol: ZMYND8
  hgvsc: ENST00000446994.2:c.935A>G
  hgvsp: ENSP00000396725.2:p.Tyr312Cys
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000418495
  ensembl transcript: ENST00000467200
  gene symbol: ZMYND8
  hgvsc: ENST00000467200.2:c.903A>G
  hgvsp: ENSP00000418495.2:p.Tyr302Cys
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000312237
  ensembl transcript: ENST00000311275
  gene symbol: ZMYND8
  hgvsc: ENST00000311275.7:c.1124A>G
  hgvsp: ENSP00000312237.7:p.Tyr375Cys
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000361093
  ensembl transcript: ENST00000372023
  gene symbol: ZMYND8
  hgvsc: ENST00000372023.3:c.1109A>G
  hgvsp: ENSP00000361093.3:p.Tyr370Cys
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000392964
  ensembl transcript: ENST00000458360
  gene symbol: ZMYND8
  hgvsc: ENST00000458360.2:c.1109A>G
  hgvsp: ENSP00000392964.2:p.Tyr370Cys
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000354166
  ensembl transcript: ENST00000360911
  gene symbol: ZMYND8
  hgvsc: ENST00000360911.3:c.1109A>G
  hgvsp: ENSP00000354166.3:p.Tyr370Cys
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000348246
  ensembl transcript: ENST00000355972
  gene symbol: ZMYND8
  hgvsc: ENST00000355972.4:c.1124A>G
  hgvsp: ENSP00000348246.4:p.Tyr375Cys
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000262975
  ensembl transcript: ENST00000262975
  gene symbol: ZMYND8
  hgvsc: ENST00000262975.4:c.1124A>G
  hgvsp: ENSP00000262975.4:p.Tyr375Cys
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101040
  ensembl transcript: ENST00000468376
  gene symbol: ZMYND8
  hgvsc: ENST00000468376.2:n.1135A>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000439800
  ensembl transcript: ENST00000536340
  gene symbol: ZMYND8
  hgvsc: ENST00000536340.1:c.1205A>G
  hgvsp: ENSP00000439800.1:p.Tyr402Cys
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000379577
  ensembl transcript: ENST00000396281
  gene symbol: ZMYND8
  hgvsc: ENST00000396281.4:c.1124A>G
  hgvsp: ENSP00000379577.4:p.Tyr375Cys
  variant of: http://identifiers.org/hgnc/9397
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 22946
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18043
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11693
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Tyr395Cys
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
reference allele: T
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: MQ

20-45905359-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45905359
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 45905359
    reference: chr 20
allele count: 2
allele frequency: 1.647283629295292e-5
allele num: 121412
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000379577
  ensembl transcript: ENST00000396281
  gene symbol: ZMYND8
  hgvsc: ENST00000396281.4:c.1119C>T
  hgvsp: ENST00000396281.4:c.1119C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000354166
  ensembl transcript: ENST00000360911
  gene symbol: ZMYND8
  hgvsc: ENST00000360911.3:c.1104C>T
  hgvsp: ENST00000360911.3:c.1104C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000312237
  ensembl transcript: ENST00000311275
  gene symbol: ZMYND8
  hgvsc: ENST00000311275.7:c.1119C>T
  hgvsp: ENST00000311275.7:c.1119C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000262975
  ensembl transcript: ENST00000262975
  gene symbol: ZMYND8
  hgvsc: ENST00000262975.4:c.1119C>T
  hgvsp: ENST00000262975.4:c.1119C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000420095
  ensembl transcript: ENST00000471951
  gene symbol: ZMYND8
  hgvsc: ENST00000471951.2:c.1179C>T
  hgvsp: ENST00000471951.2:c.1179C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000392964
  ensembl transcript: ENST00000458360
  gene symbol: ZMYND8
  hgvsc: ENST00000458360.2:c.1104C>T
  hgvsp: ENST00000458360.2:c.1104C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000439800
  ensembl transcript: ENST00000536340
  gene symbol: ZMYND8
  hgvsc: ENST00000536340.1:c.1200C>T
  hgvsp: ENST00000536340.1:c.1200C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000418210
  ensembl transcript: ENST00000461685
  gene symbol: ZMYND8
  hgvsc: ENST00000461685.1:c.1179C>T
  hgvsp: ENST00000461685.1:c.1179C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000361093
  ensembl transcript: ENST00000372023
  gene symbol: ZMYND8
  hgvsc: ENST00000372023.3:c.1104C>T
  hgvsp: ENST00000372023.3:c.1104C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000335537
  ensembl transcript: ENST00000352431
  gene symbol: ZMYND8
  hgvsc: ENST00000352431.2:c.1179C>T
  hgvsp: ENST00000352431.2:c.1179C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000396725
  ensembl transcript: ENST00000446994
  gene symbol: ZMYND8
  hgvsc: ENST00000446994.2:c.930C>T
  hgvsp: ENST00000446994.2:c.930C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000348246
  ensembl transcript: ENST00000355972
  gene symbol: ZMYND8
  hgvsc: ENST00000355972.4:c.1119C>T
  hgvsp: ENST00000355972.4:c.1119C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000418495
  ensembl transcript: ENST00000467200
  gene symbol: ZMYND8
  hgvsc: ENST00000467200.2:c.898C>T
  hgvsp: ENST00000467200.2:c.898C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101040
  ensembl transcript: ENST00000468376
  gene symbol: ZMYND8
  hgvsc: ENST00000468376.2:n.1130C>T
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000443086
  ensembl transcript: ENST00000540497
  gene symbol: ZMYND8
  hgvsc: ENST00000540497.1:c.1104C>T
  hgvsp: ENST00000540497.1:c.1104C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1808
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4316
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11695
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 841
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser393Ser
num of homozygotes: 0
population: South Asian
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum

20-45905362-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45905362
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 45905362
    reference: chr 20
allele count: 4
allele frequency: 3.311367926090268e-5
allele num: 120796
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000439800
  ensembl transcript: ENST00000536340
  gene symbol: ZMYND8
  hgvsc: ENST00000536340.1:c.1197C>T
  hgvsp: ENST00000536340.1:c.1197C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000361093
  ensembl transcript: ENST00000372023
  gene symbol: ZMYND8
  hgvsc: ENST00000372023.3:c.1101C>T
  hgvsp: ENST00000372023.3:c.1101C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000392964
  ensembl transcript: ENST00000458360
  gene symbol: ZMYND8
  hgvsc: ENST00000458360.2:c.1101C>T
  hgvsp: ENST00000458360.2:c.1101C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000335537
  ensembl transcript: ENST00000352431
  gene symbol: ZMYND8
  hgvsc: ENST00000352431.2:c.1176C>T
  hgvsp: ENST00000352431.2:c.1176C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000354166
  ensembl transcript: ENST00000360911
  gene symbol: ZMYND8
  hgvsc: ENST00000360911.3:c.1101C>T
  hgvsp: ENST00000360911.3:c.1101C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000348246
  ensembl transcript: ENST00000355972
  gene symbol: ZMYND8
  hgvsc: ENST00000355972.4:c.1116C>T
  hgvsp: ENST00000355972.4:c.1116C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000420095
  ensembl transcript: ENST00000471951
  gene symbol: ZMYND8
  hgvsc: ENST00000471951.2:c.1176C>T
  hgvsp: ENST00000471951.2:c.1176C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000396725
  ensembl transcript: ENST00000446994
  gene symbol: ZMYND8
  hgvsc: ENST00000446994.2:c.927C>T
  hgvsp: ENST00000446994.2:c.927C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000418495
  ensembl transcript: ENST00000467200
  gene symbol: ZMYND8
  hgvsc: ENST00000467200.2:c.895C>T
  hgvsp: ENST00000467200.2:c.895C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000312237
  ensembl transcript: ENST00000311275
  gene symbol: ZMYND8
  hgvsc: ENST00000311275.7:c.1116C>T
  hgvsp: ENST00000311275.7:c.1116C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000262975
  ensembl transcript: ENST00000262975
  gene symbol: ZMYND8
  hgvsc: ENST00000262975.4:c.1116C>T
  hgvsp: ENST00000262975.4:c.1116C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000418210
  ensembl transcript: ENST00000461685
  gene symbol: ZMYND8
  hgvsc: ENST00000461685.1:c.1176C>T
  hgvsp: ENST00000461685.1:c.1176C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000379577
  ensembl transcript: ENST00000396281
  gene symbol: ZMYND8
  hgvsc: ENST00000396281.4:c.1116C>T
  hgvsp: ENST00000396281.4:c.1116C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000443086
  ensembl transcript: ENST00000540497
  gene symbol: ZMYND8
  hgvsc: ENST00000540497.1:c.1101C>T
  hgvsp: ENST00000540497.1:c.1101C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101040
  ensembl transcript: ENST00000468376
  gene symbol: ZMYND8
  hgvsc: ENST00000468376.2:n.1127C>T
  variant of: http://identifiers.org/hgnc/9397
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4046
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1645
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 748
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22546
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn392Asn
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

20-45905363-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45905363
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 45905363
    reference: chr 20
allele count: 2201
allele frequency: 1.834778259419807e-2
allele num: 119960
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000354166
  ensembl transcript: ENST00000360911
  gene symbol: ZMYND8
  hgvsc: ENST00000360911.3:c.1100A>C
  hgvsp: ENSP00000354166.3:p.Asn367Thr
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000379577
  ensembl transcript: ENST00000396281
  gene symbol: ZMYND8
  hgvsc: ENST00000396281.4:c.1115A>C
  hgvsp: ENSP00000379577.4:p.Asn372Thr
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000396725
  ensembl transcript: ENST00000446994
  gene symbol: ZMYND8
  hgvsc: ENST00000446994.2:c.926A>C
  hgvsp: ENSP00000396725.2:p.Asn309Thr
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000312237
  ensembl transcript: ENST00000311275
  gene symbol: ZMYND8
  hgvsc: ENST00000311275.7:c.1115A>C
  hgvsp: ENSP00000312237.7:p.Asn372Thr
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000262975
  ensembl transcript: ENST00000262975
  gene symbol: ZMYND8
  hgvsc: ENST00000262975.4:c.1115A>C
  hgvsp: ENSP00000262975.4:p.Asn372Thr
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000348246
  ensembl transcript: ENST00000355972
  gene symbol: ZMYND8
  hgvsc: ENST00000355972.4:c.1115A>C
  hgvsp: ENSP00000348246.4:p.Asn372Thr
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000443086
  ensembl transcript: ENST00000540497
  gene symbol: ZMYND8
  hgvsc: ENST00000540497.1:c.1100A>C
  hgvsp: ENSP00000443086.1:p.Asn367Thr
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000418495
  ensembl transcript: ENST00000467200
  gene symbol: ZMYND8
  hgvsc: ENST00000467200.2:c.894A>C
  hgvsp: ENSP00000418495.2:p.Asn299Thr
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000392964
  ensembl transcript: ENST00000458360
  gene symbol: ZMYND8
  hgvsc: ENST00000458360.2:c.1100A>C
  hgvsp: ENSP00000392964.2:p.Asn367Thr
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101040
  ensembl transcript: ENST00000468376
  gene symbol: ZMYND8
  hgvsc: ENST00000468376.2:n.1126A>C
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000335537
  ensembl transcript: ENST00000352431
  gene symbol: ZMYND8
  hgvsc: ENST00000352431.2:c.1175A>C
  hgvsp: ENSP00000335537.3:p.Asn392Thr
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000418210
  ensembl transcript: ENST00000461685
  gene symbol: ZMYND8
  hgvsc: ENST00000461685.1:c.1175A>C
  hgvsp: ENSP00000418210.1:p.Asn392Thr
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000361093
  ensembl transcript: ENST00000372023
  gene symbol: ZMYND8
  hgvsc: ENST00000372023.3:c.1100A>C
  hgvsp: ENSP00000361093.3:p.Asn367Thr
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000439800
  ensembl transcript: ENST00000536340
  gene symbol: ZMYND8
  hgvsc: ENST00000536340.1:c.1196A>C
  hgvsp: ENSP00000439800.1:p.Asn399Thr
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000420095
  ensembl transcript: ENST00000471951
  gene symbol: ZMYND8
  hgvsc: ENST00000471951.2:c.1175A>C
  hgvsp: ENSP00000420095.2:p.Asn392Thr
  variant of: http://identifiers.org/hgnc/9397
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.95to100.00
genotype depth: GenotypeDepth
  all individuals: 3308
  bin: 9.75e1
  variant carriers: 2234
genotype depth: GenotypeDepth
  all individuals: 22031
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 6.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 11119
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.75e1
  variant carriers: 10
genotype quality: GenotypeQuality
hgvs: p.Asn392Thr
num of homozygotes: 0
population: East Asian
population: Latino
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: QD

20-45905368-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45905368
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 45905368
    reference: chr 20
allele count: 47
allele frequency: 3.871371618727555e-4
allele num: 121404
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000379577
  ensembl transcript: ENST00000396281
  gene symbol: ZMYND8
  hgvsc: ENST00000396281.4:c.1110A>C
  hgvsp: ENST00000396281.4:c.1110A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000439800
  ensembl transcript: ENST00000536340
  gene symbol: ZMYND8
  hgvsc: ENST00000536340.1:c.1191A>C
  hgvsp: ENST00000536340.1:c.1191A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101040
  ensembl transcript: ENST00000468376
  gene symbol: ZMYND8
  hgvsc: ENST00000468376.2:n.1121A>C
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000443086
  ensembl transcript: ENST00000540497
  gene symbol: ZMYND8
  hgvsc: ENST00000540497.1:c.1095A>C
  hgvsp: ENST00000540497.1:c.1095A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000262975
  ensembl transcript: ENST00000262975
  gene symbol: ZMYND8
  hgvsc: ENST00000262975.4:c.1110A>C
  hgvsp: ENST00000262975.4:c.1110A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000348246
  ensembl transcript: ENST00000355972
  gene symbol: ZMYND8
  hgvsc: ENST00000355972.4:c.1110A>C
  hgvsp: ENST00000355972.4:c.1110A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000361093
  ensembl transcript: ENST00000372023
  gene symbol: ZMYND8
  hgvsc: ENST00000372023.3:c.1095A>C
  hgvsp: ENST00000372023.3:c.1095A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000418210
  ensembl transcript: ENST00000461685
  gene symbol: ZMYND8
  hgvsc: ENST00000461685.1:c.1170A>C
  hgvsp: ENST00000461685.1:c.1170A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000335537
  ensembl transcript: ENST00000352431
  gene symbol: ZMYND8
  hgvsc: ENST00000352431.2:c.1170A>C
  hgvsp: ENST00000352431.2:c.1170A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000354166
  ensembl transcript: ENST00000360911
  gene symbol: ZMYND8
  hgvsc: ENST00000360911.3:c.1095A>C
  hgvsp: ENST00000360911.3:c.1095A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000312237
  ensembl transcript: ENST00000311275
  gene symbol: ZMYND8
  hgvsc: ENST00000311275.7:c.1110A>C
  hgvsp: ENST00000311275.7:c.1110A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000392964
  ensembl transcript: ENST00000458360
  gene symbol: ZMYND8
  hgvsc: ENST00000458360.2:c.1095A>C
  hgvsp: ENST00000458360.2:c.1095A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000396725
  ensembl transcript: ENST00000446994
  gene symbol: ZMYND8
  hgvsc: ENST00000446994.2:c.921A>C
  hgvsp: ENST00000446994.2:c.921A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000418495
  ensembl transcript: ENST00000467200
  gene symbol: ZMYND8
  hgvsc: ENST00000467200.2:c.889A>C
  hgvsp: ENST00000467200.2:c.889A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000420095
  ensembl transcript: ENST00000471951
  gene symbol: ZMYND8
  hgvsc: ENST00000471951.2:c.1170A>C
  hgvsp: ENST00000471951.2:c.1170A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.90to99.95
genotype depth: GenotypeDepth
  all individuals: 901
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 9.75e1
  variant carriers: 44
genotype depth: GenotypeDepth
  all individuals: 22499
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1788
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr390Thr
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
population: African
population: European (Finnish)
reference allele: T
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum

20-45905371-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45905371
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 45905371
    reference: chr 20
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101040
  ensembl transcript: ENST00000468376
  gene symbol: ZMYND8
  hgvsc: ENST00000468376.2:n.1118C>T
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000418210
  ensembl transcript: ENST00000461685
  gene symbol: ZMYND8
  hgvsc: ENST00000461685.1:c.1167C>T
  hgvsp: ENST00000461685.1:c.1167C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000348246
  ensembl transcript: ENST00000355972
  gene symbol: ZMYND8
  hgvsc: ENST00000355972.4:c.1107C>T
  hgvsp: ENST00000355972.4:c.1107C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000379577
  ensembl transcript: ENST00000396281
  gene symbol: ZMYND8
  hgvsc: ENST00000396281.4:c.1107C>T
  hgvsp: ENST00000396281.4:c.1107C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000396725
  ensembl transcript: ENST00000446994
  gene symbol: ZMYND8
  hgvsc: ENST00000446994.2:c.918C>T
  hgvsp: ENST00000446994.2:c.918C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000361093
  ensembl transcript: ENST00000372023
  gene symbol: ZMYND8
  hgvsc: ENST00000372023.3:c.1092C>T
  hgvsp: ENST00000372023.3:c.1092C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000439800
  ensembl transcript: ENST00000536340
  gene symbol: ZMYND8
  hgvsc: ENST00000536340.1:c.1188C>T
  hgvsp: ENST00000536340.1:c.1188C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000418495
  ensembl transcript: ENST00000467200
  gene symbol: ZMYND8
  hgvsc: ENST00000467200.2:c.886C>T
  hgvsp: ENST00000467200.2:c.886C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000420095
  ensembl transcript: ENST00000471951
  gene symbol: ZMYND8
  hgvsc: ENST00000471951.2:c.1167C>T
  hgvsp: ENST00000471951.2:c.1167C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000312237
  ensembl transcript: ENST00000311275
  gene symbol: ZMYND8
  hgvsc: ENST00000311275.7:c.1107C>T
  hgvsp: ENST00000311275.7:c.1107C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000443086
  ensembl transcript: ENST00000540497
  gene symbol: ZMYND8
  hgvsc: ENST00000540497.1:c.1092C>T
  hgvsp: ENST00000540497.1:c.1092C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000262975
  ensembl transcript: ENST00000262975
  gene symbol: ZMYND8
  hgvsc: ENST00000262975.4:c.1107C>T
  hgvsp: ENST00000262975.4:c.1107C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000392964
  ensembl transcript: ENST00000458360
  gene symbol: ZMYND8
  hgvsc: ENST00000458360.2:c.1092C>T
  hgvsp: ENST00000458360.2:c.1092C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000354166
  ensembl transcript: ENST00000360911
  gene symbol: ZMYND8
  hgvsc: ENST00000360911.3:c.1092C>T
  hgvsp: ENST00000360911.3:c.1092C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000335537
  ensembl transcript: ENST00000352431
  gene symbol: ZMYND8
  hgvsc: ENST00000352431.2:c.1167C>T
  hgvsp: ENST00000352431.2:c.1167C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 11604
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 901
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Tyr389Tyr
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff

