10-99212622-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 99212622
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 99212622
    reference: chr 10
allele count: 2
allele frequency: 1.647419317638919e-5
allele num: 121402
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000459777
  gene symbol: ZDHHC16
  hgvsc: ENST00000459777.1:n.249-30C>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000466895
  gene symbol: ZDHHC16
  hgvsc: ENST00000466895.1:n.248-30C>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359883
  ensembl transcript: ENST00000370846
  gene symbol: ZDHHC16
  hgvsc: ENST00000370846.4:c.528-30C>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000345383
  ensembl transcript: ENST00000352634
  gene symbol: ZDHHC16
  hgvsc: ENST00000352634.4:c.528-30C>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000398532
  ensembl transcript: ENST00000433086
  gene symbol: ZDHHC16
  hgvsc: ENST00000433086.1:c.333-30C>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000400719
  ensembl transcript: ENST00000414567
  gene symbol: ZDHHC16
  hgvsc: ENST00000414567.1:c.528-30C>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000462924
  gene symbol: ZDHHC16
  hgvsc: ENST00000462924.1:n.733C>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359891
  ensembl transcript: ENST00000370854
  gene symbol: ZDHHC16
  hgvsc: ENST00000370854.3:c.528-30C>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000323360
  ensembl transcript: ENST00000353979
  gene symbol: ZDHHC16
  hgvsc: ENST00000353979.3:c.527+362C>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000495735
  gene symbol: ZDHHC16
  hgvsc: ENST00000495735.1:n.526C>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000304487
  ensembl transcript: ENST00000345745
  gene symbol: ZDHHC16
  hgvsc: ENST00000345745.5:c.333-30C>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000377357
  ensembl transcript: ENST00000393760
  gene symbol: ZDHHC16
  hgvsc: ENST00000393760.1:c.528-30C>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359879
  ensembl transcript: ENST00000370842
  gene symbol: ZDHHC16
  hgvsc: ENST00000370842.2:c.528-30C>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000396286
  ensembl transcript: ENST00000417044
  gene symbol: ZDHHC16
  hgvsc: ENST00000417044.1:c.353-30C>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000405240
  ensembl transcript: ENST00000420089
  gene symbol: ZDHHC16
  hgvsc: ENST00000420089.1:c.455-30C>T
  variant of: http://identifiers.org/hgnc/20714
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1357
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 660
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1099
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1787
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37625
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1140
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2342
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1024
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 796
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: East Asian
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: QD

10-99212623-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 99212623
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 99212623
    reference: chr 10
allele count: 1
allele frequency: 8.237096588194593e-6
allele num: 121402
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000377357
  ensembl transcript: ENST00000393760
  gene symbol: ZDHHC16
  hgvsc: ENST00000393760.1:c.528-29G>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000323360
  ensembl transcript: ENST00000353979
  gene symbol: ZDHHC16
  hgvsc: ENST00000353979.3:c.527+363G>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359883
  ensembl transcript: ENST00000370846
  gene symbol: ZDHHC16
  hgvsc: ENST00000370846.4:c.528-29G>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000495735
  gene symbol: ZDHHC16
  hgvsc: ENST00000495735.1:n.527G>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000459777
  gene symbol: ZDHHC16
  hgvsc: ENST00000459777.1:n.249-29G>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000304487
  ensembl transcript: ENST00000345745
  gene symbol: ZDHHC16
  hgvsc: ENST00000345745.5:c.333-29G>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000400719
  ensembl transcript: ENST00000414567
  gene symbol: ZDHHC16
  hgvsc: ENST00000414567.1:c.528-29G>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000462924
  gene symbol: ZDHHC16
  hgvsc: ENST00000462924.1:n.734G>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000398532
  ensembl transcript: ENST00000433086
  gene symbol: ZDHHC16
  hgvsc: ENST00000433086.1:c.333-29G>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359891
  ensembl transcript: ENST00000370854
  gene symbol: ZDHHC16
  hgvsc: ENST00000370854.3:c.528-29G>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000466895
  gene symbol: ZDHHC16
  hgvsc: ENST00000466895.1:n.248-29G>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359879
  ensembl transcript: ENST00000370842
  gene symbol: ZDHHC16
  hgvsc: ENST00000370842.2:c.528-29G>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000396286
  ensembl transcript: ENST00000417044
  gene symbol: ZDHHC16
  hgvsc: ENST00000417044.1:c.353-29G>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000345383
  ensembl transcript: ENST00000352634
  gene symbol: ZDHHC16
  hgvsc: ENST00000352634.4:c.528-29G>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000405240
  ensembl transcript: ENST00000420089
  gene symbol: ZDHHC16
  hgvsc: ENST00000420089.1:c.455-29G>A
  variant of: http://identifiers.org/hgnc/20714
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 660
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3322
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 797
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37622
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1025
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2342
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3706
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1099
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum

10-99212637-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 99212637
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 99212637
    reference: chr 10
allele count: 1
allele frequency: 8.236825198095647e-6
allele num: 121406
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359891
  ensembl transcript: ENST00000370854
  gene symbol: ZDHHC16
  hgvsc: ENST00000370854.3:c.528-15G>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000323360
  ensembl transcript: ENST00000353979
  gene symbol: ZDHHC16
  hgvsc: ENST00000353979.3:c.527+377G>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000495735
  gene symbol: ZDHHC16
  hgvsc: ENST00000495735.1:n.541G>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000405240
  ensembl transcript: ENST00000420089
  gene symbol: ZDHHC16
  hgvsc: ENST00000420089.1:c.455-15G>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000462924
  gene symbol: ZDHHC16
  hgvsc: ENST00000462924.1:n.748G>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000400719
  ensembl transcript: ENST00000414567
  gene symbol: ZDHHC16
  hgvsc: ENST00000414567.1:c.528-15G>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000466895
  gene symbol: ZDHHC16
  hgvsc: ENST00000466895.1:n.248-15G>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000396286
  ensembl transcript: ENST00000417044
  gene symbol: ZDHHC16
  hgvsc: ENST00000417044.1:c.353-15G>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359883
  ensembl transcript: ENST00000370846
  gene symbol: ZDHHC16
  hgvsc: ENST00000370846.4:c.528-15G>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000398532
  ensembl transcript: ENST00000433086
  gene symbol: ZDHHC16
  hgvsc: ENST00000433086.1:c.333-15G>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000459777
  gene symbol: ZDHHC16
  hgvsc: ENST00000459777.1:n.249-15G>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000304487
  ensembl transcript: ENST00000345745
  gene symbol: ZDHHC16
  hgvsc: ENST00000345745.5:c.333-15G>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359879
  ensembl transcript: ENST00000370842
  gene symbol: ZDHHC16
  hgvsc: ENST00000370842.2:c.528-15G>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000345383
  ensembl transcript: ENST00000352634
  gene symbol: ZDHHC16
  hgvsc: ENST00000352634.4:c.528-15G>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000377357
  ensembl transcript: ENST00000393760
  gene symbol: ZDHHC16
  hgvsc: ENST00000393760.1:c.528-15G>A
  variant of: http://identifiers.org/hgnc/20714
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 37622
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1105
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 775
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2926
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3322
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2342
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
reference allele: G
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP

10-99212637-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 99212637
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 99212637
    reference: chr 10
allele count: 1
allele frequency: 8.236825198095647e-6
allele num: 121406
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000495735
  gene symbol: ZDHHC16
  hgvsc: ENST00000495735.1:n.541G>C
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359891
  ensembl transcript: ENST00000370854
  gene symbol: ZDHHC16
  hgvsc: ENST00000370854.3:c.528-15G>C
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000459777
  gene symbol: ZDHHC16
  hgvsc: ENST00000459777.1:n.249-15G>C
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000400719
  ensembl transcript: ENST00000414567
  gene symbol: ZDHHC16
  hgvsc: ENST00000414567.1:c.528-15G>C
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000377357
  ensembl transcript: ENST00000393760
  gene symbol: ZDHHC16
  hgvsc: ENST00000393760.1:c.528-15G>C
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000396286
  ensembl transcript: ENST00000417044
  gene symbol: ZDHHC16
  hgvsc: ENST00000417044.1:c.353-15G>C
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000398532
  ensembl transcript: ENST00000433086
  gene symbol: ZDHHC16
  hgvsc: ENST00000433086.1:c.333-15G>C
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000462924
  gene symbol: ZDHHC16
  hgvsc: ENST00000462924.1:n.748G>C
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000323360
  ensembl transcript: ENST00000353979
  gene symbol: ZDHHC16
  hgvsc: ENST00000353979.3:c.527+377G>C
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359883
  ensembl transcript: ENST00000370846
  gene symbol: ZDHHC16
  hgvsc: ENST00000370846.4:c.528-15G>C
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000466895
  gene symbol: ZDHHC16
  hgvsc: ENST00000466895.1:n.248-15G>C
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000304487
  ensembl transcript: ENST00000345745
  gene symbol: ZDHHC16
  hgvsc: ENST00000345745.5:c.333-15G>C
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000405240
  ensembl transcript: ENST00000420089
  gene symbol: ZDHHC16
  hgvsc: ENST00000420089.1:c.455-15G>C
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000345383
  ensembl transcript: ENST00000352634
  gene symbol: ZDHHC16
  hgvsc: ENST00000352634.4:c.528-15G>C
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359879
  ensembl transcript: ENST00000370842
  gene symbol: ZDHHC16
  hgvsc: ENST00000370842.2:c.528-15G>C
  variant of: http://identifiers.org/hgnc/20714
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1356
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 997
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1787
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2926
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3322
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3706
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1105
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum

http://identifiers.org/exac.variant/10-99212640-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 99212640
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 99212640
    reference: chr 10
allele count: 1
allele frequency: 8.236825198095647e-6
allele num: 121406
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000400719
  ensembl transcript: ENST00000414567
  gene symbol: ZDHHC16
  hgvsc: ENST00000414567.1:c.528-12C>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359879
  ensembl transcript: ENST00000370842
  gene symbol: ZDHHC16
  hgvsc: ENST00000370842.2:c.528-12C>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000405240
  ensembl transcript: ENST00000420089
  gene symbol: ZDHHC16
  hgvsc: ENST00000420089.1:c.455-12C>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000398532
  ensembl transcript: ENST00000433086
  gene symbol: ZDHHC16
  hgvsc: ENST00000433086.1:c.333-12C>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359883
  ensembl transcript: ENST00000370846
  gene symbol: ZDHHC16
  hgvsc: ENST00000370846.4:c.528-12C>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000377357
  ensembl transcript: ENST00000393760
  gene symbol: ZDHHC16
  hgvsc: ENST00000393760.1:c.528-12C>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000459777
  gene symbol: ZDHHC16
  hgvsc: ENST00000459777.1:n.249-12C>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000396286
  ensembl transcript: ENST00000417044
  gene symbol: ZDHHC16
  hgvsc: ENST00000417044.1:c.353-12C>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000323360
  ensembl transcript: ENST00000353979
  gene symbol: ZDHHC16
  hgvsc: ENST00000353979.3:c.527+380C>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359891
  ensembl transcript: ENST00000370854
  gene symbol: ZDHHC16
  hgvsc: ENST00000370854.3:c.528-12C>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000304487
  ensembl transcript: ENST00000345745
  gene symbol: ZDHHC16
  hgvsc: ENST00000345745.5:c.333-12C>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000462924
  gene symbol: ZDHHC16
  hgvsc: ENST00000462924.1:n.751C>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000495735
  gene symbol: ZDHHC16
  hgvsc: ENST00000495735.1:n.544C>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000466895
  gene symbol: ZDHHC16
  hgvsc: ENST00000466895.1:n.248-12C>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000345383
  ensembl transcript: ENST00000352634
  gene symbol: ZDHHC16
  hgvsc: ENST00000352634.4:c.528-12C>A
  variant of: http://identifiers.org/hgnc/20714
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 661
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1356
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1024
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 775
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1104
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3322
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ

10-99212645-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 99212645
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 99212645
    reference: chr 10
allele count: 1
allele frequency: 8.236689509752241e-6
allele num: 121408
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000400719
  ensembl transcript: ENST00000414567
  gene symbol: ZDHHC16
  hgvsc: ENST00000414567.1:c.528-7C>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359883
  ensembl transcript: ENST00000370846
  gene symbol: ZDHHC16
  hgvsc: ENST00000370846.4:c.528-7C>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000396286
  ensembl transcript: ENST00000417044
  gene symbol: ZDHHC16
  hgvsc: ENST00000417044.1:c.353-7C>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000405240
  ensembl transcript: ENST00000420089
  gene symbol: ZDHHC16
  hgvsc: ENST00000420089.1:c.455-7C>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000377357
  ensembl transcript: ENST00000393760
  gene symbol: ZDHHC16
  hgvsc: ENST00000393760.1:c.528-7C>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359879
  ensembl transcript: ENST00000370842
  gene symbol: ZDHHC16
  hgvsc: ENST00000370842.2:c.528-7C>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000466895
  gene symbol: ZDHHC16
  hgvsc: ENST00000466895.1:n.248-7C>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000462924
  gene symbol: ZDHHC16
  hgvsc: ENST00000462924.1:n.756C>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000459777
  gene symbol: ZDHHC16
  hgvsc: ENST00000459777.1:n.249-7C>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000304487
  ensembl transcript: ENST00000345745
  gene symbol: ZDHHC16
  hgvsc: ENST00000345745.5:c.333-7C>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000398532
  ensembl transcript: ENST00000433086
  gene symbol: ZDHHC16
  hgvsc: ENST00000433086.1:c.333-7C>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000345383
  ensembl transcript: ENST00000352634
  gene symbol: ZDHHC16
  hgvsc: ENST00000352634.4:c.528-7C>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000495735
  gene symbol: ZDHHC16
  hgvsc: ENST00000495735.1:n.549C>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000323360
  ensembl transcript: ENST00000353979
  gene symbol: ZDHHC16
  hgvsc: ENST00000353979.3:c.527+385C>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359891
  ensembl transcript: ENST00000370854
  gene symbol: ZDHHC16
  hgvsc: ENST00000370854.3:c.528-7C>T
  variant of: http://identifiers.org/hgnc/20714
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3322
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 775
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3706
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1787
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 661
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1142
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.528-7C>T
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: East Asian
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD

10-99212657-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 99212657
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 99212657
    reference: chr 10
allele count: 3
allele frequency: 2.471006852925672e-5
allele num: 121408
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359883
  ensembl transcript: ENST00000370846
  gene symbol: ZDHHC16
  hgvsc: ENST00000370846.4:c.533T>C
  hgvsp: ENSP00000359883.4:p.Val178Ala
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000323360
  ensembl transcript: ENST00000353979
  gene symbol: ZDHHC16
  hgvsc: ENST00000353979.3:c.527+397T>C
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000405240
  ensembl transcript: ENST00000420089
  gene symbol: ZDHHC16
  hgvsc: ENST00000420089.1:c.460T>C
  hgvsp: ENSP00000405240.1:p.Val154Ala
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000462924
  gene symbol: ZDHHC16
  hgvsc: ENST00000462924.1:n.768T>C
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000400719
  ensembl transcript: ENST00000414567
  gene symbol: ZDHHC16
  hgvsc: ENST00000414567.1:c.533T>C
  hgvsp: ENSP00000400719.1:p.Val178Ala
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359891
  ensembl transcript: ENST00000370854
  gene symbol: ZDHHC16
  hgvsc: ENST00000370854.3:c.533T>C
  hgvsp: ENSP00000359891.3:p.Val178Ala
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000377357
  ensembl transcript: ENST00000393760
  gene symbol: ZDHHC16
  hgvsc: ENST00000393760.1:c.533T>C
  hgvsp: ENSP00000377357.1:p.Val178Ala
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000396286
  ensembl transcript: ENST00000417044
  gene symbol: ZDHHC16
  hgvsc: ENST00000417044.1:c.358T>C
  hgvsp: ENSP00000396286.1:p.Val120Ala
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000304487
  ensembl transcript: ENST00000345745
  gene symbol: ZDHHC16
  hgvsc: ENST00000345745.5:c.338T>C
  hgvsp: ENSP00000304487.8:p.Val113Ala
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000398532
  ensembl transcript: ENST00000433086
  gene symbol: ZDHHC16
  hgvsc: ENST00000433086.1:c.338T>C
  hgvsp: ENSP00000398532.1:p.Val113Ala
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000345383
  ensembl transcript: ENST00000352634
  gene symbol: ZDHHC16
  hgvsc: ENST00000352634.4:c.533T>C
  hgvsp: ENSP00000345383.4:p.Val178Ala
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000495735
  gene symbol: ZDHHC16
  hgvsc: ENST00000495735.1:n.561T>C
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000459777
  gene symbol: ZDHHC16
  hgvsc: ENST00000459777.1:n.254T>C
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359879
  ensembl transcript: ENST00000370842
  gene symbol: ZDHHC16
  hgvsc: ENST00000370842.2:c.533T>C
  hgvsp: ENSP00000359879.1:p.Val178Ala
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000466895
  gene symbol: ZDHHC16
  hgvsc: ENST00000466895.1:n.253T>C
  variant of: http://identifiers.org/hgnc/20714
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3706
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37622
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1142
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 997
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2342
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2925
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val178Ala
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: ReadPosRankSum

10-99212665-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 99212665
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 99212665
    reference: chr 10
allele count: 1
allele frequency: 8.236689509752241e-6
allele num: 121408
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359879
  ensembl transcript: ENST00000370842
  gene symbol: ZDHHC16
  hgvsc: ENST00000370842.2:c.541A>T
  hgvsp: ENSP00000359879.1:p.Met181Leu
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000462924
  gene symbol: ZDHHC16
  hgvsc: ENST00000462924.1:n.776A>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000495735
  gene symbol: ZDHHC16
  hgvsc: ENST00000495735.1:n.569A>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000405240
  ensembl transcript: ENST00000420089
  gene symbol: ZDHHC16
  hgvsc: ENST00000420089.1:c.468A>T
  hgvsp: ENSP00000405240.1:p.Met157Leu
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359891
  ensembl transcript: ENST00000370854
  gene symbol: ZDHHC16
  hgvsc: ENST00000370854.3:c.541A>T
  hgvsp: ENSP00000359891.3:p.Met181Leu
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359883
  ensembl transcript: ENST00000370846
  gene symbol: ZDHHC16
  hgvsc: ENST00000370846.4:c.541A>T
  hgvsp: ENSP00000359883.4:p.Met181Leu
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000398532
  ensembl transcript: ENST00000433086
  gene symbol: ZDHHC16
  hgvsc: ENST00000433086.1:c.346A>T
  hgvsp: ENSP00000398532.1:p.Met116Leu
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000396286
  ensembl transcript: ENST00000417044
  gene symbol: ZDHHC16
  hgvsc: ENST00000417044.1:c.366A>T
  hgvsp: ENSP00000396286.1:p.Met123Leu
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000377357
  ensembl transcript: ENST00000393760
  gene symbol: ZDHHC16
  hgvsc: ENST00000393760.1:c.541A>T
  hgvsp: ENSP00000377357.1:p.Met181Leu
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000400719
  ensembl transcript: ENST00000414567
  gene symbol: ZDHHC16
  hgvsc: ENST00000414567.1:c.541A>T
  hgvsp: ENSP00000400719.1:p.Met181Leu
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000323360
  ensembl transcript: ENST00000353979
  gene symbol: ZDHHC16
  hgvsc: ENST00000353979.3:c.527+405A>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000345383
  ensembl transcript: ENST00000352634
  gene symbol: ZDHHC16
  hgvsc: ENST00000352634.4:c.541A>T
  hgvsp: ENSP00000345383.4:p.Met181Leu
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000304487
  ensembl transcript: ENST00000345745
  gene symbol: ZDHHC16
  hgvsc: ENST00000345745.5:c.346A>T
  hgvsp: ENSP00000304487.8:p.Met116Leu
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000466895
  gene symbol: ZDHHC16
  hgvsc: ENST00000466895.1:n.261A>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000459777
  gene symbol: ZDHHC16
  hgvsc: ENST00000459777.1:n.262A>T
  variant of: http://identifiers.org/hgnc/20714
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1355
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 811
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3322
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1142
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 661
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3706
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1105
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Met181Leu
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: MQ
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS

10-99212670-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 99212670
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 99212670
    reference: chr 10
allele count: 87
allele frequency: 7.165919873484449e-4
allele num: 121408
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359891
  ensembl transcript: ENST00000370854
  gene symbol: ZDHHC16
  hgvsc: ENST00000370854.3:c.546T>C
  hgvsp: ENST00000370854.3:c.546T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000377357
  ensembl transcript: ENST00000393760
  gene symbol: ZDHHC16
  hgvsc: ENST00000393760.1:c.546T>C
  hgvsp: ENST00000393760.1:c.546T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000462924
  gene symbol: ZDHHC16
  hgvsc: ENST00000462924.1:n.781T>C
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000396286
  ensembl transcript: ENST00000417044
  gene symbol: ZDHHC16
  hgvsc: ENST00000417044.1:c.371T>C
  hgvsp: ENST00000417044.1:c.371T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359883
  ensembl transcript: ENST00000370846
  gene symbol: ZDHHC16
  hgvsc: ENST00000370846.4:c.546T>C
  hgvsp: ENST00000370846.4:c.546T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000466895
  gene symbol: ZDHHC16
  hgvsc: ENST00000466895.1:n.266T>C
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000323360
  ensembl transcript: ENST00000353979
  gene symbol: ZDHHC16
  hgvsc: ENST00000353979.3:c.527+410T>C
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000405240
  ensembl transcript: ENST00000420089
  gene symbol: ZDHHC16
  hgvsc: ENST00000420089.1:c.473T>C
  hgvsp: ENST00000420089.1:c.473T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000345383
  ensembl transcript: ENST00000352634
  gene symbol: ZDHHC16
  hgvsc: ENST00000352634.4:c.546T>C
  hgvsp: ENST00000352634.4:c.546T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000304487
  ensembl transcript: ENST00000345745
  gene symbol: ZDHHC16
  hgvsc: ENST00000345745.5:c.351T>C
  hgvsp: ENST00000345745.5:c.351T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359879
  ensembl transcript: ENST00000370842
  gene symbol: ZDHHC16
  hgvsc: ENST00000370842.2:c.546T>C
  hgvsp: ENST00000370842.2:c.546T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000400719
  ensembl transcript: ENST00000414567
  gene symbol: ZDHHC16
  hgvsc: ENST00000414567.1:c.546T>C
  hgvsp: ENST00000414567.1:c.546T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000459777
  gene symbol: ZDHHC16
  hgvsc: ENST00000459777.1:n.267T>C
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000495735
  gene symbol: ZDHHC16
  hgvsc: ENST00000495735.1:n.574T>C
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000398532
  ensembl transcript: ENST00000433086
  gene symbol: ZDHHC16
  hgvsc: ENST00000433086.1:c.351T>C
  hgvsp: ENST00000433086.1:c.351T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20714
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 661
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2926
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1787
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1024
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3323
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1141
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 997
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 774
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp182Asp
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
reference allele: T
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

