12-110222104-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 110222104
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 110222104
    reference: chr 12
allele count: 2
allele frequency: 1.648396933981703e-5
allele num: 121330
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000443611
  ensembl transcript: ENST00000544971
  gene symbol: TRPV4
  hgvsc: ENST00000544971.1:c.2137+17G>A
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000406191
  ensembl transcript: ENST00000418703
  gene symbol: TRPV4
  hgvsc: ENST00000418703.2:c.2458+17G>A
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000442167
  ensembl transcript: ENST00000541794
  gene symbol: TRPV4
  hgvsc: ENST00000541794.1:c.2317+17G>A
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000261740
  ensembl transcript: ENST00000261740
  gene symbol: TRPV4
  hgvsc: ENST00000261740.2:c.2458+17G>A
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000376480
  ensembl transcript: ENST00000392719
  gene symbol: TRPV4
  hgvsc: ENST00000392719.2:c.2317+17G>A
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000442738
  ensembl transcript: ENST00000537083
  gene symbol: TRPV4
  hgvsc: ENST00000537083.1:c.2278+17G>A
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000444336
  ensembl transcript: ENST00000536838
  gene symbol: TRPV4
  hgvsc: ENST00000536838.1:c.2356+17G>A
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000319003
  ensembl transcript: ENST00000346520
  gene symbol: TRPV4
  hgvsc: ENST00000346520.2:c.2278+17G>A
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000437449
  ensembl transcript: ENST00000538125
  gene symbol: TRPV4
  hgvsc: ENST00000538125.1:c.*841+17G>A
  variant of: http://identifiers.org/hgnc/18083
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1150
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6790
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2103
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2847
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7191
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7373
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1034
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2542
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5321
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2867
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3630
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1694
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3906
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6247
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5000
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49467
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: Other
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ

12-110222106-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 110222106
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 110222106
    reference: chr 12
allele count: 4
allele frequency: 3.296902560044838e-5
allele num: 121326
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000443611
  ensembl transcript: ENST00000544971
  gene symbol: TRPV4
  hgvsc: ENST00000544971.1:c.2137+15G>A
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000437449
  ensembl transcript: ENST00000538125
  gene symbol: TRPV4
  hgvsc: ENST00000538125.1:c.*841+15G>A
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000442738
  ensembl transcript: ENST00000537083
  gene symbol: TRPV4
  hgvsc: ENST00000537083.1:c.2278+15G>A
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000376480
  ensembl transcript: ENST00000392719
  gene symbol: TRPV4
  hgvsc: ENST00000392719.2:c.2317+15G>A
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000442167
  ensembl transcript: ENST00000541794
  gene symbol: TRPV4
  hgvsc: ENST00000541794.1:c.2317+15G>A
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000319003
  ensembl transcript: ENST00000346520
  gene symbol: TRPV4
  hgvsc: ENST00000346520.2:c.2278+15G>A
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000444336
  ensembl transcript: ENST00000536838
  gene symbol: TRPV4
  hgvsc: ENST00000536838.1:c.2356+15G>A
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000261740
  ensembl transcript: ENST00000261740
  gene symbol: TRPV4
  hgvsc: ENST00000261740.2:c.2458+15G>A
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000406191
  ensembl transcript: ENST00000418703
  gene symbol: TRPV4
  hgvsc: ENST00000418703.2:c.2458+15G>A
  variant of: http://identifiers.org/hgnc/18083
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2106
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3630
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7372
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2541
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3908
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6247
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1034
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2869
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 5321
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7192
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2856
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1694
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5000
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6791
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1148
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1150
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Other
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: MQ

12-110222107-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 110222107
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 110222107
    reference: chr 12
allele count: 2
allele frequency: 1.648641519388024e-5
allele num: 121312
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000319003
  ensembl transcript: ENST00000346520
  gene symbol: TRPV4
  hgvsc: ENST00000346520.2:c.2278+14C>T
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000442738
  ensembl transcript: ENST00000537083
  gene symbol: TRPV4
  hgvsc: ENST00000537083.1:c.2278+14C>T
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000376480
  ensembl transcript: ENST00000392719
  gene symbol: TRPV4
  hgvsc: ENST00000392719.2:c.2317+14C>T
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000444336
  ensembl transcript: ENST00000536838
  gene symbol: TRPV4
  hgvsc: ENST00000536838.1:c.2356+14C>T
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000406191
  ensembl transcript: ENST00000418703
  gene symbol: TRPV4
  hgvsc: ENST00000418703.2:c.2458+14C>T
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000261740
  ensembl transcript: ENST00000261740
  gene symbol: TRPV4
  hgvsc: ENST00000261740.2:c.2458+14C>T
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000437449
  ensembl transcript: ENST00000538125
  gene symbol: TRPV4
  hgvsc: ENST00000538125.1:c.*841+14C>T
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000442167
  ensembl transcript: ENST00000541794
  gene symbol: TRPV4
  hgvsc: ENST00000541794.1:c.2317+14C>T
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000443611
  ensembl transcript: ENST00000544971
  gene symbol: TRPV4
  hgvsc: ENST00000544971.1:c.2137+14C>T
  variant of: http://identifiers.org/hgnc/18083
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2115
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5001
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7373
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3908
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2540
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1031
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1695
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1148
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2866
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6247
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2858
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6791
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7193
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3629
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5323
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2228
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1470
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
population: African
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: QD