20-45905374-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45905374
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 45905374
    reference: chr 20
allele count: 4
allele frequency: 3.294621530351701e-5
allele num: 121410
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000348246
  ensembl transcript: ENST00000355972
  gene symbol: ZMYND8
  hgvsc: ENST00000355972.4:c.1104C>G
  hgvsp: ENST00000355972.4:c.1104C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000418495
  ensembl transcript: ENST00000467200
  gene symbol: ZMYND8
  hgvsc: ENST00000467200.2:c.883C>G
  hgvsp: ENST00000467200.2:c.883C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000312237
  ensembl transcript: ENST00000311275
  gene symbol: ZMYND8
  hgvsc: ENST00000311275.7:c.1104C>G
  hgvsp: ENST00000311275.7:c.1104C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000392964
  ensembl transcript: ENST00000458360
  gene symbol: ZMYND8
  hgvsc: ENST00000458360.2:c.1089C>G
  hgvsp: ENST00000458360.2:c.1089C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000418210
  ensembl transcript: ENST00000461685
  gene symbol: ZMYND8
  hgvsc: ENST00000461685.1:c.1164C>G
  hgvsp: ENST00000461685.1:c.1164C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000396725
  ensembl transcript: ENST00000446994
  gene symbol: ZMYND8
  hgvsc: ENST00000446994.2:c.915C>G
  hgvsp: ENST00000446994.2:c.915C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000361093
  ensembl transcript: ENST00000372023
  gene symbol: ZMYND8
  hgvsc: ENST00000372023.3:c.1089C>G
  hgvsp: ENST00000372023.3:c.1089C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000354166
  ensembl transcript: ENST00000360911
  gene symbol: ZMYND8
  hgvsc: ENST00000360911.3:c.1089C>G
  hgvsp: ENST00000360911.3:c.1089C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000439800
  ensembl transcript: ENST00000536340
  gene symbol: ZMYND8
  hgvsc: ENST00000536340.1:c.1185C>G
  hgvsp: ENST00000536340.1:c.1185C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000335537
  ensembl transcript: ENST00000352431
  gene symbol: ZMYND8
  hgvsc: ENST00000352431.2:c.1164C>G
  hgvsp: ENST00000352431.2:c.1164C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000443086
  ensembl transcript: ENST00000540497
  gene symbol: ZMYND8
  hgvsc: ENST00000540497.1:c.1089C>G
  hgvsp: ENST00000540497.1:c.1089C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000262975
  ensembl transcript: ENST00000262975
  gene symbol: ZMYND8
  hgvsc: ENST00000262975.4:c.1104C>G
  hgvsp: ENST00000262975.4:c.1104C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000420095
  ensembl transcript: ENST00000471951
  gene symbol: ZMYND8
  hgvsc: ENST00000471951.2:c.1164C>G
  hgvsp: ENST00000471951.2:c.1164C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101040
  ensembl transcript: ENST00000468376
  gene symbol: ZMYND8
  hgvsc: ENST00000468376.2:n.1115C>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000379577
  ensembl transcript: ENST00000396281
  gene symbol: ZMYND8
  hgvsc: ENST00000396281.4:c.1104C>G
  hgvsp: ENST00000396281.4:c.1104C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22514
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 901
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro388Pro
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD

20-45905377-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45905377
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 45905377
    reference: chr 20
allele count: 12
allele frequency: 9.886307464162135e-5
allele num: 121380
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000439800
  ensembl transcript: ENST00000536340
  gene symbol: ZMYND8
  hgvsc: ENST00000536340.1:c.1182A>C
  hgvsp: ENST00000536340.1:c.1182A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000361093
  ensembl transcript: ENST00000372023
  gene symbol: ZMYND8
  hgvsc: ENST00000372023.3:c.1086A>C
  hgvsp: ENST00000372023.3:c.1086A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000262975
  ensembl transcript: ENST00000262975
  gene symbol: ZMYND8
  hgvsc: ENST00000262975.4:c.1101A>C
  hgvsp: ENST00000262975.4:c.1101A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000418210
  ensembl transcript: ENST00000461685
  gene symbol: ZMYND8
  hgvsc: ENST00000461685.1:c.1161A>C
  hgvsp: ENST00000461685.1:c.1161A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000443086
  ensembl transcript: ENST00000540497
  gene symbol: ZMYND8
  hgvsc: ENST00000540497.1:c.1086A>C
  hgvsp: ENST00000540497.1:c.1086A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000348246
  ensembl transcript: ENST00000355972
  gene symbol: ZMYND8
  hgvsc: ENST00000355972.4:c.1101A>C
  hgvsp: ENST00000355972.4:c.1101A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000312237
  ensembl transcript: ENST00000311275
  gene symbol: ZMYND8
  hgvsc: ENST00000311275.7:c.1101A>C
  hgvsp: ENST00000311275.7:c.1101A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000420095
  ensembl transcript: ENST00000471951
  gene symbol: ZMYND8
  hgvsc: ENST00000471951.2:c.1161A>C
  hgvsp: ENST00000471951.2:c.1161A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000335537
  ensembl transcript: ENST00000352431
  gene symbol: ZMYND8
  hgvsc: ENST00000352431.2:c.1161A>C
  hgvsp: ENST00000352431.2:c.1161A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000379577
  ensembl transcript: ENST00000396281
  gene symbol: ZMYND8
  hgvsc: ENST00000396281.4:c.1101A>C
  hgvsp: ENST00000396281.4:c.1101A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000396725
  ensembl transcript: ENST00000446994
  gene symbol: ZMYND8
  hgvsc: ENST00000446994.2:c.912A>C
  hgvsp: ENST00000446994.2:c.912A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000392964
  ensembl transcript: ENST00000458360
  gene symbol: ZMYND8
  hgvsc: ENST00000458360.2:c.1086A>C
  hgvsp: ENST00000458360.2:c.1086A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000418495
  ensembl transcript: ENST00000467200
  gene symbol: ZMYND8
  hgvsc: ENST00000467200.2:c.880A>C
  hgvsp: ENST00000467200.2:c.880A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000354166
  ensembl transcript: ENST00000360911
  gene symbol: ZMYND8
  hgvsc: ENST00000360911.3:c.1086A>C
  hgvsp: ENST00000360911.3:c.1086A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101040
  ensembl transcript: ENST00000468376
  gene symbol: ZMYND8
  hgvsc: ENST00000468376.2:n.1112A>C
  variant of: http://identifiers.org/hgnc/9397
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.95to100.00
genotype depth: GenotypeDepth
  all individuals: 22516
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11606
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 648
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 902
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr387Thr
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: MQ

20-45905378-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45905378
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 45905378
    reference: chr 20
allele count: 1
allele frequency: 8.236960890909689e-6
allele num: 121404
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000262975
  ensembl transcript: ENST00000262975
  gene symbol: ZMYND8
  hgvsc: ENST00000262975.4:c.1100C>T
  hgvsp: ENSP00000262975.4:p.Thr367Ile
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000418210
  ensembl transcript: ENST00000461685
  gene symbol: ZMYND8
  hgvsc: ENST00000461685.1:c.1160C>T
  hgvsp: ENSP00000418210.1:p.Thr387Ile
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000335537
  ensembl transcript: ENST00000352431
  gene symbol: ZMYND8
  hgvsc: ENST00000352431.2:c.1160C>T
  hgvsp: ENSP00000335537.3:p.Thr387Ile
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000392964
  ensembl transcript: ENST00000458360
  gene symbol: ZMYND8
  hgvsc: ENST00000458360.2:c.1085C>T
  hgvsp: ENSP00000392964.2:p.Thr362Ile
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000379577
  ensembl transcript: ENST00000396281
  gene symbol: ZMYND8
  hgvsc: ENST00000396281.4:c.1100C>T
  hgvsp: ENSP00000379577.4:p.Thr367Ile
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000361093
  ensembl transcript: ENST00000372023
  gene symbol: ZMYND8
  hgvsc: ENST00000372023.3:c.1085C>T
  hgvsp: ENSP00000361093.3:p.Thr362Ile
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000443086
  ensembl transcript: ENST00000540497
  gene symbol: ZMYND8
  hgvsc: ENST00000540497.1:c.1085C>T
  hgvsp: ENSP00000443086.1:p.Thr362Ile
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000420095
  ensembl transcript: ENST00000471951
  gene symbol: ZMYND8
  hgvsc: ENST00000471951.2:c.1160C>T
  hgvsp: ENSP00000420095.2:p.Thr387Ile
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000418495
  ensembl transcript: ENST00000467200
  gene symbol: ZMYND8
  hgvsc: ENST00000467200.2:c.879C>T
  hgvsp: ENSP00000418495.2:p.Thr294Ile
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000348246
  ensembl transcript: ENST00000355972
  gene symbol: ZMYND8
  hgvsc: ENST00000355972.4:c.1100C>T
  hgvsp: ENSP00000348246.4:p.Thr367Ile
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000396725
  ensembl transcript: ENST00000446994
  gene symbol: ZMYND8
  hgvsc: ENST00000446994.2:c.911C>T
  hgvsp: ENSP00000396725.2:p.Thr304Ile
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101040
  ensembl transcript: ENST00000468376
  gene symbol: ZMYND8
  hgvsc: ENST00000468376.2:n.1111C>T
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000312237
  ensembl transcript: ENST00000311275
  gene symbol: ZMYND8
  hgvsc: ENST00000311275.7:c.1100C>T
  hgvsp: ENSP00000312237.7:p.Thr367Ile
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000354166
  ensembl transcript: ENST00000360911
  gene symbol: ZMYND8
  hgvsc: ENST00000360911.3:c.1085C>T
  hgvsp: ENSP00000354166.3:p.Thr362Ile
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000439800
  ensembl transcript: ENST00000536340
  gene symbol: ZMYND8
  hgvsc: ENST00000536340.1:c.1181C>T
  hgvsp: ENSP00000439800.1:p.Thr394Ile
  variant of: http://identifiers.org/hgnc/9397
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4252
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr387Ile
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP

20-45905404-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45905404
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 45905404
    reference: chr 20
allele count: 1
allele frequency: 8.238182327451271e-6
allele num: 121386
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000396725
  ensembl transcript: ENST00000446994
  gene symbol: ZMYND8
  hgvsc: ENST00000446994.2:c.885G>A
  hgvsp: ENST00000446994.2:c.885G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000354166
  ensembl transcript: ENST00000360911
  gene symbol: ZMYND8
  hgvsc: ENST00000360911.3:c.1059G>A
  hgvsp: ENST00000360911.3:c.1059G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000379577
  ensembl transcript: ENST00000396281
  gene symbol: ZMYND8
  hgvsc: ENST00000396281.4:c.1074G>A
  hgvsp: ENST00000396281.4:c.1074G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000418495
  ensembl transcript: ENST00000467200
  gene symbol: ZMYND8
  hgvsc: ENST00000467200.2:c.853G>A
  hgvsp: ENST00000467200.2:c.853G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000418210
  ensembl transcript: ENST00000461685
  gene symbol: ZMYND8
  hgvsc: ENST00000461685.1:c.1134G>A
  hgvsp: ENST00000461685.1:c.1134G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000262975
  ensembl transcript: ENST00000262975
  gene symbol: ZMYND8
  hgvsc: ENST00000262975.4:c.1074G>A
  hgvsp: ENST00000262975.4:c.1074G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000439800
  ensembl transcript: ENST00000536340
  gene symbol: ZMYND8
  hgvsc: ENST00000536340.1:c.1155G>A
  hgvsp: ENST00000536340.1:c.1155G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000335537
  ensembl transcript: ENST00000352431
  gene symbol: ZMYND8
  hgvsc: ENST00000352431.2:c.1134G>A
  hgvsp: ENST00000352431.2:c.1134G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000420095
  ensembl transcript: ENST00000471951
  gene symbol: ZMYND8
  hgvsc: ENST00000471951.2:c.1134G>A
  hgvsp: ENST00000471951.2:c.1134G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000443086
  ensembl transcript: ENST00000540497
  gene symbol: ZMYND8
  hgvsc: ENST00000540497.1:c.1059G>A
  hgvsp: ENST00000540497.1:c.1059G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000361093
  ensembl transcript: ENST00000372023
  gene symbol: ZMYND8
  hgvsc: ENST00000372023.3:c.1059G>A
  hgvsp: ENST00000372023.3:c.1059G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000392964
  ensembl transcript: ENST00000458360
  gene symbol: ZMYND8
  hgvsc: ENST00000458360.2:c.1059G>A
  hgvsp: ENST00000458360.2:c.1059G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000312237
  ensembl transcript: ENST00000311275
  gene symbol: ZMYND8
  hgvsc: ENST00000311275.7:c.1074G>A
  hgvsp: ENST00000311275.7:c.1074G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000348246
  ensembl transcript: ENST00000355972
  gene symbol: ZMYND8
  hgvsc: ENST00000355972.4:c.1074G>A
  hgvsp: ENST00000355972.4:c.1074G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101040
  ensembl transcript: ENST00000468376
  gene symbol: ZMYND8
  hgvsc: ENST00000468376.2:n.1085G>A
  variant of: http://identifiers.org/hgnc/9397
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4249
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 649
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1796
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17140
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22516
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly378Gly
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Other
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
reference allele: C
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: FS

20-45905418-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45905418
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 45905418
    reference: chr 20
allele count: 1
allele frequency: 8.238318064983852e-6
allele num: 121384
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000361093
  ensembl transcript: ENST00000372023
  gene symbol: ZMYND8
  hgvsc: ENST00000372023.3:c.1045C>T
  hgvsp: ENSP00000361093.3:p.Arg349Cys
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000335537
  ensembl transcript: ENST00000352431
  gene symbol: ZMYND8
  hgvsc: ENST00000352431.2:c.1120C>T
  hgvsp: ENSP00000335537.3:p.Arg374Cys
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000439800
  ensembl transcript: ENST00000536340
  gene symbol: ZMYND8
  hgvsc: ENST00000536340.1:c.1141C>T
  hgvsp: ENSP00000439800.1:p.Arg381Cys
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000348246
  ensembl transcript: ENST00000355972
  gene symbol: ZMYND8
  hgvsc: ENST00000355972.4:c.1060C>T
  hgvsp: ENSP00000348246.4:p.Arg354Cys
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000396725
  ensembl transcript: ENST00000446994
  gene symbol: ZMYND8
  hgvsc: ENST00000446994.2:c.871C>T
  hgvsp: ENSP00000396725.2:p.Arg291Cys
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000354166
  ensembl transcript: ENST00000360911
  gene symbol: ZMYND8
  hgvsc: ENST00000360911.3:c.1045C>T
  hgvsp: ENSP00000354166.3:p.Arg349Cys
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000392964
  ensembl transcript: ENST00000458360
  gene symbol: ZMYND8
  hgvsc: ENST00000458360.2:c.1045C>T
  hgvsp: ENSP00000392964.2:p.Arg349Cys
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000379577
  ensembl transcript: ENST00000396281
  gene symbol: ZMYND8
  hgvsc: ENST00000396281.4:c.1060C>T
  hgvsp: ENSP00000379577.4:p.Arg354Cys
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000420095
  ensembl transcript: ENST00000471951
  gene symbol: ZMYND8
  hgvsc: ENST00000471951.2:c.1120C>T
  hgvsp: ENSP00000420095.2:p.Arg374Cys
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000262975
  ensembl transcript: ENST00000262975
  gene symbol: ZMYND8
  hgvsc: ENST00000262975.4:c.1060C>T
  hgvsp: ENSP00000262975.4:p.Arg354Cys
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000312237
  ensembl transcript: ENST00000311275
  gene symbol: ZMYND8
  hgvsc: ENST00000311275.7:c.1060C>T
  hgvsp: ENSP00000312237.7:p.Arg354Cys
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101040
  ensembl transcript: ENST00000468376
  gene symbol: ZMYND8
  hgvsc: ENST00000468376.2:n.1071C>T
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000418210
  ensembl transcript: ENST00000461685
  gene symbol: ZMYND8
  hgvsc: ENST00000461685.1:c.1120C>T
  hgvsp: ENSP00000418210.1:p.Arg374Cys
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000443086
  ensembl transcript: ENST00000540497
  gene symbol: ZMYND8
  hgvsc: ENST00000540497.1:c.1045C>T
  hgvsp: ENSP00000443086.1:p.Arg349Cys
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000418495
  ensembl transcript: ENST00000467200
  gene symbol: ZMYND8
  hgvsc: ENST00000467200.2:c.839C>T
  hgvsp: ENSP00000418495.2:p.Arg281Cys
  variant of: http://identifiers.org/hgnc/9397
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 22519
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 649
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11606
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4249
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg374Cys
num of homozygotes: 0
population: Other
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum

20-45905431-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45905431
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 45905431
    reference: chr 20
allele count: 2
allele frequency: 1.647989452867502e-5
allele num: 121360
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000335537
  ensembl transcript: ENST00000352431
  gene symbol: ZMYND8
  hgvsc: ENST00000352431.2:c.1107C>T
  hgvsp: ENST00000352431.2:c.1107C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101040
  ensembl transcript: ENST00000468376
  gene symbol: ZMYND8
  hgvsc: ENST00000468376.2:n.1058C>T
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000392964
  ensembl transcript: ENST00000458360
  gene symbol: ZMYND8
  hgvsc: ENST00000458360.2:c.1032C>T
  hgvsp: ENST00000458360.2:c.1032C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000379577
  ensembl transcript: ENST00000396281
  gene symbol: ZMYND8
  hgvsc: ENST00000396281.4:c.1047C>T
  hgvsp: ENST00000396281.4:c.1047C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000354166
  ensembl transcript: ENST00000360911
  gene symbol: ZMYND8
  hgvsc: ENST00000360911.3:c.1032C>T
  hgvsp: ENST00000360911.3:c.1032C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000418210
  ensembl transcript: ENST00000461685
  gene symbol: ZMYND8
  hgvsc: ENST00000461685.1:c.1107C>T
  hgvsp: ENST00000461685.1:c.1107C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000361093
  ensembl transcript: ENST00000372023
  gene symbol: ZMYND8
  hgvsc: ENST00000372023.3:c.1032C>T
  hgvsp: ENST00000372023.3:c.1032C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000418495
  ensembl transcript: ENST00000467200
  gene symbol: ZMYND8
  hgvsc: ENST00000467200.2:c.826C>T
  hgvsp: ENST00000467200.2:c.826C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000262975
  ensembl transcript: ENST00000262975
  gene symbol: ZMYND8
  hgvsc: ENST00000262975.4:c.1047C>T
  hgvsp: ENST00000262975.4:c.1047C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000439800
  ensembl transcript: ENST00000536340
  gene symbol: ZMYND8
  hgvsc: ENST00000536340.1:c.1128C>T
  hgvsp: ENST00000536340.1:c.1128C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000312237
  ensembl transcript: ENST00000311275
  gene symbol: ZMYND8
  hgvsc: ENST00000311275.7:c.1047C>T
  hgvsp: ENST00000311275.7:c.1047C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000348246
  ensembl transcript: ENST00000355972
  gene symbol: ZMYND8
  hgvsc: ENST00000355972.4:c.1047C>T
  hgvsp: ENST00000355972.4:c.1047C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000396725
  ensembl transcript: ENST00000446994
  gene symbol: ZMYND8
  hgvsc: ENST00000446994.2:c.858C>T
  hgvsp: ENST00000446994.2:c.858C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000420095
  ensembl transcript: ENST00000471951
  gene symbol: ZMYND8
  hgvsc: ENST00000471951.2:c.1107C>T
  hgvsp: ENST00000471951.2:c.1107C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000443086
  ensembl transcript: ENST00000540497
  gene symbol: ZMYND8
  hgvsc: ENST00000540497.1:c.1032C>T
  hgvsp: ENST00000540497.1:c.1032C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 649
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17124
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Tyr369Tyr
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
population: Latino
population: European (Finnish)
reference allele: G
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum

20-45905526-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45905526
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 45905526
    reference: chr 20
allele count: 3
allele frequency: 2.553278409477769e-5
allele num: 117496
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000439800
  ensembl transcript: ENST00000536340
  gene symbol: ZMYND8
  hgvsc: ENST00000536340.1:c.1033A>G
  hgvsp: ENSP00000439800.1:p.Ile345Val
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000418210
  ensembl transcript: ENST00000461685
  gene symbol: ZMYND8
  hgvsc: ENST00000461685.1:c.1012A>G
  hgvsp: ENSP00000418210.1:p.Ile338Val
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000418495
  ensembl transcript: ENST00000467200
  gene symbol: ZMYND8
  hgvsc: ENST00000467200.2:c.731A>G
  hgvsp: ENSP00000418495.2:p.Ile245Val
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000262975
  ensembl transcript: ENST00000262975
  gene symbol: ZMYND8
  hgvsc: ENST00000262975.4:c.952A>G
  hgvsp: ENSP00000262975.4:p.Ile318Val
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000348246
  ensembl transcript: ENST00000355972
  gene symbol: ZMYND8
  hgvsc: ENST00000355972.4:c.952A>G
  hgvsp: ENSP00000348246.4:p.Ile318Val
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000335537
  ensembl transcript: ENST00000352431
  gene symbol: ZMYND8
  hgvsc: ENST00000352431.2:c.1012A>G
  hgvsp: ENSP00000335537.3:p.Ile338Val
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101040
  ensembl transcript: ENST00000468376
  gene symbol: ZMYND8
  hgvsc: ENST00000468376.2:n.963A>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000312237
  ensembl transcript: ENST00000311275
  gene symbol: ZMYND8
  hgvsc: ENST00000311275.7:c.952A>G
  hgvsp: ENSP00000312237.7:p.Ile318Val
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000354166
  ensembl transcript: ENST00000360911
  gene symbol: ZMYND8
  hgvsc: ENST00000360911.3:c.937A>G
  hgvsp: ENSP00000354166.3:p.Ile313Val
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000392964
  ensembl transcript: ENST00000458360
  gene symbol: ZMYND8
  hgvsc: ENST00000458360.2:c.937A>G
  hgvsp: ENSP00000392964.2:p.Ile313Val
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000379577
  ensembl transcript: ENST00000396281
  gene symbol: ZMYND8
  hgvsc: ENST00000396281.4:c.952A>G
  hgvsp: ENSP00000379577.4:p.Ile318Val
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000361093
  ensembl transcript: ENST00000372023
  gene symbol: ZMYND8
  hgvsc: ENST00000372023.3:c.937A>G
  hgvsp: ENSP00000361093.3:p.Ile313Val
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000443086
  ensembl transcript: ENST00000540497
  gene symbol: ZMYND8
  hgvsc: ENST00000540497.1:c.937A>G
  hgvsp: ENSP00000443086.1:p.Ile313Val
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000396725
  ensembl transcript: ENST00000446994
  gene symbol: ZMYND8
  hgvsc: ENST00000446994.2:c.763A>G
  hgvsp: ENSP00000396725.2:p.Ile255Val
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000420095
  ensembl transcript: ENST00000471951
  gene symbol: ZMYND8
  hgvsc: ENST00000471951.2:c.1012A>G
  hgvsp: ENSP00000420095.2:p.Ile338Val
  variant of: http://identifiers.org/hgnc/9397
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1692
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21305
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2053
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile338Val
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: ClippingRankSum

20-45905527-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45905527
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 45905527
    reference: chr 20
allele count: 5
allele frequency: 4.260322762052453e-5
allele num: 117362
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000262975
  ensembl transcript: ENST00000262975
  gene symbol: ZMYND8
  hgvsc: ENST00000262975.4:c.951A>G
  hgvsp: ENST00000262975.4:c.951A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000354166
  ensembl transcript: ENST00000360911
  gene symbol: ZMYND8
  hgvsc: ENST00000360911.3:c.936A>G
  hgvsp: ENST00000360911.3:c.936A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000443086
  ensembl transcript: ENST00000540497
  gene symbol: ZMYND8
  hgvsc: ENST00000540497.1:c.936A>G
  hgvsp: ENST00000540497.1:c.936A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000312237
  ensembl transcript: ENST00000311275
  gene symbol: ZMYND8
  hgvsc: ENST00000311275.7:c.951A>G
  hgvsp: ENST00000311275.7:c.951A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000396725
  ensembl transcript: ENST00000446994
  gene symbol: ZMYND8
  hgvsc: ENST00000446994.2:c.762A>G
  hgvsp: ENST00000446994.2:c.762A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000392964
  ensembl transcript: ENST00000458360
  gene symbol: ZMYND8
  hgvsc: ENST00000458360.2:c.936A>G
  hgvsp: ENST00000458360.2:c.936A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101040
  ensembl transcript: ENST00000468376
  gene symbol: ZMYND8
  hgvsc: ENST00000468376.2:n.962A>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000439800
  ensembl transcript: ENST00000536340
  gene symbol: ZMYND8
  hgvsc: ENST00000536340.1:c.1032A>G
  hgvsp: ENST00000536340.1:c.1032A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000379577
  ensembl transcript: ENST00000396281
  gene symbol: ZMYND8
  hgvsc: ENST00000396281.4:c.951A>G
  hgvsp: ENST00000396281.4:c.951A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000420095
  ensembl transcript: ENST00000471951
  gene symbol: ZMYND8
  hgvsc: ENST00000471951.2:c.1011A>G
  hgvsp: ENST00000471951.2:c.1011A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000348246
  ensembl transcript: ENST00000355972
  gene symbol: ZMYND8
  hgvsc: ENST00000355972.4:c.951A>G
  hgvsp: ENST00000355972.4:c.951A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000418210
  ensembl transcript: ENST00000461685
  gene symbol: ZMYND8
  hgvsc: ENST00000461685.1:c.1011A>G
  hgvsp: ENST00000461685.1:c.1011A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000361093
  ensembl transcript: ENST00000372023
  gene symbol: ZMYND8
  hgvsc: ENST00000372023.3:c.936A>G
  hgvsp: ENST00000372023.3:c.936A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000418495
  ensembl transcript: ENST00000467200
  gene symbol: ZMYND8
  hgvsc: ENST00000467200.2:c.730A>G
  hgvsp: ENST00000467200.2:c.730A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000335537
  ensembl transcript: ENST00000352431
  gene symbol: ZMYND8
  hgvsc: ENST00000352431.2:c.1011A>G
  hgvsp: ENST00000352431.2:c.1011A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1746
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1793
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14128
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21247
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro337Pro
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
population: Other
reference allele: T
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum

20-45905536-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45905536
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 45905536
    reference: chr 20
allele count: 2
allele frequency: 1.730403183941859e-5
allele num: 115580
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000396725
  ensembl transcript: ENST00000446994
  gene symbol: ZMYND8
  hgvsc: ENST00000446994.2:c.753C>T
  hgvsp: ENST00000446994.2:c.753C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000348246
  ensembl transcript: ENST00000355972
  gene symbol: ZMYND8
  hgvsc: ENST00000355972.4:c.942C>T
  hgvsp: ENST00000355972.4:c.942C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000420095
  ensembl transcript: ENST00000471951
  gene symbol: ZMYND8
  hgvsc: ENST00000471951.2:c.1002C>T
  hgvsp: ENST00000471951.2:c.1002C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000418210
  ensembl transcript: ENST00000461685
  gene symbol: ZMYND8
  hgvsc: ENST00000461685.1:c.1002C>T
  hgvsp: ENST00000461685.1:c.1002C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000312237
  ensembl transcript: ENST00000311275
  gene symbol: ZMYND8
  hgvsc: ENST00000311275.7:c.942C>T
  hgvsp: ENST00000311275.7:c.942C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000379577
  ensembl transcript: ENST00000396281
  gene symbol: ZMYND8
  hgvsc: ENST00000396281.4:c.942C>T
  hgvsp: ENST00000396281.4:c.942C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000361093
  ensembl transcript: ENST00000372023
  gene symbol: ZMYND8
  hgvsc: ENST00000372023.3:c.927C>T
  hgvsp: ENST00000372023.3:c.927C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000392964
  ensembl transcript: ENST00000458360
  gene symbol: ZMYND8
  hgvsc: ENST00000458360.2:c.927C>T
  hgvsp: ENST00000458360.2:c.927C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000418495
  ensembl transcript: ENST00000467200
  gene symbol: ZMYND8
  hgvsc: ENST00000467200.2:c.721C>T
  hgvsp: ENST00000467200.2:c.721C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000262975
  ensembl transcript: ENST00000262975
  gene symbol: ZMYND8
  hgvsc: ENST00000262975.4:c.942C>T
  hgvsp: ENST00000262975.4:c.942C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101040
  ensembl transcript: ENST00000468376
  gene symbol: ZMYND8
  hgvsc: ENST00000468376.2:n.953C>T
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000439800
  ensembl transcript: ENST00000536340
  gene symbol: ZMYND8
  hgvsc: ENST00000536340.1:c.1023C>T
  hgvsp: ENST00000536340.1:c.1023C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000335537
  ensembl transcript: ENST00000352431
  gene symbol: ZMYND8
  hgvsc: ENST00000352431.2:c.1002C>T
  hgvsp: ENST00000352431.2:c.1002C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000354166
  ensembl transcript: ENST00000360911
  gene symbol: ZMYND8
  hgvsc: ENST00000360911.3:c.927C>T
  hgvsp: ENST00000360911.3:c.927C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000443086
  ensembl transcript: ENST00000540497
  gene symbol: ZMYND8
  hgvsc: ENST00000540497.1:c.927C>T
  hgvsp: ENST00000540497.1:c.927C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2366
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1781
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala334Ala
num of homozygotes: 0
population: Other
population: European (Finnish)
population: South Asian
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: ClippingRankSum

20-45905545-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45905545
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 45905545
    reference: chr 20
allele count: 1
allele frequency: 8.733777009205401e-6
allele num: 114498
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000348246
  ensembl transcript: ENST00000355972
  gene symbol: ZMYND8
  hgvsc: ENST00000355972.4:c.939-6T>C
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000262975
  ensembl transcript: ENST00000262975
  gene symbol: ZMYND8
  hgvsc: ENST00000262975.4:c.939-6T>C
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000420095
  ensembl transcript: ENST00000471951
  gene symbol: ZMYND8
  hgvsc: ENST00000471951.2:c.999-6T>C
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl transcript: ENST00000468376
  gene symbol: ZMYND8
  hgvsc: ENST00000468376.2:n.950-6T>C
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000335537
  ensembl transcript: ENST00000352431
  gene symbol: ZMYND8
  hgvsc: ENST00000352431.2:c.999-6T>C
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000312237
  ensembl transcript: ENST00000311275
  gene symbol: ZMYND8
  hgvsc: ENST00000311275.7:c.939-6T>C
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000418495
  ensembl transcript: ENST00000467200
  gene symbol: ZMYND8
  hgvsc: ENST00000467200.2:c.718-6T>C
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000361093
  ensembl transcript: ENST00000372023
  gene symbol: ZMYND8
  hgvsc: ENST00000372023.3:c.924-6T>C
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000354166
  ensembl transcript: ENST00000360911
  gene symbol: ZMYND8
  hgvsc: ENST00000360911.3:c.924-6T>C
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000418210
  ensembl transcript: ENST00000461685
  gene symbol: ZMYND8
  hgvsc: ENST00000461685.1:c.999-6T>C
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000392964
  ensembl transcript: ENST00000458360
  gene symbol: ZMYND8
  hgvsc: ENST00000458360.2:c.924-6T>C
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000443086
  ensembl transcript: ENST00000540497
  gene symbol: ZMYND8
  hgvsc: ENST00000540497.1:c.924-6T>C
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000439800
  ensembl transcript: ENST00000536340
  gene symbol: ZMYND8
  hgvsc: ENST00000536340.1:c.1020-6T>C
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000379577
  ensembl transcript: ENST00000396281
  gene symbol: ZMYND8
  hgvsc: ENST00000396281.4:c.939-6T>C
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000396725
  ensembl transcript: ENST00000446994
  gene symbol: ZMYND8
  hgvsc: ENST00000446994.2:c.750-6T>C
  variant of: http://identifiers.org/hgnc/9397
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1782
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11246
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 647
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2664
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.999-6T>C
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: A
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum

20-45905549-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45905549
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 45905549
    reference: chr 20
allele count: 1
allele frequency: 8.782869890565442e-6
allele num: 113858
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000312237
  ensembl transcript: ENST00000311275
  gene symbol: ZMYND8
  hgvsc: ENST00000311275.7:c.939-10G>A
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000392964
  ensembl transcript: ENST00000458360
  gene symbol: ZMYND8
  hgvsc: ENST00000458360.2:c.924-10G>A
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000420095
  ensembl transcript: ENST00000471951
  gene symbol: ZMYND8
  hgvsc: ENST00000471951.2:c.999-10G>A
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl transcript: ENST00000468376
  gene symbol: ZMYND8
  hgvsc: ENST00000468376.2:n.950-10G>A
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000348246
  ensembl transcript: ENST00000355972
  gene symbol: ZMYND8
  hgvsc: ENST00000355972.4:c.939-10G>A
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000439800
  ensembl transcript: ENST00000536340
  gene symbol: ZMYND8
  hgvsc: ENST00000536340.1:c.1020-10G>A
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000361093
  ensembl transcript: ENST00000372023
  gene symbol: ZMYND8
  hgvsc: ENST00000372023.3:c.924-10G>A
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000443086
  ensembl transcript: ENST00000540497
  gene symbol: ZMYND8
  hgvsc: ENST00000540497.1:c.924-10G>A
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000262975
  ensembl transcript: ENST00000262975
  gene symbol: ZMYND8
  hgvsc: ENST00000262975.4:c.939-10G>A
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000396725
  ensembl transcript: ENST00000446994
  gene symbol: ZMYND8
  hgvsc: ENST00000446994.2:c.750-10G>A
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000335537
  ensembl transcript: ENST00000352431
  gene symbol: ZMYND8
  hgvsc: ENST00000352431.2:c.999-10G>A
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000354166
  ensembl transcript: ENST00000360911
  gene symbol: ZMYND8
  hgvsc: ENST00000360911.3:c.924-10G>A
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000418210
  ensembl transcript: ENST00000461685
  gene symbol: ZMYND8
  hgvsc: ENST00000461685.1:c.999-10G>A
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000379577
  ensembl transcript: ENST00000396281
  gene symbol: ZMYND8
  hgvsc: ENST00000396281.4:c.939-10G>A
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000418495
  ensembl transcript: ENST00000467200
  gene symbol: ZMYND8
  hgvsc: ENST00000467200.2:c.718-10G>A
  variant of: http://identifiers.org/hgnc/9397
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 648
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11207
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12056
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20312
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 827
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1783
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3681
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
population: South Asian
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: ReadPosRankSum

20-45905555-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45905555
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 45905555
    reference: chr 20
allele count: 1
allele frequency: 8.844861135680169e-6
allele num: 113060
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000361093
  ensembl transcript: ENST00000372023
  gene symbol: ZMYND8
  hgvsc: ENST00000372023.3:c.924-16T>C
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000379577
  ensembl transcript: ENST00000396281
  gene symbol: ZMYND8
  hgvsc: ENST00000396281.4:c.939-16T>C
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl transcript: ENST00000468376
  gene symbol: ZMYND8
  hgvsc: ENST00000468376.2:n.950-16T>C
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000335537
  ensembl transcript: ENST00000352431
  gene symbol: ZMYND8
  hgvsc: ENST00000352431.2:c.999-16T>C
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000418495
  ensembl transcript: ENST00000467200
  gene symbol: ZMYND8
  hgvsc: ENST00000467200.2:c.718-16T>C
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000418210
  ensembl transcript: ENST00000461685
  gene symbol: ZMYND8
  hgvsc: ENST00000461685.1:c.999-16T>C
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000439800
  ensembl transcript: ENST00000536340
  gene symbol: ZMYND8
  hgvsc: ENST00000536340.1:c.1020-16T>C
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000312237
  ensembl transcript: ENST00000311275
  gene symbol: ZMYND8
  hgvsc: ENST00000311275.7:c.939-16T>C
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000262975
  ensembl transcript: ENST00000262975
  gene symbol: ZMYND8
  hgvsc: ENST00000262975.4:c.939-16T>C
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000348246
  ensembl transcript: ENST00000355972
  gene symbol: ZMYND8
  hgvsc: ENST00000355972.4:c.939-16T>C
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000354166
  ensembl transcript: ENST00000360911
  gene symbol: ZMYND8
  hgvsc: ENST00000360911.3:c.924-16T>C
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000420095
  ensembl transcript: ENST00000471951
  gene symbol: ZMYND8
  hgvsc: ENST00000471951.2:c.999-16T>C
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000396725
  ensembl transcript: ENST00000446994
  gene symbol: ZMYND8
  hgvsc: ENST00000446994.2:c.750-16T>C
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000392964
  ensembl transcript: ENST00000458360
  gene symbol: ZMYND8
  hgvsc: ENST00000458360.2:c.924-16T>C
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000443086
  ensembl transcript: ENST00000540497
  gene symbol: ZMYND8
  hgvsc: ENST00000540497.1:c.924-16T>C
  variant of: http://identifiers.org/hgnc/9397
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4174
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11701
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2961
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 905
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1089
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: A
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum

20-45905558-AAG-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45905558
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 45905556
    reference: chr 20
allele count: 1
allele frequency: 8.922994556973321e-6
allele num: 112070
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000348246
  ensembl transcript: ENST00000355972
  gene symbol: ZMYND8
  hgvsc: ENST00000355972.4:c.939-21_939-20delCT
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000392964
  ensembl transcript: ENST00000458360
  gene symbol: ZMYND8
  hgvsc: ENST00000458360.2:c.924-21_924-20delCT
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000439800
  ensembl transcript: ENST00000536340
  gene symbol: ZMYND8
  hgvsc: ENST00000536340.1:c.1020-21_1020-20delCT
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000379577
  ensembl transcript: ENST00000396281
  gene symbol: ZMYND8
  hgvsc: ENST00000396281.4:c.939-21_939-20delCT
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000443086
  ensembl transcript: ENST00000540497
  gene symbol: ZMYND8
  hgvsc: ENST00000540497.1:c.924-21_924-20delCT
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl transcript: ENST00000468376
  gene symbol: ZMYND8
  hgvsc: ENST00000468376.2:n.950-21_950-20delCT
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000312237
  ensembl transcript: ENST00000311275
  gene symbol: ZMYND8
  hgvsc: ENST00000311275.7:c.939-21_939-20delCT
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000418210
  ensembl transcript: ENST00000461685
  gene symbol: ZMYND8
  hgvsc: ENST00000461685.1:c.999-21_999-20delCT
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000335537
  ensembl transcript: ENST00000352431
  gene symbol: ZMYND8
  hgvsc: ENST00000352431.2:c.999-21_999-20delCT
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000262975
  ensembl transcript: ENST00000262975
  gene symbol: ZMYND8
  hgvsc: ENST00000262975.4:c.939-21_939-20delCT
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000361093
  ensembl transcript: ENST00000372023
  gene symbol: ZMYND8
  hgvsc: ENST00000372023.3:c.924-21_924-20delCT
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000354166
  ensembl transcript: ENST00000360911
  gene symbol: ZMYND8
  hgvsc: ENST00000360911.3:c.924-21_924-20delCT
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000396725
  ensembl transcript: ENST00000446994
  gene symbol: ZMYND8
  hgvsc: ENST00000446994.2:c.750-21_750-20delCT
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000418495
  ensembl transcript: ENST00000467200
  gene symbol: ZMYND8
  hgvsc: ENST00000467200.2:c.718-21_718-20delCT
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000420095
  ensembl transcript: ENST00000471951
  gene symbol: ZMYND8
  hgvsc: ENST00000471951.2:c.999-21_999-20delCT
  variant of: http://identifiers.org/hgnc/9397
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11073
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 841
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19661
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3974
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1371
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 905
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4169
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1783
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Other
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: AAG
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: MQ

http://identifiers.org/exac.variant/20-45905582-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45905582
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 45905582
    reference: chr 20
allele count: 1
allele frequency: 9.218968950512574e-6
allele num: 108472
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000348246
  ensembl transcript: ENST00000355972
  gene symbol: ZMYND8
  hgvsc: ENST00000355972.4:c.939-43T>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000418495
  ensembl transcript: ENST00000467200
  gene symbol: ZMYND8
  hgvsc: ENST00000467200.2:c.718-43T>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000392964
  ensembl transcript: ENST00000458360
  gene symbol: ZMYND8
  hgvsc: ENST00000458360.2:c.924-43T>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000312237
  ensembl transcript: ENST00000311275
  gene symbol: ZMYND8
  hgvsc: ENST00000311275.7:c.939-43T>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000262975
  ensembl transcript: ENST00000262975
  gene symbol: ZMYND8
  hgvsc: ENST00000262975.4:c.939-43T>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000418210
  ensembl transcript: ENST00000461685
  gene symbol: ZMYND8
  hgvsc: ENST00000461685.1:c.999-43T>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000396725
  ensembl transcript: ENST00000446994
  gene symbol: ZMYND8
  hgvsc: ENST00000446994.2:c.750-43T>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000361093
  ensembl transcript: ENST00000372023
  gene symbol: ZMYND8
  hgvsc: ENST00000372023.3:c.924-43T>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000354166
  ensembl transcript: ENST00000360911
  gene symbol: ZMYND8
  hgvsc: ENST00000360911.3:c.924-43T>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl transcript: ENST00000468376
  gene symbol: ZMYND8
  hgvsc: ENST00000468376.2:n.950-43T>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000420095
  ensembl transcript: ENST00000471951
  gene symbol: ZMYND8
  hgvsc: ENST00000471951.2:c.999-43T>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000443086
  ensembl transcript: ENST00000540497
  gene symbol: ZMYND8
  hgvsc: ENST00000540497.1:c.924-43T>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000335537
  ensembl transcript: ENST00000352431
  gene symbol: ZMYND8
  hgvsc: ENST00000352431.2:c.999-43T>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000439800
  ensembl transcript: ENST00000536340
  gene symbol: ZMYND8
  hgvsc: ENST00000536340.1:c.1020-43T>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000379577
  ensembl transcript: ENST00000396281
  gene symbol: ZMYND8
  hgvsc: ENST00000396281.4:c.939-43T>G
  variant of: http://identifiers.org/hgnc/9397
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3378
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2120
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11274
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4043
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9737
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 905
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4073
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4458
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: African
population: Other
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: A
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff

20-45910797-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45910797
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 45910797
    reference: chr 20
allele count: 1
allele frequency: 8.42971305256769e-6
allele num: 118628
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000443086
  ensembl transcript: ENST00000540497
  gene symbol: ZMYND8
  hgvsc: ENST00000540497.1:c.923+49A>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000312237
  ensembl transcript: ENST00000311275
  gene symbol: ZMYND8
  hgvsc: ENST00000311275.7:c.938+49A>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000348246
  ensembl transcript: ENST00000355972
  gene symbol: ZMYND8
  hgvsc: ENST00000355972.4:c.938+49A>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000354166
  ensembl transcript: ENST00000360911
  gene symbol: ZMYND8
  hgvsc: ENST00000360911.3:c.923+49A>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000418210
  ensembl transcript: ENST00000461685
  gene symbol: ZMYND8
  hgvsc: ENST00000461685.1:c.998+49A>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl transcript: ENST00000468376
  gene symbol: ZMYND8
  hgvsc: ENST00000468376.2:n.949+49A>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000439800
  ensembl transcript: ENST00000536340
  gene symbol: ZMYND8
  hgvsc: ENST00000536340.1:c.1019+49A>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000379577
  ensembl transcript: ENST00000396281
  gene symbol: ZMYND8
  hgvsc: ENST00000396281.4:c.938+49A>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000335537
  ensembl transcript: ENST00000352431
  gene symbol: ZMYND8
  hgvsc: ENST00000352431.2:c.998+49A>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000418495
  ensembl transcript: ENST00000467200
  gene symbol: ZMYND8
  hgvsc: ENST00000467200.2:c.717+49A>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000392964
  ensembl transcript: ENST00000458360
  gene symbol: ZMYND8
  hgvsc: ENST00000458360.2:c.923+49A>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000262975
  ensembl transcript: ENST00000262975
  gene symbol: ZMYND8
  hgvsc: ENST00000262975.4:c.938+49A>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000420095
  ensembl transcript: ENST00000471951
  gene symbol: ZMYND8
  hgvsc: ENST00000471951.2:c.998+49A>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000361093
  ensembl transcript: ENST00000372023
  gene symbol: ZMYND8
  hgvsc: ENST00000372023.3:c.923+49A>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000396725
  ensembl transcript: ENST00000446994
  gene symbol: ZMYND8
  hgvsc: ENST00000446994.2:c.749+49A>G
  variant of: http://identifiers.org/hgnc/9397
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1631
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1411
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21720
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 618
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4956
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15420
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2621
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 922
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: T
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: MQ

http://identifiers.org/exac.variant/20-45910801-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45910801
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 45910801
    reference: chr 20
allele count: 2
allele frequency: 1.684948356332878e-5
allele num: 118698
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000348246
  ensembl transcript: ENST00000355972
  gene symbol: ZMYND8
  hgvsc: ENST00000355972.4:c.938+45T>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000312237
  ensembl transcript: ENST00000311275
  gene symbol: ZMYND8
  hgvsc: ENST00000311275.7:c.938+45T>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000439800
  ensembl transcript: ENST00000536340
  gene symbol: ZMYND8
  hgvsc: ENST00000536340.1:c.1019+45T>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000418210
  ensembl transcript: ENST00000461685
  gene symbol: ZMYND8
  hgvsc: ENST00000461685.1:c.998+45T>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000420095
  ensembl transcript: ENST00000471951
  gene symbol: ZMYND8
  hgvsc: ENST00000471951.2:c.998+45T>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000443086
  ensembl transcript: ENST00000540497
  gene symbol: ZMYND8
  hgvsc: ENST00000540497.1:c.923+45T>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl transcript: ENST00000468376
  gene symbol: ZMYND8
  hgvsc: ENST00000468376.2:n.949+45T>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000361093
  ensembl transcript: ENST00000372023
  gene symbol: ZMYND8
  hgvsc: ENST00000372023.3:c.923+45T>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000379577
  ensembl transcript: ENST00000396281
  gene symbol: ZMYND8
  hgvsc: ENST00000396281.4:c.938+45T>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000392964
  ensembl transcript: ENST00000458360
  gene symbol: ZMYND8
  hgvsc: ENST00000458360.2:c.923+45T>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000335537
  ensembl transcript: ENST00000352431
  gene symbol: ZMYND8
  hgvsc: ENST00000352431.2:c.998+45T>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000354166
  ensembl transcript: ENST00000360911
  gene symbol: ZMYND8
  hgvsc: ENST00000360911.3:c.923+45T>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000418495
  ensembl transcript: ENST00000467200
  gene symbol: ZMYND8
  hgvsc: ENST00000467200.2:c.717+45T>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000262975
  ensembl transcript: ENST00000262975
  gene symbol: ZMYND8
  hgvsc: ENST00000262975.4:c.938+45T>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000396725
  ensembl transcript: ENST00000446994
  gene symbol: ZMYND8
  hgvsc: ENST00000446994.2:c.749+45T>G
  variant of: http://identifiers.org/hgnc/9397
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5482
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2620
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5249
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21763
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15417
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 922
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1410
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1339
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: Other
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD

20-45910802-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45910802
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 45910802
    reference: chr 20
allele count: 6
allele frequency: 5.054248938607723e-5
allele num: 118712
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000418495
  ensembl transcript: ENST00000467200
  gene symbol: ZMYND8
  hgvsc: ENST00000467200.2:c.717+44C>T
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl transcript: ENST00000468376
  gene symbol: ZMYND8
  hgvsc: ENST00000468376.2:n.949+44C>T
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000379577
  ensembl transcript: ENST00000396281
  gene symbol: ZMYND8
  hgvsc: ENST00000396281.4:c.938+44C>T
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000262975
  ensembl transcript: ENST00000262975
  gene symbol: ZMYND8
  hgvsc: ENST00000262975.4:c.938+44C>T
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000361093
  ensembl transcript: ENST00000372023
  gene symbol: ZMYND8
  hgvsc: ENST00000372023.3:c.923+44C>T
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000418210
  ensembl transcript: ENST00000461685
  gene symbol: ZMYND8
  hgvsc: ENST00000461685.1:c.998+44C>T
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000348246
  ensembl transcript: ENST00000355972
  gene symbol: ZMYND8
  hgvsc: ENST00000355972.4:c.938+44C>T
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000392964
  ensembl transcript: ENST00000458360
  gene symbol: ZMYND8
  hgvsc: ENST00000458360.2:c.923+44C>T
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000312237
  ensembl transcript: ENST00000311275
  gene symbol: ZMYND8
  hgvsc: ENST00000311275.7:c.938+44C>T
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000396725
  ensembl transcript: ENST00000446994
  gene symbol: ZMYND8
  hgvsc: ENST00000446994.2:c.749+44C>T
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000443086
  ensembl transcript: ENST00000540497
  gene symbol: ZMYND8
  hgvsc: ENST00000540497.1:c.923+44C>T
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000335537
  ensembl transcript: ENST00000352431
  gene symbol: ZMYND8
  hgvsc: ENST00000352431.2:c.998+44C>T
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000420095
  ensembl transcript: ENST00000471951
  gene symbol: ZMYND8
  hgvsc: ENST00000471951.2:c.998+44C>T
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000354166
  ensembl transcript: ENST00000360911
  gene symbol: ZMYND8
  hgvsc: ENST00000360911.3:c.923+44C>T
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000439800
  ensembl transcript: ENST00000536340
  gene symbol: ZMYND8
  hgvsc: ENST00000536340.1:c.1019+44C>T
  variant of: http://identifiers.org/hgnc/9397
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 923
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21766
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1172
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2315
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15423
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2620
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1409
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5305
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1287
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
population: South Asian
reference allele: G
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD

http://identifiers.org/exac.variant/20-45910817-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45910817
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 45910817
    reference: chr 20
allele count: 1
allele frequency: 8.405197774303629e-6
allele num: 118974
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000418210
  ensembl transcript: ENST00000461685
  gene symbol: ZMYND8
  hgvsc: ENST00000461685.1:c.998+29G>T
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000354166
  ensembl transcript: ENST00000360911
  gene symbol: ZMYND8
  hgvsc: ENST00000360911.3:c.923+29G>T
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000361093
  ensembl transcript: ENST00000372023
  gene symbol: ZMYND8
  hgvsc: ENST00000372023.3:c.923+29G>T
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000312237
  ensembl transcript: ENST00000311275
  gene symbol: ZMYND8
  hgvsc: ENST00000311275.7:c.938+29G>T
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl transcript: ENST00000468376
  gene symbol: ZMYND8
  hgvsc: ENST00000468376.2:n.949+29G>T
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000418495
  ensembl transcript: ENST00000467200
  gene symbol: ZMYND8
  hgvsc: ENST00000467200.2:c.717+29G>T
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000392964
  ensembl transcript: ENST00000458360
  gene symbol: ZMYND8
  hgvsc: ENST00000458360.2:c.923+29G>T
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000262975
  ensembl transcript: ENST00000262975
  gene symbol: ZMYND8
  hgvsc: ENST00000262975.4:c.938+29G>T
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000443086
  ensembl transcript: ENST00000540497
  gene symbol: ZMYND8
  hgvsc: ENST00000540497.1:c.923+29G>T
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000348246
  ensembl transcript: ENST00000355972
  gene symbol: ZMYND8
  hgvsc: ENST00000355972.4:c.938+29G>T
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000439800
  ensembl transcript: ENST00000536340
  gene symbol: ZMYND8
  hgvsc: ENST00000536340.1:c.1019+29G>T
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000396725
  ensembl transcript: ENST00000446994
  gene symbol: ZMYND8
  hgvsc: ENST00000446994.2:c.749+29G>T
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000335537
  ensembl transcript: ENST00000352431
  gene symbol: ZMYND8
  hgvsc: ENST00000352431.2:c.998+29G>T
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000420095
  ensembl transcript: ENST00000471951
  gene symbol: ZMYND8
  hgvsc: ENST00000471951.2:c.998+29G>T
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000379577
  ensembl transcript: ENST00000396281
  gene symbol: ZMYND8
  hgvsc: ENST00000396281.4:c.938+29G>T
  variant of: http://identifiers.org/hgnc/9397
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 617
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6516
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15435
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2618
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1758
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21987
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 921
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: QD

20-45910824-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45910824
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 45910824
    reference: chr 20
allele count: 3
allele frequency: 2.515512326010398e-5
allele num: 119260
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000361093
  ensembl transcript: ENST00000372023
  gene symbol: ZMYND8
  hgvsc: ENST00000372023.3:c.923+22G>A
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl transcript: ENST00000468376
  gene symbol: ZMYND8
  hgvsc: ENST00000468376.2:n.949+22G>A
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000312237
  ensembl transcript: ENST00000311275
  gene symbol: ZMYND8
  hgvsc: ENST00000311275.7:c.938+22G>A
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000354166
  ensembl transcript: ENST00000360911
  gene symbol: ZMYND8
  hgvsc: ENST00000360911.3:c.923+22G>A
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000418495
  ensembl transcript: ENST00000467200
  gene symbol: ZMYND8
  hgvsc: ENST00000467200.2:c.717+22G>A
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000396725
  ensembl transcript: ENST00000446994
  gene symbol: ZMYND8
  hgvsc: ENST00000446994.2:c.749+22G>A
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000443086
  ensembl transcript: ENST00000540497
  gene symbol: ZMYND8
  hgvsc: ENST00000540497.1:c.923+22G>A
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000262975
  ensembl transcript: ENST00000262975
  gene symbol: ZMYND8
  hgvsc: ENST00000262975.4:c.938+22G>A
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000439800
  ensembl transcript: ENST00000536340
  gene symbol: ZMYND8
  hgvsc: ENST00000536340.1:c.1019+22G>A
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000348246
  ensembl transcript: ENST00000355972
  gene symbol: ZMYND8
  hgvsc: ENST00000355972.4:c.938+22G>A
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000392964
  ensembl transcript: ENST00000458360
  gene symbol: ZMYND8
  hgvsc: ENST00000458360.2:c.923+22G>A
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000418210
  ensembl transcript: ENST00000461685
  gene symbol: ZMYND8
  hgvsc: ENST00000461685.1:c.998+22G>A
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000420095
  ensembl transcript: ENST00000471951
  gene symbol: ZMYND8
  hgvsc: ENST00000471951.2:c.998+22G>A
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000335537
  ensembl transcript: ENST00000352431
  gene symbol: ZMYND8
  hgvsc: ENST00000352431.2:c.998+22G>A
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000379577
  ensembl transcript: ENST00000396281
  gene symbol: ZMYND8
  hgvsc: ENST00000396281.4:c.938+22G>A
  variant of: http://identifiers.org/hgnc/9397
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 921
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 972
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2616
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1365
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22124
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1405
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
reference allele: C
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/20-45910825-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45910825
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 45910825
    reference: chr 20
allele count: 1
allele frequency: 8.377033524888167e-6
allele num: 119374
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000418210
  ensembl transcript: ENST00000461685
  gene symbol: ZMYND8
  hgvsc: ENST00000461685.1:c.998+21T>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000312237
  ensembl transcript: ENST00000311275
  gene symbol: ZMYND8
  hgvsc: ENST00000311275.7:c.938+21T>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000439800
  ensembl transcript: ENST00000536340
  gene symbol: ZMYND8
  hgvsc: ENST00000536340.1:c.1019+21T>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000361093
  ensembl transcript: ENST00000372023
  gene symbol: ZMYND8
  hgvsc: ENST00000372023.3:c.923+21T>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000354166
  ensembl transcript: ENST00000360911
  gene symbol: ZMYND8
  hgvsc: ENST00000360911.3:c.923+21T>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000348246
  ensembl transcript: ENST00000355972
  gene symbol: ZMYND8
  hgvsc: ENST00000355972.4:c.938+21T>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000420095
  ensembl transcript: ENST00000471951
  gene symbol: ZMYND8
  hgvsc: ENST00000471951.2:c.998+21T>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000262975
  ensembl transcript: ENST00000262975
  gene symbol: ZMYND8
  hgvsc: ENST00000262975.4:c.938+21T>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000392964
  ensembl transcript: ENST00000458360
  gene symbol: ZMYND8
  hgvsc: ENST00000458360.2:c.923+21T>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl transcript: ENST00000468376
  gene symbol: ZMYND8
  hgvsc: ENST00000468376.2:n.949+21T>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000396725
  ensembl transcript: ENST00000446994
  gene symbol: ZMYND8
  hgvsc: ENST00000446994.2:c.749+21T>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000379577
  ensembl transcript: ENST00000396281
  gene symbol: ZMYND8
  hgvsc: ENST00000396281.4:c.938+21T>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000418495
  ensembl transcript: ENST00000467200
  gene symbol: ZMYND8
  hgvsc: ENST00000467200.2:c.717+21T>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000335537
  ensembl transcript: ENST00000352431
  gene symbol: ZMYND8
  hgvsc: ENST00000352431.2:c.998+21T>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000443086
  ensembl transcript: ENST00000540497
  gene symbol: ZMYND8
  hgvsc: ENST00000540497.1:c.923+21T>G
  variant of: http://identifiers.org/hgnc/9397
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 953
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2614
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15455
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1279
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 922
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7154
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1406
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Latino
reference allele: A
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum

20-45910827-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45910827
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 45910827
    reference: chr 20
allele count: 1
allele frequency: 8.370442294170824e-6
allele num: 119468
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000312237
  ensembl transcript: ENST00000311275
  gene symbol: ZMYND8
  hgvsc: ENST00000311275.7:c.938+19C>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl transcript: ENST00000468376
  gene symbol: ZMYND8
  hgvsc: ENST00000468376.2:n.949+19C>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000348246
  ensembl transcript: ENST00000355972
  gene symbol: ZMYND8
  hgvsc: ENST00000355972.4:c.938+19C>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000392964
  ensembl transcript: ENST00000458360
  gene symbol: ZMYND8
  hgvsc: ENST00000458360.2:c.923+19C>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000354166
  ensembl transcript: ENST00000360911
  gene symbol: ZMYND8
  hgvsc: ENST00000360911.3:c.923+19C>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000418210
  ensembl transcript: ENST00000461685
  gene symbol: ZMYND8
  hgvsc: ENST00000461685.1:c.998+19C>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000262975
  ensembl transcript: ENST00000262975
  gene symbol: ZMYND8
  hgvsc: ENST00000262975.4:c.938+19C>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000443086
  ensembl transcript: ENST00000540497
  gene symbol: ZMYND8
  hgvsc: ENST00000540497.1:c.923+19C>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000439800
  ensembl transcript: ENST00000536340
  gene symbol: ZMYND8
  hgvsc: ENST00000536340.1:c.1019+19C>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000361093
  ensembl transcript: ENST00000372023
  gene symbol: ZMYND8
  hgvsc: ENST00000372023.3:c.923+19C>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000420095
  ensembl transcript: ENST00000471951
  gene symbol: ZMYND8
  hgvsc: ENST00000471951.2:c.998+19C>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000335537
  ensembl transcript: ENST00000352431
  gene symbol: ZMYND8
  hgvsc: ENST00000352431.2:c.998+19C>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000379577
  ensembl transcript: ENST00000396281
  gene symbol: ZMYND8
  hgvsc: ENST00000396281.4:c.938+19C>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000418495
  ensembl transcript: ENST00000467200
  gene symbol: ZMYND8
  hgvsc: ENST00000467200.2:c.717+19C>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000396725
  ensembl transcript: ENST00000446994
  gene symbol: ZMYND8
  hgvsc: ENST00000446994.2:c.749+19C>G
  variant of: http://identifiers.org/hgnc/9397
canonical: true
consequence: intron
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 7331
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 904
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15464
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1148
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5482
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2614
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1406
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum

20-45910827-GC-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45910827
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 45910826
    reference: chr 20
allele count: 1
allele frequency: 8.370442294170824e-6
allele num: 119468
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000335537
  ensembl transcript: ENST00000352431
  gene symbol: ZMYND8
  hgvsc: ENST00000352431.2:c.998+18delG
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000262975
  ensembl transcript: ENST00000262975
  gene symbol: ZMYND8
  hgvsc: ENST00000262975.4:c.938+18delG
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000348246
  ensembl transcript: ENST00000355972
  gene symbol: ZMYND8
  hgvsc: ENST00000355972.4:c.938+18delG
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000420095
  ensembl transcript: ENST00000471951
  gene symbol: ZMYND8
  hgvsc: ENST00000471951.2:c.998+18delG
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000361093
  ensembl transcript: ENST00000372023
  gene symbol: ZMYND8
  hgvsc: ENST00000372023.3:c.923+18delG
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000379577
  ensembl transcript: ENST00000396281
  gene symbol: ZMYND8
  hgvsc: ENST00000396281.4:c.938+18delG
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000354166
  ensembl transcript: ENST00000360911
  gene symbol: ZMYND8
  hgvsc: ENST00000360911.3:c.923+18delG
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000418210
  ensembl transcript: ENST00000461685
  gene symbol: ZMYND8
  hgvsc: ENST00000461685.1:c.998+18delG
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl transcript: ENST00000468376
  gene symbol: ZMYND8
  hgvsc: ENST00000468376.2:n.949+18delG
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000396725
  ensembl transcript: ENST00000446994
  gene symbol: ZMYND8
  hgvsc: ENST00000446994.2:c.749+18delG
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000392964
  ensembl transcript: ENST00000458360
  gene symbol: ZMYND8
  hgvsc: ENST00000458360.2:c.923+18delG
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000439800
  ensembl transcript: ENST00000536340
  gene symbol: ZMYND8
  hgvsc: ENST00000536340.1:c.1019+18delG
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000312237
  ensembl transcript: ENST00000311275
  gene symbol: ZMYND8
  hgvsc: ENST00000311275.7:c.938+18delG
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000443086
  ensembl transcript: ENST00000540497
  gene symbol: ZMYND8
  hgvsc: ENST00000540497.1:c.923+18delG
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000418495
  ensembl transcript: ENST00000467200
  gene symbol: ZMYND8
  hgvsc: ENST00000467200.2:c.717+18delG
  variant of: http://identifiers.org/hgnc/9397
canonical: true
consequence: intron
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 7331
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 904
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15464
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 922
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5482
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1148
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 616
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: Other
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: GC
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS

20-45910835-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45910835
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 45910835
    reference: chr 20
allele count: 2
allele frequency: 1.667055646317474e-5
allele num: 119972
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000439800
  ensembl transcript: ENST00000536340
  gene symbol: ZMYND8
  hgvsc: ENST00000536340.1:c.1019+11A>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000443086
  ensembl transcript: ENST00000540497
  gene symbol: ZMYND8
  hgvsc: ENST00000540497.1:c.923+11A>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000335537
  ensembl transcript: ENST00000352431
  gene symbol: ZMYND8
  hgvsc: ENST00000352431.2:c.998+11A>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000348246
  ensembl transcript: ENST00000355972
  gene symbol: ZMYND8
  hgvsc: ENST00000355972.4:c.938+11A>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000312237
  ensembl transcript: ENST00000311275
  gene symbol: ZMYND8
  hgvsc: ENST00000311275.7:c.938+11A>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000379577
  ensembl transcript: ENST00000396281
  gene symbol: ZMYND8
  hgvsc: ENST00000396281.4:c.938+11A>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl transcript: ENST00000468376
  gene symbol: ZMYND8
  hgvsc: ENST00000468376.2:n.949+11A>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000361093
  ensembl transcript: ENST00000372023
  gene symbol: ZMYND8
  hgvsc: ENST00000372023.3:c.923+11A>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000354166
  ensembl transcript: ENST00000360911
  gene symbol: ZMYND8
  hgvsc: ENST00000360911.3:c.923+11A>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000418495
  ensembl transcript: ENST00000467200
  gene symbol: ZMYND8
  hgvsc: ENST00000467200.2:c.717+11A>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000418210
  ensembl transcript: ENST00000461685
  gene symbol: ZMYND8
  hgvsc: ENST00000461685.1:c.998+11A>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000392964
  ensembl transcript: ENST00000458360
  gene symbol: ZMYND8
  hgvsc: ENST00000458360.2:c.923+11A>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000396725
  ensembl transcript: ENST00000446994
  gene symbol: ZMYND8
  hgvsc: ENST00000446994.2:c.749+11A>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000420095
  ensembl transcript: ENST00000471951
  gene symbol: ZMYND8
  hgvsc: ENST00000471951.2:c.998+11A>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000262975
  ensembl transcript: ENST00000262975
  gene symbol: ZMYND8
  hgvsc: ENST00000262975.4:c.938+11A>G
  variant of: http://identifiers.org/hgnc/9397
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 616
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7809
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 750
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2614
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22381
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
population: Other
population: African
population: European (Non-Finnish)
reference allele: T
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: DP

20-45910838-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45910838
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 45910838
    reference: chr 20
allele count: 1
allele frequency: 8.32514693884347e-6
allele num: 120118
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000396725
  ensembl transcript: ENST00000446994
  gene symbol: ZMYND8
  hgvsc: ENST00000446994.2:c.749+8T>C
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000262975
  ensembl transcript: ENST00000262975
  gene symbol: ZMYND8
  hgvsc: ENST00000262975.4:c.938+8T>C
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000418495
  ensembl transcript: ENST00000467200
  gene symbol: ZMYND8
  hgvsc: ENST00000467200.2:c.717+8T>C
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000420095
  ensembl transcript: ENST00000471951
  gene symbol: ZMYND8
  hgvsc: ENST00000471951.2:c.998+8T>C
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000348246
  ensembl transcript: ENST00000355972
  gene symbol: ZMYND8
  hgvsc: ENST00000355972.4:c.938+8T>C
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000335537
  ensembl transcript: ENST00000352431
  gene symbol: ZMYND8
  hgvsc: ENST00000352431.2:c.998+8T>C
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000392964
  ensembl transcript: ENST00000458360
  gene symbol: ZMYND8
  hgvsc: ENST00000458360.2:c.923+8T>C
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000361093
  ensembl transcript: ENST00000372023
  gene symbol: ZMYND8
  hgvsc: ENST00000372023.3:c.923+8T>C
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000443086
  ensembl transcript: ENST00000540497
  gene symbol: ZMYND8
  hgvsc: ENST00000540497.1:c.923+8T>C
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl transcript: ENST00000468376
  gene symbol: ZMYND8
  hgvsc: ENST00000468376.2:n.949+8T>C
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000354166
  ensembl transcript: ENST00000360911
  gene symbol: ZMYND8
  hgvsc: ENST00000360911.3:c.923+8T>C
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000418210
  ensembl transcript: ENST00000461685
  gene symbol: ZMYND8
  hgvsc: ENST00000461685.1:c.998+8T>C
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000312237
  ensembl transcript: ENST00000311275
  gene symbol: ZMYND8
  hgvsc: ENST00000311275.7:c.938+8T>C
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000439800
  ensembl transcript: ENST00000536340
  gene symbol: ZMYND8
  hgvsc: ENST00000536340.1:c.1019+8T>C
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000379577
  ensembl transcript: ENST00000396281
  gene symbol: ZMYND8
  hgvsc: ENST00000396281.4:c.938+8T>C
  variant of: http://identifiers.org/hgnc/9397
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22441
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 613
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15486
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1406
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7978
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 921
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 638
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.998+8T>C
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
population: East Asian
population: European (Finnish)
population: Other
reference allele: A
site quality: DP
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum

20-45910854-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45910854
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 45910854
    reference: chr 20
allele count: 74
allele frequency: 6.123293338849814e-4
allele num: 120850
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000312237
  ensembl transcript: ENST00000311275
  gene symbol: ZMYND8
  hgvsc: ENST00000311275.7:c.930A>G
  hgvsp: ENST00000311275.7:c.930A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000354166
  ensembl transcript: ENST00000360911
  gene symbol: ZMYND8
  hgvsc: ENST00000360911.3:c.915A>G
  hgvsp: ENST00000360911.3:c.915A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000418210
  ensembl transcript: ENST00000461685
  gene symbol: ZMYND8
  hgvsc: ENST00000461685.1:c.990A>G
  hgvsp: ENST00000461685.1:c.990A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000443086
  ensembl transcript: ENST00000540497
  gene symbol: ZMYND8
  hgvsc: ENST00000540497.1:c.915A>G
  hgvsp: ENST00000540497.1:c.915A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000396725
  ensembl transcript: ENST00000446994
  gene symbol: ZMYND8
  hgvsc: ENST00000446994.2:c.741A>G
  hgvsp: ENST00000446994.2:c.741A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000335537
  ensembl transcript: ENST00000352431
  gene symbol: ZMYND8
  hgvsc: ENST00000352431.2:c.990A>G
  hgvsp: ENST00000352431.2:c.990A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000420095
  ensembl transcript: ENST00000471951
  gene symbol: ZMYND8
  hgvsc: ENST00000471951.2:c.990A>G
  hgvsp: ENST00000471951.2:c.990A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000439800
  ensembl transcript: ENST00000536340
  gene symbol: ZMYND8
  hgvsc: ENST00000536340.1:c.1011A>G
  hgvsp: ENST00000536340.1:c.1011A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000262975
  ensembl transcript: ENST00000262975
  gene symbol: ZMYND8
  hgvsc: ENST00000262975.4:c.930A>G
  hgvsp: ENST00000262975.4:c.930A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000348246
  ensembl transcript: ENST00000355972
  gene symbol: ZMYND8
  hgvsc: ENST00000355972.4:c.930A>G
  hgvsp: ENST00000355972.4:c.930A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000418495
  ensembl transcript: ENST00000467200
  gene symbol: ZMYND8
  hgvsc: ENST00000467200.2:c.709A>G
  hgvsp: ENST00000467200.2:c.709A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000361093
  ensembl transcript: ENST00000372023
  gene symbol: ZMYND8
  hgvsc: ENST00000372023.3:c.915A>G
  hgvsp: ENST00000372023.3:c.915A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101040
  ensembl transcript: ENST00000468376
  gene symbol: ZMYND8
  hgvsc: ENST00000468376.2:n.941A>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000392964
  ensembl transcript: ENST00000458360
  gene symbol: ZMYND8
  hgvsc: ENST00000458360.2:c.915A>G
  hgvsp: ENST00000458360.2:c.915A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000379577
  ensembl transcript: ENST00000396281
  gene symbol: ZMYND8
  hgvsc: ENST00000396281.4:c.930A>G
  hgvsp: ENST00000396281.4:c.930A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 15541
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5482
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8440
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 914
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1399
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22836
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 9.75e1
  variant carriers: 48
genotype quality: GenotypeQuality
hgvs: p.Gln330Gln
num of homozygotes: 1
population: Latino
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: T
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD

20-45910881-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45910881
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 45910881
    reference: chr 20
allele count: 1
allele frequency: 8.244838730954422e-6
allele num: 121288
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000262975
  ensembl transcript: ENST00000262975
  gene symbol: ZMYND8
  hgvsc: ENST00000262975.4:c.903G>C
  hgvsp: ENST00000262975.4:c.903G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000418495
  ensembl transcript: ENST00000467200
  gene symbol: ZMYND8
  hgvsc: ENST00000467200.2:c.682G>C
  hgvsp: ENST00000467200.2:c.682G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000312237
  ensembl transcript: ENST00000311275
  gene symbol: ZMYND8
  hgvsc: ENST00000311275.7:c.903G>C
  hgvsp: ENST00000311275.7:c.903G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000420095
  ensembl transcript: ENST00000471951
  gene symbol: ZMYND8
  hgvsc: ENST00000471951.2:c.963G>C
  hgvsp: ENST00000471951.2:c.963G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000392964
  ensembl transcript: ENST00000458360
  gene symbol: ZMYND8
  hgvsc: ENST00000458360.2:c.888G>C
  hgvsp: ENST00000458360.2:c.888G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000439800
  ensembl transcript: ENST00000536340
  gene symbol: ZMYND8
  hgvsc: ENST00000536340.1:c.984G>C
  hgvsp: ENST00000536340.1:c.984G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000348246
  ensembl transcript: ENST00000355972
  gene symbol: ZMYND8
  hgvsc: ENST00000355972.4:c.903G>C
  hgvsp: ENST00000355972.4:c.903G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000361093
  ensembl transcript: ENST00000372023
  gene symbol: ZMYND8
  hgvsc: ENST00000372023.3:c.888G>C
  hgvsp: ENST00000372023.3:c.888G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000418210
  ensembl transcript: ENST00000461685
  gene symbol: ZMYND8
  hgvsc: ENST00000461685.1:c.963G>C
  hgvsp: ENST00000461685.1:c.963G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000379577
  ensembl transcript: ENST00000396281
  gene symbol: ZMYND8
  hgvsc: ENST00000396281.4:c.903G>C
  hgvsp: ENST00000396281.4:c.903G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101040
  ensembl transcript: ENST00000468376
  gene symbol: ZMYND8
  hgvsc: ENST00000468376.2:n.914G>C
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000354166
  ensembl transcript: ENST00000360911
  gene symbol: ZMYND8
  hgvsc: ENST00000360911.3:c.888G>C
  hgvsp: ENST00000360911.3:c.888G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000396725
  ensembl transcript: ENST00000446994
  gene symbol: ZMYND8
  hgvsc: ENST00000446994.2:c.714G>C
  hgvsp: ENST00000446994.2:c.714G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000443086
  ensembl transcript: ENST00000540497
  gene symbol: ZMYND8
  hgvsc: ENST00000540497.1:c.888G>C
  hgvsp: ENST00000540497.1:c.888G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000335537
  ensembl transcript: ENST00000352431
  gene symbol: ZMYND8
  hgvsc: ENST00000352431.2:c.963G>C
  hgvsp: ENST00000352431.2:c.963G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2613
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 918
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15588
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 608
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8594
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly321Gly
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: Latino
population: African
population: South Asian
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD

20-45910884-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45910884
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 45910884
    reference: chr 20
allele count: 8
allele frequency: 6.595218466611707e-5
allele num: 121300
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000418495
  ensembl transcript: ENST00000467200
  gene symbol: ZMYND8
  hgvsc: ENST00000467200.2:c.679C>T
  hgvsp: ENST00000467200.2:c.679C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000262975
  ensembl transcript: ENST00000262975
  gene symbol: ZMYND8
  hgvsc: ENST00000262975.4:c.900C>T
  hgvsp: ENST00000262975.4:c.900C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000348246
  ensembl transcript: ENST00000355972
  gene symbol: ZMYND8
  hgvsc: ENST00000355972.4:c.900C>T
  hgvsp: ENST00000355972.4:c.900C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000392964
  ensembl transcript: ENST00000458360
  gene symbol: ZMYND8
  hgvsc: ENST00000458360.2:c.885C>T
  hgvsp: ENST00000458360.2:c.885C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000379577
  ensembl transcript: ENST00000396281
  gene symbol: ZMYND8
  hgvsc: ENST00000396281.4:c.900C>T
  hgvsp: ENST00000396281.4:c.900C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000312237
  ensembl transcript: ENST00000311275
  gene symbol: ZMYND8
  hgvsc: ENST00000311275.7:c.900C>T
  hgvsp: ENST00000311275.7:c.900C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000439800
  ensembl transcript: ENST00000536340
  gene symbol: ZMYND8
  hgvsc: ENST00000536340.1:c.981C>T
  hgvsp: ENST00000536340.1:c.981C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000354166
  ensembl transcript: ENST00000360911
  gene symbol: ZMYND8
  hgvsc: ENST00000360911.3:c.885C>T
  hgvsp: ENST00000360911.3:c.885C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101040
  ensembl transcript: ENST00000468376
  gene symbol: ZMYND8
  hgvsc: ENST00000468376.2:n.911C>T
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000418210
  ensembl transcript: ENST00000461685
  gene symbol: ZMYND8
  hgvsc: ENST00000461685.1:c.960C>T
  hgvsp: ENST00000461685.1:c.960C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000420095
  ensembl transcript: ENST00000471951
  gene symbol: ZMYND8
  hgvsc: ENST00000471951.2:c.960C>T
  hgvsp: ENST00000471951.2:c.960C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000396725
  ensembl transcript: ENST00000446994
  gene symbol: ZMYND8
  hgvsc: ENST00000446994.2:c.711C>T
  hgvsp: ENST00000446994.2:c.711C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000361093
  ensembl transcript: ENST00000372023
  gene symbol: ZMYND8
  hgvsc: ENST00000372023.3:c.885C>T
  hgvsp: ENST00000372023.3:c.885C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000335537
  ensembl transcript: ENST00000352431
  gene symbol: ZMYND8
  hgvsc: ENST00000352431.2:c.960C>T
  hgvsp: ENST00000352431.2:c.960C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000443086
  ensembl transcript: ENST00000540497
  gene symbol: ZMYND8
  hgvsc: ENST00000540497.1:c.885C>T
  hgvsp: ENST00000540497.1:c.885C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1400
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15592
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5494
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8604
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp320Asp
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: G
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: QD