10-99212679-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 99212679
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 99212679
    reference: chr 10
allele count: 1
allele frequency: 8.236825198095647e-6
allele num: 121406
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000398532
  ensembl transcript: ENST00000433086
  gene symbol: ZDHHC16
  hgvsc: ENST00000433086.1:c.360C>T
  hgvsp: ENST00000433086.1:c.360C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000466895
  gene symbol: ZDHHC16
  hgvsc: ENST00000466895.1:n.275C>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359891
  ensembl transcript: ENST00000370854
  gene symbol: ZDHHC16
  hgvsc: ENST00000370854.3:c.555C>T
  hgvsp: ENST00000370854.3:c.555C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359879
  ensembl transcript: ENST00000370842
  gene symbol: ZDHHC16
  hgvsc: ENST00000370842.2:c.555C>T
  hgvsp: ENST00000370842.2:c.555C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000345383
  ensembl transcript: ENST00000352634
  gene symbol: ZDHHC16
  hgvsc: ENST00000352634.4:c.555C>T
  hgvsp: ENST00000352634.4:c.555C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000377357
  ensembl transcript: ENST00000393760
  gene symbol: ZDHHC16
  hgvsc: ENST00000393760.1:c.555C>T
  hgvsp: ENST00000393760.1:c.555C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000396286
  ensembl transcript: ENST00000417044
  gene symbol: ZDHHC16
  hgvsc: ENST00000417044.1:c.380C>T
  hgvsp: ENST00000417044.1:c.380C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000304487
  ensembl transcript: ENST00000345745
  gene symbol: ZDHHC16
  hgvsc: ENST00000345745.5:c.360C>T
  hgvsp: ENST00000345745.5:c.360C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000495735
  gene symbol: ZDHHC16
  hgvsc: ENST00000495735.1:n.583C>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000462924
  gene symbol: ZDHHC16
  hgvsc: ENST00000462924.1:n.790C>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359883
  ensembl transcript: ENST00000370846
  gene symbol: ZDHHC16
  hgvsc: ENST00000370846.4:c.555C>T
  hgvsp: ENST00000370846.4:c.555C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000400719
  ensembl transcript: ENST00000414567
  gene symbol: ZDHHC16
  hgvsc: ENST00000414567.1:c.555C>T
  hgvsp: ENST00000414567.1:c.555C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000323360
  ensembl transcript: ENST00000353979
  gene symbol: ZDHHC16
  hgvsc: ENST00000353979.3:c.527+419C>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000459777
  gene symbol: ZDHHC16
  hgvsc: ENST00000459777.1:n.276C>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000405240
  ensembl transcript: ENST00000420089
  gene symbol: ZDHHC16
  hgvsc: ENST00000420089.1:c.482C>T
  hgvsp: ENST00000420089.1:c.482C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20714
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3324
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2925
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1105
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2342
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.555C>T
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: DP

10-99212680-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 99212680
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 99212680
    reference: chr 10
allele count: 2
allele frequency: 1.647365039619129e-5
allele num: 121406
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000396286
  ensembl transcript: ENST00000417044
  gene symbol: ZDHHC16
  hgvsc: ENST00000417044.1:c.381C>T
  hgvsp: ENSP00000396286.1:p.Pro128Ser
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000459777
  gene symbol: ZDHHC16
  hgvsc: ENST00000459777.1:n.277C>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000398532
  ensembl transcript: ENST00000433086
  gene symbol: ZDHHC16
  hgvsc: ENST00000433086.1:c.361C>T
  hgvsp: ENSP00000398532.1:p.Pro121Ser
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000462924
  gene symbol: ZDHHC16
  hgvsc: ENST00000462924.1:n.791C>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000323360
  ensembl transcript: ENST00000353979
  gene symbol: ZDHHC16
  hgvsc: ENST00000353979.3:c.527+420C>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000345383
  ensembl transcript: ENST00000352634
  gene symbol: ZDHHC16
  hgvsc: ENST00000352634.4:c.556C>T
  hgvsp: ENSP00000345383.4:p.Pro186Ser
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000405240
  ensembl transcript: ENST00000420089
  gene symbol: ZDHHC16
  hgvsc: ENST00000420089.1:c.483C>T
  hgvsp: ENSP00000405240.1:p.Pro162Ser
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000304487
  ensembl transcript: ENST00000345745
  gene symbol: ZDHHC16
  hgvsc: ENST00000345745.5:c.361C>T
  hgvsp: ENSP00000304487.8:p.Pro121Ser
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359879
  ensembl transcript: ENST00000370842
  gene symbol: ZDHHC16
  hgvsc: ENST00000370842.2:c.556C>T
  hgvsp: ENSP00000359879.1:p.Pro186Ser
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359891
  ensembl transcript: ENST00000370854
  gene symbol: ZDHHC16
  hgvsc: ENST00000370854.3:c.556C>T
  hgvsp: ENSP00000359891.3:p.Pro186Ser
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000495735
  gene symbol: ZDHHC16
  hgvsc: ENST00000495735.1:n.584C>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359883
  ensembl transcript: ENST00000370846
  gene symbol: ZDHHC16
  hgvsc: ENST00000370846.4:c.556C>T
  hgvsp: ENSP00000359883.4:p.His186Tyr
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000400719
  ensembl transcript: ENST00000414567
  gene symbol: ZDHHC16
  hgvsc: ENST00000414567.1:c.556C>T
  hgvsp: ENSP00000400719.1:p.Pro186Ser
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000377357
  ensembl transcript: ENST00000393760
  gene symbol: ZDHHC16
  hgvsc: ENST00000393760.1:c.556C>T
  hgvsp: ENSP00000377357.1:p.Pro186Ser
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000466895
  gene symbol: ZDHHC16
  hgvsc: ENST00000466895.1:n.276C>T
  variant of: http://identifiers.org/hgnc/20714
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 814
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1355
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 774
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro186Ser
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: C
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: ClippingRankSum

10-99212681-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 99212681
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 99212681
    reference: chr 10
allele count: 1
allele frequency: 8.236825198095647e-6
allele num: 121406
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359879
  ensembl transcript: ENST00000370842
  gene symbol: ZDHHC16
  hgvsc: ENST00000370842.2:c.556+1G>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000398532
  ensembl transcript: ENST00000433086
  gene symbol: ZDHHC16
  hgvsc: ENST00000433086.1:c.361+1G>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000462924
  gene symbol: ZDHHC16
  hgvsc: ENST00000462924.1:n.791+1G>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000466895
  gene symbol: ZDHHC16
  hgvsc: ENST00000466895.1:n.276+1G>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359883
  ensembl transcript: ENST00000370846
  gene symbol: ZDHHC16
  hgvsc: ENST00000370846.4:c.556+1G>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000323360
  ensembl transcript: ENST00000353979
  gene symbol: ZDHHC16
  hgvsc: ENST00000353979.3:c.527+421G>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000396286
  ensembl transcript: ENST00000417044
  gene symbol: ZDHHC16
  hgvsc: ENST00000417044.1:c.381+1G>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000495735
  gene symbol: ZDHHC16
  hgvsc: ENST00000495735.1:n.584+1G>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: true
  consequence: splice_donor_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000377357
  ensembl transcript: ENST00000393760
  gene symbol: ZDHHC16
  hgvsc: ENST00000393760.1:c.556+1G>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000459777
  gene symbol: ZDHHC16
  hgvsc: ENST00000459777.1:n.277+1G>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000345383
  ensembl transcript: ENST00000352634
  gene symbol: ZDHHC16
  hgvsc: ENST00000352634.4:c.556+1G>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359891
  ensembl transcript: ENST00000370854
  gene symbol: ZDHHC16
  hgvsc: ENST00000370854.3:c.556+1G>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000405240
  ensembl transcript: ENST00000420089
  gene symbol: ZDHHC16
  hgvsc: ENST00000420089.1:c.483+1G>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000400719
  ensembl transcript: ENST00000414567
  gene symbol: ZDHHC16
  hgvsc: ENST00000414567.1:c.556+1G>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000304487
  ensembl transcript: ENST00000345745
  gene symbol: ZDHHC16
  hgvsc: ENST00000345745.5:c.361+1G>A
  variant of: http://identifiers.org/hgnc/20714
canonical: true
consequence: splice donor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 701
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1025
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37619
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1141
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2925
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1355
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2342
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.556+1G>A
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: African
population: South Asian
population: Other
reference allele: G
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: ClippingRankSum

10-99212693-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 99212693
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 99212693
    reference: chr 10
allele count: 1
allele frequency: 8.236825198095647e-6
allele num: 121406
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000495735
  gene symbol: ZDHHC16
  hgvsc: ENST00000495735.1:n.584+13T>C
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359883
  ensembl transcript: ENST00000370846
  gene symbol: ZDHHC16
  hgvsc: ENST00000370846.4:c.556+13T>C
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000400719
  ensembl transcript: ENST00000414567
  gene symbol: ZDHHC16
  hgvsc: ENST00000414567.1:c.556+13T>C
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000396286
  ensembl transcript: ENST00000417044
  gene symbol: ZDHHC16
  hgvsc: ENST00000417044.1:c.381+13T>C
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359891
  ensembl transcript: ENST00000370854
  gene symbol: ZDHHC16
  hgvsc: ENST00000370854.3:c.556+13T>C
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000462924
  gene symbol: ZDHHC16
  hgvsc: ENST00000462924.1:n.791+13T>C
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000398532
  ensembl transcript: ENST00000433086
  gene symbol: ZDHHC16
  hgvsc: ENST00000433086.1:c.361+13T>C
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000377357
  ensembl transcript: ENST00000393760
  gene symbol: ZDHHC16
  hgvsc: ENST00000393760.1:c.556+13T>C
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000466895
  gene symbol: ZDHHC16
  hgvsc: ENST00000466895.1:n.276+13T>C
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000323360
  ensembl transcript: ENST00000353979
  gene symbol: ZDHHC16
  hgvsc: ENST00000353979.3:c.527+433T>C
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000345383
  ensembl transcript: ENST00000352634
  gene symbol: ZDHHC16
  hgvsc: ENST00000352634.4:c.556+13T>C
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359879
  ensembl transcript: ENST00000370842
  gene symbol: ZDHHC16
  hgvsc: ENST00000370842.2:c.556+13T>C
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000459777
  gene symbol: ZDHHC16
  hgvsc: ENST00000459777.1:n.277+13T>C
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000405240
  ensembl transcript: ENST00000420089
  gene symbol: ZDHHC16
  hgvsc: ENST00000420089.1:c.483+13T>C
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000304487
  ensembl transcript: ENST00000345745
  gene symbol: ZDHHC16
  hgvsc: ENST00000345745.5:c.361+13T>C
  variant of: http://identifiers.org/hgnc/20714
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 774
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 997
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 816
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1103
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1141
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3324
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1355
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: T
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff

10-99212696-CTCT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 99212696
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 99212693
    reference: chr 10
allele count: 1
allele frequency: 8.236689509752241e-6
allele num: 121408
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359883
  ensembl transcript: ENST00000370846
  gene symbol: ZDHHC16
  hgvsc: ENST00000370846.4:c.556+20_556+22delTCT
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000377357
  ensembl transcript: ENST00000393760
  gene symbol: ZDHHC16
  hgvsc: ENST00000393760.1:c.556+20_556+22delTCT
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359879
  ensembl transcript: ENST00000370842
  gene symbol: ZDHHC16
  hgvsc: ENST00000370842.2:c.556+20_556+22delTCT
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000396286
  ensembl transcript: ENST00000417044
  gene symbol: ZDHHC16
  hgvsc: ENST00000417044.1:c.381+20_381+22delTCT
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000400719
  ensembl transcript: ENST00000414567
  gene symbol: ZDHHC16
  hgvsc: ENST00000414567.1:c.556+20_556+22delTCT
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000323360
  ensembl transcript: ENST00000353979
  gene symbol: ZDHHC16
  hgvsc: ENST00000353979.3:c.527+440_527+442delTCT
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000462924
  gene symbol: ZDHHC16
  hgvsc: ENST00000462924.1:n.791+20_791+22delTCT
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000495735
  gene symbol: ZDHHC16
  hgvsc: ENST00000495735.1:n.584+20_584+22delTCT
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000345383
  ensembl transcript: ENST00000352634
  gene symbol: ZDHHC16
  hgvsc: ENST00000352634.4:c.556+20_556+22delTCT
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000398532
  ensembl transcript: ENST00000433086
  gene symbol: ZDHHC16
  hgvsc: ENST00000433086.1:c.361+20_361+22delTCT
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000405240
  ensembl transcript: ENST00000420089
  gene symbol: ZDHHC16
  hgvsc: ENST00000420089.1:c.483+20_483+22delTCT
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000466895
  gene symbol: ZDHHC16
  hgvsc: ENST00000466895.1:n.276+20_276+22delTCT
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359891
  ensembl transcript: ENST00000370854
  gene symbol: ZDHHC16
  hgvsc: ENST00000370854.3:c.556+20_556+22delTCT
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000459777
  gene symbol: ZDHHC16
  hgvsc: ENST00000459777.1:n.277+20_277+22delTCT
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000304487
  ensembl transcript: ENST00000345745
  gene symbol: ZDHHC16
  hgvsc: ENST00000345745.5:c.361+20_361+22delTCT
  variant of: http://identifiers.org/hgnc/20714
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 701
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1141
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1104
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 997
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1355
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 815
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1025
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37619
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2925
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2342
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1787
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 774
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
population: African
population: East Asian
population: South Asian
reference allele: CTCT
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: MQRankSum

10-99212700-TCTGC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 99212700
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 99212696
    reference: chr 10
allele count: 1
allele frequency: 8.236825198095647e-6
allele num: 121406
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000398532
  ensembl transcript: ENST00000433086
  gene symbol: ZDHHC16
  hgvsc: ENST00000433086.1:c.361+24_361+27delCCTG
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000396286
  ensembl transcript: ENST00000417044
  gene symbol: ZDHHC16
  hgvsc: ENST00000417044.1:c.381+24_381+27delCCTG
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000495735
  gene symbol: ZDHHC16
  hgvsc: ENST00000495735.1:n.584+24_584+27delCCTG
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000323360
  ensembl transcript: ENST00000353979
  gene symbol: ZDHHC16
  hgvsc: ENST00000353979.3:c.527+444_527+447delCCTG
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000462924
  gene symbol: ZDHHC16
  hgvsc: ENST00000462924.1:n.791+24_791+27delCCTG
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000405240
  ensembl transcript: ENST00000420089
  gene symbol: ZDHHC16
  hgvsc: ENST00000420089.1:c.483+24_483+27delCCTG
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359883
  ensembl transcript: ENST00000370846
  gene symbol: ZDHHC16
  hgvsc: ENST00000370846.4:c.556+24_556+27delCCTG
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359891
  ensembl transcript: ENST00000370854
  gene symbol: ZDHHC16
  hgvsc: ENST00000370854.3:c.556+24_556+27delCCTG
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000377357
  ensembl transcript: ENST00000393760
  gene symbol: ZDHHC16
  hgvsc: ENST00000393760.1:c.556+24_556+27delCCTG
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000466895
  gene symbol: ZDHHC16
  hgvsc: ENST00000466895.1:n.276+24_276+27delCCTG
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000345383
  ensembl transcript: ENST00000352634
  gene symbol: ZDHHC16
  hgvsc: ENST00000352634.4:c.556+24_556+27delCCTG
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000400719
  ensembl transcript: ENST00000414567
  gene symbol: ZDHHC16
  hgvsc: ENST00000414567.1:c.556+24_556+27delCCTG
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359879
  ensembl transcript: ENST00000370842
  gene symbol: ZDHHC16
  hgvsc: ENST00000370842.2:c.556+24_556+27delCCTG
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000304487
  ensembl transcript: ENST00000345745
  gene symbol: ZDHHC16
  hgvsc: ENST00000345745.5:c.361+24_361+27delCCTG
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000459777
  gene symbol: ZDHHC16
  hgvsc: ENST00000459777.1:n.277+24_277+27delCCTG
  variant of: http://identifiers.org/hgnc/20714
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1355
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 701
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3707
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3324
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1103
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1025
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1142
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 814
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
reference allele: TCTGC
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum

10-99212701-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 99212701
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 99212701
    reference: chr 10
allele count: 1
allele frequency: 8.236825198095647e-6
allele num: 121406
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359883
  ensembl transcript: ENST00000370846
  gene symbol: ZDHHC16
  hgvsc: ENST00000370846.4:c.556+21C>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000396286
  ensembl transcript: ENST00000417044
  gene symbol: ZDHHC16
  hgvsc: ENST00000417044.1:c.381+21C>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000459777
  gene symbol: ZDHHC16
  hgvsc: ENST00000459777.1:n.277+21C>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000304487
  ensembl transcript: ENST00000345745
  gene symbol: ZDHHC16
  hgvsc: ENST00000345745.5:c.361+21C>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000495735
  gene symbol: ZDHHC16
  hgvsc: ENST00000495735.1:n.584+21C>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359891
  ensembl transcript: ENST00000370854
  gene symbol: ZDHHC16
  hgvsc: ENST00000370854.3:c.556+21C>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000400719
  ensembl transcript: ENST00000414567
  gene symbol: ZDHHC16
  hgvsc: ENST00000414567.1:c.556+21C>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000377357
  ensembl transcript: ENST00000393760
  gene symbol: ZDHHC16
  hgvsc: ENST00000393760.1:c.556+21C>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359879
  ensembl transcript: ENST00000370842
  gene symbol: ZDHHC16
  hgvsc: ENST00000370842.2:c.556+21C>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000398532
  ensembl transcript: ENST00000433086
  gene symbol: ZDHHC16
  hgvsc: ENST00000433086.1:c.361+21C>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000466895
  gene symbol: ZDHHC16
  hgvsc: ENST00000466895.1:n.276+21C>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000462924
  gene symbol: ZDHHC16
  hgvsc: ENST00000462924.1:n.791+21C>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000405240
  ensembl transcript: ENST00000420089
  gene symbol: ZDHHC16
  hgvsc: ENST00000420089.1:c.483+21C>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000323360
  ensembl transcript: ENST00000353979
  gene symbol: ZDHHC16
  hgvsc: ENST00000353979.3:c.527+441C>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000345383
  ensembl transcript: ENST00000352634
  gene symbol: ZDHHC16
  hgvsc: ENST00000352634.4:c.556+21C>G
  variant of: http://identifiers.org/hgnc/20714
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1141
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37618
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1355
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1787
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 997
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2925
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 701
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1103
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
population: African
reference allele: C
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP

10-99212709-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 99212709
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 99212709
    reference: chr 10
allele count: 1
allele frequency: 8.236689509752241e-6
allele num: 121408
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000396286
  ensembl transcript: ENST00000417044
  gene symbol: ZDHHC16
  hgvsc: ENST00000417044.1:c.381+29G>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000377357
  ensembl transcript: ENST00000393760
  gene symbol: ZDHHC16
  hgvsc: ENST00000393760.1:c.556+29G>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000345383
  ensembl transcript: ENST00000352634
  gene symbol: ZDHHC16
  hgvsc: ENST00000352634.4:c.556+29G>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359891
  ensembl transcript: ENST00000370854
  gene symbol: ZDHHC16
  hgvsc: ENST00000370854.3:c.556+29G>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000462924
  gene symbol: ZDHHC16
  hgvsc: ENST00000462924.1:n.791+29G>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000459777
  gene symbol: ZDHHC16
  hgvsc: ENST00000459777.1:n.277+29G>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359879
  ensembl transcript: ENST00000370842
  gene symbol: ZDHHC16
  hgvsc: ENST00000370842.2:c.556+29G>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000466895
  gene symbol: ZDHHC16
  hgvsc: ENST00000466895.1:n.276+29G>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000398532
  ensembl transcript: ENST00000433086
  gene symbol: ZDHHC16
  hgvsc: ENST00000433086.1:c.361+29G>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000304487
  ensembl transcript: ENST00000345745
  gene symbol: ZDHHC16
  hgvsc: ENST00000345745.5:c.361+29G>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000405240
  ensembl transcript: ENST00000420089
  gene symbol: ZDHHC16
  hgvsc: ENST00000420089.1:c.483+29G>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000495735
  gene symbol: ZDHHC16
  hgvsc: ENST00000495735.1:n.584+29G>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000400719
  ensembl transcript: ENST00000414567
  gene symbol: ZDHHC16
  hgvsc: ENST00000414567.1:c.556+29G>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000323360
  ensembl transcript: ENST00000353979
  gene symbol: ZDHHC16
  hgvsc: ENST00000353979.3:c.527+449G>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359883
  ensembl transcript: ENST00000370846
  gene symbol: ZDHHC16
  hgvsc: ENST00000370846.4:c.556+29G>T
  variant of: http://identifiers.org/hgnc/20714
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1103
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1024
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 774
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1355
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2342
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 701
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3707
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3326
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum

10-99212715-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 99212715
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 99212715
    reference: chr 10
allele count: 6
allele frequency: 4.942095118857387e-5
allele num: 121406
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000398532
  ensembl transcript: ENST00000433086
  gene symbol: ZDHHC16
  hgvsc: ENST00000433086.1:c.361+35C>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000466895
  gene symbol: ZDHHC16
  hgvsc: ENST00000466895.1:n.276+35C>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359879
  ensembl transcript: ENST00000370842
  gene symbol: ZDHHC16
  hgvsc: ENST00000370842.2:c.556+35C>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000396286
  ensembl transcript: ENST00000417044
  gene symbol: ZDHHC16
  hgvsc: ENST00000417044.1:c.381+35C>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000304487
  ensembl transcript: ENST00000345745
  gene symbol: ZDHHC16
  hgvsc: ENST00000345745.5:c.361+35C>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000459777
  gene symbol: ZDHHC16
  hgvsc: ENST00000459777.1:n.277+35C>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000405240
  ensembl transcript: ENST00000420089
  gene symbol: ZDHHC16
  hgvsc: ENST00000420089.1:c.483+35C>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000462924
  gene symbol: ZDHHC16
  hgvsc: ENST00000462924.1:n.791+35C>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359891
  ensembl transcript: ENST00000370854
  gene symbol: ZDHHC16
  hgvsc: ENST00000370854.3:c.556+35C>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359883
  ensembl transcript: ENST00000370846
  gene symbol: ZDHHC16
  hgvsc: ENST00000370846.4:c.556+35C>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000345383
  ensembl transcript: ENST00000352634
  gene symbol: ZDHHC16
  hgvsc: ENST00000352634.4:c.556+35C>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000400719
  ensembl transcript: ENST00000414567
  gene symbol: ZDHHC16
  hgvsc: ENST00000414567.1:c.556+35C>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000495735
  gene symbol: ZDHHC16
  hgvsc: ENST00000495735.1:n.584+35C>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000323360
  ensembl transcript: ENST00000353979
  gene symbol: ZDHHC16
  hgvsc: ENST00000353979.3:c.527+455C>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000377357
  ensembl transcript: ENST00000393760
  gene symbol: ZDHHC16
  hgvsc: ENST00000393760.1:c.556+35C>G
  variant of: http://identifiers.org/hgnc/20714
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37617
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 774
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1143
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1106
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1025
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1355
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 997
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3707
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD

10-99212728-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 99212728
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 99212728
    reference: chr 10
allele count: 1
allele frequency: 8.236689509752241e-6
allele num: 121408
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000398532
  ensembl transcript: ENST00000433086
  gene symbol: ZDHHC16
  hgvsc: ENST00000433086.1:c.361+48G>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000396286
  ensembl transcript: ENST00000417044
  gene symbol: ZDHHC16
  hgvsc: ENST00000417044.1:c.381+48G>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000462924
  gene symbol: ZDHHC16
  hgvsc: ENST00000462924.1:n.791+48G>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359879
  ensembl transcript: ENST00000370842
  gene symbol: ZDHHC16
  hgvsc: ENST00000370842.2:c.556+48G>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000466895
  gene symbol: ZDHHC16
  hgvsc: ENST00000466895.1:n.276+48G>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000323360
  ensembl transcript: ENST00000353979
  gene symbol: ZDHHC16
  hgvsc: ENST00000353979.3:c.527+468G>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000405240
  ensembl transcript: ENST00000420089
  gene symbol: ZDHHC16
  hgvsc: ENST00000420089.1:c.483+48G>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000345383
  ensembl transcript: ENST00000352634
  gene symbol: ZDHHC16
  hgvsc: ENST00000352634.4:c.556+48G>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000304487
  ensembl transcript: ENST00000345745
  gene symbol: ZDHHC16
  hgvsc: ENST00000345745.5:c.361+48G>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000459777
  gene symbol: ZDHHC16
  hgvsc: ENST00000459777.1:n.277+48G>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359891
  ensembl transcript: ENST00000370854
  gene symbol: ZDHHC16
  hgvsc: ENST00000370854.3:c.556+48G>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000400719
  ensembl transcript: ENST00000414567
  gene symbol: ZDHHC16
  hgvsc: ENST00000414567.1:c.556+48G>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359883
  ensembl transcript: ENST00000370846
  gene symbol: ZDHHC16
  hgvsc: ENST00000370846.4:c.556+48G>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000377357
  ensembl transcript: ENST00000393760
  gene symbol: ZDHHC16
  hgvsc: ENST00000393760.1:c.556+48G>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000495735
  gene symbol: ZDHHC16
  hgvsc: ENST00000495735.1:n.584+48G>A
  variant of: http://identifiers.org/hgnc/20714
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 997
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1097
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2925
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3327
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 793
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37615
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1024
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1787
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1149
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
population: African
population: Latino
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/10-99213237-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 99213237
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 99213237
    reference: chr 10
allele count: 1
allele frequency: 8.404067568703253e-6
allele num: 118990
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000398532
  ensembl transcript: ENST00000433086
  gene symbol: ZDHHC16
  hgvsc: ENST00000433086.1:c.362-50C>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000405240
  ensembl transcript: ENST00000420089
  gene symbol: ZDHHC16
  hgvsc: ENST00000420089.1:c.484-50C>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000377357
  ensembl transcript: ENST00000393760
  gene symbol: ZDHHC16
  hgvsc: ENST00000393760.1:c.557-50C>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000345383
  ensembl transcript: ENST00000352634
  gene symbol: ZDHHC16
  hgvsc: ENST00000352634.4:c.557-50C>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000323360
  ensembl transcript: ENST00000353979
  gene symbol: ZDHHC16
  hgvsc: ENST00000353979.3:c.528-138C>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359879
  ensembl transcript: ENST00000370842
  gene symbol: ZDHHC16
  hgvsc: ENST00000370842.2:c.557-50C>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000466895
  gene symbol: ZDHHC16
  hgvsc: ENST00000466895.1:n.277-50C>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000459777
  gene symbol: ZDHHC16
  hgvsc: ENST00000459777.1:n.278-50C>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000396286
  ensembl transcript: ENST00000417044
  gene symbol: ZDHHC16
  hgvsc: ENST00000417044.1:c.382-50C>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359891
  ensembl transcript: ENST00000370854
  gene symbol: ZDHHC16
  hgvsc: ENST00000370854.3:c.557-50C>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000495735
  gene symbol: ZDHHC16
  hgvsc: ENST00000495735.1:n.585-50C>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000304487
  ensembl transcript: ENST00000345745
  gene symbol: ZDHHC16
  hgvsc: ENST00000345745.5:c.362-50C>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000462924
  gene symbol: ZDHHC16
  hgvsc: ENST00000462924.1:n.791+557C>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000400719
  ensembl transcript: ENST00000414567
  gene symbol: ZDHHC16
  hgvsc: ENST00000414567.1:c.557-50C>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359883
  ensembl transcript: ENST00000370846
  gene symbol: ZDHHC16
  hgvsc: ENST00000370846.4:c.556+557C>A
  variant of: http://identifiers.org/hgnc/20714
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2140
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6161
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5311
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4592
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 867
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3145
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3623
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2186
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 948
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1550
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1561
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: DP

10-99213240-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 99213240
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 99213240
    reference: chr 10
allele count: 1
allele frequency: 8.395882659143956e-6
allele num: 119106
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000396286
  ensembl transcript: ENST00000417044
  gene symbol: ZDHHC16
  hgvsc: ENST00000417044.1:c.382-47C>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000462924
  gene symbol: ZDHHC16
  hgvsc: ENST00000462924.1:n.791+560C>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359891
  ensembl transcript: ENST00000370854
  gene symbol: ZDHHC16
  hgvsc: ENST00000370854.3:c.557-47C>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000466895
  gene symbol: ZDHHC16
  hgvsc: ENST00000466895.1:n.277-47C>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359879
  ensembl transcript: ENST00000370842
  gene symbol: ZDHHC16
  hgvsc: ENST00000370842.2:c.557-47C>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000459777
  gene symbol: ZDHHC16
  hgvsc: ENST00000459777.1:n.278-47C>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000345383
  ensembl transcript: ENST00000352634
  gene symbol: ZDHHC16
  hgvsc: ENST00000352634.4:c.557-47C>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000323360
  ensembl transcript: ENST00000353979
  gene symbol: ZDHHC16
  hgvsc: ENST00000353979.3:c.528-135C>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000400719
  ensembl transcript: ENST00000414567
  gene symbol: ZDHHC16
  hgvsc: ENST00000414567.1:c.557-47C>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359883
  ensembl transcript: ENST00000370846
  gene symbol: ZDHHC16
  hgvsc: ENST00000370846.4:c.556+560C>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000304487
  ensembl transcript: ENST00000345745
  gene symbol: ZDHHC16
  hgvsc: ENST00000345745.5:c.362-47C>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000398532
  ensembl transcript: ENST00000433086
  gene symbol: ZDHHC16
  hgvsc: ENST00000433086.1:c.362-47C>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000405240
  ensembl transcript: ENST00000420089
  gene symbol: ZDHHC16
  hgvsc: ENST00000420089.1:c.484-47C>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000495735
  gene symbol: ZDHHC16
  hgvsc: ENST00000495735.1:n.585-47C>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000377357
  ensembl transcript: ENST00000393760
  gene symbol: ZDHHC16
  hgvsc: ENST00000393760.1:c.557-47C>T
  variant of: http://identifiers.org/hgnc/20714
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2734
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6162
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2109
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2186
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 999
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1503
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1456
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3145
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2094
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 940
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1568
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: East Asian
population: African
population: Other
reference allele: C
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD

10-99213241-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 99213241
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 99213241
    reference: chr 10
allele count: 11
allele frequency: 9.225092250922509e-5
allele num: 119240
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359891
  ensembl transcript: ENST00000370854
  gene symbol: ZDHHC16
  hgvsc: ENST00000370854.3:c.557-46G>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000398532
  ensembl transcript: ENST00000433086
  gene symbol: ZDHHC16
  hgvsc: ENST00000433086.1:c.362-46G>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000405240
  ensembl transcript: ENST00000420089
  gene symbol: ZDHHC16
  hgvsc: ENST00000420089.1:c.484-46G>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000377357
  ensembl transcript: ENST00000393760
  gene symbol: ZDHHC16
  hgvsc: ENST00000393760.1:c.557-46G>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000462924
  gene symbol: ZDHHC16
  hgvsc: ENST00000462924.1:n.791+561G>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000400719
  ensembl transcript: ENST00000414567
  gene symbol: ZDHHC16
  hgvsc: ENST00000414567.1:c.557-46G>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000495735
  gene symbol: ZDHHC16
  hgvsc: ENST00000495735.1:n.585-46G>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000466895
  gene symbol: ZDHHC16
  hgvsc: ENST00000466895.1:n.277-46G>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000345383
  ensembl transcript: ENST00000352634
  gene symbol: ZDHHC16
  hgvsc: ENST00000352634.4:c.557-46G>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000459777
  gene symbol: ZDHHC16
  hgvsc: ENST00000459777.1:n.278-46G>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000304487
  ensembl transcript: ENST00000345745
  gene symbol: ZDHHC16
  hgvsc: ENST00000345745.5:c.362-46G>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000396286
  ensembl transcript: ENST00000417044
  gene symbol: ZDHHC16
  hgvsc: ENST00000417044.1:c.382-46G>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359883
  ensembl transcript: ENST00000370846
  gene symbol: ZDHHC16
  hgvsc: ENST00000370846.4:c.556+561G>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359879
  ensembl transcript: ENST00000370842
  gene symbol: ZDHHC16
  hgvsc: ENST00000370842.2:c.557-46G>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000323360
  ensembl transcript: ENST00000353979
  gene symbol: ZDHHC16
  hgvsc: ENST00000353979.3:c.528-134G>A
  variant of: http://identifiers.org/hgnc/20714
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1330
  bin: 1.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1144
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4597
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1503
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5552
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4848
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3623
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2096
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2094
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1578
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2734
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: European (Finnish)
population: African
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum

10-99213251-GTGTT-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 99213251
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 99213247
    reference: chr 10
allele count: 1
allele frequency: 8.364281173675934e-6
allele num: 119556
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000377357
  ensembl transcript: ENST00000393760
  gene symbol: ZDHHC16
  hgvsc: ENST00000393760.1:c.557-33_557-30delTTTG
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000398532
  ensembl transcript: ENST00000433086
  gene symbol: ZDHHC16
  hgvsc: ENST00000433086.1:c.362-33_362-30delTTTG
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000323360
  ensembl transcript: ENST00000353979
  gene symbol: ZDHHC16
  hgvsc: ENST00000353979.3:c.528-121_528-118delTTTG
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359879
  ensembl transcript: ENST00000370842
  gene symbol: ZDHHC16
  hgvsc: ENST00000370842.2:c.557-33_557-30delTTTG
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000400719
  ensembl transcript: ENST00000414567
  gene symbol: ZDHHC16
  hgvsc: ENST00000414567.1:c.557-33_557-30delTTTG
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000459777
  gene symbol: ZDHHC16
  hgvsc: ENST00000459777.1:n.278-33_278-30delTTTG
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000396286
  ensembl transcript: ENST00000417044
  gene symbol: ZDHHC16
  hgvsc: ENST00000417044.1:c.382-33_382-30delTTTG
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000304487
  ensembl transcript: ENST00000345745
  gene symbol: ZDHHC16
  hgvsc: ENST00000345745.5:c.362-33_362-30delTTTG
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000466895
  gene symbol: ZDHHC16
  hgvsc: ENST00000466895.1:n.277-33_277-30delTTTG
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000405240
  ensembl transcript: ENST00000420089
  gene symbol: ZDHHC16
  hgvsc: ENST00000420089.1:c.484-33_484-30delTTTG
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000345383
  ensembl transcript: ENST00000352634
  gene symbol: ZDHHC16
  hgvsc: ENST00000352634.4:c.557-33_557-30delTTTG
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000495735
  gene symbol: ZDHHC16
  hgvsc: ENST00000495735.1:n.585-33_585-30delTTTG
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359883
  ensembl transcript: ENST00000370846
  gene symbol: ZDHHC16
  hgvsc: ENST00000370846.4:c.556+574_556+577delTTTG
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000462924
  gene symbol: ZDHHC16
  hgvsc: ENST00000462924.1:n.791+574_791+577delTTTG
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359891
  ensembl transcript: ENST00000370854
  gene symbol: ZDHHC16
  hgvsc: ENST00000370854.3:c.557-33_557-30delTTTG
  variant of: http://identifiers.org/hgnc/20714
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4598
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 856
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5311
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1518
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2481
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6070
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3148
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2094
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4845
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3624
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5552
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: GTGTT
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff

10-99213258-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 99213258
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 99213258
    reference: chr 10
allele count: 1
allele frequency: 8.343623802689983e-6
allele num: 119852
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000466895
  gene symbol: ZDHHC16
  hgvsc: ENST00000466895.1:n.277-29A>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000495735
  gene symbol: ZDHHC16
  hgvsc: ENST00000495735.1:n.585-29A>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000462924
  gene symbol: ZDHHC16
  hgvsc: ENST00000462924.1:n.791+578A>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000459777
  gene symbol: ZDHHC16
  hgvsc: ENST00000459777.1:n.278-29A>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000405240
  ensembl transcript: ENST00000420089
  gene symbol: ZDHHC16
  hgvsc: ENST00000420089.1:c.484-29A>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000396286
  ensembl transcript: ENST00000417044
  gene symbol: ZDHHC16
  hgvsc: ENST00000417044.1:c.382-29A>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000345383
  ensembl transcript: ENST00000352634
  gene symbol: ZDHHC16
  hgvsc: ENST00000352634.4:c.557-29A>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359879
  ensembl transcript: ENST00000370842
  gene symbol: ZDHHC16
  hgvsc: ENST00000370842.2:c.557-29A>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000398532
  ensembl transcript: ENST00000433086
  gene symbol: ZDHHC16
  hgvsc: ENST00000433086.1:c.362-29A>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000377357
  ensembl transcript: ENST00000393760
  gene symbol: ZDHHC16
  hgvsc: ENST00000393760.1:c.557-29A>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359883
  ensembl transcript: ENST00000370846
  gene symbol: ZDHHC16
  hgvsc: ENST00000370846.4:c.556+578A>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000400719
  ensembl transcript: ENST00000414567
  gene symbol: ZDHHC16
  hgvsc: ENST00000414567.1:c.557-29A>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000304487
  ensembl transcript: ENST00000345745
  gene symbol: ZDHHC16
  hgvsc: ENST00000345745.5:c.362-29A>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000323360
  ensembl transcript: ENST00000353979
  gene symbol: ZDHHC16
  hgvsc: ENST00000353979.3:c.528-117A>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359891
  ensembl transcript: ENST00000370854
  gene symbol: ZDHHC16
  hgvsc: ENST00000370854.3:c.557-29A>G
  variant of: http://identifiers.org/hgnc/20714
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2094
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4592
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2734
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6163
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1146
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4599
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3625
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1032
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2255
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3146
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
reference allele: A
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum

10-99213265-TC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 99213265
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 99213264
    reference: chr 10
allele count: 1
allele frequency: 8.319329129299013e-6
allele num: 120202
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000398532
  ensembl transcript: ENST00000433086
  gene symbol: ZDHHC16
  hgvsc: ENST00000433086.1:c.362-20delC
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000495735
  gene symbol: ZDHHC16
  hgvsc: ENST00000495735.1:n.585-20delC
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000400719
  ensembl transcript: ENST00000414567
  gene symbol: ZDHHC16
  hgvsc: ENST00000414567.1:c.557-20delC
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000304487
  ensembl transcript: ENST00000345745
  gene symbol: ZDHHC16
  hgvsc: ENST00000345745.5:c.362-20delC
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000462924
  gene symbol: ZDHHC16
  hgvsc: ENST00000462924.1:n.791+587delC
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000466895
  gene symbol: ZDHHC16
  hgvsc: ENST00000466895.1:n.277-20delC
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000396286
  ensembl transcript: ENST00000417044
  gene symbol: ZDHHC16
  hgvsc: ENST00000417044.1:c.382-20delC
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000405240
  ensembl transcript: ENST00000420089
  gene symbol: ZDHHC16
  hgvsc: ENST00000420089.1:c.484-20delC
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359883
  ensembl transcript: ENST00000370846
  gene symbol: ZDHHC16
  hgvsc: ENST00000370846.4:c.556+587delC
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359879
  ensembl transcript: ENST00000370842
  gene symbol: ZDHHC16
  hgvsc: ENST00000370842.2:c.557-20delC
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000377357
  ensembl transcript: ENST00000393760
  gene symbol: ZDHHC16
  hgvsc: ENST00000393760.1:c.557-20delC
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000345383
  ensembl transcript: ENST00000352634
  gene symbol: ZDHHC16
  hgvsc: ENST00000352634.4:c.557-20delC
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000323360
  ensembl transcript: ENST00000353979
  gene symbol: ZDHHC16
  hgvsc: ENST00000353979.3:c.528-108delC
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000459777
  gene symbol: ZDHHC16
  hgvsc: ENST00000459777.1:n.278-20delC
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359891
  ensembl transcript: ENST00000370854
  gene symbol: ZDHHC16
  hgvsc: ENST00000370854.3:c.557-20delC
  variant of: http://identifiers.org/hgnc/20714
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6163
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2094
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2734
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3152
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4592
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5552
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2041
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3625
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: Other
reference allele: TC
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ

10-99213266-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 99213266
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 99213266
    reference: chr 10
allele count: 1
allele frequency: 8.316284949187499e-6
allele num: 120246
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000495735
  gene symbol: ZDHHC16
  hgvsc: ENST00000495735.1:n.585-21C>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000396286
  ensembl transcript: ENST00000417044
  gene symbol: ZDHHC16
  hgvsc: ENST00000417044.1:c.382-21C>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359891
  ensembl transcript: ENST00000370854
  gene symbol: ZDHHC16
  hgvsc: ENST00000370854.3:c.557-21C>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000466895
  gene symbol: ZDHHC16
  hgvsc: ENST00000466895.1:n.277-21C>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000345383
  ensembl transcript: ENST00000352634
  gene symbol: ZDHHC16
  hgvsc: ENST00000352634.4:c.557-21C>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359879
  ensembl transcript: ENST00000370842
  gene symbol: ZDHHC16
  hgvsc: ENST00000370842.2:c.557-21C>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359883
  ensembl transcript: ENST00000370846
  gene symbol: ZDHHC16
  hgvsc: ENST00000370846.4:c.556+586C>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000462924
  gene symbol: ZDHHC16
  hgvsc: ENST00000462924.1:n.791+586C>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000398532
  ensembl transcript: ENST00000433086
  gene symbol: ZDHHC16
  hgvsc: ENST00000433086.1:c.362-21C>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000377357
  ensembl transcript: ENST00000393760
  gene symbol: ZDHHC16
  hgvsc: ENST00000393760.1:c.557-21C>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000405240
  ensembl transcript: ENST00000420089
  gene symbol: ZDHHC16
  hgvsc: ENST00000420089.1:c.484-21C>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000304487
  ensembl transcript: ENST00000345745
  gene symbol: ZDHHC16
  hgvsc: ENST00000345745.5:c.362-21C>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000459777
  gene symbol: ZDHHC16
  hgvsc: ENST00000459777.1:n.278-21C>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000400719
  ensembl transcript: ENST00000414567
  gene symbol: ZDHHC16
  hgvsc: ENST00000414567.1:c.557-21C>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000323360
  ensembl transcript: ENST00000353979
  gene symbol: ZDHHC16
  hgvsc: ENST00000353979.3:c.528-109C>T
  variant of: http://identifiers.org/hgnc/20714
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2094
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4592
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 558
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2090
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2734
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 531
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4602
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1503
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6163
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5552
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6070
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
reference allele: C
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: DP

10-99213267-CTTAATCA-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 99213267
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 99213260
    reference: chr 10
allele count: 1
allele frequency: 8.311584686736373e-6
allele num: 120314
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000400719
  ensembl transcript: ENST00000414567
  gene symbol: ZDHHC16
  hgvsc: ENST00000414567.1:c.557-17_557-11delAATCATT
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000459777
  gene symbol: ZDHHC16
  hgvsc: ENST00000459777.1:n.278-17_278-11delAATCATT
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000304487
  ensembl transcript: ENST00000345745
  gene symbol: ZDHHC16
  hgvsc: ENST00000345745.5:c.362-17_362-11delAATCATT
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000377357
  ensembl transcript: ENST00000393760
  gene symbol: ZDHHC16
  hgvsc: ENST00000393760.1:c.557-17_557-11delAATCATT
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000462924
  gene symbol: ZDHHC16
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000323360
  ensembl transcript: ENST00000353979
  gene symbol: ZDHHC16
  hgvsc: ENST00000353979.3:c.528-105_528-99delAATCATT
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359879
  ensembl transcript: ENST00000370842
  gene symbol: ZDHHC16
  hgvsc: ENST00000370842.2:c.557-17_557-11delAATCATT
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000398532
  ensembl transcript: ENST00000433086
  gene symbol: ZDHHC16
  hgvsc: ENST00000433086.1:c.362-17_362-11delAATCATT
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000345383
  ensembl transcript: ENST00000352634
  gene symbol: ZDHHC16
  hgvsc: ENST00000352634.4:c.557-17_557-11delAATCATT
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000495735
  gene symbol: ZDHHC16
  hgvsc: ENST00000495735.1:n.585-17_585-11delAATCATT
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000396286
  ensembl transcript: ENST00000417044
  gene symbol: ZDHHC16
  hgvsc: ENST00000417044.1:c.382-17_382-11delAATCATT
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000466895
  gene symbol: ZDHHC16
  hgvsc: ENST00000466895.1:n.277-17_277-11delAATCATT
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000405240
  ensembl transcript: ENST00000420089
  gene symbol: ZDHHC16
  hgvsc: ENST00000420089.1:c.484-17_484-11delAATCATT
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359891
  ensembl transcript: ENST00000370854
  gene symbol: ZDHHC16
  hgvsc: ENST00000370854.3:c.557-17_557-11delAATCATT
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359883
  ensembl transcript: ENST00000370846
  gene symbol: ZDHHC16
  variant of: http://identifiers.org/hgnc/20714
canonical: true
consequence: intron
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 2094
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5311
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3154
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4592
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2734
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5552
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2370
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6163
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6070
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1503
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: Latino
population: African
reference allele: CTTAATCA
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: MQ