12-110222110-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 110222110
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 110222110
    reference: chr 12
allele count: 2
allele frequency: 1.648233917357551e-5
allele num: 121342
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000319003
  ensembl transcript: ENST00000346520
  gene symbol: TRPV4
  hgvsc: ENST00000346520.2:c.2278+11G>A
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000261740
  ensembl transcript: ENST00000261740
  gene symbol: TRPV4
  hgvsc: ENST00000261740.2:c.2458+11G>A
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000406191
  ensembl transcript: ENST00000418703
  gene symbol: TRPV4
  hgvsc: ENST00000418703.2:c.2458+11G>A
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000442738
  ensembl transcript: ENST00000537083
  gene symbol: TRPV4
  hgvsc: ENST00000537083.1:c.2278+11G>A
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000444336
  ensembl transcript: ENST00000536838
  gene symbol: TRPV4
  hgvsc: ENST00000536838.1:c.2356+11G>A
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000437449
  ensembl transcript: ENST00000538125
  gene symbol: TRPV4
  hgvsc: ENST00000538125.1:c.*841+11G>A
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000442167
  ensembl transcript: ENST00000541794
  gene symbol: TRPV4
  hgvsc: ENST00000541794.1:c.2317+11G>A
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000376480
  ensembl transcript: ENST00000392719
  gene symbol: TRPV4
  hgvsc: ENST00000392719.2:c.2317+11G>A
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000443611
  ensembl transcript: ENST00000544971
  gene symbol: TRPV4
  hgvsc: ENST00000544971.1:c.2137+11G>A
  variant of: http://identifiers.org/hgnc/18083
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2866
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3629
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1046
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4999
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6247
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1695
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5327
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6791
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2128
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2539
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2857
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7192
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1148
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3906
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7372
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 757
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1471
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1428
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: MQ

12-110222118-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 110222118
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 110222118
    reference: chr 12
allele count: 1
allele frequency: 8.241305422778968e-6
allele num: 121340
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000261740
  ensembl transcript: ENST00000261740
  gene symbol: TRPV4
  hgvsc: ENST00000261740.2:c.2458+3G>C
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000319003
  ensembl transcript: ENST00000346520
  gene symbol: TRPV4
  hgvsc: ENST00000346520.2:c.2278+3G>C
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000442738
  ensembl transcript: ENST00000537083
  gene symbol: TRPV4
  hgvsc: ENST00000537083.1:c.2278+3G>C
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000376480
  ensembl transcript: ENST00000392719
  gene symbol: TRPV4
  hgvsc: ENST00000392719.2:c.2317+3G>C
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000443611
  ensembl transcript: ENST00000544971
  gene symbol: TRPV4
  hgvsc: ENST00000544971.1:c.2137+3G>C
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000437449
  ensembl transcript: ENST00000538125
  gene symbol: TRPV4
  hgvsc: ENST00000538125.1:c.*841+3G>C
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000444336
  ensembl transcript: ENST00000536838
  gene symbol: TRPV4
  hgvsc: ENST00000536838.1:c.2356+3G>C
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000442167
  ensembl transcript: ENST00000541794
  gene symbol: TRPV4
  hgvsc: ENST00000541794.1:c.2317+3G>C
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000406191
  ensembl transcript: ENST00000418703
  gene symbol: TRPV4
  hgvsc: ENST00000418703.2:c.2458+3G>C
  variant of: http://identifiers.org/hgnc/18083
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7373
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1695
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3630
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2538
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2866
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3913
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2855
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6791
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7192
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5332
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2129
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6244
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4997
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1148
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1022
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49455
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1473
  bin: 7.75e1
  variant carriers: 0
hgvs: c.2458+3G>C
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: European (Finnish)
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP

http://identifiers.org/exac.variant/12-110222121-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 110222121
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 110222121
    reference: chr 12
allele count: 1
allele frequency: 8.241577108195424e-6
allele num: 121336
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000443611
  ensembl transcript: ENST00000544971
  gene symbol: TRPV4
  hgvsc: ENST00000544971.1:c.2137G>T
  hgvsp: ENSP00000443611.1:p.Asp713Tyr
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000376480
  ensembl transcript: ENST00000392719
  gene symbol: TRPV4
  hgvsc: ENST00000392719.2:c.2317G>T
  hgvsp: ENSP00000376480.2:p.Asp773Tyr
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000261740
  ensembl transcript: ENST00000261740
  gene symbol: TRPV4
  hgvsc: ENST00000261740.2:c.2458G>T
  hgvsp: ENSP00000261740.2:p.Asp820Tyr
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000442167
  ensembl transcript: ENST00000541794
  gene symbol: TRPV4
  hgvsc: ENST00000541794.1:c.2317G>T
  hgvsp: ENSP00000442167.1:p.Asp773Tyr
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000442738
  ensembl transcript: ENST00000537083
  gene symbol: TRPV4
  hgvsc: ENST00000537083.1:c.2278G>T
  hgvsp: ENSP00000442738.1:p.Asp760Tyr
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000444336
  ensembl transcript: ENST00000536838
  gene symbol: TRPV4
  hgvsc: ENST00000536838.1:c.2356G>T
  hgvsp: ENSP00000444336.1:p.Asp786Tyr
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000319003
  ensembl transcript: ENST00000346520
  gene symbol: TRPV4
  hgvsc: ENST00000346520.2:c.2278G>T
  hgvsp: ENSP00000319003.2:p.Asp760Tyr
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000406191
  ensembl transcript: ENST00000418703
  gene symbol: TRPV4
  hgvsc: ENST00000418703.2:c.2458G>T
  hgvsp: ENSP00000406191.2:p.Asp820Tyr
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000437449
  ensembl transcript: ENST00000538125
  gene symbol: TRPV4
  hgvsc: ENST00000538125.1:c.*841G>T
  variant of: http://identifiers.org/hgnc/18083
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7190
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5324
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1693
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7368
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6246
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2177
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3628
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6788
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2537
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4993
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2873
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3894
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2864
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1148
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1009
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Asp820Tyr
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
population: African
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum

12-110222127-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 110222127
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 110222127
    reference: chr 12
allele count: 1
allele frequency: 8.240626287597857e-6
allele num: 121350
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000261740
  ensembl transcript: ENST00000261740
  gene symbol: TRPV4
  hgvsc: ENST00000261740.2:c.2452C>T
  hgvsp: ENSP00000261740.2:p.Arg818Cys
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000319003
  ensembl transcript: ENST00000346520
  gene symbol: TRPV4
  hgvsc: ENST00000346520.2:c.2272C>T
  hgvsp: ENSP00000319003.2:p.Arg758Cys
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000376480
  ensembl transcript: ENST00000392719
  gene symbol: TRPV4
  hgvsc: ENST00000392719.2:c.2311C>T
  hgvsp: ENSP00000376480.2:p.Arg771Cys
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000437449
  ensembl transcript: ENST00000538125
  gene symbol: TRPV4
  hgvsc: ENST00000538125.1:c.*835C>T
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000406191
  ensembl transcript: ENST00000418703
  gene symbol: TRPV4
  hgvsc: ENST00000418703.2:c.2452C>T
  hgvsp: ENSP00000406191.2:p.Arg818Cys
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000444336
  ensembl transcript: ENST00000536838
  gene symbol: TRPV4
  hgvsc: ENST00000536838.1:c.2350C>T
  hgvsp: ENSP00000444336.1:p.Arg784Cys
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000443611
  ensembl transcript: ENST00000544971
  gene symbol: TRPV4
  hgvsc: ENST00000544971.1:c.2131C>T
  hgvsp: ENSP00000443611.1:p.Arg711Cys
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000442738
  ensembl transcript: ENST00000537083
  gene symbol: TRPV4
  hgvsc: ENST00000537083.1:c.2272C>T
  hgvsp: ENSP00000442738.1:p.Arg758Cys
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000442167
  ensembl transcript: ENST00000541794
  gene symbol: TRPV4
  hgvsc: ENST00000541794.1:c.2311C>T
  hgvsp: ENSP00000442167.1:p.Arg771Cys
  variant of: http://identifiers.org/hgnc/18083
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2875
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1013
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3893
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7368
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2182
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7189
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6785
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4995
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1693
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5327
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1148
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2537
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6246
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2864
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3628
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1464
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Arg818Cys
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD

12-110222133-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 110222133
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 110222133
    reference: chr 12
allele count: 2
allele frequency: 1.648070932972955e-5
allele num: 121354
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000261740
  ensembl transcript: ENST00000261740
  gene symbol: TRPV4
  hgvsc: ENST00000261740.2:c.2446C>T
  hgvsp: ENSP00000261740.2:p.Arg816Cys
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000443611
  ensembl transcript: ENST00000544971
  gene symbol: TRPV4
  hgvsc: ENST00000544971.1:c.2125C>T
  hgvsp: ENSP00000443611.1:p.Arg709Cys
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000376480
  ensembl transcript: ENST00000392719
  gene symbol: TRPV4
  hgvsc: ENST00000392719.2:c.2305C>T
  hgvsp: ENSP00000376480.2:p.Arg769Cys
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000406191
  ensembl transcript: ENST00000418703
  gene symbol: TRPV4
  hgvsc: ENST00000418703.2:c.2446C>T
  hgvsp: ENSP00000406191.2:p.Arg816Cys
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000442167
  ensembl transcript: ENST00000541794
  gene symbol: TRPV4
  hgvsc: ENST00000541794.1:c.2305C>T
  hgvsp: ENSP00000442167.1:p.Arg769Cys
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000444336
  ensembl transcript: ENST00000536838
  gene symbol: TRPV4
  hgvsc: ENST00000536838.1:c.2344C>T
  hgvsp: ENSP00000444336.1:p.Arg782Cys
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000319003
  ensembl transcript: ENST00000346520
  gene symbol: TRPV4
  hgvsc: ENST00000346520.2:c.2266C>T
  hgvsp: ENSP00000319003.2:p.Arg756Cys
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000437449
  ensembl transcript: ENST00000538125
  gene symbol: TRPV4
  hgvsc: ENST00000538125.1:c.*829C>T
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000442738
  ensembl transcript: ENST00000537083
  gene symbol: TRPV4
  hgvsc: ENST00000537083.1:c.2266C>T
  hgvsp: ENSP00000442738.1:p.Arg756Cys
  variant of: http://identifiers.org/hgnc/18083
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2182
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5328
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7192
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3893
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2537
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1147
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3628
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1010
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6785
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6246
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2878
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2864
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1693
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7367
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4994
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 977
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Arg816Cys
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Other
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD

http://identifiers.org/exac.variant/12-110222139-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 110222139
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 110222139
    reference: chr 12
allele count: 1
allele frequency: 8.241305422778968e-6
allele num: 121340
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000261740
  ensembl transcript: ENST00000261740
  gene symbol: TRPV4
  hgvsc: ENST00000261740.2:c.2440G>T
  hgvsp: ENSP00000261740.2:p.Val814Leu
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000444336
  ensembl transcript: ENST00000536838
  gene symbol: TRPV4
  hgvsc: ENST00000536838.1:c.2338G>T
  hgvsp: ENSP00000444336.1:p.Val780Leu
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000442167
  ensembl transcript: ENST00000541794
  gene symbol: TRPV4
  hgvsc: ENST00000541794.1:c.2299G>T
  hgvsp: ENSP00000442167.1:p.Val767Leu
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000406191
  ensembl transcript: ENST00000418703
  gene symbol: TRPV4
  hgvsc: ENST00000418703.2:c.2440G>T
  hgvsp: ENSP00000406191.2:p.Val814Leu
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000319003
  ensembl transcript: ENST00000346520
  gene symbol: TRPV4
  hgvsc: ENST00000346520.2:c.2260G>T
  hgvsp: ENSP00000319003.2:p.Val754Leu
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000376480
  ensembl transcript: ENST00000392719
  gene symbol: TRPV4
  hgvsc: ENST00000392719.2:c.2299G>T
  hgvsp: ENSP00000376480.2:p.Val767Leu
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000437449
  ensembl transcript: ENST00000538125
  gene symbol: TRPV4
  hgvsc: ENST00000538125.1:c.*823G>T
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000442738
  ensembl transcript: ENST00000537083
  gene symbol: TRPV4
  hgvsc: ENST00000537083.1:c.2260G>T
  hgvsp: ENSP00000442738.1:p.Val754Leu
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000443611
  ensembl transcript: ENST00000544971
  gene symbol: TRPV4
  hgvsc: ENST00000544971.1:c.2119G>T
  hgvsp: ENSP00000443611.1:p.Val707Leu
  variant of: http://identifiers.org/hgnc/18083
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6245
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2876
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5326
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1025
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6785
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4995
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1694
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2539
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2176
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3629
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3889
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7371
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7195
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2863
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1146
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1602
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2257
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Val814Leu
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: African
population: Other
reference allele: C
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum

12-110222139-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 110222139
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 110222139
    reference: chr 12
allele count: 1
allele frequency: 8.241305422778968e-6
allele num: 121340
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000442738
  ensembl transcript: ENST00000537083
  gene symbol: TRPV4
  hgvsc: ENST00000537083.1:c.2260G>A
  hgvsp: ENSP00000442738.1:p.Val754Met
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000261740
  ensembl transcript: ENST00000261740
  gene symbol: TRPV4
  hgvsc: ENST00000261740.2:c.2440G>A
  hgvsp: ENSP00000261740.2:p.Val814Met
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000444336
  ensembl transcript: ENST00000536838
  gene symbol: TRPV4
  hgvsc: ENST00000536838.1:c.2338G>A
  hgvsp: ENSP00000444336.1:p.Val780Met
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000437449
  ensembl transcript: ENST00000538125
  gene symbol: TRPV4
  hgvsc: ENST00000538125.1:c.*823G>A
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000442167
  ensembl transcript: ENST00000541794
  gene symbol: TRPV4
  hgvsc: ENST00000541794.1:c.2299G>A
  hgvsp: ENSP00000442167.1:p.Val767Met
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000376480
  ensembl transcript: ENST00000392719
  gene symbol: TRPV4
  hgvsc: ENST00000392719.2:c.2299G>A
  hgvsp: ENSP00000376480.2:p.Val767Met
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000406191
  ensembl transcript: ENST00000418703
  gene symbol: TRPV4
  hgvsc: ENST00000418703.2:c.2440G>A
  hgvsp: ENSP00000406191.2:p.Val814Met
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000443611
  ensembl transcript: ENST00000544971
  gene symbol: TRPV4
  hgvsc: ENST00000544971.1:c.2119G>A
  hgvsp: ENSP00000443611.1:p.Val707Met
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000319003
  ensembl transcript: ENST00000346520
  gene symbol: TRPV4
  hgvsc: ENST00000346520.2:c.2260G>A
  hgvsp: ENSP00000319003.2:p.Val754Met
  variant of: http://identifiers.org/hgnc/18083
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6785
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3629
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1694
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1025
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6245
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5326
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3889
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2176
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2863
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2539
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7371
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4995
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7195
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2876
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1146
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Val814Met
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum

12-110222140-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 110222140
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 110222140
    reference: chr 12
allele count: 3
allele frequency: 2.47222863170386e-5
allele num: 121348
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000442738
  ensembl transcript: ENST00000537083
  gene symbol: TRPV4
  hgvsc: ENST00000537083.1:c.2259C>T
  hgvsp: ENST00000537083.1:c.2259C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000442167
  ensembl transcript: ENST00000541794
  gene symbol: TRPV4
  hgvsc: ENST00000541794.1:c.2298C>T
  hgvsp: ENST00000541794.1:c.2298C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000444336
  ensembl transcript: ENST00000536838
  gene symbol: TRPV4
  hgvsc: ENST00000536838.1:c.2337C>T
  hgvsp: ENST00000536838.1:c.2337C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000443611
  ensembl transcript: ENST00000544971
  gene symbol: TRPV4
  hgvsc: ENST00000544971.1:c.2118C>T
  hgvsp: ENST00000544971.1:c.2118C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000376480
  ensembl transcript: ENST00000392719
  gene symbol: TRPV4
  hgvsc: ENST00000392719.2:c.2298C>T
  hgvsp: ENST00000392719.2:c.2298C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000319003
  ensembl transcript: ENST00000346520
  gene symbol: TRPV4
  hgvsc: ENST00000346520.2:c.2259C>T
  hgvsp: ENST00000346520.2:c.2259C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000437449
  ensembl transcript: ENST00000538125
  gene symbol: TRPV4
  hgvsc: ENST00000538125.1:c.*822C>T
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000406191
  ensembl transcript: ENST00000418703
  gene symbol: TRPV4
  hgvsc: ENST00000418703.2:c.2439C>T
  hgvsp: ENST00000418703.2:c.2439C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000261740
  ensembl transcript: ENST00000261740
  gene symbol: TRPV4
  hgvsc: ENST00000261740.2:c.2439C>T
  hgvsp: ENST00000261740.2:c.2439C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2876
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1147
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6786
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6246
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2538
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2861
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7371
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4995
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3631
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3888
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2172
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1694
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1036
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5326
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7196
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 984
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Thr813Thr
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
population: South Asian
population: Latino
reference allele: G
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD

12-110222140-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 110222140
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 110222140
    reference: chr 12
allele count: 1
allele frequency: 8.240762105679534e-6
allele num: 121348
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000443611
  ensembl transcript: ENST00000544971
  gene symbol: TRPV4
  hgvsc: ENST00000544971.1:c.2118C>A
  hgvsp: ENST00000544971.1:c.2118C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000376480
  ensembl transcript: ENST00000392719
  gene symbol: TRPV4
  hgvsc: ENST00000392719.2:c.2298C>A
  hgvsp: ENST00000392719.2:c.2298C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000261740
  ensembl transcript: ENST00000261740
  gene symbol: TRPV4
  hgvsc: ENST00000261740.2:c.2439C>A
  hgvsp: ENST00000261740.2:c.2439C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000444336
  ensembl transcript: ENST00000536838
  gene symbol: TRPV4
  hgvsc: ENST00000536838.1:c.2337C>A
  hgvsp: ENST00000536838.1:c.2337C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000442738
  ensembl transcript: ENST00000537083
  gene symbol: TRPV4
  hgvsc: ENST00000537083.1:c.2259C>A
  hgvsp: ENST00000537083.1:c.2259C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000406191
  ensembl transcript: ENST00000418703
  gene symbol: TRPV4
  hgvsc: ENST00000418703.2:c.2439C>A
  hgvsp: ENST00000418703.2:c.2439C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000442167
  ensembl transcript: ENST00000541794
  gene symbol: TRPV4
  hgvsc: ENST00000541794.1:c.2298C>A
  hgvsp: ENST00000541794.1:c.2298C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000319003
  ensembl transcript: ENST00000346520
  gene symbol: TRPV4
  hgvsc: ENST00000346520.2:c.2259C>A
  hgvsp: ENST00000346520.2:c.2259C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000437449
  ensembl transcript: ENST00000538125
  gene symbol: TRPV4
  hgvsc: ENST00000538125.1:c.*822C>A
  variant of: http://identifiers.org/hgnc/18083
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1036
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4995
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3888
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7371
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5326
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1147
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7196
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2538
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2876
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6246
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2861
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6786
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3631
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1694
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2172
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1455
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Thr813Thr
num of homozygotes: 0
population: African
population: Other
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP

12-110222145-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 110222145
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 110222145
    reference: chr 12
allele count: 1
allele frequency: 8.239947264337508e-6
allele num: 121360
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000261740
  ensembl transcript: ENST00000261740
  gene symbol: TRPV4
  hgvsc: ENST00000261740.2:c.2434C>T
  hgvsp: ENSP00000261740.2:p.His812Tyr
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000443611
  ensembl transcript: ENST00000544971
  gene symbol: TRPV4
  hgvsc: ENST00000544971.1:c.2113C>T
  hgvsp: ENSP00000443611.1:p.His705Tyr
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000437449
  ensembl transcript: ENST00000538125
  gene symbol: TRPV4
  hgvsc: ENST00000538125.1:c.*817C>T
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000376480
  ensembl transcript: ENST00000392719
  gene symbol: TRPV4
  hgvsc: ENST00000392719.2:c.2293C>T
  hgvsp: ENSP00000376480.2:p.His765Tyr
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000406191
  ensembl transcript: ENST00000418703
  gene symbol: TRPV4
  hgvsc: ENST00000418703.2:c.2434C>T
  hgvsp: ENSP00000406191.2:p.His812Tyr
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000442738
  ensembl transcript: ENST00000537083
  gene symbol: TRPV4
  hgvsc: ENST00000537083.1:c.2254C>T
  hgvsp: ENSP00000442738.1:p.His752Tyr
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000444336
  ensembl transcript: ENST00000536838
  gene symbol: TRPV4
  hgvsc: ENST00000536838.1:c.2332C>T
  hgvsp: ENSP00000444336.1:p.His778Tyr
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000442167
  ensembl transcript: ENST00000541794
  gene symbol: TRPV4
  hgvsc: ENST00000541794.1:c.2293C>T
  hgvsp: ENSP00000442167.1:p.His765Tyr
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000319003
  ensembl transcript: ENST00000346520
  gene symbol: TRPV4
  hgvsc: ENST00000346520.2:c.2254C>T
  hgvsp: ENSP00000319003.2:p.His752Tyr
  variant of: http://identifiers.org/hgnc/18083
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 7371
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5329
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3888
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1059
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3631
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7195
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2878
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4996
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2175
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6787
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2860
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1146
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2537
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1694
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6248
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2285
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
hgvs: p.His812Tyr
num of homozygotes: 0
population: Other
population: African
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum

http://identifiers.org/exac.variant/12-110222146-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 110222146
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 110222146
    reference: chr 12
allele count: 3
allele frequency: 2.472269378471478e-5
allele num: 121346
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000437449
  ensembl transcript: ENST00000538125
  gene symbol: TRPV4
  hgvsc: ENST00000538125.1:c.*816G>T
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000319003
  ensembl transcript: ENST00000346520
  gene symbol: TRPV4
  hgvsc: ENST00000346520.2:c.2253G>T
  hgvsp: ENST00000346520.2:c.2253G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000443611
  ensembl transcript: ENST00000544971
  gene symbol: TRPV4
  hgvsc: ENST00000544971.1:c.2112G>T
  hgvsp: ENST00000544971.1:c.2112G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000376480
  ensembl transcript: ENST00000392719
  gene symbol: TRPV4
  hgvsc: ENST00000392719.2:c.2292G>T
  hgvsp: ENST00000392719.2:c.2292G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000442167
  ensembl transcript: ENST00000541794
  gene symbol: TRPV4
  hgvsc: ENST00000541794.1:c.2292G>T
  hgvsp: ENST00000541794.1:c.2292G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000261740
  ensembl transcript: ENST00000261740
  gene symbol: TRPV4
  hgvsc: ENST00000261740.2:c.2433G>T
  hgvsp: ENST00000261740.2:c.2433G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000444336
  ensembl transcript: ENST00000536838
  gene symbol: TRPV4
  hgvsc: ENST00000536838.1:c.2331G>T
  hgvsp: ENST00000536838.1:c.2331G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000442738
  ensembl transcript: ENST00000537083
  gene symbol: TRPV4
  hgvsc: ENST00000537083.1:c.2253G>T
  hgvsp: ENST00000537083.1:c.2253G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000406191
  ensembl transcript: ENST00000418703
  gene symbol: TRPV4
  hgvsc: ENST00000418703.2:c.2433G>T
  hgvsp: ENST00000418703.2:c.2433G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6191
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 697
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2171
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1095
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1035
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1630
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7308
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6741
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5299
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2464
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2862
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3869
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3542
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3580
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7132
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4936
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 972
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Ser811Ser
num of homozygotes: 0
population: Other
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
reference allele: C
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: DP