20-45910890-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45910890
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 45910890
    reference: chr 20
allele count: 1
allele frequency: 8.243071698237632e-6
allele num: 121314
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000418495
  ensembl transcript: ENST00000467200
  gene symbol: ZMYND8
  hgvsc: ENST00000467200.2:c.673T>C
  hgvsp: ENST00000467200.2:c.673T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000354166
  ensembl transcript: ENST00000360911
  gene symbol: ZMYND8
  hgvsc: ENST00000360911.3:c.879T>C
  hgvsp: ENST00000360911.3:c.879T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000312237
  ensembl transcript: ENST00000311275
  gene symbol: ZMYND8
  hgvsc: ENST00000311275.7:c.894T>C
  hgvsp: ENST00000311275.7:c.894T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000262975
  ensembl transcript: ENST00000262975
  gene symbol: ZMYND8
  hgvsc: ENST00000262975.4:c.894T>C
  hgvsp: ENST00000262975.4:c.894T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000361093
  ensembl transcript: ENST00000372023
  gene symbol: ZMYND8
  hgvsc: ENST00000372023.3:c.879T>C
  hgvsp: ENST00000372023.3:c.879T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000420095
  ensembl transcript: ENST00000471951
  gene symbol: ZMYND8
  hgvsc: ENST00000471951.2:c.954T>C
  hgvsp: ENST00000471951.2:c.954T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101040
  ensembl transcript: ENST00000468376
  gene symbol: ZMYND8
  hgvsc: ENST00000468376.2:n.905T>C
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000379577
  ensembl transcript: ENST00000396281
  gene symbol: ZMYND8
  hgvsc: ENST00000396281.4:c.894T>C
  hgvsp: ENST00000396281.4:c.894T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000396725
  ensembl transcript: ENST00000446994
  gene symbol: ZMYND8
  hgvsc: ENST00000446994.2:c.705T>C
  hgvsp: ENST00000446994.2:c.705T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000418210
  ensembl transcript: ENST00000461685
  gene symbol: ZMYND8
  hgvsc: ENST00000461685.1:c.954T>C
  hgvsp: ENST00000461685.1:c.954T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000443086
  ensembl transcript: ENST00000540497
  gene symbol: ZMYND8
  hgvsc: ENST00000540497.1:c.879T>C
  hgvsp: ENST00000540497.1:c.879T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000348246
  ensembl transcript: ENST00000355972
  gene symbol: ZMYND8
  hgvsc: ENST00000355972.4:c.894T>C
  hgvsp: ENST00000355972.4:c.894T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000335537
  ensembl transcript: ENST00000352431
  gene symbol: ZMYND8
  hgvsc: ENST00000352431.2:c.954T>C
  hgvsp: ENST00000352431.2:c.954T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000392964
  ensembl transcript: ENST00000458360
  gene symbol: ZMYND8
  hgvsc: ENST00000458360.2:c.879T>C
  hgvsp: ENST00000458360.2:c.879T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000439800
  ensembl transcript: ENST00000536340
  gene symbol: ZMYND8
  hgvsc: ENST00000536340.1:c.975T>C
  hgvsp: ENST00000536340.1:c.975T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1400
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 608
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 918
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8611
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp318Asp
num of homozygotes: 0
population: Latino
population: Other
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: African
reference allele: A
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum

20-45910896-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45910896
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 45910896
    reference: chr 20
allele count: 2
allele frequency: 1.648559982854976e-5
allele num: 121318
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000361093
  ensembl transcript: ENST00000372023
  gene symbol: ZMYND8
  hgvsc: ENST00000372023.3:c.873A>G
  hgvsp: ENST00000372023.3:c.873A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000354166
  ensembl transcript: ENST00000360911
  gene symbol: ZMYND8
  hgvsc: ENST00000360911.3:c.873A>G
  hgvsp: ENST00000360911.3:c.873A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000418210
  ensembl transcript: ENST00000461685
  gene symbol: ZMYND8
  hgvsc: ENST00000461685.1:c.948A>G
  hgvsp: ENST00000461685.1:c.948A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000262975
  ensembl transcript: ENST00000262975
  gene symbol: ZMYND8
  hgvsc: ENST00000262975.4:c.888A>G
  hgvsp: ENST00000262975.4:c.888A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000348246
  ensembl transcript: ENST00000355972
  gene symbol: ZMYND8
  hgvsc: ENST00000355972.4:c.888A>G
  hgvsp: ENST00000355972.4:c.888A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000418495
  ensembl transcript: ENST00000467200
  gene symbol: ZMYND8
  hgvsc: ENST00000467200.2:c.667A>G
  hgvsp: ENST00000467200.2:c.667A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000312237
  ensembl transcript: ENST00000311275
  gene symbol: ZMYND8
  hgvsc: ENST00000311275.7:c.888A>G
  hgvsp: ENST00000311275.7:c.888A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000396725
  ensembl transcript: ENST00000446994
  gene symbol: ZMYND8
  hgvsc: ENST00000446994.2:c.699A>G
  hgvsp: ENST00000446994.2:c.699A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000439800
  ensembl transcript: ENST00000536340
  gene symbol: ZMYND8
  hgvsc: ENST00000536340.1:c.969A>G
  hgvsp: ENST00000536340.1:c.969A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000335537
  ensembl transcript: ENST00000352431
  gene symbol: ZMYND8
  hgvsc: ENST00000352431.2:c.948A>G
  hgvsp: ENST00000352431.2:c.948A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000379577
  ensembl transcript: ENST00000396281
  gene symbol: ZMYND8
  hgvsc: ENST00000396281.4:c.888A>G
  hgvsp: ENST00000396281.4:c.888A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000420095
  ensembl transcript: ENST00000471951
  gene symbol: ZMYND8
  hgvsc: ENST00000471951.2:c.948A>G
  hgvsp: ENST00000471951.2:c.948A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000443086
  ensembl transcript: ENST00000540497
  gene symbol: ZMYND8
  hgvsc: ENST00000540497.1:c.873A>G
  hgvsp: ENST00000540497.1:c.873A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000392964
  ensembl transcript: ENST00000458360
  gene symbol: ZMYND8
  hgvsc: ENST00000458360.2:c.873A>G
  hgvsp: ENST00000458360.2:c.873A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101040
  ensembl transcript: ENST00000468376
  gene symbol: ZMYND8
  hgvsc: ENST00000468376.2:n.899A>G
  variant of: http://identifiers.org/hgnc/9397
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23127
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5495
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2610
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu316Leu
num of homozygotes: 0
population: Latino
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: T
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: BaseQRankSum

20-45910908-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45910908
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 45910908
    reference: chr 20
allele count: 1
allele frequency: 8.244430886935875e-6
allele num: 121294
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101040
  ensembl transcript: ENST00000468376
  gene symbol: ZMYND8
  hgvsc: ENST00000468376.2:n.887T>C
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000418210
  ensembl transcript: ENST00000461685
  gene symbol: ZMYND8
  hgvsc: ENST00000461685.1:c.936T>C
  hgvsp: ENST00000461685.1:c.936T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000396725
  ensembl transcript: ENST00000446994
  gene symbol: ZMYND8
  hgvsc: ENST00000446994.2:c.687T>C
  hgvsp: ENST00000446994.2:c.687T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000354166
  ensembl transcript: ENST00000360911
  gene symbol: ZMYND8
  hgvsc: ENST00000360911.3:c.861T>C
  hgvsp: ENST00000360911.3:c.861T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000379577
  ensembl transcript: ENST00000396281
  gene symbol: ZMYND8
  hgvsc: ENST00000396281.4:c.876T>C
  hgvsp: ENST00000396281.4:c.876T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000361093
  ensembl transcript: ENST00000372023
  gene symbol: ZMYND8
  hgvsc: ENST00000372023.3:c.861T>C
  hgvsp: ENST00000372023.3:c.861T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000262975
  ensembl transcript: ENST00000262975
  gene symbol: ZMYND8
  hgvsc: ENST00000262975.4:c.876T>C
  hgvsp: ENST00000262975.4:c.876T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000312237
  ensembl transcript: ENST00000311275
  gene symbol: ZMYND8
  hgvsc: ENST00000311275.7:c.876T>C
  hgvsp: ENST00000311275.7:c.876T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000418495
  ensembl transcript: ENST00000467200
  gene symbol: ZMYND8
  hgvsc: ENST00000467200.2:c.655T>C
  hgvsp: ENST00000467200.2:c.655T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000443086
  ensembl transcript: ENST00000540497
  gene symbol: ZMYND8
  hgvsc: ENST00000540497.1:c.861T>C
  hgvsp: ENST00000540497.1:c.861T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000348246
  ensembl transcript: ENST00000355972
  gene symbol: ZMYND8
  hgvsc: ENST00000355972.4:c.876T>C
  hgvsp: ENST00000355972.4:c.876T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000392964
  ensembl transcript: ENST00000458360
  gene symbol: ZMYND8
  hgvsc: ENST00000458360.2:c.861T>C
  hgvsp: ENST00000458360.2:c.861T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000439800
  ensembl transcript: ENST00000536340
  gene symbol: ZMYND8
  hgvsc: ENST00000536340.1:c.957T>C
  hgvsp: ENST00000536340.1:c.957T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000420095
  ensembl transcript: ENST00000471951
  gene symbol: ZMYND8
  hgvsc: ENST00000471951.2:c.936T>C
  hgvsp: ENST00000471951.2:c.936T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000335537
  ensembl transcript: ENST00000352431
  gene symbol: ZMYND8
  hgvsc: ENST00000352431.2:c.936T>C
  hgvsp: ENST00000352431.2:c.936T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 23128
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5494
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1400
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro312Pro
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: South Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum

20-45910935-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45910935
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 45910935
    reference: chr 20
allele count: 1
allele frequency: 8.254094030639197e-6
allele num: 121152
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000312237
  ensembl transcript: ENST00000311275
  gene symbol: ZMYND8
  hgvsc: ENST00000311275.7:c.849C>T
  hgvsp: ENST00000311275.7:c.849C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000354166
  ensembl transcript: ENST00000360911
  gene symbol: ZMYND8
  hgvsc: ENST00000360911.3:c.834C>T
  hgvsp: ENST00000360911.3:c.834C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000439800
  ensembl transcript: ENST00000536340
  gene symbol: ZMYND8
  hgvsc: ENST00000536340.1:c.930C>T
  hgvsp: ENST00000536340.1:c.930C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000396725
  ensembl transcript: ENST00000446994
  gene symbol: ZMYND8
  hgvsc: ENST00000446994.2:c.660C>T
  hgvsp: ENST00000446994.2:c.660C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000443086
  ensembl transcript: ENST00000540497
  gene symbol: ZMYND8
  hgvsc: ENST00000540497.1:c.834C>T
  hgvsp: ENST00000540497.1:c.834C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000418495
  ensembl transcript: ENST00000467200
  gene symbol: ZMYND8
  hgvsc: ENST00000467200.2:c.628C>T
  hgvsp: ENST00000467200.2:c.628C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000418210
  ensembl transcript: ENST00000461685
  gene symbol: ZMYND8
  hgvsc: ENST00000461685.1:c.909C>T
  hgvsp: ENST00000461685.1:c.909C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000361093
  ensembl transcript: ENST00000372023
  gene symbol: ZMYND8
  hgvsc: ENST00000372023.3:c.834C>T
  hgvsp: ENST00000372023.3:c.834C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000392964
  ensembl transcript: ENST00000458360
  gene symbol: ZMYND8
  hgvsc: ENST00000458360.2:c.834C>T
  hgvsp: ENST00000458360.2:c.834C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000348246
  ensembl transcript: ENST00000355972
  gene symbol: ZMYND8
  hgvsc: ENST00000355972.4:c.849C>T
  hgvsp: ENST00000355972.4:c.849C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000379577
  ensembl transcript: ENST00000396281
  gene symbol: ZMYND8
  hgvsc: ENST00000396281.4:c.849C>T
  hgvsp: ENST00000396281.4:c.849C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000262975
  ensembl transcript: ENST00000262975
  gene symbol: ZMYND8
  hgvsc: ENST00000262975.4:c.849C>T
  hgvsp: ENST00000262975.4:c.849C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000335537
  ensembl transcript: ENST00000352431
  gene symbol: ZMYND8
  hgvsc: ENST00000352431.2:c.909C>T
  hgvsp: ENST00000352431.2:c.909C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101040
  ensembl transcript: ENST00000468376
  gene symbol: ZMYND8
  hgvsc: ENST00000468376.2:n.860C>T
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000420095
  ensembl transcript: ENST00000471951
  gene symbol: ZMYND8
  hgvsc: ENST00000471951.2:c.909C>T
  hgvsp: ENST00000471951.2:c.909C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9397
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1399
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Ala303Ala
num of homozygotes: 0
population: African
population: Other
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum

20-45910949-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45910949
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 45910949
    reference: chr 20
allele count: 1
allele frequency: 8.271298593879239e-6
allele num: 120900
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000420095
  ensembl transcript: ENST00000471951
  gene symbol: ZMYND8
  hgvsc: ENST00000471951.2:c.895C>A
  hgvsp: ENSP00000420095.2:p.Pro299Thr
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000348246
  ensembl transcript: ENST00000355972
  gene symbol: ZMYND8
  hgvsc: ENST00000355972.4:c.835C>A
  hgvsp: ENSP00000348246.4:p.Pro279Thr
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000335537
  ensembl transcript: ENST00000352431
  gene symbol: ZMYND8
  hgvsc: ENST00000352431.2:c.895C>A
  hgvsp: ENSP00000335537.3:p.Pro299Thr
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000396725
  ensembl transcript: ENST00000446994
  gene symbol: ZMYND8
  hgvsc: ENST00000446994.2:c.646C>A
  hgvsp: ENSP00000396725.2:p.Pro216Thr
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000379577
  ensembl transcript: ENST00000396281
  gene symbol: ZMYND8
  hgvsc: ENST00000396281.4:c.835C>A
  hgvsp: ENSP00000379577.4:p.Pro279Thr
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000439800
  ensembl transcript: ENST00000536340
  gene symbol: ZMYND8
  hgvsc: ENST00000536340.1:c.916C>A
  hgvsp: ENSP00000439800.1:p.Pro306Thr
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000392964
  ensembl transcript: ENST00000458360
  gene symbol: ZMYND8
  hgvsc: ENST00000458360.2:c.820C>A
  hgvsp: ENSP00000392964.2:p.Pro274Thr
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000361093
  ensembl transcript: ENST00000372023
  gene symbol: ZMYND8
  hgvsc: ENST00000372023.3:c.820C>A
  hgvsp: ENSP00000361093.3:p.Pro274Thr
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000443086
  ensembl transcript: ENST00000540497
  gene symbol: ZMYND8
  hgvsc: ENST00000540497.1:c.820C>A
  hgvsp: ENSP00000443086.1:p.Pro274Thr
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000418210
  ensembl transcript: ENST00000461685
  gene symbol: ZMYND8
  hgvsc: ENST00000461685.1:c.895C>A
  hgvsp: ENSP00000418210.1:p.Pro299Thr
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000354166
  ensembl transcript: ENST00000360911
  gene symbol: ZMYND8
  hgvsc: ENST00000360911.3:c.820C>A
  hgvsp: ENSP00000354166.3:p.Pro274Thr
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000418495
  ensembl transcript: ENST00000467200
  gene symbol: ZMYND8
  hgvsc: ENST00000467200.2:c.614C>A
  hgvsp: ENSP00000418495.2:p.Pro206Thr
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000312237
  ensembl transcript: ENST00000311275
  gene symbol: ZMYND8
  hgvsc: ENST00000311275.7:c.835C>A
  hgvsp: ENSP00000312237.7:p.Pro279Thr
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000262975
  ensembl transcript: ENST00000262975
  gene symbol: ZMYND8
  hgvsc: ENST00000262975.4:c.835C>A
  hgvsp: ENSP00000262975.4:p.Pro279Thr
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101040
  ensembl transcript: ENST00000468376
  gene symbol: ZMYND8
  hgvsc: ENST00000468376.2:n.846C>A
  variant of: http://identifiers.org/hgnc/9397
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5489
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2611
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22972
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro299Thr
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: South Asian
population: Latino
population: African
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum

20-45910971-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45910971
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 45910971
    reference: chr 20
allele count: 4
allele frequency: 3.333222225925803e-5
allele num: 120004
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000361093
  ensembl transcript: ENST00000372023
  gene symbol: ZMYND8
  hgvsc: ENST00000372023.3:c.808-10C>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000348246
  ensembl transcript: ENST00000355972
  gene symbol: ZMYND8
  hgvsc: ENST00000355972.4:c.823-10C>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000392964
  ensembl transcript: ENST00000458360
  gene symbol: ZMYND8
  hgvsc: ENST00000458360.2:c.808-10C>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000335537
  ensembl transcript: ENST00000352431
  gene symbol: ZMYND8
  hgvsc: ENST00000352431.2:c.883-10C>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000418210
  ensembl transcript: ENST00000461685
  gene symbol: ZMYND8
  hgvsc: ENST00000461685.1:c.883-10C>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000379577
  ensembl transcript: ENST00000396281
  gene symbol: ZMYND8
  hgvsc: ENST00000396281.4:c.823-10C>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000443086
  ensembl transcript: ENST00000540497
  gene symbol: ZMYND8
  hgvsc: ENST00000540497.1:c.808-10C>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000420095
  ensembl transcript: ENST00000471951
  gene symbol: ZMYND8
  hgvsc: ENST00000471951.2:c.883-10C>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl transcript: ENST00000468376
  gene symbol: ZMYND8
  hgvsc: ENST00000468376.2:n.834-10C>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000439800
  ensembl transcript: ENST00000536340
  gene symbol: ZMYND8
  hgvsc: ENST00000536340.1:c.904-10C>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000418495
  ensembl transcript: ENST00000467200
  gene symbol: ZMYND8
  hgvsc: ENST00000467200.2:c.602-10C>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000354166
  ensembl transcript: ENST00000360911
  gene symbol: ZMYND8
  hgvsc: ENST00000360911.3:c.808-10C>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000312237
  ensembl transcript: ENST00000311275
  gene symbol: ZMYND8
  hgvsc: ENST00000311275.7:c.823-10C>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000396725
  ensembl transcript: ENST00000446994
  gene symbol: ZMYND8
  hgvsc: ENST00000446994.2:c.634-10C>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000262975
  ensembl transcript: ENST00000262975
  gene symbol: ZMYND8
  hgvsc: ENST00000262975.4:c.823-10C>G
  variant of: http://identifiers.org/hgnc/9397
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 919
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2597
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7222
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22477
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1532
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15241
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1397
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 1
population: African
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD

http://identifiers.org/exac.variant/20-45910978-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45910978
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 45910978
    reference: chr 20
allele count: 2
allele frequency: 1.672716324038606e-5
allele num: 119566
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl transcript: ENST00000468376
  gene symbol: ZMYND8
  hgvsc: ENST00000468376.2:n.834-17T>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000348246
  ensembl transcript: ENST00000355972
  gene symbol: ZMYND8
  hgvsc: ENST00000355972.4:c.823-17T>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000418210
  ensembl transcript: ENST00000461685
  gene symbol: ZMYND8
  hgvsc: ENST00000461685.1:c.883-17T>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000418495
  ensembl transcript: ENST00000467200
  gene symbol: ZMYND8
  hgvsc: ENST00000467200.2:c.602-17T>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000420095
  ensembl transcript: ENST00000471951
  gene symbol: ZMYND8
  hgvsc: ENST00000471951.2:c.883-17T>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000312237
  ensembl transcript: ENST00000311275
  gene symbol: ZMYND8
  hgvsc: ENST00000311275.7:c.823-17T>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000443086
  ensembl transcript: ENST00000540497
  gene symbol: ZMYND8
  hgvsc: ENST00000540497.1:c.808-17T>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000439800
  ensembl transcript: ENST00000536340
  gene symbol: ZMYND8
  hgvsc: ENST00000536340.1:c.904-17T>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000354166
  ensembl transcript: ENST00000360911
  gene symbol: ZMYND8
  hgvsc: ENST00000360911.3:c.808-17T>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000361093
  ensembl transcript: ENST00000372023
  gene symbol: ZMYND8
  hgvsc: ENST00000372023.3:c.808-17T>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000379577
  ensembl transcript: ENST00000396281
  gene symbol: ZMYND8
  hgvsc: ENST00000396281.4:c.823-17T>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000396725
  ensembl transcript: ENST00000446994
  gene symbol: ZMYND8
  hgvsc: ENST00000446994.2:c.634-17T>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000335537
  ensembl transcript: ENST00000352431
  gene symbol: ZMYND8
  hgvsc: ENST00000352431.2:c.883-17T>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000262975
  ensembl transcript: ENST00000262975
  gene symbol: ZMYND8
  hgvsc: ENST00000262975.4:c.823-17T>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000392964
  ensembl transcript: ENST00000458360
  gene symbol: ZMYND8
  hgvsc: ENST00000458360.2:c.808-17T>G
  variant of: http://identifiers.org/hgnc/9397
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5358
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 915
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21893
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6671
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 749
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 608
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2504
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1394
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14894
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 819
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
population: African
population: European (Finnish)
reference allele: A
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: BaseQRankSum