10-99213297-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 99213297
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 99213297
    reference: chr 10
allele count: 2
allele frequency: 1.648587160803192e-5
allele num: 121316
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000398532
  ensembl transcript: ENST00000433086
  gene symbol: ZDHHC16
  hgvsc: ENST00000433086.1:c.372C>T
  hgvsp: ENST00000433086.1:c.372C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359879
  ensembl transcript: ENST00000370842
  gene symbol: ZDHHC16
  hgvsc: ENST00000370842.2:c.567C>T
  hgvsp: ENST00000370842.2:c.567C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000400719
  ensembl transcript: ENST00000414567
  gene symbol: ZDHHC16
  hgvsc: ENST00000414567.1:c.567C>T
  hgvsp: ENST00000414567.1:c.567C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000377357
  ensembl transcript: ENST00000393760
  gene symbol: ZDHHC16
  hgvsc: ENST00000393760.1:c.567C>T
  hgvsp: ENST00000393760.1:c.567C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000459777
  gene symbol: ZDHHC16
  hgvsc: ENST00000459777.1:n.288C>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000304487
  ensembl transcript: ENST00000345745
  gene symbol: ZDHHC16
  hgvsc: ENST00000345745.5:c.372C>T
  hgvsp: ENST00000345745.5:c.372C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000466895
  gene symbol: ZDHHC16
  hgvsc: ENST00000466895.1:n.287C>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000345383
  ensembl transcript: ENST00000352634
  gene symbol: ZDHHC16
  hgvsc: ENST00000352634.4:c.567C>T
  hgvsp: ENST00000352634.4:c.567C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359883
  ensembl transcript: ENST00000370846
  gene symbol: ZDHHC16
  hgvsc: ENST00000370846.4:c.556+617C>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000323360
  ensembl transcript: ENST00000353979
  gene symbol: ZDHHC16
  hgvsc: ENST00000353979.3:c.528-78C>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000405240
  ensembl transcript: ENST00000420089
  gene symbol: ZDHHC16
  hgvsc: ENST00000420089.1:c.494C>T
  hgvsp: ENST00000420089.1:c.494C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000495735
  gene symbol: ZDHHC16
  hgvsc: ENST00000495735.1:n.595C>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000396286
  ensembl transcript: ENST00000417044
  gene symbol: ZDHHC16
  hgvsc: ENST00000417044.1:c.392C>T
  hgvsp: ENST00000417044.1:c.392C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000462924
  gene symbol: ZDHHC16
  hgvsc: ENST00000462924.1:n.791+617C>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359891
  ensembl transcript: ENST00000370854
  gene symbol: ZDHHC16
  hgvsc: ENST00000370854.3:c.567C>T
  hgvsp: ENST00000370854.3:c.567C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20714
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3207
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3898
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6070
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4841
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2734
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4592
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1503
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn189Asn
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Other
population: East Asian
population: African
population: Latino
population: European (Finnish)
reference allele: C
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ

10-99213302-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 99213302
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 99213302
    reference: chr 10
allele count: 1
allele frequency: 8.240490473993011e-6
allele num: 121352
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000466895
  gene symbol: ZDHHC16
  hgvsc: ENST00000466895.1:n.292G>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000323360
  ensembl transcript: ENST00000353979
  gene symbol: ZDHHC16
  hgvsc: ENST00000353979.3:c.528-73G>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359891
  ensembl transcript: ENST00000370854
  gene symbol: ZDHHC16
  hgvsc: ENST00000370854.3:c.572G>A
  hgvsp: ENSP00000359891.3:p.Cys191Tyr
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000377357
  ensembl transcript: ENST00000393760
  gene symbol: ZDHHC16
  hgvsc: ENST00000393760.1:c.572G>A
  hgvsp: ENSP00000377357.1:p.Cys191Tyr
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000398532
  ensembl transcript: ENST00000433086
  gene symbol: ZDHHC16
  hgvsc: ENST00000433086.1:c.377G>A
  hgvsp: ENSP00000398532.1:p.Cys126Tyr
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000304487
  ensembl transcript: ENST00000345745
  gene symbol: ZDHHC16
  hgvsc: ENST00000345745.5:c.377G>A
  hgvsp: ENSP00000304487.8:p.Cys126Tyr
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000345383
  ensembl transcript: ENST00000352634
  gene symbol: ZDHHC16
  hgvsc: ENST00000352634.4:c.572G>A
  hgvsp: ENSP00000345383.4:p.Cys191Tyr
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000462924
  gene symbol: ZDHHC16
  hgvsc: ENST00000462924.1:n.791+622G>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359879
  ensembl transcript: ENST00000370842
  gene symbol: ZDHHC16
  hgvsc: ENST00000370842.2:c.572G>A
  hgvsp: ENSP00000359879.1:p.Cys191Tyr
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000396286
  ensembl transcript: ENST00000417044
  gene symbol: ZDHHC16
  hgvsc: ENST00000417044.1:c.397G>A
  hgvsp: ENSP00000396286.1:p.Cys133Tyr
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000459777
  gene symbol: ZDHHC16
  hgvsc: ENST00000459777.1:n.293G>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000495735
  gene symbol: ZDHHC16
  hgvsc: ENST00000495735.1:n.600G>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359883
  ensembl transcript: ENST00000370846
  gene symbol: ZDHHC16
  hgvsc: ENST00000370846.4:c.556+622G>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000400719
  ensembl transcript: ENST00000414567
  gene symbol: ZDHHC16
  hgvsc: ENST00000414567.1:c.572G>A
  hgvsp: ENSP00000400719.1:p.Cys191Tyr
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000405240
  ensembl transcript: ENST00000420089
  gene symbol: ZDHHC16
  hgvsc: ENST00000420089.1:c.499G>A
  hgvsp: ENSP00000405240.1:p.Cys167Tyr
  variant of: http://identifiers.org/hgnc/20714
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4841
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3914
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1503
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6070
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2575
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4592
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3627
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Cys191Tyr
num of homozygotes: 0
population: South Asian
population: Other
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
population: Latino
reference allele: G
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD

10-99213303-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 99213303
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 99213303
    reference: chr 10
allele count: 3
allele frequency: 2.472147142197904e-5
allele num: 121352
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000345383
  ensembl transcript: ENST00000352634
  gene symbol: ZDHHC16
  hgvsc: ENST00000352634.4:c.573T>C
  hgvsp: ENST00000352634.4:c.573T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000398532
  ensembl transcript: ENST00000433086
  gene symbol: ZDHHC16
  hgvsc: ENST00000433086.1:c.378T>C
  hgvsp: ENST00000433086.1:c.378T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000396286
  ensembl transcript: ENST00000417044
  gene symbol: ZDHHC16
  hgvsc: ENST00000417044.1:c.398T>C
  hgvsp: ENST00000417044.1:c.398T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000462924
  gene symbol: ZDHHC16
  hgvsc: ENST00000462924.1:n.791+623T>C
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359879
  ensembl transcript: ENST00000370842
  gene symbol: ZDHHC16
  hgvsc: ENST00000370842.2:c.573T>C
  hgvsp: ENST00000370842.2:c.573T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000377357
  ensembl transcript: ENST00000393760
  gene symbol: ZDHHC16
  hgvsc: ENST00000393760.1:c.573T>C
  hgvsp: ENST00000393760.1:c.573T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000459777
  gene symbol: ZDHHC16
  hgvsc: ENST00000459777.1:n.294T>C
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359883
  ensembl transcript: ENST00000370846
  gene symbol: ZDHHC16
  hgvsc: ENST00000370846.4:c.556+623T>C
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000400719
  ensembl transcript: ENST00000414567
  gene symbol: ZDHHC16
  hgvsc: ENST00000414567.1:c.573T>C
  hgvsp: ENST00000414567.1:c.573T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000304487
  ensembl transcript: ENST00000345745
  gene symbol: ZDHHC16
  hgvsc: ENST00000345745.5:c.378T>C
  hgvsp: ENST00000345745.5:c.378T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000405240
  ensembl transcript: ENST00000420089
  gene symbol: ZDHHC16
  hgvsc: ENST00000420089.1:c.500T>C
  hgvsp: ENST00000420089.1:c.500T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000495735
  gene symbol: ZDHHC16
  hgvsc: ENST00000495735.1:n.601T>C
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359891
  ensembl transcript: ENST00000370854
  gene symbol: ZDHHC16
  hgvsc: ENST00000370854.3:c.573T>C
  hgvsp: ENST00000370854.3:c.573T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000323360
  ensembl transcript: ENST00000353979
  gene symbol: ZDHHC16
  hgvsc: ENST00000353979.3:c.528-72T>C
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000466895
  gene symbol: ZDHHC16
  hgvsc: ENST00000466895.1:n.293T>C
  variant of: http://identifiers.org/hgnc/20714
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3917
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6164
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5313
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2734
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2095
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6070
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2576
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Cys191Cys
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: Latino
population: South Asian
reference allele: T
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: DP

10-99213306-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 99213306
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 99213306
    reference: chr 10
allele count: 1
allele frequency: 8.239404126293587e-6
allele num: 121368
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000400719
  ensembl transcript: ENST00000414567
  gene symbol: ZDHHC16
  hgvsc: ENST00000414567.1:c.576G>A
  hgvsp: ENST00000414567.1:c.576G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000377357
  ensembl transcript: ENST00000393760
  gene symbol: ZDHHC16
  hgvsc: ENST00000393760.1:c.576G>A
  hgvsp: ENST00000393760.1:c.576G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000459777
  gene symbol: ZDHHC16
  hgvsc: ENST00000459777.1:n.297G>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359891
  ensembl transcript: ENST00000370854
  gene symbol: ZDHHC16
  hgvsc: ENST00000370854.3:c.576G>A
  hgvsp: ENST00000370854.3:c.576G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000462924
  gene symbol: ZDHHC16
  hgvsc: ENST00000462924.1:n.791+626G>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000396286
  ensembl transcript: ENST00000417044
  gene symbol: ZDHHC16
  hgvsc: ENST00000417044.1:c.401G>A
  hgvsp: ENST00000417044.1:c.401G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000495735
  gene symbol: ZDHHC16
  hgvsc: ENST00000495735.1:n.604G>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000323360
  ensembl transcript: ENST00000353979
  gene symbol: ZDHHC16
  hgvsc: ENST00000353979.3:c.528-69G>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359883
  ensembl transcript: ENST00000370846
  gene symbol: ZDHHC16
  hgvsc: ENST00000370846.4:c.556+626G>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000405240
  ensembl transcript: ENST00000420089
  gene symbol: ZDHHC16
  hgvsc: ENST00000420089.1:c.503G>A
  hgvsp: ENST00000420089.1:c.503G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000345383
  ensembl transcript: ENST00000352634
  gene symbol: ZDHHC16
  hgvsc: ENST00000352634.4:c.576G>A
  hgvsp: ENST00000352634.4:c.576G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000398532
  ensembl transcript: ENST00000433086
  gene symbol: ZDHHC16
  hgvsc: ENST00000433086.1:c.381G>A
  hgvsp: ENST00000433086.1:c.381G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000304487
  ensembl transcript: ENST00000345745
  gene symbol: ZDHHC16
  hgvsc: ENST00000345745.5:c.381G>A
  hgvsp: ENST00000345745.5:c.381G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359879
  ensembl transcript: ENST00000370842
  gene symbol: ZDHHC16
  hgvsc: ENST00000370842.2:c.576G>A
  hgvsp: ENST00000370842.2:c.576G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000466895
  gene symbol: ZDHHC16
  hgvsc: ENST00000466895.1:n.296G>A
  variant of: http://identifiers.org/hgnc/20714
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2734
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3916
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6164
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4838
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6071
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5556
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4624
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val192Val
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: QD

10-99213314-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 99213314
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 99213314
    reference: chr 10
allele count: 1
allele frequency: 8.238318064983852e-6
allele num: 121384
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359883
  ensembl transcript: ENST00000370846
  gene symbol: ZDHHC16
  hgvsc: ENST00000370846.4:c.556+634A>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000396286
  ensembl transcript: ENST00000417044
  gene symbol: ZDHHC16
  hgvsc: ENST00000417044.1:c.409A>G
  hgvsp: ENSP00000396286.1:p.Tyr137Cys
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000487315
  gene symbol: ZDHHC16
  hgvsc: ENST00000487315.1:n.4A>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000398532
  ensembl transcript: ENST00000433086
  gene symbol: ZDHHC16
  hgvsc: ENST00000433086.1:c.389A>G
  hgvsp: ENSP00000398532.1:p.Tyr130Cys
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000405240
  ensembl transcript: ENST00000420089
  gene symbol: ZDHHC16
  hgvsc: ENST00000420089.1:c.511A>G
  hgvsp: ENSP00000405240.1:p.Tyr171Cys
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000377357
  ensembl transcript: ENST00000393760
  gene symbol: ZDHHC16
  hgvsc: ENST00000393760.1:c.584A>G
  hgvsp: ENSP00000377357.1:p.Tyr195Cys
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000304487
  ensembl transcript: ENST00000345745
  gene symbol: ZDHHC16
  hgvsc: ENST00000345745.5:c.389A>G
  hgvsp: ENSP00000304487.8:p.Tyr130Cys
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359891
  ensembl transcript: ENST00000370854
  gene symbol: ZDHHC16
  hgvsc: ENST00000370854.3:c.584A>G
  hgvsp: ENSP00000359891.3:p.Tyr195Cys
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359879
  ensembl transcript: ENST00000370842
  gene symbol: ZDHHC16
  hgvsc: ENST00000370842.2:c.584A>G
  hgvsp: ENSP00000359879.1:p.Tyr195Cys
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000400719
  ensembl transcript: ENST00000414567
  gene symbol: ZDHHC16
  hgvsc: ENST00000414567.1:c.584A>G
  hgvsp: ENSP00000400719.1:p.Tyr195Cys
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000345383
  ensembl transcript: ENST00000352634
  gene symbol: ZDHHC16
  hgvsc: ENST00000352634.4:c.584A>G
  hgvsp: ENSP00000345383.4:p.Tyr195Cys
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000459777
  gene symbol: ZDHHC16
  hgvsc: ENST00000459777.1:n.305A>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000495735
  gene symbol: ZDHHC16
  hgvsc: ENST00000495735.1:n.612A>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000466895
  gene symbol: ZDHHC16
  hgvsc: ENST00000466895.1:n.304A>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000323360
  ensembl transcript: ENST00000353979
  gene symbol: ZDHHC16
  hgvsc: ENST00000353979.3:c.528-61A>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000462924
  gene symbol: ZDHHC16
  hgvsc: ENST00000462924.1:n.791+634A>G
  variant of: http://identifiers.org/hgnc/20714
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2690
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2095
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5555
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6164
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6072
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3893
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Tyr195Cys
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
population: Other
population: African
reference allele: A
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ

10-99213322-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 99213322
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 99213322
    reference: chr 10
allele count: 1
allele frequency: 8.237639422047218e-6
allele num: 121394
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000487315
  gene symbol: ZDHHC16
  hgvsc: ENST00000487315.1:n.12C>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000405240
  ensembl transcript: ENST00000420089
  gene symbol: ZDHHC16
  hgvsc: ENST00000420089.1:c.519C>T
  hgvsp: ENSP00000405240.1:p.Arg174Trp
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000377357
  ensembl transcript: ENST00000393760
  gene symbol: ZDHHC16
  hgvsc: ENST00000393760.1:c.592C>T
  hgvsp: ENSP00000377357.1:p.Arg198Trp
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000466895
  gene symbol: ZDHHC16
  hgvsc: ENST00000466895.1:n.312C>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000396286
  ensembl transcript: ENST00000417044
  gene symbol: ZDHHC16
  hgvsc: ENST00000417044.1:c.417C>T
  hgvsp: ENSP00000396286.1:p.Arg140Trp
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000398532
  ensembl transcript: ENST00000433086
  gene symbol: ZDHHC16
  hgvsc: ENST00000433086.1:c.397C>T
  hgvsp: ENSP00000398532.1:p.Arg133Trp
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000323360
  ensembl transcript: ENST00000353979
  gene symbol: ZDHHC16
  hgvsc: ENST00000353979.3:c.528-53C>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000345383
  ensembl transcript: ENST00000352634
  gene symbol: ZDHHC16
  hgvsc: ENST00000352634.4:c.592C>T
  hgvsp: ENSP00000345383.4:p.Arg198Trp
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000459777
  gene symbol: ZDHHC16
  hgvsc: ENST00000459777.1:n.313C>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000304487
  ensembl transcript: ENST00000345745
  gene symbol: ZDHHC16
  hgvsc: ENST00000345745.5:c.397C>T
  hgvsp: ENSP00000304487.8:p.Arg133Trp
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359879
  ensembl transcript: ENST00000370842
  gene symbol: ZDHHC16
  hgvsc: ENST00000370842.2:c.592C>T
  hgvsp: ENSP00000359879.1:p.Arg198Trp
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000462924
  gene symbol: ZDHHC16
  hgvsc: ENST00000462924.1:n.791+642C>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000495735
  gene symbol: ZDHHC16
  hgvsc: ENST00000495735.1:n.620C>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000400719
  ensembl transcript: ENST00000414567
  gene symbol: ZDHHC16
  hgvsc: ENST00000414567.1:c.592C>T
  hgvsp: ENSP00000400719.1:p.Arg198Trp
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359883
  ensembl transcript: ENST00000370846
  gene symbol: ZDHHC16
  hgvsc: ENST00000370846.4:c.556+642C>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359891
  ensembl transcript: ENST00000370854
  gene symbol: ZDHHC16
  hgvsc: ENST00000370854.3:c.592C>T
  hgvsp: ENSP00000359891.3:p.Arg198Trp
  variant of: http://identifiers.org/hgnc/20714
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2690
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3206
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2095
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3627
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1503
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3895
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg198Trp
num of homozygotes: 0
population: African
population: Latino
population: Other
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: DP

10-99213332-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 99213332
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 99213332
    reference: chr 10
allele count: 1
allele frequency: 8.236825198095647e-6
allele num: 121406
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000462924
  gene symbol: ZDHHC16
  hgvsc: ENST00000462924.1:n.791+652T>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000466895
  gene symbol: ZDHHC16
  hgvsc: ENST00000466895.1:n.322T>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359883
  ensembl transcript: ENST00000370846
  gene symbol: ZDHHC16
  hgvsc: ENST00000370846.4:c.556+652T>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000487315
  gene symbol: ZDHHC16
  hgvsc: ENST00000487315.1:n.22T>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000304487
  ensembl transcript: ENST00000345745
  gene symbol: ZDHHC16
  hgvsc: ENST00000345745.5:c.407T>A
  hgvsp: ENSP00000304487.8:p.Phe136Tyr
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000405240
  ensembl transcript: ENST00000420089
  gene symbol: ZDHHC16
  hgvsc: ENST00000420089.1:c.529T>A
  hgvsp: ENSP00000405240.1:p.Phe177Tyr
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000396286
  ensembl transcript: ENST00000417044
  gene symbol: ZDHHC16
  hgvsc: ENST00000417044.1:c.427T>A
  hgvsp: ENSP00000396286.1:p.Phe143Tyr
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000377357
  ensembl transcript: ENST00000393760
  gene symbol: ZDHHC16
  hgvsc: ENST00000393760.1:c.602T>A
  hgvsp: ENSP00000377357.1:p.Phe201Tyr
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000398532
  ensembl transcript: ENST00000433086
  gene symbol: ZDHHC16
  hgvsc: ENST00000433086.1:c.407T>A
  hgvsp: ENSP00000398532.1:p.Phe136Tyr
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000400719
  ensembl transcript: ENST00000414567
  gene symbol: ZDHHC16
  hgvsc: ENST00000414567.1:c.602T>A
  hgvsp: ENSP00000400719.1:p.Phe201Tyr
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359891
  ensembl transcript: ENST00000370854
  gene symbol: ZDHHC16
  hgvsc: ENST00000370854.3:c.602T>A
  hgvsp: ENSP00000359891.3:p.Phe201Tyr
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000495735
  gene symbol: ZDHHC16
  hgvsc: ENST00000495735.1:n.630T>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000345383
  ensembl transcript: ENST00000352634
  gene symbol: ZDHHC16
  hgvsc: ENST00000352634.4:c.602T>A
  hgvsp: ENSP00000345383.4:p.Phe201Tyr
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000323360
  ensembl transcript: ENST00000353979
  gene symbol: ZDHHC16
  hgvsc: ENST00000353979.3:c.528-43T>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359879
  ensembl transcript: ENST00000370842
  gene symbol: ZDHHC16
  hgvsc: ENST00000370842.2:c.602T>A
  hgvsp: ENSP00000359879.1:p.Phe201Tyr
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000459777
  gene symbol: ZDHHC16
  hgvsc: ENST00000459777.1:n.323T>A
  variant of: http://identifiers.org/hgnc/20714
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4837
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3207
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2689
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2641
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4621
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Phe201Tyr
num of homozygotes: 0
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
reference allele: T
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ

10-99213362-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 99213362
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 99213362
    reference: chr 10
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359879
  ensembl transcript: ENST00000370842
  gene symbol: ZDHHC16
  hgvsc: ENST00000370842.2:c.632G>T
  hgvsp: ENSP00000359879.1:p.Cys211Phe
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000495735
  gene symbol: ZDHHC16
  hgvsc: ENST00000495735.1:n.660G>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000396286
  ensembl transcript: ENST00000417044
  gene symbol: ZDHHC16
  hgvsc: ENST00000417044.1:c.457G>T
  hgvsp: ENSP00000396286.1:p.Cys153Phe
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000323360
  ensembl transcript: ENST00000353979
  gene symbol: ZDHHC16
  hgvsc: ENST00000353979.3:c.528-13G>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000400719
  ensembl transcript: ENST00000414567
  gene symbol: ZDHHC16
  hgvsc: ENST00000414567.1:c.632G>T
  hgvsp: ENSP00000400719.1:p.Cys211Phe
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000398532
  ensembl transcript: ENST00000433086
  gene symbol: ZDHHC16
  hgvsc: ENST00000433086.1:c.437G>T
  hgvsp: ENSP00000398532.1:p.Cys146Phe
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000345383
  ensembl transcript: ENST00000352634
  gene symbol: ZDHHC16
  hgvsc: ENST00000352634.4:c.632G>T
  hgvsp: ENSP00000345383.4:p.Cys211Phe
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000304487
  ensembl transcript: ENST00000345745
  gene symbol: ZDHHC16
  hgvsc: ENST00000345745.5:c.437G>T
  hgvsp: ENSP00000304487.8:p.Cys146Phe
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000462924
  gene symbol: ZDHHC16
  hgvsc: ENST00000462924.1:n.791+682G>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000487315
  gene symbol: ZDHHC16
  hgvsc: ENST00000487315.1:n.52G>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000377357
  ensembl transcript: ENST00000393760
  gene symbol: ZDHHC16
  hgvsc: ENST00000393760.1:c.632G>T
  hgvsp: ENSP00000377357.1:p.Cys211Phe
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000466895
  gene symbol: ZDHHC16
  hgvsc: ENST00000466895.1:n.352G>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000405240
  ensembl transcript: ENST00000420089
  gene symbol: ZDHHC16
  hgvsc: ENST00000420089.1:c.559G>T
  hgvsp: ENSP00000405240.1:p.Cys187Phe
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359891
  ensembl transcript: ENST00000370854
  gene symbol: ZDHHC16
  hgvsc: ENST00000370854.3:c.632G>T
  hgvsp: ENSP00000359891.3:p.Cys211Phe
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359883
  ensembl transcript: ENST00000370846
  gene symbol: ZDHHC16
  hgvsc: ENST00000370846.4:c.556+682G>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000459777
  gene symbol: ZDHHC16
  hgvsc: ENST00000459777.1:n.353G>T
  variant of: http://identifiers.org/hgnc/20714
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2095
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1503
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1144
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6164
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4621
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5556
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Cys211Phe
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
population: Other
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