12-110222146-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 110222146
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 110222146
    reference: chr 12
allele count: 1215
allele frequency: 1.001269098280949e-2
allele num: 121346
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000443611
  ensembl transcript: ENST00000544971
  gene symbol: TRPV4
  hgvsc: ENST00000544971.1:c.2112G>C
  hgvsp: ENST00000544971.1:c.2112G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000442738
  ensembl transcript: ENST00000537083
  gene symbol: TRPV4
  hgvsc: ENST00000537083.1:c.2253G>C
  hgvsp: ENST00000537083.1:c.2253G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000261740
  ensembl transcript: ENST00000261740
  gene symbol: TRPV4
  hgvsc: ENST00000261740.2:c.2433G>C
  hgvsp: ENST00000261740.2:c.2433G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000376480
  ensembl transcript: ENST00000392719
  gene symbol: TRPV4
  hgvsc: ENST00000392719.2:c.2292G>C
  hgvsp: ENST00000392719.2:c.2292G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000319003
  ensembl transcript: ENST00000346520
  gene symbol: TRPV4
  hgvsc: ENST00000346520.2:c.2253G>C
  hgvsp: ENST00000346520.2:c.2253G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000444336
  ensembl transcript: ENST00000536838
  gene symbol: TRPV4
  hgvsc: ENST00000536838.1:c.2331G>C
  hgvsp: ENST00000536838.1:c.2331G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000442167
  ensembl transcript: ENST00000541794
  gene symbol: TRPV4
  hgvsc: ENST00000541794.1:c.2292G>C
  hgvsp: ENST00000541794.1:c.2292G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000437449
  ensembl transcript: ENST00000538125
  gene symbol: TRPV4
  hgvsc: ENST00000538125.1:c.*816G>C
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000406191
  ensembl transcript: ENST00000418703
  gene symbol: TRPV4
  hgvsc: ENST00000418703.2:c.2433G>C
  hgvsp: ENST00000418703.2:c.2433G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2171
  bin: 2.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 6741
  bin: 4.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1035
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 5299
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1630
  bin: 8.25e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2862
  bin: 3.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 3869
  bin: 3.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 6191
  bin: 6.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7308
  bin: 5.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 1095
  bin: 8.75e1
  variant carriers: 31
genotype depth: GenotypeDepth
  all individuals: 2464
  bin: 7.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7132
  bin: 5.75e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 4936
  bin: 6.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 3580
  bin: 7.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 3542
  bin: 9.75e1
  variant carriers: 1029
genotype depth: GenotypeDepth
  all individuals: 697
  bin: 9.25e1
  variant carriers: 22
genotype quality: GenotypeQuality
  all individuals: 1145
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2255
  bin: 6.25e1
  variant carriers: 1
hgvs: p.Ser811Ser
num of homozygotes: 12
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff

12-110222146-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 110222146
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 110222146
    reference: chr 12
allele count: 1
allele frequency: 8.240897928238261e-6
allele num: 121346
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000444336
  ensembl transcript: ENST00000536838
  gene symbol: TRPV4
  hgvsc: ENST00000536838.1:c.2331G>A
  hgvsp: ENST00000536838.1:c.2331G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000261740
  ensembl transcript: ENST00000261740
  gene symbol: TRPV4
  hgvsc: ENST00000261740.2:c.2433G>A
  hgvsp: ENST00000261740.2:c.2433G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000437449
  ensembl transcript: ENST00000538125
  gene symbol: TRPV4
  hgvsc: ENST00000538125.1:c.*816G>A
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000443611
  ensembl transcript: ENST00000544971
  gene symbol: TRPV4
  hgvsc: ENST00000544971.1:c.2112G>A
  hgvsp: ENST00000544971.1:c.2112G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000442167
  ensembl transcript: ENST00000541794
  gene symbol: TRPV4
  hgvsc: ENST00000541794.1:c.2292G>A
  hgvsp: ENST00000541794.1:c.2292G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000406191
  ensembl transcript: ENST00000418703
  gene symbol: TRPV4
  hgvsc: ENST00000418703.2:c.2433G>A
  hgvsp: ENST00000418703.2:c.2433G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000376480
  ensembl transcript: ENST00000392719
  gene symbol: TRPV4
  hgvsc: ENST00000392719.2:c.2292G>A
  hgvsp: ENST00000392719.2:c.2292G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000442738
  ensembl transcript: ENST00000537083
  gene symbol: TRPV4
  hgvsc: ENST00000537083.1:c.2253G>A
  hgvsp: ENST00000537083.1:c.2253G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000319003
  ensembl transcript: ENST00000346520
  gene symbol: TRPV4
  hgvsc: ENST00000346520.2:c.2253G>A
  hgvsp: ENST00000346520.2:c.2253G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2862
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2171
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3542
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2464
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6191
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3869
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4936
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7308
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1035
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7132
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3580
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1630
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 697
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6741
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1095
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5299
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49508
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2255
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Ser811Ser
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: Other
population: European (Non-Finnish)
population: East Asian
population: Latino
reference allele: C
site quality: MQ
site quality: DP
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