20-45910980-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45910980
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 45910980
    reference: chr 20
allele count: 1
allele frequency: 8.372965369415233e-6
allele num: 119432
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000312237
  ensembl transcript: ENST00000311275
  gene symbol: ZMYND8
  hgvsc: ENST00000311275.7:c.823-19C>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl transcript: ENST00000468376
  gene symbol: ZMYND8
  hgvsc: ENST00000468376.2:n.834-19C>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000418210
  ensembl transcript: ENST00000461685
  gene symbol: ZMYND8
  hgvsc: ENST00000461685.1:c.883-19C>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000420095
  ensembl transcript: ENST00000471951
  gene symbol: ZMYND8
  hgvsc: ENST00000471951.2:c.883-19C>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000354166
  ensembl transcript: ENST00000360911
  gene symbol: ZMYND8
  hgvsc: ENST00000360911.3:c.808-19C>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000348246
  ensembl transcript: ENST00000355972
  gene symbol: ZMYND8
  hgvsc: ENST00000355972.4:c.823-19C>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000262975
  ensembl transcript: ENST00000262975
  gene symbol: ZMYND8
  hgvsc: ENST00000262975.4:c.823-19C>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000335537
  ensembl transcript: ENST00000352431
  gene symbol: ZMYND8
  hgvsc: ENST00000352431.2:c.883-19C>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000379577
  ensembl transcript: ENST00000396281
  gene symbol: ZMYND8
  hgvsc: ENST00000396281.4:c.823-19C>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000361093
  ensembl transcript: ENST00000372023
  gene symbol: ZMYND8
  hgvsc: ENST00000372023.3:c.808-19C>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000418495
  ensembl transcript: ENST00000467200
  gene symbol: ZMYND8
  hgvsc: ENST00000467200.2:c.602-19C>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000392964
  ensembl transcript: ENST00000458360
  gene symbol: ZMYND8
  hgvsc: ENST00000458360.2:c.808-19C>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000443086
  ensembl transcript: ENST00000540497
  gene symbol: ZMYND8
  hgvsc: ENST00000540497.1:c.808-19C>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000439800
  ensembl transcript: ENST00000536340
  gene symbol: ZMYND8
  hgvsc: ENST00000536340.1:c.904-19C>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000396725
  ensembl transcript: ENST00000446994
  gene symbol: ZMYND8
  hgvsc: ENST00000446994.2:c.634-19C>G
  variant of: http://identifiers.org/hgnc/9397
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14696
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2581
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2907
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1395
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 875
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 608
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6524
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 915
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 501
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
population: Latino
population: East Asian
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: ReadPosRankSum

20-45910995-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45910995
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 45910995
    reference: chr 20
allele count: 1
allele frequency: 8.45337120443633e-6
allele num: 118296
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000443086
  ensembl transcript: ENST00000540497
  gene symbol: ZMYND8
  hgvsc: ENST00000540497.1:c.808-34G>A
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000396725
  ensembl transcript: ENST00000446994
  gene symbol: ZMYND8
  hgvsc: ENST00000446994.2:c.634-34G>A
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000379577
  ensembl transcript: ENST00000396281
  gene symbol: ZMYND8
  hgvsc: ENST00000396281.4:c.823-34G>A
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000312237
  ensembl transcript: ENST00000311275
  gene symbol: ZMYND8
  hgvsc: ENST00000311275.7:c.823-34G>A
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl transcript: ENST00000468376
  gene symbol: ZMYND8
  hgvsc: ENST00000468376.2:n.834-34G>A
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000361093
  ensembl transcript: ENST00000372023
  gene symbol: ZMYND8
  hgvsc: ENST00000372023.3:c.808-34G>A
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000418210
  ensembl transcript: ENST00000461685
  gene symbol: ZMYND8
  hgvsc: ENST00000461685.1:c.883-34G>A
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000348246
  ensembl transcript: ENST00000355972
  gene symbol: ZMYND8
  hgvsc: ENST00000355972.4:c.823-34G>A
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000354166
  ensembl transcript: ENST00000360911
  gene symbol: ZMYND8
  hgvsc: ENST00000360911.3:c.808-34G>A
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000262975
  ensembl transcript: ENST00000262975
  gene symbol: ZMYND8
  hgvsc: ENST00000262975.4:c.823-34G>A
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000420095
  ensembl transcript: ENST00000471951
  gene symbol: ZMYND8
  hgvsc: ENST00000471951.2:c.883-34G>A
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000392964
  ensembl transcript: ENST00000458360
  gene symbol: ZMYND8
  hgvsc: ENST00000458360.2:c.808-34G>A
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000439800
  ensembl transcript: ENST00000536340
  gene symbol: ZMYND8
  hgvsc: ENST00000536340.1:c.904-34G>A
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000418495
  ensembl transcript: ENST00000467200
  gene symbol: ZMYND8
  hgvsc: ENST00000467200.2:c.602-34G>A
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000335537
  ensembl transcript: ENST00000352431
  gene symbol: ZMYND8
  hgvsc: ENST00000352431.2:c.883-34G>A
  variant of: http://identifiers.org/hgnc/9397
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5751
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5884
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11644
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5707
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 608
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17992
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1209
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD

20-45910996-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45910996
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 45910996
    reference: chr 20
allele count: 1
allele frequency: 8.444662129068216e-6
allele num: 118418
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000418210
  ensembl transcript: ENST00000461685
  gene symbol: ZMYND8
  hgvsc: ENST00000461685.1:c.883-35T>C
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000418495
  ensembl transcript: ENST00000467200
  gene symbol: ZMYND8
  hgvsc: ENST00000467200.2:c.602-35T>C
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000420095
  ensembl transcript: ENST00000471951
  gene symbol: ZMYND8
  hgvsc: ENST00000471951.2:c.883-35T>C
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000379577
  ensembl transcript: ENST00000396281
  gene symbol: ZMYND8
  hgvsc: ENST00000396281.4:c.823-35T>C
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000335537
  ensembl transcript: ENST00000352431
  gene symbol: ZMYND8
  hgvsc: ENST00000352431.2:c.883-35T>C
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000396725
  ensembl transcript: ENST00000446994
  gene symbol: ZMYND8
  hgvsc: ENST00000446994.2:c.634-35T>C
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000361093
  ensembl transcript: ENST00000372023
  gene symbol: ZMYND8
  hgvsc: ENST00000372023.3:c.808-35T>C
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000348246
  ensembl transcript: ENST00000355972
  gene symbol: ZMYND8
  hgvsc: ENST00000355972.4:c.823-35T>C
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl transcript: ENST00000468376
  gene symbol: ZMYND8
  hgvsc: ENST00000468376.2:n.834-35T>C
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000392964
  ensembl transcript: ENST00000458360
  gene symbol: ZMYND8
  hgvsc: ENST00000458360.2:c.808-35T>C
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000312237
  ensembl transcript: ENST00000311275
  gene symbol: ZMYND8
  hgvsc: ENST00000311275.7:c.823-35T>C
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000354166
  ensembl transcript: ENST00000360911
  gene symbol: ZMYND8
  hgvsc: ENST00000360911.3:c.808-35T>C
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000262975
  ensembl transcript: ENST00000262975
  gene symbol: ZMYND8
  hgvsc: ENST00000262975.4:c.823-35T>C
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000443086
  ensembl transcript: ENST00000540497
  gene symbol: ZMYND8
  hgvsc: ENST00000540497.1:c.808-35T>C
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000439800
  ensembl transcript: ENST00000536340
  gene symbol: ZMYND8
  hgvsc: ENST00000536340.1:c.904-35T>C
  variant of: http://identifiers.org/hgnc/9397
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1222
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2495
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5848
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5819
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1378
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18007
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4646
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5732
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 501
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQ

20-45910997-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45910997
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 45910997
    reference: chr 20
allele count: 1
allele frequency: 8.451370812345762e-6
allele num: 118324
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000361093
  ensembl transcript: ENST00000372023
  gene symbol: ZMYND8
  hgvsc: ENST00000372023.3:c.808-36A>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000418210
  ensembl transcript: ENST00000461685
  gene symbol: ZMYND8
  hgvsc: ENST00000461685.1:c.883-36A>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000335537
  ensembl transcript: ENST00000352431
  gene symbol: ZMYND8
  hgvsc: ENST00000352431.2:c.883-36A>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000348246
  ensembl transcript: ENST00000355972
  gene symbol: ZMYND8
  hgvsc: ENST00000355972.4:c.823-36A>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000420095
  ensembl transcript: ENST00000471951
  gene symbol: ZMYND8
  hgvsc: ENST00000471951.2:c.883-36A>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000439800
  ensembl transcript: ENST00000536340
  gene symbol: ZMYND8
  hgvsc: ENST00000536340.1:c.904-36A>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000262975
  ensembl transcript: ENST00000262975
  gene symbol: ZMYND8
  hgvsc: ENST00000262975.4:c.823-36A>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000312237
  ensembl transcript: ENST00000311275
  gene symbol: ZMYND8
  hgvsc: ENST00000311275.7:c.823-36A>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000379577
  ensembl transcript: ENST00000396281
  gene symbol: ZMYND8
  hgvsc: ENST00000396281.4:c.823-36A>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000354166
  ensembl transcript: ENST00000360911
  gene symbol: ZMYND8
  hgvsc: ENST00000360911.3:c.808-36A>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl transcript: ENST00000468376
  gene symbol: ZMYND8
  hgvsc: ENST00000468376.2:n.834-36A>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000392964
  ensembl transcript: ENST00000458360
  gene symbol: ZMYND8
  hgvsc: ENST00000458360.2:c.808-36A>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000396725
  ensembl transcript: ENST00000446994
  gene symbol: ZMYND8
  hgvsc: ENST00000446994.2:c.634-36A>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000418495
  ensembl transcript: ENST00000467200
  gene symbol: ZMYND8
  hgvsc: ENST00000467200.2:c.602-36A>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000443086
  ensembl transcript: ENST00000540497
  gene symbol: ZMYND8
  hgvsc: ENST00000540497.1:c.808-36A>G
  variant of: http://identifiers.org/hgnc/9397
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11339
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4620
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 608
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 501
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6551
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1248
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5777
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1378
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: East Asian
population: African
population: Latino
population: South Asian
reference allele: T
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum

20-45911003-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45911003
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 45911003
    reference: chr 20
allele count: 1
allele frequency: 8.512956720128034e-6
allele num: 117468
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000335537
  ensembl transcript: ENST00000352431
  gene symbol: ZMYND8
  hgvsc: ENST00000352431.2:c.883-42T>A
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000418210
  ensembl transcript: ENST00000461685
  gene symbol: ZMYND8
  hgvsc: ENST00000461685.1:c.883-42T>A
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000418495
  ensembl transcript: ENST00000467200
  gene symbol: ZMYND8
  hgvsc: ENST00000467200.2:c.602-42T>A
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl transcript: ENST00000468376
  gene symbol: ZMYND8
  hgvsc: ENST00000468376.2:n.834-42T>A
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000361093
  ensembl transcript: ENST00000372023
  gene symbol: ZMYND8
  hgvsc: ENST00000372023.3:c.808-42T>A
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000348246
  ensembl transcript: ENST00000355972
  gene symbol: ZMYND8
  hgvsc: ENST00000355972.4:c.823-42T>A
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000420095
  ensembl transcript: ENST00000471951
  gene symbol: ZMYND8
  hgvsc: ENST00000471951.2:c.883-42T>A
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000312237
  ensembl transcript: ENST00000311275
  gene symbol: ZMYND8
  hgvsc: ENST00000311275.7:c.823-42T>A
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000354166
  ensembl transcript: ENST00000360911
  gene symbol: ZMYND8
  hgvsc: ENST00000360911.3:c.808-42T>A
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000262975
  ensembl transcript: ENST00000262975
  gene symbol: ZMYND8
  hgvsc: ENST00000262975.4:c.823-42T>A
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000439800
  ensembl transcript: ENST00000536340
  gene symbol: ZMYND8
  hgvsc: ENST00000536340.1:c.904-42T>A
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000392964
  ensembl transcript: ENST00000458360
  gene symbol: ZMYND8
  hgvsc: ENST00000458360.2:c.808-42T>A
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000396725
  ensembl transcript: ENST00000446994
  gene symbol: ZMYND8
  hgvsc: ENST00000446994.2:c.634-42T>A
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000443086
  ensembl transcript: ENST00000540497
  gene symbol: ZMYND8
  hgvsc: ENST00000540497.1:c.808-42T>A
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000379577
  ensembl transcript: ENST00000396281
  gene symbol: ZMYND8
  hgvsc: ENST00000396281.4:c.823-42T>A
  variant of: http://identifiers.org/hgnc/9397
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5628
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4432
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13240
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2480
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9290
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8689
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 608
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9983
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: MQ

http://identifiers.org/exac.variant/20-45911009-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45911009
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 45911009
    reference: chr 20
allele count: 2
allele frequency: 1.712798026856673e-5
allele num: 116768
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000418495
  ensembl transcript: ENST00000467200
  gene symbol: ZMYND8
  hgvsc: ENST00000467200.2:c.602-48T>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000443086
  ensembl transcript: ENST00000540497
  gene symbol: ZMYND8
  hgvsc: ENST00000540497.1:c.808-48T>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000418210
  ensembl transcript: ENST00000461685
  gene symbol: ZMYND8
  hgvsc: ENST00000461685.1:c.883-48T>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000262975
  ensembl transcript: ENST00000262975
  gene symbol: ZMYND8
  hgvsc: ENST00000262975.4:c.823-48T>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000335537
  ensembl transcript: ENST00000352431
  gene symbol: ZMYND8
  hgvsc: ENST00000352431.2:c.883-48T>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000354166
  ensembl transcript: ENST00000360911
  gene symbol: ZMYND8
  hgvsc: ENST00000360911.3:c.808-48T>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000361093
  ensembl transcript: ENST00000372023
  gene symbol: ZMYND8
  hgvsc: ENST00000372023.3:c.808-48T>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000348246
  ensembl transcript: ENST00000355972
  gene symbol: ZMYND8
  hgvsc: ENST00000355972.4:c.823-48T>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000312237
  ensembl transcript: ENST00000311275
  gene symbol: ZMYND8
  hgvsc: ENST00000311275.7:c.823-48T>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000420095
  ensembl transcript: ENST00000471951
  gene symbol: ZMYND8
  hgvsc: ENST00000471951.2:c.883-48T>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000439800
  ensembl transcript: ENST00000536340
  gene symbol: ZMYND8
  hgvsc: ENST00000536340.1:c.904-48T>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl transcript: ENST00000468376
  gene symbol: ZMYND8
  hgvsc: ENST00000468376.2:n.834-48T>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000392964
  ensembl transcript: ENST00000458360
  gene symbol: ZMYND8
  hgvsc: ENST00000458360.2:c.808-48T>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000379577
  ensembl transcript: ENST00000396281
  gene symbol: ZMYND8
  hgvsc: ENST00000396281.4:c.823-48T>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000396725
  ensembl transcript: ENST00000446994
  gene symbol: ZMYND8
  hgvsc: ENST00000446994.2:c.634-48T>G
  variant of: http://identifiers.org/hgnc/9397
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11845
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2459
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9803
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5629
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1804
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1372
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
population: Latino
reference allele: A
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: DP

20-45911012-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45911012
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 45911012
    reference: chr 20
allele count: 2
allele frequency: 1.71847880256397e-5
allele num: 116382
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000420095
  ensembl transcript: ENST00000471951
  gene symbol: ZMYND8
  hgvsc: ENST00000471951.2:c.883-51A>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000439800
  ensembl transcript: ENST00000536340
  gene symbol: ZMYND8
  hgvsc: ENST00000536340.1:c.904-51A>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000361093
  ensembl transcript: ENST00000372023
  gene symbol: ZMYND8
  hgvsc: ENST00000372023.3:c.808-51A>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000392964
  ensembl transcript: ENST00000458360
  gene symbol: ZMYND8
  hgvsc: ENST00000458360.2:c.808-51A>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl transcript: ENST00000468376
  gene symbol: ZMYND8
  hgvsc: ENST00000468376.2:n.834-51A>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000396725
  ensembl transcript: ENST00000446994
  gene symbol: ZMYND8
  hgvsc: ENST00000446994.2:c.634-51A>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000312237
  ensembl transcript: ENST00000311275
  gene symbol: ZMYND8
  hgvsc: ENST00000311275.7:c.823-51A>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000418210
  ensembl transcript: ENST00000461685
  gene symbol: ZMYND8
  hgvsc: ENST00000461685.1:c.883-51A>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000354166
  ensembl transcript: ENST00000360911
  gene symbol: ZMYND8
  hgvsc: ENST00000360911.3:c.808-51A>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000348246
  ensembl transcript: ENST00000355972
  gene symbol: ZMYND8
  hgvsc: ENST00000355972.4:c.823-51A>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000262975
  ensembl transcript: ENST00000262975
  gene symbol: ZMYND8
  hgvsc: ENST00000262975.4:c.823-51A>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000379577
  ensembl transcript: ENST00000396281
  gene symbol: ZMYND8
  hgvsc: ENST00000396281.4:c.823-51A>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000443086
  ensembl transcript: ENST00000540497
  gene symbol: ZMYND8
  hgvsc: ENST00000540497.1:c.808-51A>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000418495
  ensembl transcript: ENST00000467200
  gene symbol: ZMYND8
  hgvsc: ENST00000467200.2:c.602-51A>G
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000335537
  ensembl transcript: ENST00000352431
  gene symbol: ZMYND8
  hgvsc: ENST00000352431.2:c.883-51A>G
  variant of: http://identifiers.org/hgnc/9397
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 915
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11342
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7682
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5608
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 608
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1874
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: T
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD

20-45912276-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45912276
    reference: chr 20
  end: Position
    type: ExactPosition
    position: 45912276
    reference: chr 20
allele count: 1
allele frequency: 8.310479514667997e-6
allele num: 120330
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000418495
  ensembl transcript: ENST00000467200
  gene symbol: ZMYND8
  hgvsc: ENST00000467200.2:c.601+39C>T
  variant of: http://identifiers.org/hgnc/9397
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101040
  ensembl protein: ENSP00000348246
  ensembl transcript: ENST00000355972
  gene symbol: ZMYND8
  hgvsc: ENST00000355972.4:c.822+39C>T
  variant of: http://identifiers.org/hgnc/9397
canonical: true
consequence: intron
filter: PASS
num of homozygotes: 0
reference allele: G

GenotypeDepth
all individuals: 4
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 12
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1782
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 22908
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 41
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 21
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 44
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 22
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 820
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 29
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 3
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9520
bin: 6.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 3
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3805
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4450
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 33495
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3107
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3428
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1554
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 10
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1313
bin: 8.75e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498486528606108e-5
allele num: 66734
num of homozygotes: 0

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

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

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

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.78e-1

QD
type: SiteQuality
SIO_000300: 1.306e1

MQRankSum
type: SiteQuality
SIO_000300: 4.62e-1

FS
type: SiteQuality
SIO_000300: 1.2194e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -3.57e0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.98e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.881e0

DP
type: SiteQuality
SIO_000300: 1.725256e6

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

GenotypeDepth
all individuals: 22910
bin: 2.75e1
variant carriers: 0

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

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

GenotypeDepth
all individuals: 819
bin: 4.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 28
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 115
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 43
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 21
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 451
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3430
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 9519
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3
bin: 3.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 3806
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3108
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1312
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4449
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 33506
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1553
bin: 9.25e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66736
num of homozygotes: 0

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

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

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: 3.28e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.98e1

FS
type: SiteQuality
SIO_000300: 2.795e0

DP
type: SiteQuality
SIO_000300: 1.725391e6

MQRankSum
type: SiteQuality
SIO_000300: 2.89e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.03e0

VQSLOD
type: SiteQuality
SIO_000300: 7.05e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.66e-1

QD
type: SiteQuality
SIO_000300: 9.289999999999999e0

GenotypeDepth
all individuals: 11688
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1783
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 18152
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 12
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4321
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 30
bin: 9.75e1
variant carriers: 2

GenotypeDepth
all individuals: 22910
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 60
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 22
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 44
bin: 7.75e1
variant carriers: 1

GenotypeDepth
all individuals: 819
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33513
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3432
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 4448
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 3.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 2
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1553
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3108
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3805
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1312
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 9519
bin: 6.75e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.495324862143371e-5
allele num: 66736
num of homozygotes: 0

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

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

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 1.725615e6

VQSLOD
type: SiteQuality
SIO_000300: -1.114e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 8.057e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.75e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.38e0

QD
type: SiteQuality
SIO_000300: 1.639e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.73e0

MQRankSum
type: SiteQuality
SIO_000300: 2.22e-1

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

GenotypeDepth
all individuals: 22910
bin: 2.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 60
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 22
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 819
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 12
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 30
bin: 9.75e1
variant carriers: 2

GenotypeDepth
all individuals: 43
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 115
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 21
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9519
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3107
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 2.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 1553
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 2.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 1313
bin: 8.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 33515
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3433
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 3805
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4448
bin: 7.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498441620714457e-5
allele num: 66736
num of homozygotes: 0

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

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

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

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

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

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

MQRankSum
type: SiteQuality
SIO_000300: 4.96e-1

QD
type: SiteQuality
SIO_000300: 1.375e1

MQ
type: SiteQuality
SIO_000300: 5.981e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.43e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.71e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.35e0

DP
type: SiteQuality
SIO_000300: 1.725634e6

FS
type: SiteQuality
SIO_000300: 7.06e0

VQSLOD
type: SiteQuality
SIO_000300: 2.0e-3

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

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
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 386

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 10406
num of homozygotes: 0

South Asian
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allele count: 14
allele frequency: 8.478682170542636e-4
allele num: 16512
num of homozygotes: 0

Other
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allele count: 3
allele frequency: 3.303964757709251e-3
allele num: 908
num of homozygotes: 0

European (Non-Finnish)
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allele count: 9
allele frequency: 1.348597458643011e-4
allele num: 66736
num of homozygotes: 0

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

East Asian
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allele count: 370
allele frequency: 4.277456647398844e-2
allele num: 8650
num of homozygotes: 16

Latino
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allele count: 6
allele frequency: 5.182242183451373e-4
allele num: 11578
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.83e-1

MQRankSum
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SIO_000300: 2.44e-1

InbreedingCoeff
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SIO_000300: 5.46e-2

ClippingRankSum
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QD
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SIO_000300: 1.309e1

VQSLOD
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SIO_000300: 4.79e0

FS
type: SiteQuality
SIO_000300: 5.36e-1

MQ
type: SiteQuality
SIO_000300: 5.971e1

BaseQRankSum
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SIO_000300: -6.392e0

DP
type: SiteQuality
SIO_000300: 1.780863e6

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

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66736
num of homozygotes: 0

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

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

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

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

VQSLOD
type: SiteQuality
SIO_000300: 1.53e0

MQ
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SIO_000300: 5.981e1

ClippingRankSum
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SIO_000300: -2.22e-1

InbreedingCoeff
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SIO_000300: -2.0e-4

DP
type: SiteQuality
SIO_000300: 1.728647e6

MQRankSum
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SIO_000300: 1.07e0

QD
type: SiteQuality
SIO_000300: 1.424e1

ReadPosRankSum
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SIO_000300: 1.63e0

FS
type: SiteQuality
SIO_000300: 1.746e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.75e0

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

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

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

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

African
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allele count: 1
allele frequency: 9.609840476648087e-5
allele num: 10406
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66738
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.7e-1

BaseQRankSum
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SIO_000300: -4.082e0

MQRankSum
type: SiteQuality
SIO_000300: -2.161e0

InbreedingCoeff
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SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 6.179e1

VQSLOD
type: SiteQuality
SIO_000300: -6.024e-1

QD
type: SiteQuality
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FS
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SIO_000300: 0.0e0

ClippingRankSum
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SIO_000300: 1.73e0

DP
type: SiteQuality
SIO_000300: 1.728682e6

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498441620714457e-5
allele num: 66736
num of homozygotes: 0

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

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

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

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

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

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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num of homozygotes: 0

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

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

South Asian
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Latino
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allele frequency: 8.637070305752289e-5
allele num: 11578
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 (Non-Finnish)
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allele count: 1
allele frequency: 1.498351813005694e-5
allele num: 66740
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.4e-2

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66740
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
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African
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Other
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Latino
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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: 3.466605038132656e-4
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InbreedingCoeff
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MQRankSum
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BaseQRankSum
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ClippingRankSum
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ReadPosRankSum
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MQ
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QD
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FS
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VQSLOD
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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African
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European (Non-Finnish)
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East Asian
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Other
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European (Finnish)
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VQSLOD
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InbreedingCoeff
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MQ
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MQRankSum
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ReadPosRankSum
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BaseQRankSum
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FS
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ClippingRankSum
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DP
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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num of homozygotes: 0

European (Non-Finnish)
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Other
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South Asian
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European (Finnish)
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Latino
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African
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VQSLOD
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ReadPosRankSum
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FS
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MQRankSum
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MQ
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BaseQRankSum
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InbreedingCoeff
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ClippingRankSum
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QD
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DP
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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
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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Latino
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European (Finnish)
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Other
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European (Non-Finnish)
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BaseQRankSum
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MQ
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InbreedingCoeff
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ClippingRankSum
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QD
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MQRankSum
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DP
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FS
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ReadPosRankSum
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VQSLOD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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Other
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African
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European (Non-Finnish)
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East Asian
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South Asian
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MQRankSum
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MQ
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BaseQRankSum
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QD
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ClippingRankSum
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InbreedingCoeff
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VQSLOD
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FS
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DP
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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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European (Finnish)
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South Asian
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European (Non-Finnish)
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Latino
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African
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East Asian
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MQRankSum
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VQSLOD
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QD
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InbreedingCoeff
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DP
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FS
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MQ
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ClippingRankSum
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GenotypeQuality
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European (Finnish)
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European (Non-Finnish)
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FS
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ReadPosRankSum
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VQSLOD
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InbreedingCoeff
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ClippingRankSum
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MQ
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DP
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African
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East Asian
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European (Finnish)
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VQSLOD
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QD
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MQRankSum
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MQ
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DP
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FS
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InbreedingCoeff
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ClippingRankSum
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Latino
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East Asian
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European (Non-Finnish)
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African
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European (Finnish)
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VQSLOD
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BaseQRankSum
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ClippingRankSum
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MQRankSum
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DP
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FS
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QD
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MQ
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East Asian
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African
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European (Non-Finnish)
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European (Finnish)
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ReadPosRankSum
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VQSLOD
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QD
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BaseQRankSum
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InbreedingCoeff
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MQ
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MQRankSum
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FS
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DP
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ClippingRankSum
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GenotypeDepth
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Latino
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European (Non-Finnish)
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East Asian
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South Asian
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European (Finnish)
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InbreedingCoeff
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FS
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MQ
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MQRankSum
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VQSLOD
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ReadPosRankSum
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MQ
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MQRankSum
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VQSLOD
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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Latino
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European (Non-Finnish)
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allele frequency: 2.846868444710818e-4
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Other
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East Asian
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African
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European (Finnish)
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allele frequency: 1.663641863278887e-3
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VQSLOD
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ClippingRankSum
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FS
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InbreedingCoeff
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QD
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MQ
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MQRankSum
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BaseQRankSum
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DP
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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African
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East Asian
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Latino
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European (Non-Finnish)
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Other
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VQSLOD
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ClippingRankSum
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MQ
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ReadPosRankSum
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QD
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DP
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BaseQRankSum
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MQRankSum
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FS
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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South Asian
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European (Finnish)
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Other
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DP
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VQSLOD
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FS
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BaseQRankSum
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ReadPosRankSum
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ClippingRankSum
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MQ
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InbreedingCoeff
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MQRankSum
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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East Asian
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Latino
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European (Non-Finnish)
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European (Finnish)
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InbreedingCoeff
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BaseQRankSum
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MQRankSum
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ClippingRankSum
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QD
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FS
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VQSLOD
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ReadPosRankSum
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DP
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MQ
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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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African
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East Asian
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Other
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European (Non-Finnish)
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European (Finnish)
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ClippingRankSum
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ReadPosRankSum
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VQSLOD
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FS
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QD
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MQ
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BaseQRankSum
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MQRankSum
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InbreedingCoeff
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DP
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South Asian
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European (Non-Finnish)
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African
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Latino
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VQSLOD
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MQRankSum
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QD
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DP
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MQ
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ReadPosRankSum
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FS
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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East Asian
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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: 0.0e0
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Latino
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allele num: 11578
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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African
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InbreedingCoeff
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SIO_000300: -2.0e-4

FS
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DP
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QD
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BaseQRankSum
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MQ
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VQSLOD
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ReadPosRankSum
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SIO_000300: 1.33e0

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

European (Non-Finnish)
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allele count: 2
allele frequency: 2.996703626011388e-5
allele num: 66740
num of homozygotes: 0

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

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

DP
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SIO_000300: 1.791074e6

InbreedingCoeff
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VQSLOD
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MQ
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SIO_000300: 5.97e1

ClippingRankSum
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FS
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QD
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BaseQRankSum
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SIO_000300: 3.0e-3

MQRankSum
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SIO_000300: 4.4e-1

ReadPosRankSum
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SIO_000300: 2.47e0

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
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 9728
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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allele 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: 6586
num of homozygotes: 0

East Asian
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allele count: 1
allele frequency: 1.17426021606388e-4
allele num: 8516
num of homozygotes: 0

European (Non-Finnish)
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allele count: 2
allele frequency: 3.053808098699078e-5
allele num: 65492
num of homozygotes: 0

Other
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allele count: 0
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MQRankSum
type: SiteQuality
SIO_000300: 5.620000000000001e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.61e-1

InbreedingCoeff
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SIO_000300: 1.0e-4

DP
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SIO_000300: 1.732022e6

BaseQRankSum
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SIO_000300: 3.68e0

ReadPosRankSum
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SIO_000300: 1.2e0

FS
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SIO_000300: 1.383e0

QD
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SIO_000300: 1.26e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
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SIO_000300: -3.87e-1

GenotypeDepth
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variant carriers: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
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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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European (Non-Finnish)
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allele count: 3
allele frequency: 4.583791712504584e-5
allele num: 65448
num of homozygotes: 0

Latino
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allele count: 1
allele frequency: 8.713837574067619e-5
allele num: 11476
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.77323218639935e-5
allele num: 14764
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
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MQRankSum
type: SiteQuality
SIO_000300: 2.31e-1

ClippingRankSum
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FS
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SIO_000300: 1.94e0

InbreedingCoeff
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DP
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QD
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VQSLOD
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ReadPosRankSum
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MQ
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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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allele num: 850
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European (Finnish)
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South Asian
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African
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East Asian
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Latino
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European (Non-Finnish)
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MQRankSum
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ReadPosRankSum
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BaseQRankSum
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MQ
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QD
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InbreedingCoeff
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VQSLOD
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FS
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DP
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
allele num: 6580
num of homozygotes: 0

African
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East Asian
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Latino
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European (Non-Finnish)
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Other
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South Asian
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DP
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QD
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MQRankSum
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InbreedingCoeff
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BaseQRankSum
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MQ
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VQSLOD
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ClippingRankSum
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FS
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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East Asian
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South Asian
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European (Finnish)
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BaseQRankSum
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VQSLOD
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ClippingRankSum
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FS
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QD
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MQRankSum
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MQ
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DP
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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European (Finnish)
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Latino
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European (Non-Finnish)
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Other
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South Asian
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FS
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QD
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InbreedingCoeff
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BaseQRankSum
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ClippingRankSum
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MQ
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VQSLOD
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MQRankSum
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DP
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ReadPosRankSum
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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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Other
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East Asian
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Latino
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African
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European (Finnish)
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European (Non-Finnish)
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QD
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ReadPosRankSum
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VQSLOD
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InbreedingCoeff
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MQRankSum
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BaseQRankSum
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ClippingRankSum
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FS
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DP
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MQ
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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African
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Other
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East Asian
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European (Finnish)
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Latino
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European (Non-Finnish)
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FS
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VQSLOD
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MQ
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MQRankSum
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DP
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ReadPosRankSum
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BaseQRankSum
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QD
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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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GenotypeQuality
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GenotypeQuality
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African
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Latino
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South Asian
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European (Non-Finnish)
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European (Finnish)
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QD
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ReadPosRankSum
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BaseQRankSum
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DP
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VQSLOD
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FS
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ClippingRankSum
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MQ
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African
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Latino
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East Asian
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South Asian
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QD
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MQ
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DP
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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European (Finnish)
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 7.574609907589759e-5
allele num: 66010
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African
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allele frequency: 9.633911368015414e-5
allele num: 10380
num of homozygotes: 0

Latino
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num of homozygotes: 0

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

Other
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num of homozygotes: 0

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

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

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

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

Latino
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allele frequency: 0.0e0
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South Asian
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African
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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

Other
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DP
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FS
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QD
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InbreedingCoeff
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ClippingRankSum
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ReadPosRankSum
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MQ
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BaseQRankSum
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VQSLOD
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MQRankSum
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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

Latino
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allele frequency: 2.592464569650881e-4
allele num: 11572
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.502313562886846e-5
allele num: 66564
num of homozygotes: 0

African
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allele count: 69
allele frequency: 6.6320645905421e-3
allele num: 10404
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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 count: 0
allele frequency: 0.0e0
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South Asian
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allele count: 1
allele frequency: 6.196554715578138e-5
allele num: 16138
num of homozygotes: 0

ClippingRankSum
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SIO_000300: -3.78e-1

BaseQRankSum
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ReadPosRankSum
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DP
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VQSLOD
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FS
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MQRankSum
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MQ
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SIO_000300: 5.966e1

InbreedingCoeff
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SIO_000300: 2.7e-2

QD
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GenotypeDepth
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variant carriers: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.499880009599232e-5
allele num: 66672
num of homozygotes: 0

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

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

Other
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South Asian
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European (Finnish)
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East Asian
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European (Non-Finnish)
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African
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InbreedingCoeff
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BaseQRankSum
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DP
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QD
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MQ
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FS
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MQRankSum
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VQSLOD
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ReadPosRankSum
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ClippingRankSum
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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European (Finnish)
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 2.999220202747286e-5
allele num: 66684
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East Asian
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South Asian
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ClippingRankSum
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InbreedingCoeff
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FS
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ReadPosRankSum
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MQ
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VQSLOD
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MQRankSum
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QD
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DP
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele frequency: 0.0e0
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African
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South Asian
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Other
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European (Finnish)
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European (Non-Finnish)
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FS
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MQ
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VQSLOD
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BaseQRankSum
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QD
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ReadPosRankSum
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InbreedingCoeff
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ClippingRankSum
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DP
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MQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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Other
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Latino
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allele frequency: 0.0e0
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European (Finnish)
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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: 66592
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MQ
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BaseQRankSum
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ReadPosRankSum
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FS
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DP
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QD
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MQRankSum
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VQSLOD
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InbreedingCoeff
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
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Other
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European (Finnish)
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South Asian
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Latino
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African
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FS
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MQRankSum
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InbreedingCoeff
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QD
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VQSLOD
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ReadPosRankSum
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MQ
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BaseQRankSum
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DP
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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East Asian
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South Asian
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European (Finnish)
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Latino
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European (Non-Finnish)
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FS
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InbreedingCoeff
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QD
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MQ
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DP
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BaseQRankSum
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ReadPosRankSum
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MQRankSum
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VQSLOD
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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South Asian
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European (Non-Finnish)
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Latino
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East Asian
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African
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European (Finnish)
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ReadPosRankSum
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ClippingRankSum
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MQ
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FS
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InbreedingCoeff
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VQSLOD
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DP
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QD
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BaseQRankSum
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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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Other
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European (Non-Finnish)
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South Asian
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Latino
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East Asian
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FS
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DP
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VQSLOD
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InbreedingCoeff
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BaseQRankSum
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MQRankSum
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QD
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MQ
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ReadPosRankSum
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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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European (Finnish)
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South Asian
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African
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Latino
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East Asian
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European (Non-Finnish)
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MQ
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VQSLOD
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MQRankSum
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FS
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ClippingRankSum
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ReadPosRankSum
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BaseQRankSum
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DP
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InbreedingCoeff
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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European (Finnish)
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African
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East Asian
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European (Non-Finnish)
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Other
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BaseQRankSum
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ClippingRankSum
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FS
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InbreedingCoeff
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QD
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VQSLOD
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MQRankSum
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DP
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ReadPosRankSum
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MQ
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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European (Non-Finnish)
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Other
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East Asian
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African
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Latino
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South Asian
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FS
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DP
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InbreedingCoeff
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QD
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ClippingRankSum
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MQRankSum
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MQ
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ReadPosRankSum
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VQSLOD
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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European (Finnish)
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African
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Latino
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South Asian
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East Asian
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MQRankSum
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ReadPosRankSum
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ClippingRankSum
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QD
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FS
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InbreedingCoeff
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DP
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VQSLOD
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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European (Non-Finnish)
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African
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European (Finnish)
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Other
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QD
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InbreedingCoeff
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MQ
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FS
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VQSLOD
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DP
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GenotypeQuality
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African
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South Asian
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East Asian
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European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 11270
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6564
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.664953e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 9.13e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.57e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.66e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.6e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.75e0

QD
type: SiteQuality
SIO_000300: 1.067e1