10-99213363-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 99213363
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 99213363
    reference: chr 10
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000462924
  gene symbol: ZDHHC16
  hgvsc: ENST00000462924.1:n.791+683T>C
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000495735
  gene symbol: ZDHHC16
  hgvsc: ENST00000495735.1:n.661T>C
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000304487
  ensembl transcript: ENST00000345745
  gene symbol: ZDHHC16
  hgvsc: ENST00000345745.5:c.438T>C
  hgvsp: ENST00000345745.5:c.438T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000400719
  ensembl transcript: ENST00000414567
  gene symbol: ZDHHC16
  hgvsc: ENST00000414567.1:c.633T>C
  hgvsp: ENST00000414567.1:c.633T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359883
  ensembl transcript: ENST00000370846
  gene symbol: ZDHHC16
  hgvsc: ENST00000370846.4:c.556+683T>C
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000396286
  ensembl transcript: ENST00000417044
  gene symbol: ZDHHC16
  hgvsc: ENST00000417044.1:c.458T>C
  hgvsp: ENST00000417044.1:c.458T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000398532
  ensembl transcript: ENST00000433086
  gene symbol: ZDHHC16
  hgvsc: ENST00000433086.1:c.438T>C
  hgvsp: ENST00000433086.1:c.438T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359879
  ensembl transcript: ENST00000370842
  gene symbol: ZDHHC16
  hgvsc: ENST00000370842.2:c.633T>C
  hgvsp: ENST00000370842.2:c.633T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000377357
  ensembl transcript: ENST00000393760
  gene symbol: ZDHHC16
  hgvsc: ENST00000393760.1:c.633T>C
  hgvsp: ENST00000393760.1:c.633T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000459777
  gene symbol: ZDHHC16
  hgvsc: ENST00000459777.1:n.354T>C
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000405240
  ensembl transcript: ENST00000420089
  gene symbol: ZDHHC16
  hgvsc: ENST00000420089.1:c.560T>C
  hgvsp: ENST00000420089.1:c.560T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000345383
  ensembl transcript: ENST00000352634
  gene symbol: ZDHHC16
  hgvsc: ENST00000352634.4:c.633T>C
  hgvsp: ENST00000352634.4:c.633T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000487315
  gene symbol: ZDHHC16
  hgvsc: ENST00000487315.1:n.53T>C
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000323360
  ensembl transcript: ENST00000353979
  gene symbol: ZDHHC16
  hgvsc: ENST00000353979.3:c.528-12T>C
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359891
  ensembl transcript: ENST00000370854
  gene symbol: ZDHHC16
  hgvsc: ENST00000370854.3:c.633T>C
  hgvsp: ENST00000370854.3:c.633T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000466895
  gene symbol: ZDHHC16
  hgvsc: ENST00000466895.1:n.353T>C
  variant of: http://identifiers.org/hgnc/20714
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2646
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3627
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1504
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5556
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6164
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Cys211Cys
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: DP
site quality: QD
site quality: VQSLOD

10-99213377-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 99213377
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 99213377
    reference: chr 10
allele count: 1
allele frequency: 8.237232289950576e-6
allele num: 121400
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000459777
  gene symbol: ZDHHC16
  hgvsc: ENST00000459777.1:n.368A>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000377357
  ensembl transcript: ENST00000393760
  gene symbol: ZDHHC16
  hgvsc: ENST00000393760.1:c.647A>G
  hgvsp: ENSP00000377357.1:p.Tyr216Cys
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000304487
  ensembl transcript: ENST00000345745
  gene symbol: ZDHHC16
  hgvsc: ENST00000345745.5:c.452A>G
  hgvsp: ENSP00000304487.8:p.Tyr151Cys
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000323360
  ensembl transcript: ENST00000353979
  gene symbol: ZDHHC16
  hgvsc: ENST00000353979.3:c.530A>G
  hgvsp: ENSP00000323360.3:p.Tyr177Cys
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000462924
  gene symbol: ZDHHC16
  hgvsc: ENST00000462924.1:n.791+697A>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000487315
  gene symbol: ZDHHC16
  hgvsc: ENST00000487315.1:n.67A>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000396286
  ensembl transcript: ENST00000417044
  gene symbol: ZDHHC16
  hgvsc: ENST00000417044.1:c.472A>G
  hgvsp: ENSP00000396286.1:p.Tyr158Cys
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359879
  ensembl transcript: ENST00000370842
  gene symbol: ZDHHC16
  hgvsc: ENST00000370842.2:c.647A>G
  hgvsp: ENSP00000359879.1:p.Tyr216Cys
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000405240
  ensembl transcript: ENST00000420089
  gene symbol: ZDHHC16
  hgvsc: ENST00000420089.1:c.574A>G
  hgvsp: ENSP00000405240.1:p.Tyr192Cys
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000495735
  gene symbol: ZDHHC16
  hgvsc: ENST00000495735.1:n.675A>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359891
  ensembl transcript: ENST00000370854
  gene symbol: ZDHHC16
  hgvsc: ENST00000370854.3:c.647A>G
  hgvsp: ENSP00000359891.3:p.Tyr216Cys
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000398532
  ensembl transcript: ENST00000433086
  gene symbol: ZDHHC16
  hgvsc: ENST00000433086.1:c.452A>G
  hgvsp: ENSP00000398532.1:p.Tyr151Cys
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000345383
  ensembl transcript: ENST00000352634
  gene symbol: ZDHHC16
  hgvsc: ENST00000352634.4:c.647A>G
  hgvsp: ENSP00000345383.4:p.Tyr216Cys
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359883
  ensembl transcript: ENST00000370846
  gene symbol: ZDHHC16
  hgvsc: ENST00000370846.4:c.556+697A>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000466895
  gene symbol: ZDHHC16
  hgvsc: ENST00000466895.1:n.367A>G
  variant of: http://identifiers.org/hgnc/20714
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5556
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3901
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4620
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3627
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5315
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2684
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2644
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1144
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Tyr216Cys
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
population: European (Finnish)
population: Latino
reference allele: A
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum

10-99213380-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 99213380
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 99213380
    reference: chr 10
allele count: 1
allele frequency: 8.237232289950576e-6
allele num: 121400
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359891
  ensembl transcript: ENST00000370854
  gene symbol: ZDHHC16
  hgvsc: ENST00000370854.3:c.650G>A
  hgvsp: ENSP00000359891.3:p.Gly217Glu
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000405240
  ensembl transcript: ENST00000420089
  gene symbol: ZDHHC16
  hgvsc: ENST00000420089.1:c.577G>A
  hgvsp: ENSP00000405240.1:p.Gly193Glu
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000396286
  ensembl transcript: ENST00000417044
  gene symbol: ZDHHC16
  hgvsc: ENST00000417044.1:c.475G>A
  hgvsp: ENSP00000396286.1:p.Gly159Glu
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000377357
  ensembl transcript: ENST00000393760
  gene symbol: ZDHHC16
  hgvsc: ENST00000393760.1:c.650G>A
  hgvsp: ENSP00000377357.1:p.Gly217Glu
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000459777
  gene symbol: ZDHHC16
  hgvsc: ENST00000459777.1:n.371G>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000304487
  ensembl transcript: ENST00000345745
  gene symbol: ZDHHC16
  hgvsc: ENST00000345745.5:c.455G>A
  hgvsp: ENSP00000304487.8:p.Gly152Glu
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359879
  ensembl transcript: ENST00000370842
  gene symbol: ZDHHC16
  hgvsc: ENST00000370842.2:c.650G>A
  hgvsp: ENSP00000359879.1:p.Gly217Glu
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000495735
  gene symbol: ZDHHC16
  hgvsc: ENST00000495735.1:n.678G>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359883
  ensembl transcript: ENST00000370846
  gene symbol: ZDHHC16
  hgvsc: ENST00000370846.4:c.556+700G>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000462924
  gene symbol: ZDHHC16
  hgvsc: ENST00000462924.1:n.791+700G>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000398532
  ensembl transcript: ENST00000433086
  gene symbol: ZDHHC16
  hgvsc: ENST00000433086.1:c.455G>A
  hgvsp: ENSP00000398532.1:p.Gly152Glu
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000487315
  gene symbol: ZDHHC16
  hgvsc: ENST00000487315.1:n.70G>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000466895
  gene symbol: ZDHHC16
  hgvsc: ENST00000466895.1:n.370G>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000323360
  ensembl transcript: ENST00000353979
  gene symbol: ZDHHC16
  hgvsc: ENST00000353979.3:c.533G>A
  hgvsp: ENSP00000323360.3:p.Gly178Glu
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000345383
  ensembl transcript: ENST00000352634
  gene symbol: ZDHHC16
  hgvsc: ENST00000352634.4:c.650G>A
  hgvsp: ENSP00000345383.4:p.Gly217Glu
  variant of: http://identifiers.org/hgnc/20714
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4591
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3900
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4834
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5555
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4622
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5315
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2644
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly217Glu
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: Other
population: European (Finnish)
reference allele: G
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum

10-99213394-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 99213394
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 99213394
    reference: chr 10
allele count: 1
allele frequency: 8.237910865804433e-6
allele num: 121390
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000495735
  gene symbol: ZDHHC16
  hgvsc: ENST00000495735.1:n.692T>C
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359879
  ensembl transcript: ENST00000370842
  gene symbol: ZDHHC16
  hgvsc: ENST00000370842.2:c.664T>C
  hgvsp: ENSP00000359879.1:p.Phe222Leu
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000398532
  ensembl transcript: ENST00000433086
  gene symbol: ZDHHC16
  hgvsc: ENST00000433086.1:c.469T>C
  hgvsp: ENSP00000398532.1:p.Phe157Leu
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000323360
  ensembl transcript: ENST00000353979
  gene symbol: ZDHHC16
  hgvsc: ENST00000353979.3:c.547T>C
  hgvsp: ENSP00000323360.3:p.Phe183Leu
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000345383
  ensembl transcript: ENST00000352634
  gene symbol: ZDHHC16
  hgvsc: ENST00000352634.4:c.664T>C
  hgvsp: ENSP00000345383.4:p.Phe222Leu
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000487315
  gene symbol: ZDHHC16
  hgvsc: ENST00000487315.1:n.84T>C
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000405240
  ensembl transcript: ENST00000420089
  gene symbol: ZDHHC16
  hgvsc: ENST00000420089.1:c.591T>C
  hgvsp: ENSP00000405240.1:p.Phe198Leu
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000396286
  ensembl transcript: ENST00000417044
  gene symbol: ZDHHC16
  hgvsc: ENST00000417044.1:c.489T>C
  hgvsp: ENSP00000396286.1:p.Phe164Leu
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000466895
  gene symbol: ZDHHC16
  hgvsc: ENST00000466895.1:n.384T>C
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000304487
  ensembl transcript: ENST00000345745
  gene symbol: ZDHHC16
  hgvsc: ENST00000345745.5:c.469T>C
  hgvsp: ENSP00000304487.8:p.Phe157Leu
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000459777
  gene symbol: ZDHHC16
  hgvsc: ENST00000459777.1:n.385T>C
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000462924
  gene symbol: ZDHHC16
  hgvsc: ENST00000462924.1:n.791+714T>C
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359883
  ensembl transcript: ENST00000370846
  gene symbol: ZDHHC16
  hgvsc: ENST00000370846.4:c.556+714T>C
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359891
  ensembl transcript: ENST00000370854
  gene symbol: ZDHHC16
  hgvsc: ENST00000370854.3:c.664T>C
  hgvsp: ENSP00000359891.3:p.Phe222Leu
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000377357
  ensembl transcript: ENST00000393760
  gene symbol: ZDHHC16
  hgvsc: ENST00000393760.1:c.664T>C
  hgvsp: ENSP00000377357.1:p.Phe222Leu
  variant of: http://identifiers.org/hgnc/20714
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3902
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3190
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3627
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6069
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5314
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4617
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2618
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Phe222Leu
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
population: Other
reference allele: T
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: ClippingRankSum

10-99213395-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 99213395
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 99213395
    reference: chr 10
allele count: 1
allele frequency: 8.238046594391538e-6
allele num: 121388
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000304487
  ensembl transcript: ENST00000345745
  gene symbol: ZDHHC16
  hgvsc: ENST00000345745.5:c.470T>C
  hgvsp: ENSP00000304487.8:p.Phe157Ser
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000323360
  ensembl transcript: ENST00000353979
  gene symbol: ZDHHC16
  hgvsc: ENST00000353979.3:c.548T>C
  hgvsp: ENSP00000323360.3:p.Phe183Ser
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000462924
  gene symbol: ZDHHC16
  hgvsc: ENST00000462924.1:n.791+715T>C
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000459777
  gene symbol: ZDHHC16
  hgvsc: ENST00000459777.1:n.386T>C
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000405240
  ensembl transcript: ENST00000420089
  gene symbol: ZDHHC16
  hgvsc: ENST00000420089.1:c.592T>C
  hgvsp: ENSP00000405240.1:p.Phe198Ser
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359891
  ensembl transcript: ENST00000370854
  gene symbol: ZDHHC16
  hgvsc: ENST00000370854.3:c.665T>C
  hgvsp: ENSP00000359891.3:p.Phe222Ser
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000345383
  ensembl transcript: ENST00000352634
  gene symbol: ZDHHC16
  hgvsc: ENST00000352634.4:c.665T>C
  hgvsp: ENSP00000345383.4:p.Phe222Ser
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359879
  ensembl transcript: ENST00000370842
  gene symbol: ZDHHC16
  hgvsc: ENST00000370842.2:c.665T>C
  hgvsp: ENSP00000359879.1:p.Phe222Ser
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359883
  ensembl transcript: ENST00000370846
  gene symbol: ZDHHC16
  hgvsc: ENST00000370846.4:c.556+715T>C
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000466895
  gene symbol: ZDHHC16
  hgvsc: ENST00000466895.1:n.385T>C
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000377357
  ensembl transcript: ENST00000393760
  gene symbol: ZDHHC16
  hgvsc: ENST00000393760.1:c.665T>C
  hgvsp: ENSP00000377357.1:p.Phe222Ser
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000487315
  gene symbol: ZDHHC16
  hgvsc: ENST00000487315.1:n.85T>C
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000398532
  ensembl transcript: ENST00000433086
  gene symbol: ZDHHC16
  hgvsc: ENST00000433086.1:c.470T>C
  hgvsp: ENSP00000398532.1:p.Phe157Ser
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000396286
  ensembl transcript: ENST00000417044
  gene symbol: ZDHHC16
  hgvsc: ENST00000417044.1:c.490T>C
  hgvsp: ENSP00000396286.1:p.Phe164Ser
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000495735
  gene symbol: ZDHHC16
  hgvsc: ENST00000495735.1:n.693T>C
  variant of: http://identifiers.org/hgnc/20714
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2638
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6161
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4590
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4616
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3628
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1144
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2095
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Phe222Ser
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
population: Latino
reference allele: T
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD

10-99213397-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 99213397
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 99213397
    reference: chr 10
allele count: 1
allele frequency: 8.238318064983852e-6
allele num: 121384
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000377357
  ensembl transcript: ENST00000393760
  gene symbol: ZDHHC16
  hgvsc: ENST00000393760.1:c.667C>T
  hgvsp: ENSP00000377357.1:p.Arg223Trp
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000405240
  ensembl transcript: ENST00000420089
  gene symbol: ZDHHC16
  hgvsc: ENST00000420089.1:c.594C>T
  hgvsp: ENSP00000405240.1:p.Arg199Trp
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359879
  ensembl transcript: ENST00000370842
  gene symbol: ZDHHC16
  hgvsc: ENST00000370842.2:c.667C>T
  hgvsp: ENSP00000359879.1:p.Arg223Trp
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000323360
  ensembl transcript: ENST00000353979
  gene symbol: ZDHHC16
  hgvsc: ENST00000353979.3:c.550C>T
  hgvsp: ENSP00000323360.3:p.Arg184Trp
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000466895
  gene symbol: ZDHHC16
  hgvsc: ENST00000466895.1:n.387C>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000487315
  gene symbol: ZDHHC16
  hgvsc: ENST00000487315.1:n.87C>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000398532
  ensembl transcript: ENST00000433086
  gene symbol: ZDHHC16
  hgvsc: ENST00000433086.1:c.472C>T
  hgvsp: ENSP00000398532.1:p.Arg158Trp
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000495735
  gene symbol: ZDHHC16
  hgvsc: ENST00000495735.1:n.695C>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000304487
  ensembl transcript: ENST00000345745
  gene symbol: ZDHHC16
  hgvsc: ENST00000345745.5:c.472C>T
  hgvsp: ENSP00000304487.8:p.Arg158Trp
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000396286
  ensembl transcript: ENST00000417044
  gene symbol: ZDHHC16
  hgvsc: ENST00000417044.1:c.492C>T
  hgvsp: ENSP00000396286.1:p.Arg165Trp
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000459777
  gene symbol: ZDHHC16
  hgvsc: ENST00000459777.1:n.388C>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359883
  ensembl transcript: ENST00000370846
  gene symbol: ZDHHC16
  hgvsc: ENST00000370846.4:c.556+717C>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000462924
  gene symbol: ZDHHC16
  hgvsc: ENST00000462924.1:n.791+717C>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359891
  ensembl transcript: ENST00000370854
  gene symbol: ZDHHC16
  hgvsc: ENST00000370854.3:c.667C>T
  hgvsp: ENSP00000359891.3:p.Arg223Trp
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000345383
  ensembl transcript: ENST00000352634
  gene symbol: ZDHHC16
  hgvsc: ENST00000352634.4:c.667C>T
  hgvsp: ENSP00000345383.4:p.Arg223Trp
  variant of: http://identifiers.org/hgnc/20714
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4832
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2603
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3905
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6070
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2633
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2095
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6160
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg223Trp
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: East Asian
population: Latino
population: African
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff

10-99213398-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 99213398
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 99213398
    reference: chr 10
allele count: 1
allele frequency: 8.2387253044209e-6
allele num: 121378
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000487315
  gene symbol: ZDHHC16
  hgvsc: ENST00000487315.1:n.88G>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359883
  ensembl transcript: ENST00000370846
  gene symbol: ZDHHC16
  hgvsc: ENST00000370846.4:c.556+718G>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000345383
  ensembl transcript: ENST00000352634
  gene symbol: ZDHHC16
  hgvsc: ENST00000352634.4:c.668G>A
  hgvsp: ENSP00000345383.4:p.Arg223Gln
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000459777
  gene symbol: ZDHHC16
  hgvsc: ENST00000459777.1:n.389G>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000462924
  gene symbol: ZDHHC16
  hgvsc: ENST00000462924.1:n.791+718G>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359891
  ensembl transcript: ENST00000370854
  gene symbol: ZDHHC16
  hgvsc: ENST00000370854.3:c.668G>A
  hgvsp: ENSP00000359891.3:p.Arg223Gln
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000304487
  ensembl transcript: ENST00000345745
  gene symbol: ZDHHC16
  hgvsc: ENST00000345745.5:c.473G>A
  hgvsp: ENSP00000304487.8:p.Arg158Gln
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000396286
  ensembl transcript: ENST00000417044
  gene symbol: ZDHHC16
  hgvsc: ENST00000417044.1:c.493G>A
  hgvsp: ENSP00000396286.1:p.Arg165Gln
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000377357
  ensembl transcript: ENST00000393760
  gene symbol: ZDHHC16
  hgvsc: ENST00000393760.1:c.668G>A
  hgvsp: ENSP00000377357.1:p.Arg223Gln
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359879
  ensembl transcript: ENST00000370842
  gene symbol: ZDHHC16
  hgvsc: ENST00000370842.2:c.668G>A
  hgvsp: ENSP00000359879.1:p.Arg223Gln
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000495735
  gene symbol: ZDHHC16
  hgvsc: ENST00000495735.1:n.696G>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000323360
  ensembl transcript: ENST00000353979
  gene symbol: ZDHHC16
  hgvsc: ENST00000353979.3:c.551G>A
  hgvsp: ENSP00000323360.3:p.Arg184Gln
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000466895
  gene symbol: ZDHHC16
  hgvsc: ENST00000466895.1:n.388G>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000398532
  ensembl transcript: ENST00000433086
  gene symbol: ZDHHC16
  hgvsc: ENST00000433086.1:c.473G>A
  hgvsp: ENSP00000398532.1:p.Arg158Gln
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000405240
  ensembl transcript: ENST00000420089
  gene symbol: ZDHHC16
  hgvsc: ENST00000420089.1:c.595G>A
  hgvsp: ENSP00000405240.1:p.Arg199Gln
  variant of: http://identifiers.org/hgnc/20714
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4612
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3628
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6156
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4832
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3185
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2605
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1504
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg223Gln
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: DP
site quality: ClippingRankSum