12-110222147-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 110222147
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 110222147
    reference: chr 12
allele count: 8
allele frequency: 6.592175088170342e-5
allele num: 121356
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000443611
  ensembl transcript: ENST00000544971
  gene symbol: TRPV4
  hgvsc: ENST00000544971.1:c.2111C>T
  hgvsp: ENSP00000443611.1:p.Ser704Leu
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000319003
  ensembl transcript: ENST00000346520
  gene symbol: TRPV4
  hgvsc: ENST00000346520.2:c.2252C>T
  hgvsp: ENSP00000319003.2:p.Ser751Leu
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000444336
  ensembl transcript: ENST00000536838
  gene symbol: TRPV4
  hgvsc: ENST00000536838.1:c.2330C>T
  hgvsp: ENSP00000444336.1:p.Ser777Leu
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000261740
  ensembl transcript: ENST00000261740
  gene symbol: TRPV4
  hgvsc: ENST00000261740.2:c.2432C>T
  hgvsp: ENSP00000261740.2:p.Ser811Leu
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000442738
  ensembl transcript: ENST00000537083
  gene symbol: TRPV4
  hgvsc: ENST00000537083.1:c.2252C>T
  hgvsp: ENSP00000442738.1:p.Ser751Leu
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000376480
  ensembl transcript: ENST00000392719
  gene symbol: TRPV4
  hgvsc: ENST00000392719.2:c.2291C>T
  hgvsp: ENSP00000376480.2:p.Ser764Leu
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000437449
  ensembl transcript: ENST00000538125
  gene symbol: TRPV4
  hgvsc: ENST00000538125.1:c.*815C>T
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000442167
  ensembl transcript: ENST00000541794
  gene symbol: TRPV4
  hgvsc: ENST00000541794.1:c.2291C>T
  hgvsp: ENSP00000442167.1:p.Ser764Leu
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000406191
  ensembl transcript: ENST00000418703
  gene symbol: TRPV4
  hgvsc: ENST00000418703.2:c.2432C>T
  hgvsp: ENSP00000406191.2:p.Ser811Leu
  variant of: http://identifiers.org/hgnc/18083
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 7441
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2193
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2604
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6295
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3631
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3951
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1043
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5028
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2920
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1108
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2502
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6860
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5408
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1652
  bin: 8.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 7235
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 699
  bin: 9.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1633
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1509
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Ser811Leu
num of homozygotes: 0
population: African
population: Other
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: G
site quality: MQRankSum
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

12-110222149-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 110222149
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 110222149
    reference: chr 12
allele count: 308
allele frequency: 2.664313766197817e-3
allele num: 115602
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000406191
  ensembl transcript: ENST00000418703
  gene symbol: TRPV4
  hgvsc: ENST00000418703.2:c.2430C>T
  hgvsp: ENST00000418703.2:c.2430C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000437449
  ensembl transcript: ENST00000538125
  gene symbol: TRPV4
  hgvsc: ENST00000538125.1:c.*813C>T
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000261740
  ensembl transcript: ENST00000261740
  gene symbol: TRPV4
  hgvsc: ENST00000261740.2:c.2430C>T
  hgvsp: ENST00000261740.2:c.2430C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000442167
  ensembl transcript: ENST00000541794
  gene symbol: TRPV4
  hgvsc: ENST00000541794.1:c.2289C>T
  hgvsp: ENST00000541794.1:c.2289C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000376480
  ensembl transcript: ENST00000392719
  gene symbol: TRPV4
  hgvsc: ENST00000392719.2:c.2289C>T
  hgvsp: ENST00000392719.2:c.2289C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000444336
  ensembl transcript: ENST00000536838
  gene symbol: TRPV4
  hgvsc: ENST00000536838.1:c.2328C>T
  hgvsp: ENST00000536838.1:c.2328C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000442738
  ensembl transcript: ENST00000537083
  gene symbol: TRPV4
  hgvsc: ENST00000537083.1:c.2250C>T
  hgvsp: ENST00000537083.1:c.2250C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000443611
  ensembl transcript: ENST00000544971
  gene symbol: TRPV4
  hgvsc: ENST00000544971.1:c.2109C>T
  hgvsp: ENST00000544971.1:c.2109C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000319003
  ensembl transcript: ENST00000346520
  gene symbol: TRPV4
  hgvsc: ENST00000346520.2:c.2250C>T
  hgvsp: ENST00000346520.2:c.2250C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.95to100.00
genotype depth: GenotypeDepth
  all individuals: 1617
  bin: 8.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7265
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 970
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1066
  bin: 8.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 3327
  bin: 9.75e1
  variant carriers: 271
genotype depth: GenotypeDepth
  all individuals: 5026
  bin: 6.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 3594
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 6862
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 668
  bin: 9.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 2741
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1986
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5385
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3878
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2452
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 7467
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6311
  bin: 6.25e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 876
  bin: 7.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 1106
  bin: 8.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 3.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 5.25e1
  variant carriers: 3
hgvs: p.Phe810Phe
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: Other
population: East Asian
population: African
population: European (Finnish)
population: South Asian
reference allele: G
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum

12-110222154-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 110222154
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 110222154
    reference: chr 12
allele count: 1
allele frequency: 8.237639422047218e-6
allele num: 121394
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000442738
  ensembl transcript: ENST00000537083
  gene symbol: TRPV4
  hgvsc: ENST00000537083.1:c.2245G>A
  hgvsp: ENSP00000442738.1:p.Gly749Ser
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000406191
  ensembl transcript: ENST00000418703
  gene symbol: TRPV4
  hgvsc: ENST00000418703.2:c.2425G>A
  hgvsp: ENSP00000406191.2:p.Gly809Ser
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000444336
  ensembl transcript: ENST00000536838
  gene symbol: TRPV4
  hgvsc: ENST00000536838.1:c.2323G>A
  hgvsp: ENSP00000444336.1:p.Gly775Ser
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000376480
  ensembl transcript: ENST00000392719
  gene symbol: TRPV4
  hgvsc: ENST00000392719.2:c.2284G>A
  hgvsp: ENSP00000376480.2:p.Gly762Ser
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000443611
  ensembl transcript: ENST00000544971
  gene symbol: TRPV4
  hgvsc: ENST00000544971.1:c.2104G>A
  hgvsp: ENSP00000443611.1:p.Gly702Ser
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000261740
  ensembl transcript: ENST00000261740
  gene symbol: TRPV4
  hgvsc: ENST00000261740.2:c.2425G>A
  hgvsp: ENSP00000261740.2:p.Gly809Ser
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000319003
  ensembl transcript: ENST00000346520
  gene symbol: TRPV4
  hgvsc: ENST00000346520.2:c.2245G>A
  hgvsp: ENSP00000319003.2:p.Gly749Ser
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000442167
  ensembl transcript: ENST00000541794
  gene symbol: TRPV4
  hgvsc: ENST00000541794.1:c.2284G>A
  hgvsp: ENSP00000442167.1:p.Gly762Ser
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000437449
  ensembl transcript: ENST00000538125
  gene symbol: TRPV4
  hgvsc: ENST00000538125.1:c.*808G>A
  variant of: http://identifiers.org/hgnc/18083
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2526
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2277
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6876
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7259
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2210
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3685
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1688
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5397
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3975
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7440
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2997
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 740
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1054
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5068
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1157
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6318
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2168
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2418
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Gly809Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: Other
reference allele: C
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: ReadPosRankSum