10-99213416-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 99213416
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 99213416
    reference: chr 10
allele count: 7
allele frequency: 5.768058142026072e-5
allele num: 121358
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000396286
  ensembl transcript: ENST00000417044
  gene symbol: ZDHHC16
  hgvsc: ENST00000417044.1:c.511T>C
  hgvsp: ENSP00000396286.1:p.Ile171Thr
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000323360
  ensembl transcript: ENST00000353979
  gene symbol: ZDHHC16
  hgvsc: ENST00000353979.3:c.569T>C
  hgvsp: ENSP00000323360.3:p.Ile190Thr
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359883
  ensembl transcript: ENST00000370846
  gene symbol: ZDHHC16
  hgvsc: ENST00000370846.4:c.556+736T>C
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000377357
  ensembl transcript: ENST00000393760
  gene symbol: ZDHHC16
  hgvsc: ENST00000393760.1:c.686T>C
  hgvsp: ENSP00000377357.1:p.Ile229Thr
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000462924
  gene symbol: ZDHHC16
  hgvsc: ENST00000462924.1:n.791+736T>C
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359891
  ensembl transcript: ENST00000370854
  gene symbol: ZDHHC16
  hgvsc: ENST00000370854.3:c.686T>C
  hgvsp: ENSP00000359891.3:p.Ile229Thr
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000304487
  ensembl transcript: ENST00000345745
  gene symbol: ZDHHC16
  hgvsc: ENST00000345745.5:c.491T>C
  hgvsp: ENSP00000304487.8:p.Ile164Thr
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359879
  ensembl transcript: ENST00000370842
  gene symbol: ZDHHC16
  hgvsc: ENST00000370842.2:c.686T>C
  hgvsp: ENSP00000359879.1:p.Ile229Thr
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000487315
  gene symbol: ZDHHC16
  hgvsc: ENST00000487315.1:n.106T>C
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000398532
  ensembl transcript: ENST00000433086
  gene symbol: ZDHHC16
  hgvsc: ENST00000433086.1:c.491T>C
  hgvsp: ENSP00000398532.1:p.Ile164Thr
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000459777
  gene symbol: ZDHHC16
  hgvsc: ENST00000459777.1:n.407T>C
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000405240
  ensembl transcript: ENST00000420089
  gene symbol: ZDHHC16
  hgvsc: ENST00000420089.1:c.613T>C
  hgvsp: ENSP00000405240.1:p.Ile205Thr
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000345383
  ensembl transcript: ENST00000352634
  gene symbol: ZDHHC16
  hgvsc: ENST00000352634.4:c.686T>C
  hgvsp: ENSP00000345383.4:p.Ile229Thr
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000495735
  gene symbol: ZDHHC16
  hgvsc: ENST00000495735.1:n.714T>C
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000466895
  gene symbol: ZDHHC16
  hgvsc: ENST00000466895.1:n.406T>C
  variant of: http://identifiers.org/hgnc/20714
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6154
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2735
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2094
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1143
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5314
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2499
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3172
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3966
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile229Thr
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: T
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: ClippingRankSum

10-99213417-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 99213417
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 99213417
    reference: chr 10
allele count: 1
allele frequency: 8.240083060037246e-6
allele num: 121358
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359883
  ensembl transcript: ENST00000370846
  gene symbol: ZDHHC16
  hgvsc: ENST00000370846.4:c.556+737T>C
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000304487
  ensembl transcript: ENST00000345745
  gene symbol: ZDHHC16
  hgvsc: ENST00000345745.5:c.492T>C
  hgvsp: ENST00000345745.5:c.492T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000396286
  ensembl transcript: ENST00000417044
  gene symbol: ZDHHC16
  hgvsc: ENST00000417044.1:c.512T>C
  hgvsp: ENST00000417044.1:c.512T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000459777
  gene symbol: ZDHHC16
  hgvsc: ENST00000459777.1:n.408T>C
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000487315
  gene symbol: ZDHHC16
  hgvsc: ENST00000487315.1:n.107T>C
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359879
  ensembl transcript: ENST00000370842
  gene symbol: ZDHHC16
  hgvsc: ENST00000370842.2:c.687T>C
  hgvsp: ENST00000370842.2:c.687T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000323360
  ensembl transcript: ENST00000353979
  gene symbol: ZDHHC16
  hgvsc: ENST00000353979.3:c.570T>C
  hgvsp: ENST00000353979.3:c.570T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000345383
  ensembl transcript: ENST00000352634
  gene symbol: ZDHHC16
  hgvsc: ENST00000352634.4:c.687T>C
  hgvsp: ENST00000352634.4:c.687T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359891
  ensembl transcript: ENST00000370854
  gene symbol: ZDHHC16
  hgvsc: ENST00000370854.3:c.687T>C
  hgvsp: ENST00000370854.3:c.687T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000466895
  gene symbol: ZDHHC16
  hgvsc: ENST00000466895.1:n.407T>C
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000462924
  gene symbol: ZDHHC16
  hgvsc: ENST00000462924.1:n.791+737T>C
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000377357
  ensembl transcript: ENST00000393760
  gene symbol: ZDHHC16
  hgvsc: ENST00000393760.1:c.687T>C
  hgvsp: ENST00000393760.1:c.687T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000398532
  ensembl transcript: ENST00000433086
  gene symbol: ZDHHC16
  hgvsc: ENST00000433086.1:c.492T>C
  hgvsp: ENST00000433086.1:c.492T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000405240
  ensembl transcript: ENST00000420089
  gene symbol: ZDHHC16
  hgvsc: ENST00000420089.1:c.614T>C
  hgvsp: ENST00000420089.1:c.614T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000495735
  gene symbol: ZDHHC16
  hgvsc: ENST00000495735.1:n.715T>C
  variant of: http://identifiers.org/hgnc/20714
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4589
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6066
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3171
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2092
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5315
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5548
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2537
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile229Ile
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: T
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum

10-99213431-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 99213431
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 99213431
    reference: chr 10
allele count: 1
allele frequency: 8.241169586787756e-6
allele num: 121342
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000377357
  ensembl transcript: ENST00000393760
  gene symbol: ZDHHC16
  hgvsc: ENST00000393760.1:c.690+11C>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000459777
  gene symbol: ZDHHC16
  hgvsc: ENST00000459777.1:n.411+11C>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000398532
  ensembl transcript: ENST00000433086
  gene symbol: ZDHHC16
  hgvsc: ENST00000433086.1:c.495+11C>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000304487
  ensembl transcript: ENST00000345745
  gene symbol: ZDHHC16
  hgvsc: ENST00000345745.5:c.495+11C>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000396286
  ensembl transcript: ENST00000417044
  gene symbol: ZDHHC16
  hgvsc: ENST00000417044.1:c.515+11C>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000345383
  ensembl transcript: ENST00000352634
  gene symbol: ZDHHC16
  hgvsc: ENST00000352634.4:c.690+11C>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000323360
  ensembl transcript: ENST00000353979
  gene symbol: ZDHHC16
  hgvsc: ENST00000353979.3:c.573+11C>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000405240
  ensembl transcript: ENST00000420089
  gene symbol: ZDHHC16
  hgvsc: ENST00000420089.1:c.617+11C>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359879
  ensembl transcript: ENST00000370842
  gene symbol: ZDHHC16
  hgvsc: ENST00000370842.2:c.690+11C>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359891
  ensembl transcript: ENST00000370854
  gene symbol: ZDHHC16
  hgvsc: ENST00000370854.3:c.690+11C>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000487315
  gene symbol: ZDHHC16
  hgvsc: ENST00000487315.1:n.110+11C>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000466895
  gene symbol: ZDHHC16
  hgvsc: ENST00000466895.1:n.410+11C>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000462924
  gene symbol: ZDHHC16
  hgvsc: ENST00000462924.1:n.791+751C>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000495735
  gene symbol: ZDHHC16
  hgvsc: ENST00000495735.1:n.718+11C>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359883
  ensembl transcript: ENST00000370846
  gene symbol: ZDHHC16
  hgvsc: ENST00000370846.4:c.556+751C>T
  variant of: http://identifiers.org/hgnc/20714
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5543
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2092
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4833
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6148
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2524
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1503
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4589
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2735
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3982
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3168
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1143
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5314
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ

10-99213432-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 99213432
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 99213432
    reference: chr 10
allele count: 1
allele frequency: 8.241033755274261e-6
allele num: 121344
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359891
  ensembl transcript: ENST00000370854
  gene symbol: ZDHHC16
  hgvsc: ENST00000370854.3:c.690+12A>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359883
  ensembl transcript: ENST00000370846
  gene symbol: ZDHHC16
  hgvsc: ENST00000370846.4:c.556+752A>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000487315
  gene symbol: ZDHHC16
  hgvsc: ENST00000487315.1:n.110+12A>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000323360
  ensembl transcript: ENST00000353979
  gene symbol: ZDHHC16
  hgvsc: ENST00000353979.3:c.573+12A>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000466895
  gene symbol: ZDHHC16
  hgvsc: ENST00000466895.1:n.410+12A>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359879
  ensembl transcript: ENST00000370842
  gene symbol: ZDHHC16
  hgvsc: ENST00000370842.2:c.690+12A>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000345383
  ensembl transcript: ENST00000352634
  gene symbol: ZDHHC16
  hgvsc: ENST00000352634.4:c.690+12A>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000459777
  gene symbol: ZDHHC16
  hgvsc: ENST00000459777.1:n.411+12A>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000396286
  ensembl transcript: ENST00000417044
  gene symbol: ZDHHC16
  hgvsc: ENST00000417044.1:c.515+12A>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000377357
  ensembl transcript: ENST00000393760
  gene symbol: ZDHHC16
  hgvsc: ENST00000393760.1:c.690+12A>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000398532
  ensembl transcript: ENST00000433086
  gene symbol: ZDHHC16
  hgvsc: ENST00000433086.1:c.495+12A>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000405240
  ensembl transcript: ENST00000420089
  gene symbol: ZDHHC16
  hgvsc: ENST00000420089.1:c.617+12A>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000462924
  gene symbol: ZDHHC16
  hgvsc: ENST00000462924.1:n.791+752A>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000495735
  gene symbol: ZDHHC16
  hgvsc: ENST00000495735.1:n.718+12A>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000304487
  ensembl transcript: ENST00000345745
  gene symbol: ZDHHC16
  hgvsc: ENST00000345745.5:c.495+12A>G
  variant of: http://identifiers.org/hgnc/20714
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1143
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5313
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2409
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6149
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3983
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2092
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2520
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1503
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: A
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: DP

10-99213433-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 99213433
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 99213433
    reference: chr 10
allele count: 2
allele frequency: 1.648179585647652e-5
allele num: 121346
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359879
  ensembl transcript: ENST00000370842
  gene symbol: ZDHHC16
  hgvsc: ENST00000370842.2:c.690+13G>C
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359883
  ensembl transcript: ENST00000370846
  gene symbol: ZDHHC16
  hgvsc: ENST00000370846.4:c.556+753G>C
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000304487
  ensembl transcript: ENST00000345745
  gene symbol: ZDHHC16
  hgvsc: ENST00000345745.5:c.495+13G>C
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000466895
  gene symbol: ZDHHC16
  hgvsc: ENST00000466895.1:n.410+13G>C
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000405240
  ensembl transcript: ENST00000420089
  gene symbol: ZDHHC16
  hgvsc: ENST00000420089.1:c.617+13G>C
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000345383
  ensembl transcript: ENST00000352634
  gene symbol: ZDHHC16
  hgvsc: ENST00000352634.4:c.690+13G>C
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000396286
  ensembl transcript: ENST00000417044
  gene symbol: ZDHHC16
  hgvsc: ENST00000417044.1:c.515+13G>C
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000377357
  ensembl transcript: ENST00000393760
  gene symbol: ZDHHC16
  hgvsc: ENST00000393760.1:c.690+13G>C
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359891
  ensembl transcript: ENST00000370854
  gene symbol: ZDHHC16
  hgvsc: ENST00000370854.3:c.690+13G>C
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000459777
  gene symbol: ZDHHC16
  hgvsc: ENST00000459777.1:n.411+13G>C
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000487315
  gene symbol: ZDHHC16
  hgvsc: ENST00000487315.1:n.110+13G>C
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000398532
  ensembl transcript: ENST00000433086
  gene symbol: ZDHHC16
  hgvsc: ENST00000433086.1:c.495+13G>C
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000462924
  gene symbol: ZDHHC16
  hgvsc: ENST00000462924.1:n.791+753G>C
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000323360
  ensembl transcript: ENST00000353979
  gene symbol: ZDHHC16
  hgvsc: ENST00000353979.3:c.573+13G>C
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000495735
  gene symbol: ZDHHC16
  hgvsc: ENST00000495735.1:n.718+13G>C
  variant of: http://identifiers.org/hgnc/20714
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3630
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1503
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3981
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6066
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5545
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4833
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4588
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2092
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2522
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD

10-99213434-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 99213434
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 99213434
    reference: chr 10
allele count: 3
allele frequency: 2.472310126582278e-5
allele num: 121344
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000466895
  gene symbol: ZDHHC16
  hgvsc: ENST00000466895.1:n.410+14G>C
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000396286
  ensembl transcript: ENST00000417044
  gene symbol: ZDHHC16
  hgvsc: ENST00000417044.1:c.515+14G>C
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000462924
  gene symbol: ZDHHC16
  hgvsc: ENST00000462924.1:n.791+754G>C
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000487315
  gene symbol: ZDHHC16
  hgvsc: ENST00000487315.1:n.110+14G>C
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000377357
  ensembl transcript: ENST00000393760
  gene symbol: ZDHHC16
  hgvsc: ENST00000393760.1:c.690+14G>C
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000398532
  ensembl transcript: ENST00000433086
  gene symbol: ZDHHC16
  hgvsc: ENST00000433086.1:c.495+14G>C
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000345383
  ensembl transcript: ENST00000352634
  gene symbol: ZDHHC16
  hgvsc: ENST00000352634.4:c.690+14G>C
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000304487
  ensembl transcript: ENST00000345745
  gene symbol: ZDHHC16
  hgvsc: ENST00000345745.5:c.495+14G>C
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359879
  ensembl transcript: ENST00000370842
  gene symbol: ZDHHC16
  hgvsc: ENST00000370842.2:c.690+14G>C
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000323360
  ensembl transcript: ENST00000353979
  gene symbol: ZDHHC16
  hgvsc: ENST00000353979.3:c.573+14G>C
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000495735
  gene symbol: ZDHHC16
  hgvsc: ENST00000495735.1:n.718+14G>C
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359883
  ensembl transcript: ENST00000370846
  gene symbol: ZDHHC16
  hgvsc: ENST00000370846.4:c.556+754G>C
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359891
  ensembl transcript: ENST00000370854
  gene symbol: ZDHHC16
  hgvsc: ENST00000370854.3:c.690+14G>C
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000459777
  gene symbol: ZDHHC16
  hgvsc: ENST00000459777.1:n.411+14G>C
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000405240
  ensembl transcript: ENST00000420089
  gene symbol: ZDHHC16
  hgvsc: ENST00000420089.1:c.617+14G>C
  variant of: http://identifiers.org/hgnc/20714
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3629
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6151
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2516
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1143
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4589
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4590
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6065
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2735
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2092
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: Other
reference allele: G
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: DP

10-99213450-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 99213450
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 99213450
    reference: chr 10
allele count: 2
allele frequency: 1.648179585647652e-5
allele num: 121346
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000398532
  ensembl transcript: ENST00000433086
  gene symbol: ZDHHC16
  hgvsc: ENST00000433086.1:c.495+30T>C
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000345383
  ensembl transcript: ENST00000352634
  gene symbol: ZDHHC16
  hgvsc: ENST00000352634.4:c.690+30T>C
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000495735
  gene symbol: ZDHHC16
  hgvsc: ENST00000495735.1:n.718+30T>C
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000466895
  gene symbol: ZDHHC16
  hgvsc: ENST00000466895.1:n.410+30T>C
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000459777
  gene symbol: ZDHHC16
  hgvsc: ENST00000459777.1:n.411+30T>C
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000377357
  ensembl transcript: ENST00000393760
  gene symbol: ZDHHC16
  hgvsc: ENST00000393760.1:c.690+30T>C
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359891
  ensembl transcript: ENST00000370854
  gene symbol: ZDHHC16
  hgvsc: ENST00000370854.3:c.690+30T>C
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000487315
  gene symbol: ZDHHC16
  hgvsc: ENST00000487315.1:n.110+30T>C
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000462924
  gene symbol: ZDHHC16
  hgvsc: ENST00000462924.1:n.791+770T>C
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000405240
  ensembl transcript: ENST00000420089
  gene symbol: ZDHHC16
  hgvsc: ENST00000420089.1:c.617+30T>C
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000323360
  ensembl transcript: ENST00000353979
  gene symbol: ZDHHC16
  hgvsc: ENST00000353979.3:c.573+30T>C
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359883
  ensembl transcript: ENST00000370846
  gene symbol: ZDHHC16
  hgvsc: ENST00000370846.4:c.556+770T>C
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000304487
  ensembl transcript: ENST00000345745
  gene symbol: ZDHHC16
  hgvsc: ENST00000345745.5:c.495+30T>C
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000396286
  ensembl transcript: ENST00000417044
  gene symbol: ZDHHC16
  hgvsc: ENST00000417044.1:c.515+30T>C
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359879
  ensembl transcript: ENST00000370842
  gene symbol: ZDHHC16
  hgvsc: ENST00000370842.2:c.690+30T>C
  variant of: http://identifiers.org/hgnc/20714
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4597
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3194
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5547
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2092
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2406
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6064
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3905
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4590
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4833
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: South Asian
population: African
population: Latino
reference allele: T
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP

10-99213453-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 99213453
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 99213453
    reference: chr 10
allele count: 2
allele frequency: 1.648070932972955e-5
allele num: 121354
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000377357
  ensembl transcript: ENST00000393760
  gene symbol: ZDHHC16
  hgvsc: ENST00000393760.1:c.690+33T>C
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000466895
  gene symbol: ZDHHC16
  hgvsc: ENST00000466895.1:n.410+33T>C
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000396286
  ensembl transcript: ENST00000417044
  gene symbol: ZDHHC16
  hgvsc: ENST00000417044.1:c.515+33T>C
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000405240
  ensembl transcript: ENST00000420089
  gene symbol: ZDHHC16
  hgvsc: ENST00000420089.1:c.617+33T>C
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000459777
  gene symbol: ZDHHC16
  hgvsc: ENST00000459777.1:n.411+33T>C
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000462924
  gene symbol: ZDHHC16
  hgvsc: ENST00000462924.1:n.791+773T>C
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000345383
  ensembl transcript: ENST00000352634
  gene symbol: ZDHHC16
  hgvsc: ENST00000352634.4:c.690+33T>C
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000398532
  ensembl transcript: ENST00000433086
  gene symbol: ZDHHC16
  hgvsc: ENST00000433086.1:c.495+33T>C
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000323360
  ensembl transcript: ENST00000353979
  gene symbol: ZDHHC16
  hgvsc: ENST00000353979.3:c.573+33T>C
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000487315
  gene symbol: ZDHHC16
  hgvsc: ENST00000487315.1:n.110+33T>C
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359879
  ensembl transcript: ENST00000370842
  gene symbol: ZDHHC16
  hgvsc: ENST00000370842.2:c.690+33T>C
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359883
  ensembl transcript: ENST00000370846
  gene symbol: ZDHHC16
  hgvsc: ENST00000370846.4:c.556+773T>C
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000304487
  ensembl transcript: ENST00000345745
  gene symbol: ZDHHC16
  hgvsc: ENST00000345745.5:c.495+33T>C
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359891
  ensembl transcript: ENST00000370854
  gene symbol: ZDHHC16
  hgvsc: ENST00000370854.3:c.690+33T>C
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000495735
  gene symbol: ZDHHC16
  hgvsc: ENST00000495735.1:n.718+33T>C
  variant of: http://identifiers.org/hgnc/20714
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2092
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3898
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6147
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5316
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4598
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5550
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6064
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1503
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2419
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2735
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
population: Other
reference allele: T
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum

10-99213453-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 99213453
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 99213453
    reference: chr 10
allele count: 3
allele frequency: 2.472106399459433e-5
allele num: 121354
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000377357
  ensembl transcript: ENST00000393760
  gene symbol: ZDHHC16
  hgvsc: ENST00000393760.1:c.690+33T>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000487315
  gene symbol: ZDHHC16
  hgvsc: ENST00000487315.1:n.110+33T>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359879
  ensembl transcript: ENST00000370842
  gene symbol: ZDHHC16
  hgvsc: ENST00000370842.2:c.690+33T>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000466895
  gene symbol: ZDHHC16
  hgvsc: ENST00000466895.1:n.410+33T>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359891
  ensembl transcript: ENST00000370854
  gene symbol: ZDHHC16
  hgvsc: ENST00000370854.3:c.690+33T>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000345383
  ensembl transcript: ENST00000352634
  gene symbol: ZDHHC16
  hgvsc: ENST00000352634.4:c.690+33T>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000459777
  gene symbol: ZDHHC16
  hgvsc: ENST00000459777.1:n.411+33T>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000398532
  ensembl transcript: ENST00000433086
  gene symbol: ZDHHC16
  hgvsc: ENST00000433086.1:c.495+33T>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359883
  ensembl transcript: ENST00000370846
  gene symbol: ZDHHC16
  hgvsc: ENST00000370846.4:c.556+773T>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000304487
  ensembl transcript: ENST00000345745
  gene symbol: ZDHHC16
  hgvsc: ENST00000345745.5:c.495+33T>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000396286
  ensembl transcript: ENST00000417044
  gene symbol: ZDHHC16
  hgvsc: ENST00000417044.1:c.515+33T>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000495735
  gene symbol: ZDHHC16
  hgvsc: ENST00000495735.1:n.718+33T>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000462924
  gene symbol: ZDHHC16
  hgvsc: ENST00000462924.1:n.791+773T>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000405240
  ensembl transcript: ENST00000420089
  gene symbol: ZDHHC16
  hgvsc: ENST00000420089.1:c.617+33T>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000323360
  ensembl transcript: ENST00000353979
  gene symbol: ZDHHC16
  hgvsc: ENST00000353979.3:c.573+33T>G
  variant of: http://identifiers.org/hgnc/20714
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4833
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4591
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6147
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3628
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2419
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1143
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4598
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5550
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3199
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: T
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum

10-99213454-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 99213454
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 99213454
    reference: chr 10
allele count: 1
allele frequency: 8.240626287597857e-6
allele num: 121350
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000396286
  ensembl transcript: ENST00000417044
  gene symbol: ZDHHC16
  hgvsc: ENST00000417044.1:c.515+34G>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000345383
  ensembl transcript: ENST00000352634
  gene symbol: ZDHHC16
  hgvsc: ENST00000352634.4:c.690+34G>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359883
  ensembl transcript: ENST00000370846
  gene symbol: ZDHHC16
  hgvsc: ENST00000370846.4:c.556+774G>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000462924
  gene symbol: ZDHHC16
  hgvsc: ENST00000462924.1:n.791+774G>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000459777
  gene symbol: ZDHHC16
  hgvsc: ENST00000459777.1:n.411+34G>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000466895
  gene symbol: ZDHHC16
  hgvsc: ENST00000466895.1:n.410+34G>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000487315
  gene symbol: ZDHHC16
  hgvsc: ENST00000487315.1:n.110+34G>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000377357
  ensembl transcript: ENST00000393760
  gene symbol: ZDHHC16
  hgvsc: ENST00000393760.1:c.690+34G>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359891
  ensembl transcript: ENST00000370854
  gene symbol: ZDHHC16
  hgvsc: ENST00000370854.3:c.690+34G>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000323360
  ensembl transcript: ENST00000353979
  gene symbol: ZDHHC16
  hgvsc: ENST00000353979.3:c.573+34G>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000398532
  ensembl transcript: ENST00000433086
  gene symbol: ZDHHC16
  hgvsc: ENST00000433086.1:c.495+34G>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000495735
  gene symbol: ZDHHC16
  hgvsc: ENST00000495735.1:n.718+34G>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359879
  ensembl transcript: ENST00000370842
  gene symbol: ZDHHC16
  hgvsc: ENST00000370842.2:c.690+34G>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000304487
  ensembl transcript: ENST00000345745
  gene symbol: ZDHHC16
  hgvsc: ENST00000345745.5:c.495+34G>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000405240
  ensembl transcript: ENST00000420089
  gene symbol: ZDHHC16
  hgvsc: ENST00000420089.1:c.617+34G>A
  variant of: http://identifiers.org/hgnc/20714
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6146
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6064
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3201
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1143
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2559
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3880
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5548
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4601
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3628
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2092
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: African
population: Latino
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: QD

10-99213460-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 99213460
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 99213460
    reference: chr 10
allele count: 4
allele frequency: 3.296359171295305e-5
allele num: 121346
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000377357
  ensembl transcript: ENST00000393760
  gene symbol: ZDHHC16
  hgvsc: ENST00000393760.1:c.690+40C>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000345383
  ensembl transcript: ENST00000352634
  gene symbol: ZDHHC16
  hgvsc: ENST00000352634.4:c.690+40C>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000466895
  gene symbol: ZDHHC16
  hgvsc: ENST00000466895.1:n.410+40C>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000396286
  ensembl transcript: ENST00000417044
  gene symbol: ZDHHC16
  hgvsc: ENST00000417044.1:c.515+40C>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000405240
  ensembl transcript: ENST00000420089
  gene symbol: ZDHHC16
  hgvsc: ENST00000420089.1:c.617+40C>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359883
  ensembl transcript: ENST00000370846
  gene symbol: ZDHHC16
  hgvsc: ENST00000370846.4:c.556+780C>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000487315
  gene symbol: ZDHHC16
  hgvsc: ENST00000487315.1:n.110+40C>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359879
  ensembl transcript: ENST00000370842
  gene symbol: ZDHHC16
  hgvsc: ENST00000370842.2:c.690+40C>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000462924
  gene symbol: ZDHHC16
  hgvsc: ENST00000462924.1:n.791+780C>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000495735
  gene symbol: ZDHHC16
  hgvsc: ENST00000495735.1:n.718+40C>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359891
  ensembl transcript: ENST00000370854
  gene symbol: ZDHHC16
  hgvsc: ENST00000370854.3:c.690+40C>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000459777
  gene symbol: ZDHHC16
  hgvsc: ENST00000459777.1:n.411+40C>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000323360
  ensembl transcript: ENST00000353979
  gene symbol: ZDHHC16
  hgvsc: ENST00000353979.3:c.573+40C>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000304487
  ensembl transcript: ENST00000345745
  gene symbol: ZDHHC16
  hgvsc: ENST00000345745.5:c.495+40C>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000398532
  ensembl transcript: ENST00000433086
  gene symbol: ZDHHC16
  hgvsc: ENST00000433086.1:c.495+40C>G
  variant of: http://identifiers.org/hgnc/20714
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2092
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5548
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2579
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2408
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3212
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6065
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5315
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1503
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3894
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: African
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ

10-99213463-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 99213463
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 99213463
    reference: chr 10
allele count: 209
allele frequency: 1.722262509064539e-3
allele num: 121352
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000462924
  gene symbol: ZDHHC16
  hgvsc: ENST00000462924.1:n.791+783C>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000345383
  ensembl transcript: ENST00000352634
  gene symbol: ZDHHC16
  hgvsc: ENST00000352634.4:c.690+43C>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000487315
  gene symbol: ZDHHC16
  hgvsc: ENST00000487315.1:n.110+43C>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359879
  ensembl transcript: ENST00000370842
  gene symbol: ZDHHC16
  hgvsc: ENST00000370842.2:c.690+43C>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000398532
  ensembl transcript: ENST00000433086
  gene symbol: ZDHHC16
  hgvsc: ENST00000433086.1:c.495+43C>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000466895
  gene symbol: ZDHHC16
  hgvsc: ENST00000466895.1:n.410+43C>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000495735
  gene symbol: ZDHHC16
  hgvsc: ENST00000495735.1:n.718+43C>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000304487
  ensembl transcript: ENST00000345745
  gene symbol: ZDHHC16
  hgvsc: ENST00000345745.5:c.495+43C>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359891
  ensembl transcript: ENST00000370854
  gene symbol: ZDHHC16
  hgvsc: ENST00000370854.3:c.690+43C>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000396286
  ensembl transcript: ENST00000417044
  gene symbol: ZDHHC16
  hgvsc: ENST00000417044.1:c.515+43C>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000377357
  ensembl transcript: ENST00000393760
  gene symbol: ZDHHC16
  hgvsc: ENST00000393760.1:c.690+43C>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359883
  ensembl transcript: ENST00000370846
  gene symbol: ZDHHC16
  hgvsc: ENST00000370846.4:c.556+783C>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000323360
  ensembl transcript: ENST00000353979
  gene symbol: ZDHHC16
  hgvsc: ENST00000353979.3:c.573+43C>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000459777
  gene symbol: ZDHHC16
  hgvsc: ENST00000459777.1:n.411+43C>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000405240
  ensembl transcript: ENST00000420089
  gene symbol: ZDHHC16
  hgvsc: ENST00000420089.1:c.617+43C>T
  variant of: http://identifiers.org/hgnc/20714
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3206
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 4595
  bin: 6.75e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 1512
  bin: 8.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5551
  bin: 4.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2593
  bin: 3.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 3882
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3631
  bin: 7.25e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 1145
  bin: 9.25e1
  variant carriers: 6
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
population: African
population: Latino
reference allele: C
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS

10-99213464-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 99213464
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 99213464
    reference: chr 10
allele count: 1482
allele frequency: 1.221421860319449e-2
allele num: 121334
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000396286
  ensembl transcript: ENST00000417044
  gene symbol: ZDHHC16
  hgvsc: ENST00000417044.1:c.515+44G>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000398532
  ensembl transcript: ENST00000433086
  gene symbol: ZDHHC16
  hgvsc: ENST00000433086.1:c.495+44G>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000304487
  ensembl transcript: ENST00000345745
  gene symbol: ZDHHC16
  hgvsc: ENST00000345745.5:c.495+44G>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000345383
  ensembl transcript: ENST00000352634
  gene symbol: ZDHHC16
  hgvsc: ENST00000352634.4:c.690+44G>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000459777
  gene symbol: ZDHHC16
  hgvsc: ENST00000459777.1:n.411+44G>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000462924
  gene symbol: ZDHHC16
  hgvsc: ENST00000462924.1:n.791+784G>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359879
  ensembl transcript: ENST00000370842
  gene symbol: ZDHHC16
  hgvsc: ENST00000370842.2:c.690+44G>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000377357
  ensembl transcript: ENST00000393760
  gene symbol: ZDHHC16
  hgvsc: ENST00000393760.1:c.690+44G>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359891
  ensembl transcript: ENST00000370854
  gene symbol: ZDHHC16
  hgvsc: ENST00000370854.3:c.690+44G>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000487315
  gene symbol: ZDHHC16
  hgvsc: ENST00000487315.1:n.110+44G>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000495735
  gene symbol: ZDHHC16
  hgvsc: ENST00000495735.1:n.718+44G>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000466895
  gene symbol: ZDHHC16
  hgvsc: ENST00000466895.1:n.410+44G>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359883
  ensembl transcript: ENST00000370846
  gene symbol: ZDHHC16
  hgvsc: ENST00000370846.4:c.556+784G>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000405240
  ensembl transcript: ENST00000420089
  gene symbol: ZDHHC16
  hgvsc: ENST00000420089.1:c.617+44G>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000323360
  ensembl transcript: ENST00000353979
  gene symbol: ZDHHC16
  hgvsc: ENST00000353979.3:c.573+44G>A
  variant of: http://identifiers.org/hgnc/20714
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2369
  bin: 2.75e1
  variant carriers: 35
genotype depth: GenotypeDepth
  all individuals: 3694
  bin: 7.25e1
  variant carriers: 123
genotype depth: GenotypeDepth
  all individuals: 6107
  bin: 5.25e1
  variant carriers: 118
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3767
  bin: 2.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 4613
  bin: 6.75e1
  variant carriers: 117
genotype depth: GenotypeDepth
  all individuals: 5541
  bin: 4.75e1
  variant carriers: 123
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 6050
  bin: 5.75e1
  variant carriers: 132
genotype depth: GenotypeDepth
  all individuals: 1519
  bin: 8.75e1
  variant carriers: 32
genotype depth: GenotypeDepth
  all individuals: 2572
  bin: 3.25e1
  variant carriers: 49
genotype quality: GenotypeQuality
num of homozygotes: 35
population: East Asian
population: African
population: South Asian
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

10-99213469-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 99213469
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 99213469
    reference: chr 10
allele count: 6
allele frequency: 4.943561011782154e-5
allele num: 121370
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000345383
  ensembl transcript: ENST00000352634
  gene symbol: ZDHHC16
  hgvsc: ENST00000352634.4:c.690+49G>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000405240
  ensembl transcript: ENST00000420089
  gene symbol: ZDHHC16
  hgvsc: ENST00000420089.1:c.617+49G>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000323360
  ensembl transcript: ENST00000353979
  gene symbol: ZDHHC16
  hgvsc: ENST00000353979.3:c.573+49G>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359883
  ensembl transcript: ENST00000370846
  gene symbol: ZDHHC16
  hgvsc: ENST00000370846.4:c.556+789G>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000304487
  ensembl transcript: ENST00000345745
  gene symbol: ZDHHC16
  hgvsc: ENST00000345745.5:c.495+49G>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000396286
  ensembl transcript: ENST00000417044
  gene symbol: ZDHHC16
  hgvsc: ENST00000417044.1:c.515+49G>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359891
  ensembl transcript: ENST00000370854
  gene symbol: ZDHHC16
  hgvsc: ENST00000370854.3:c.690+49G>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000377357
  ensembl transcript: ENST00000393760
  gene symbol: ZDHHC16
  hgvsc: ENST00000393760.1:c.690+49G>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000466895
  gene symbol: ZDHHC16
  hgvsc: ENST00000466895.1:n.410+49G>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000487315
  gene symbol: ZDHHC16
  hgvsc: ENST00000487315.1:n.110+49G>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359879
  ensembl transcript: ENST00000370842
  gene symbol: ZDHHC16
  hgvsc: ENST00000370842.2:c.690+49G>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000459777
  gene symbol: ZDHHC16
  hgvsc: ENST00000459777.1:n.411+49G>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000398532
  ensembl transcript: ENST00000433086
  gene symbol: ZDHHC16
  hgvsc: ENST00000433086.1:c.495+49G>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000495735
  gene symbol: ZDHHC16
  hgvsc: ENST00000495735.1:n.718+49G>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000462924
  gene symbol: ZDHHC16
  hgvsc: ENST00000462924.1:n.791+789G>A
  variant of: http://identifiers.org/hgnc/20714
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2399
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4631
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2584
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2123
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3689
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3186
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4927
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5524
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
population: Other
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP

10-99213469-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 99213469
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 99213469
    reference: chr 10
allele count: 1
allele frequency: 8.239268352970255e-6
allele num: 121370
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000495735
  gene symbol: ZDHHC16
  hgvsc: ENST00000495735.1:n.718+49G>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000345383
  ensembl transcript: ENST00000352634
  gene symbol: ZDHHC16
  hgvsc: ENST00000352634.4:c.690+49G>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000487315
  gene symbol: ZDHHC16
  hgvsc: ENST00000487315.1:n.110+49G>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000304487
  ensembl transcript: ENST00000345745
  gene symbol: ZDHHC16
  hgvsc: ENST00000345745.5:c.495+49G>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359883
  ensembl transcript: ENST00000370846
  gene symbol: ZDHHC16
  hgvsc: ENST00000370846.4:c.556+789G>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000398532
  ensembl transcript: ENST00000433086
  gene symbol: ZDHHC16
  hgvsc: ENST00000433086.1:c.495+49G>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000396286
  ensembl transcript: ENST00000417044
  gene symbol: ZDHHC16
  hgvsc: ENST00000417044.1:c.515+49G>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000466895
  gene symbol: ZDHHC16
  hgvsc: ENST00000466895.1:n.410+49G>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359879
  ensembl transcript: ENST00000370842
  gene symbol: ZDHHC16
  hgvsc: ENST00000370842.2:c.690+49G>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000405240
  ensembl transcript: ENST00000420089
  gene symbol: ZDHHC16
  hgvsc: ENST00000420089.1:c.617+49G>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000459777
  gene symbol: ZDHHC16
  hgvsc: ENST00000459777.1:n.411+49G>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000323360
  ensembl transcript: ENST00000353979
  gene symbol: ZDHHC16
  hgvsc: ENST00000353979.3:c.573+49G>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359891
  ensembl transcript: ENST00000370854
  gene symbol: ZDHHC16
  hgvsc: ENST00000370854.3:c.690+49G>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000377357
  ensembl transcript: ENST00000393760
  gene symbol: ZDHHC16
  hgvsc: ENST00000393760.1:c.690+49G>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000462924
  gene symbol: ZDHHC16
  hgvsc: ENST00000462924.1:n.791+789G>T
  variant of: http://identifiers.org/hgnc/20714
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5524
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3770
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4927
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2783
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3186
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5336
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6109
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1154
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4598
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2399
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ

10-99213508-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 99213508
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 99213508
    reference: chr 10
allele count: 32
allele frequency: 2.636001186200534e-4
allele num: 121396
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000345383
  ensembl transcript: ENST00000352634
  gene symbol: ZDHHC16
  hgvsc: ENST00000352634.4:c.690+88A>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000487315
  gene symbol: ZDHHC16
  hgvsc: ENST00000487315.1:n.110+88A>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000495735
  gene symbol: ZDHHC16
  hgvsc: ENST00000495735.1:n.719-48A>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359883
  ensembl transcript: ENST00000370846
  gene symbol: ZDHHC16
  hgvsc: ENST00000370846.4:c.556+828A>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000398532
  ensembl transcript: ENST00000433086
  gene symbol: ZDHHC16
  hgvsc: ENST00000433086.1:c.496-48A>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000466895
  gene symbol: ZDHHC16
  hgvsc: ENST00000466895.1:n.411-48A>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000405240
  ensembl transcript: ENST00000420089
  gene symbol: ZDHHC16
  hgvsc: ENST00000420089.1:c.617+88A>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359879
  ensembl transcript: ENST00000370842
  gene symbol: ZDHHC16
  hgvsc: ENST00000370842.2:c.690+88A>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000459777
  gene symbol: ZDHHC16
  hgvsc: ENST00000459777.1:n.412-48A>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000396286
  ensembl transcript: ENST00000417044
  gene symbol: ZDHHC16
  hgvsc: ENST00000417044.1:c.516-48A>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000462924
  gene symbol: ZDHHC16
  hgvsc: ENST00000462924.1:n.791+828A>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000323360
  ensembl transcript: ENST00000353979
  gene symbol: ZDHHC16
  hgvsc: ENST00000353979.3:c.574-48A>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359891
  ensembl transcript: ENST00000370854
  gene symbol: ZDHHC16
  hgvsc: ENST00000370854.3:c.691-48A>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000377357
  ensembl transcript: ENST00000393760
  gene symbol: ZDHHC16
  hgvsc: ENST00000393760.1:c.691-48A>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000304487
  ensembl transcript: ENST00000345745
  gene symbol: ZDHHC16
  hgvsc: ENST00000345745.5:c.495+88A>G
  variant of: http://identifiers.org/hgnc/20714
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7630
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2943
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 875
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4977
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1220
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6669
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4010
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7895
  bin: 4.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Other
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
reference allele: A
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum

10-99213516-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 99213516
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 99213516
    reference: chr 10
allele count: 1
allele frequency: 8.237775141689733e-6
allele num: 121392
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000495735
  gene symbol: ZDHHC16
  hgvsc: ENST00000495735.1:n.719-40G>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359891
  ensembl transcript: ENST00000370854
  gene symbol: ZDHHC16
  hgvsc: ENST00000370854.3:c.691-40G>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000466895
  gene symbol: ZDHHC16
  hgvsc: ENST00000466895.1:n.411-40G>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000323360
  ensembl transcript: ENST00000353979
  gene symbol: ZDHHC16
  hgvsc: ENST00000353979.3:c.574-40G>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000377357
  ensembl transcript: ENST00000393760
  gene symbol: ZDHHC16
  hgvsc: ENST00000393760.1:c.691-40G>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000396286
  ensembl transcript: ENST00000417044
  gene symbol: ZDHHC16
  hgvsc: ENST00000417044.1:c.516-40G>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000398532
  ensembl transcript: ENST00000433086
  gene symbol: ZDHHC16
  hgvsc: ENST00000433086.1:c.496-40G>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000462924
  gene symbol: ZDHHC16
  hgvsc: ENST00000462924.1:n.791+836G>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000459777
  gene symbol: ZDHHC16
  hgvsc: ENST00000459777.1:n.412-40G>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359879
  ensembl transcript: ENST00000370842
  gene symbol: ZDHHC16
  hgvsc: ENST00000370842.2:c.690+96G>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000304487
  ensembl transcript: ENST00000345745
  gene symbol: ZDHHC16
  hgvsc: ENST00000345745.5:c.495+96G>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000345383
  ensembl transcript: ENST00000352634
  gene symbol: ZDHHC16
  hgvsc: ENST00000352634.4:c.690+96G>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000487315
  gene symbol: ZDHHC16
  hgvsc: ENST00000487315.1:n.110+96G>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359883
  ensembl transcript: ENST00000370846
  gene symbol: ZDHHC16
  hgvsc: ENST00000370846.4:c.556+836G>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000405240
  ensembl transcript: ENST00000420089
  gene symbol: ZDHHC16
  hgvsc: ENST00000420089.1:c.617+96G>T
  variant of: http://identifiers.org/hgnc/20714
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4991
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1254
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6673
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7900
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7633
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 702
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2940
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7230
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP

10-99213522-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 99213522
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 99213522
    reference: chr 10
allele count: 1
allele frequency: 8.237775141689733e-6
allele num: 121392
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359883
  ensembl transcript: ENST00000370846
  gene symbol: ZDHHC16
  hgvsc: ENST00000370846.4:c.556+842A>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000398532
  ensembl transcript: ENST00000433086
  gene symbol: ZDHHC16
  hgvsc: ENST00000433086.1:c.496-34A>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000323360
  ensembl transcript: ENST00000353979
  gene symbol: ZDHHC16
  hgvsc: ENST00000353979.3:c.574-34A>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000396286
  ensembl transcript: ENST00000417044
  gene symbol: ZDHHC16
  hgvsc: ENST00000417044.1:c.516-34A>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000466895
  gene symbol: ZDHHC16
  hgvsc: ENST00000466895.1:n.411-34A>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000495735
  gene symbol: ZDHHC16
  hgvsc: ENST00000495735.1:n.719-34A>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000462924
  gene symbol: ZDHHC16
  hgvsc: ENST00000462924.1:n.791+842A>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000459777
  gene symbol: ZDHHC16
  hgvsc: ENST00000459777.1:n.412-34A>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000487315
  gene symbol: ZDHHC16
  hgvsc: ENST00000487315.1:n.110+102A>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359891
  ensembl transcript: ENST00000370854
  gene symbol: ZDHHC16
  hgvsc: ENST00000370854.3:c.691-34A>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359879
  ensembl transcript: ENST00000370842
  gene symbol: ZDHHC16
  hgvsc: ENST00000370842.2:c.690+102A>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000304487
  ensembl transcript: ENST00000345745
  gene symbol: ZDHHC16
  hgvsc: ENST00000345745.5:c.495+102A>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000405240
  ensembl transcript: ENST00000420089
  gene symbol: ZDHHC16
  hgvsc: ENST00000420089.1:c.617+102A>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000345383
  ensembl transcript: ENST00000352634
  gene symbol: ZDHHC16
  hgvsc: ENST00000352634.4:c.690+102A>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000377357
  ensembl transcript: ENST00000393760
  gene symbol: ZDHHC16
  hgvsc: ENST00000393760.1:c.691-34A>G
  variant of: http://identifiers.org/hgnc/20714
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1344
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5394
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7225
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4999
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7634
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 873
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6722
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4011
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1280
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum

10-99213524-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 99213524
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 99213524
    reference: chr 10
allele count: 1
allele frequency: 8.237775141689733e-6
allele num: 121392
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000459777
  gene symbol: ZDHHC16
  hgvsc: ENST00000459777.1:n.412-32A>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000323360
  ensembl transcript: ENST00000353979
  gene symbol: ZDHHC16
  hgvsc: ENST00000353979.3:c.574-32A>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000487315
  gene symbol: ZDHHC16
  hgvsc: ENST00000487315.1:n.110+104A>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000398532
  ensembl transcript: ENST00000433086
  gene symbol: ZDHHC16
  hgvsc: ENST00000433086.1:c.496-32A>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000377357
  ensembl transcript: ENST00000393760
  gene symbol: ZDHHC16
  hgvsc: ENST00000393760.1:c.691-32A>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000462924
  gene symbol: ZDHHC16
  hgvsc: ENST00000462924.1:n.791+844A>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359891
  ensembl transcript: ENST00000370854
  gene symbol: ZDHHC16
  hgvsc: ENST00000370854.3:c.691-32A>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000396286
  ensembl transcript: ENST00000417044
  gene symbol: ZDHHC16
  hgvsc: ENST00000417044.1:c.516-32A>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359879
  ensembl transcript: ENST00000370842
  gene symbol: ZDHHC16
  hgvsc: ENST00000370842.2:c.690+104A>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000495735
  gene symbol: ZDHHC16
  hgvsc: ENST00000495735.1:n.719-32A>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000345383
  ensembl transcript: ENST00000352634
  gene symbol: ZDHHC16
  hgvsc: ENST00000352634.4:c.690+104A>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000466895
  gene symbol: ZDHHC16
  hgvsc: ENST00000466895.1:n.411-32A>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359883
  ensembl transcript: ENST00000370846
  gene symbol: ZDHHC16
  hgvsc: ENST00000370846.4:c.556+844A>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000405240
  ensembl transcript: ENST00000420089
  gene symbol: ZDHHC16
  hgvsc: ENST00000420089.1:c.617+104A>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000304487
  ensembl transcript: ENST00000345745
  gene symbol: ZDHHC16
  hgvsc: ENST00000345745.5:c.495+104A>G
  variant of: http://identifiers.org/hgnc/20714
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6722
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7225
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 873
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5395
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5003
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1285
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7899
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 702
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
population: Latino
population: Other
reference allele: A
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

10-99213536-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 99213536
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 99213536
    reference: chr 10
allele count: 1
allele frequency: 8.238996819747227e-6
allele num: 121374
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000405240
  ensembl transcript: ENST00000420089
  gene symbol: ZDHHC16
  hgvsc: ENST00000420089.1:c.617+116A>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000345383
  ensembl transcript: ENST00000352634
  gene symbol: ZDHHC16
  hgvsc: ENST00000352634.4:c.690+116A>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000323360
  ensembl transcript: ENST00000353979
  gene symbol: ZDHHC16
  hgvsc: ENST00000353979.3:c.574-20A>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000398532
  ensembl transcript: ENST00000433086
  gene symbol: ZDHHC16
  hgvsc: ENST00000433086.1:c.496-20A>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000466895
  gene symbol: ZDHHC16
  hgvsc: ENST00000466895.1:n.411-20A>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359883
  ensembl transcript: ENST00000370846
  gene symbol: ZDHHC16
  hgvsc: ENST00000370846.4:c.556+856A>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000377357
  ensembl transcript: ENST00000393760
  gene symbol: ZDHHC16
  hgvsc: ENST00000393760.1:c.691-20A>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000459777
  gene symbol: ZDHHC16
  hgvsc: ENST00000459777.1:n.412-20A>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000487315
  gene symbol: ZDHHC16
  hgvsc: ENST00000487315.1:n.110+116A>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000304487
  ensembl transcript: ENST00000345745
  gene symbol: ZDHHC16
  hgvsc: ENST00000345745.5:c.495+116A>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000462924
  gene symbol: ZDHHC16
  hgvsc: ENST00000462924.1:n.791+856A>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359879
  ensembl transcript: ENST00000370842
  gene symbol: ZDHHC16
  hgvsc: ENST00000370842.2:c.690+116A>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000396286
  ensembl transcript: ENST00000417044
  gene symbol: ZDHHC16
  hgvsc: ENST00000417044.1:c.516-20A>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359891
  ensembl transcript: ENST00000370854
  gene symbol: ZDHHC16
  hgvsc: ENST00000370854.3:c.691-20A>G
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000495735
  gene symbol: ZDHHC16
  hgvsc: ENST00000495735.1:n.719-20A>G
  variant of: http://identifiers.org/hgnc/20714
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7902
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1305
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7633
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 873
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5394
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 702
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4011
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6671
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5008
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: South Asian
population: Other
population: East Asian
reference allele: A
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum

10-99213545-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 99213545
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 99213545
    reference: chr 10
allele count: 9
allele frequency: 7.415097137772504e-5
allele num: 121374
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000398532
  ensembl transcript: ENST00000433086
  gene symbol: ZDHHC16
  hgvsc: ENST00000433086.1:c.496-11C>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000459777
  gene symbol: ZDHHC16
  hgvsc: ENST00000459777.1:n.412-11C>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359879
  ensembl transcript: ENST00000370842
  gene symbol: ZDHHC16
  hgvsc: ENST00000370842.2:c.690+125C>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000345383
  ensembl transcript: ENST00000352634
  gene symbol: ZDHHC16
  hgvsc: ENST00000352634.4:c.690+125C>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000323360
  ensembl transcript: ENST00000353979
  gene symbol: ZDHHC16
  hgvsc: ENST00000353979.3:c.574-11C>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000495735
  gene symbol: ZDHHC16
  hgvsc: ENST00000495735.1:n.719-11C>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000466895
  gene symbol: ZDHHC16
  hgvsc: ENST00000466895.1:n.411-11C>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359891
  ensembl transcript: ENST00000370854
  gene symbol: ZDHHC16
  hgvsc: ENST00000370854.3:c.691-11C>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000462924
  gene symbol: ZDHHC16
  hgvsc: ENST00000462924.1:n.791+865C>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000396286
  ensembl transcript: ENST00000417044
  gene symbol: ZDHHC16
  hgvsc: ENST00000417044.1:c.516-11C>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359883
  ensembl transcript: ENST00000370846
  gene symbol: ZDHHC16
  hgvsc: ENST00000370846.4:c.556+865C>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000304487
  ensembl transcript: ENST00000345745
  gene symbol: ZDHHC16
  hgvsc: ENST00000345745.5:c.495+125C>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000405240
  ensembl transcript: ENST00000420089
  gene symbol: ZDHHC16
  hgvsc: ENST00000420089.1:c.617+125C>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000487315
  gene symbol: ZDHHC16
  hgvsc: ENST00000487315.1:n.110+125C>T
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000377357
  ensembl transcript: ENST00000393760
  gene symbol: ZDHHC16
  hgvsc: ENST00000393760.1:c.691-11C>T
  variant of: http://identifiers.org/hgnc/20714
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4010
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7634
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 873
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5010
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5394
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7216
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6659
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1343
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1965
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: African
population: East Asian
reference allele: C
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff

10-99213546-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 99213546
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 99213546
    reference: chr 10
allele count: 7
allele frequency: 5.767392808885081e-5
allele num: 121372
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359891
  ensembl transcript: ENST00000370854
  gene symbol: ZDHHC16
  hgvsc: ENST00000370854.3:c.691-10G>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000466895
  gene symbol: ZDHHC16
  hgvsc: ENST00000466895.1:n.411-10G>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359883
  ensembl transcript: ENST00000370846
  gene symbol: ZDHHC16
  hgvsc: ENST00000370846.4:c.556+866G>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000304487
  ensembl transcript: ENST00000345745
  gene symbol: ZDHHC16
  hgvsc: ENST00000345745.5:c.495+126G>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000405240
  ensembl transcript: ENST00000420089
  gene symbol: ZDHHC16
  hgvsc: ENST00000420089.1:c.617+126G>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000359879
  ensembl transcript: ENST00000370842
  gene symbol: ZDHHC16
  hgvsc: ENST00000370842.2:c.690+126G>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000495735
  gene symbol: ZDHHC16
  hgvsc: ENST00000495735.1:n.719-10G>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000398532
  ensembl transcript: ENST00000433086
  gene symbol: ZDHHC16
  hgvsc: ENST00000433086.1:c.496-10G>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000323360
  ensembl transcript: ENST00000353979
  gene symbol: ZDHHC16
  hgvsc: ENST00000353979.3:c.574-10G>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000377357
  ensembl transcript: ENST00000393760
  gene symbol: ZDHHC16
  hgvsc: ENST00000393760.1:c.691-10G>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000487315
  gene symbol: ZDHHC16
  hgvsc: ENST00000487315.1:n.110+126G>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000462924
  gene symbol: ZDHHC16
  hgvsc: ENST00000462924.1:n.791+866G>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000396286
  ensembl transcript: ENST00000417044
  gene symbol: ZDHHC16
  hgvsc: ENST00000417044.1:c.516-10G>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl transcript: ENST00000459777
  gene symbol: ZDHHC16
  hgvsc: ENST00000459777.1:n.412-10G>A
  variant of: http://identifiers.org/hgnc/20714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171307
  ensembl protein: ENSP00000345383
  ensembl transcript: ENST00000352634
  gene symbol: ZDHHC16
  hgvsc: ENST00000352634.4:c.690+126G>A
  variant of: http://identifiers.org/hgnc/20714
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4011
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 701
  bin: 9.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 6653
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7894
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1341
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5397
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1966
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum

http://identifiers.org/exac.variant/10-99213558-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 99213558
allele count: 1
allele frequency: 8.239675686364985e-6
allele num: 121364
alternate allele: C
canonical: true
consequence: missense
filter: PASS
hgvs: p.Lys231Asn
num of homozygotes: 0
reference allele: A

GenotypeDepth
all individuals: 2924
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3322
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 701
bin: 5.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 776
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3704
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 997
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 414
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 294
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 483
bin: 6.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 310
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 643
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 497
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 4.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 11
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 504
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 502
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 57419
bin: 9.75e1
variant carriers: 2

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498531439189594e-5
allele num: 66732
num of homozygotes: 0

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.3e-2

MQRankSum
type: SiteQuality
SIO_000300: 2.15e-1

MQ
type: SiteQuality
SIO_000300: 5.949e1

VQSLOD
type: SiteQuality
SIO_000300: 8.5e-1

FS
type: SiteQuality
SIO_000300: 6.32e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.36e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 6.615136e6

BaseQRankSum
type: SiteQuality
SIO_000300: -3.729e0

QD
type: SiteQuality
SIO_000300: 1.219e1

GenotypeDepth
all individuals: 11
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 701
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1143
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 775
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2925
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1356
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 997
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1787
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 57421
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 5
bin: 4.75e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 293
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 503
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 483
bin: 6.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 310
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 647
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 505
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 498
bin: 7.75e1
variant carriers: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66732
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.637070305752289e-5
allele num: 11578
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: 4.15e-1

FS
type: SiteQuality
SIO_000300: 5.95e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.77e-1

DP
type: SiteQuality
SIO_000300: 6.615076e6

VQSLOD
type: SiteQuality
SIO_000300: 8.62e-1

QD
type: SiteQuality
SIO_000300: 1.255e1

MQ
type: SiteQuality
SIO_000300: 5.91e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.051e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.28e0

GenotypeDepth
all individuals: 3706
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1024
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 807
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 997
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 660
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1142
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1787
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1356
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 505
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 2.25e1
variant carriers: 0

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

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: 11560
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.5109391998066e-5
allele num: 66184
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
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num of homozygotes: 0

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

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

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

MQRankSum
type: SiteQuality
SIO_000300: -1.58e-1

InbreedingCoeff
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SIO_000300: -4.0e-4

DP
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SIO_000300: 3.552185e6

VQSLOD
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FS
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SIO_000300: 2.11e0

MQ
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SIO_000300: 5.961e1

ClippingRankSum
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SIO_000300: -2.2e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.56e-1

BaseQRankSum
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SIO_000300: 2.07e0

QD
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SIO_000300: 1.524e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 10

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

European (Non-Finnish)
type: Population
allele count: 9
allele frequency: 1.359147059711861e-4
allele num: 66218
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 896
num of homozygotes: 0

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

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

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

South Asian
type: Population
allele count: 2
allele frequency: 1.341381623071764e-4
allele num: 14910
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.18e0

VQSLOD
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SIO_000300: 4.38e0

DP
type: SiteQuality
SIO_000300: 3.553296e6

MQRankSum
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SIO_000300: 3.22e-1

FS
type: SiteQuality
SIO_000300: 7.9e-1

QD
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ClippingRankSum
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SIO_000300: -5.92e-1

MQ
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SIO_000300: 5.985e1

InbreedingCoeff
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SIO_000300: -3.0e-4

ReadPosRankSum
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SIO_000300: 5.97e-1

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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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bin: 7.75e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.508159140952553e-5
allele num: 66306
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 15124
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.491e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.67e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.31e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.81e-1

DP
type: SiteQuality
SIO_000300: 3.565529e6

MQRankSum
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SIO_000300: -3.597e0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 1.51e0

QD
type: SiteQuality
SIO_000300: 1.316e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.5e-3

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11566
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.506931886678722e-5
allele num: 66360
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 15356
num of homozygotes: 0

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: 1.09e-1

MQ
type: SiteQuality
SIO_000300: 5.973e1

DP
type: SiteQuality
SIO_000300: 3.573887e6

VQSLOD
type: SiteQuality
SIO_000300: 9.85e-1

QD
type: SiteQuality
SIO_000300: 1.418e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 8.63e-1

FS
type: SiteQuality
SIO_000300: 2.447e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.27e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.31e-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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.505751972535084e-5
allele num: 66412
num of homozygotes: 0

South Asian
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num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

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

Other
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allele count: 0
allele frequency: 0.0e0
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VQSLOD
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DP
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InbreedingCoeff
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BaseQRankSum
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ClippingRankSum
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QD
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SIO_000300: 1.461e1

MQRankSum
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FS
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ReadPosRankSum
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MQ
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.505661286437003e-5
allele num: 66416
num of homozygotes: 0

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

South Asian
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European (Finnish)
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East Asian
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Other
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VQSLOD
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MQ
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QD
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InbreedingCoeff
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ReadPosRankSum
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ClippingRankSum
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BaseQRankSum
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MQRankSum
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FS
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele count: 1
allele frequency: 6.356470887363335e-5
allele num: 15732
num of homozygotes: 0

East Asian
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allele count: 0
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num of homozygotes: 0

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

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

African
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allele frequency: 0.0e0
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MQRankSum
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ReadPosRankSum
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VQSLOD
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BaseQRankSum
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ClippingRankSum
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DP
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QD
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FS
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InbreedingCoeff
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MQ
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GenotypeDepth
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variant carriers: 0

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

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

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

South Asian
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allele num: 16494
num of homozygotes: 0

Other
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num of homozygotes: 0

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

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

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

GenotypeDepth
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variant carriers: 0

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

European (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 num: 66700
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African
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East Asian
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Other
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Latino
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South Asian
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QD
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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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InbreedingCoeff
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BaseQRankSum
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MQ
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DP
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GenotypeDepth
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variant carriers: 0

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

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

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

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

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

European (Finnish)
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 0
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African
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Other
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South Asian
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Latino
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MQRankSum
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ClippingRankSum
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BaseQRankSum
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FS
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MQ
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DP
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VQSLOD
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InbreedingCoeff
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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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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 (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66722
num of homozygotes: 0

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

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

African
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allele count: 0
allele frequency: 0.0e0
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South Asian
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ClippingRankSum
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VQSLOD
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MQRankSum
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MQ
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QD
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ReadPosRankSum
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BaseQRankSum
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DP
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FS
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InbreedingCoeff
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SIO_000300: -5.999999999999999e-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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

Latino
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num of homozygotes: 0

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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele frequency: 1.157407407407407e-4
allele num: 8640
num of homozygotes: 0

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

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

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

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

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

FS
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SIO_000300: 3.253e0

VQSLOD
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SIO_000300: 9.51e-1

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

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

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

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

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

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

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

MQRankSum
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SIO_000300: 8.92e-1

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

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

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

Latino
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allele frequency: 1.728011059270779e-4
allele num: 11574
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66700
num of homozygotes: 0

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

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

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

South Asian
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MQRankSum
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QD
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ClippingRankSum
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ReadPosRankSum
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BaseQRankSum
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MQ
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DP
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InbreedingCoeff
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FS
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VQSLOD
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SIO_000300: 6.899999999999999e-1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66702
num of homozygotes: 0

South Asian
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allele count: 3
allele frequency: 1.817300702689605e-4
allele num: 16508
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African
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele count: 0
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Latino
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Other
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VQSLOD
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SIO_000300: 7.31e-1

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

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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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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allele count: 2
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Other
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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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MQRankSum
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BaseQRankSum
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MQ
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VQSLOD
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QD
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InbreedingCoeff
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FS
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ClippingRankSum
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ReadPosRankSum
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DP
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GenotypeDepth
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variant carriers: 0

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

East Asian
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European (Non-Finnish)
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African
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European (Finnish)
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South Asian
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Other
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MQ
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QD
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BaseQRankSum
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ClippingRankSum
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VQSLOD
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InbreedingCoeff
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FS
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MQRankSum
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele frequency: 1.921968095329617e-4
allele num: 10406
num of homozygotes: 0

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

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

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

DP
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SIO_000300: 3.597993e6

ClippingRankSum
type: SiteQuality
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InbreedingCoeff
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SIO_000300: 1.2e-2

FS
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MQ
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VQSLOD
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QD
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MQRankSum
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SIO_000300: 3.72e-1

ReadPosRankSum
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SIO_000300: -1.93e-1

BaseQRankSum
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SIO_000300: 7.02e-1

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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: 8642
num of homozygotes: 0

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

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

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

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

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

VQSLOD
type: SiteQuality
SIO_000300: -5.351e-1

InbreedingCoeff
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FS
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SIO_000300: 3.476e0

ReadPosRankSum
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MQRankSum
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BaseQRankSum
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DP
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MQ
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ClippingRankSum
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SIO_000300: 8.66e-1

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

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

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

European (Non-Finnish)
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allele count: 2
allele frequency: 2.998320940273447e-5
allele num: 66704
num of homozygotes: 0

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

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

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

European (Finnish)
type: Population
allele count: 2
allele frequency: 3.024803387779795e-4
allele num: 6612
num of homozygotes: 0

BaseQRankSum
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SIO_000300: 1.62e0

QD
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SIO_000300: 1.648e1

FS
type: SiteQuality
SIO_000300: 1.6434e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.6e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.6e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -4.11e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.59e-1

DP
type: SiteQuality
SIO_000300: 3.599114e6

VQSLOD
type: SiteQuality
SIO_000300: -2.052e0

MQ
type: SiteQuality
SIO_000300: 5.949e1

GenotypeDepth
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variant carriers: 3

GenotypeDepth
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variant carriers: 17

GenotypeDepth
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GenotypeDepth
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variant carriers: 19

GenotypeDepth
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variant carriers: 18

GenotypeDepth
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variant carriers: 38

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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variant carriers: 210

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 63
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variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 191
allele frequency: 2.863224800623614e-3
allele num: 66708
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.05913717886573e-5
allele num: 16504
num of homozygotes: 0

European (Finnish)
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allele count: 3
allele frequency: 4.537205081669691e-4
allele num: 6612
num of homozygotes: 0

Other
type: Population
allele count: 2
allele frequency: 2.207505518763797e-3
allele num: 906
num of homozygotes: 0

African
type: Population
allele count: 4
allele frequency: 3.844675124951942e-4
allele num: 10404
num of homozygotes: 0

Latino
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allele count: 8
allele frequency: 6.912044237083118e-4
allele num: 11574
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.474e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.17e-1

InbreedingCoeff
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SIO_000300: 3.6e-3

MQRankSum
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DP
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VQSLOD
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SIO_000300: 5.33e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.49e-1

BaseQRankSum
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SIO_000300: -7.8e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

GenotypeDepth
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variant carriers: 74

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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
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num of homozygotes: 0

African
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allele count: 853
allele frequency: 8.201923076923077e-2
allele num: 10400
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South Asian
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allele count: 274
allele frequency: 1.660404799418252e-2
allele num: 16502
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European (Finnish)
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allele count: 1
allele frequency: 1.512401693889897e-4
allele num: 6612
num of homozygotes: 0

Other
type: Population
allele count: 9
allele frequency: 9.933774834437087e-3
allele num: 906
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Latino
type: Population
allele count: 108
allele frequency: 9.331259720062209e-3
allele num: 11574
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 237
allele frequency: 3.553436487945304e-3
allele num: 66696
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.37e-2

BaseQRankSum
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MQ
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QD
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VQSLOD
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FS
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DP
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MQRankSum
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ClippingRankSum
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SIO_000300: -2.19e-1

ReadPosRankSum
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SIO_000300: 4.23e-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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 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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European (Non-Finnish)
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allele count: 4
allele frequency: 5.995743022454058e-5
allele num: 66714
num of homozygotes: 0

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

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

South Asian
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African
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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European (Non-Finnish)
type: Population
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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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ReadPosRankSum
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SIO_000300: 1.71e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 4.9e-1

InbreedingCoeff
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SIO_000300: 7.8e-3

VQSLOD
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DP
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SIO_000300: 3.617465e6

QD
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BaseQRankSum
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SIO_000300: -4.118e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.65e-1

MQ
type: SiteQuality
SIO_000300: 5.975e1

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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variant carriers: 3

GenotypeDepth
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GenotypeDepth
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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: 32

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 32
allele frequency: 1.938454082868912e-3
allele num: 16508
num of homozygotes: 0

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

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

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

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

QD
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SIO_000300: 1.262e1

ClippingRankSum
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SIO_000300: -4.4e-2

DP
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FS
type: SiteQuality
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ReadPosRankSum
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VQSLOD
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MQ
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BaseQRankSum
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InbreedingCoeff
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SIO_000300: 0.0e0

MQRankSum
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SIO_000300: -2.93e-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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10404
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 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: 66730
num of homozygotes: 0

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

South Asian
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allele count: 0
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num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 5.97e-1

ReadPosRankSum
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BaseQRankSum
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SIO_000300: -2.271e0

VQSLOD
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SIO_000300: 1.76e-1

QD
type: SiteQuality
SIO_000300: 1.258e1

MQ
type: SiteQuality
SIO_000300: 5.969e1

FS
type: SiteQuality
SIO_000300: 3.924e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.5e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.9e-3

DP
type: SiteQuality
SIO_000300: 2.917213e6

GenotypeDepth
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variant carriers: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10402
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

South Asian
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allele count: 1
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allele num: 16508
num of homozygotes: 0

Latino
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allele count: 0
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num of homozygotes: 0

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

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

Other
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num of homozygotes: 0

InbreedingCoeff
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SIO_000300: 0.0e0

MQRankSum
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ClippingRankSum
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SIO_000300: -3.55e-1

MQ
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 1.0012e1

DP
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QD
type: SiteQuality
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VQSLOD
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ReadPosRankSum
type: SiteQuality
SIO_000300: 9.8e-1

BaseQRankSum
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GenotypeDepth
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variant carriers: 0

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

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

European (Non-Finnish)
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allele count: 1
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allele num: 66728
num of homozygotes: 0

African
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South Asian
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East Asian
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Latino
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num of homozygotes: 0

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

European (Non-Finnish)
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African
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European (Finnish)
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Latino
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South Asian
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Other
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East Asian
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InbreedingCoeff
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FS
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ReadPosRankSum
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QD
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DP
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VQSLOD
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BaseQRankSum
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MQ
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

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

GenotypeDepth
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variant carriers: 0

GenotypeDepth
all individuals: 362
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5017
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7216
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6723
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7633
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 870
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5841
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 37
bin: 2.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 19
bin: 3.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 3337
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3578
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2982
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3201
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1954
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1763
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37929
bin: 9.75e1
variant carriers: 7

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

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.495577609210566e-5
allele num: 66706
num of homozygotes: 0

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

Latino
type: Population
allele count: 2
allele frequency: 1.727414061150458e-4
allele num: 11578
num of homozygotes: 0

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.35e-1

FS
type: SiteQuality
SIO_000300: 5.33e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.71e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.971e1

VQSLOD
type: SiteQuality
SIO_000300: 7.65e-1

DP
type: SiteQuality
SIO_000300: 2.916693e6

QD
type: SiteQuality
SIO_000300: 1.122e1

MQRankSum
type: SiteQuality
SIO_000300: 8.87e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.51e-1