12-110222169-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 110222169
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 110222169
    reference: chr 12
allele count: 0
allele frequency: 0.0e0
allele num: 121386
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000261740
  ensembl transcript: ENST00000261740
  gene symbol: TRPV4
  hgvsc: ENST00000261740.2:c.2410A>C
  hgvsp: ENSP00000261740.2:p.Thr804Pro
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000406191
  ensembl transcript: ENST00000418703
  gene symbol: TRPV4
  hgvsc: ENST00000418703.2:c.2410A>C
  hgvsp: ENSP00000406191.2:p.Thr804Pro
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000437449
  ensembl transcript: ENST00000538125
  gene symbol: TRPV4
  hgvsc: ENST00000538125.1:c.*793A>C
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000444336
  ensembl transcript: ENST00000536838
  gene symbol: TRPV4
  hgvsc: ENST00000536838.1:c.2308A>C
  hgvsp: ENSP00000444336.1:p.Thr770Pro
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000443611
  ensembl transcript: ENST00000544971
  gene symbol: TRPV4
  hgvsc: ENST00000544971.1:c.2089A>C
  hgvsp: ENSP00000443611.1:p.Thr697Pro
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000442167
  ensembl transcript: ENST00000541794
  gene symbol: TRPV4
  hgvsc: ENST00000541794.1:c.2269A>C
  hgvsp: ENSP00000442167.1:p.Thr757Pro
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000319003
  ensembl transcript: ENST00000346520
  gene symbol: TRPV4
  hgvsc: ENST00000346520.2:c.2230A>C
  hgvsp: ENSP00000319003.2:p.Thr744Pro
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000376480
  ensembl transcript: ENST00000392719
  gene symbol: TRPV4
  hgvsc: ENST00000392719.2:c.2269A>C
  hgvsp: ENSP00000376480.2:p.Thr757Pro
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000442738
  ensembl transcript: ENST00000537083
  gene symbol: TRPV4
  hgvsc: ENST00000537083.1:c.2230A>C
  hgvsp: ENSP00000442738.1:p.Thr744Pro
  variant of: http://identifiers.org/hgnc/18083
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.90to99.95
genotype depth: GenotypeDepth
  all individuals: 5067
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3977
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1049
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 741
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3685
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7440
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6876
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6318
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5399
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2275
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1689
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7261
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2998
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2206
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1156
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2524
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1162
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2169
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Thr804Pro
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: VQSLOD

12-110222170-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 110222170
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 110222170
    reference: chr 12
allele count: 1
allele frequency: 8.237639422047218e-6
allele num: 121394
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000319003
  ensembl transcript: ENST00000346520
  gene symbol: TRPV4
  hgvsc: ENST00000346520.2:c.2229G>C
  hgvsp: ENSP00000319003.2:p.Glu743Asp
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000442738
  ensembl transcript: ENST00000537083
  gene symbol: TRPV4
  hgvsc: ENST00000537083.1:c.2229G>C
  hgvsp: ENSP00000442738.1:p.Glu743Asp
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000376480
  ensembl transcript: ENST00000392719
  gene symbol: TRPV4
  hgvsc: ENST00000392719.2:c.2268G>C
  hgvsp: ENSP00000376480.2:p.Glu756Asp
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000444336
  ensembl transcript: ENST00000536838
  gene symbol: TRPV4
  hgvsc: ENST00000536838.1:c.2307G>C
  hgvsp: ENSP00000444336.1:p.Glu769Asp
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000406191
  ensembl transcript: ENST00000418703
  gene symbol: TRPV4
  hgvsc: ENST00000418703.2:c.2409G>C
  hgvsp: ENSP00000406191.2:p.Glu803Asp
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000443611
  ensembl transcript: ENST00000544971
  gene symbol: TRPV4
  hgvsc: ENST00000544971.1:c.2088G>C
  hgvsp: ENSP00000443611.1:p.Glu696Asp
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000442167
  ensembl transcript: ENST00000541794
  gene symbol: TRPV4
  hgvsc: ENST00000541794.1:c.2268G>C
  hgvsp: ENSP00000442167.1:p.Glu756Asp
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000437449
  ensembl transcript: ENST00000538125
  gene symbol: TRPV4
  hgvsc: ENST00000538125.1:c.*792G>C
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000261740
  ensembl transcript: ENST00000261740
  gene symbol: TRPV4
  hgvsc: ENST00000261740.2:c.2409G>C
  hgvsp: ENSP00000261740.2:p.Glu803Asp
  variant of: http://identifiers.org/hgnc/18083
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1156
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2282
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1054
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5398
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5065
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6875
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3003
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6316
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1688
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2207
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2523
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3978
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7257
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3682
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7439
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 739
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1509
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Glu803Asp
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

http://identifiers.org/exac.variant/12-110222173-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 110222173
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 110222173
    reference: chr 12
allele count: 2
allele frequency: 1.647527884409444e-5
allele num: 121394
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000442738
  ensembl transcript: ENST00000537083
  gene symbol: TRPV4
  hgvsc: ENST00000537083.1:c.2226T>G
  hgvsp: ENSP00000442738.1:p.Asn742Lys
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000319003
  ensembl transcript: ENST00000346520
  gene symbol: TRPV4
  hgvsc: ENST00000346520.2:c.2226T>G
  hgvsp: ENSP00000319003.2:p.Asn742Lys
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000376480
  ensembl transcript: ENST00000392719
  gene symbol: TRPV4
  hgvsc: ENST00000392719.2:c.2265T>G
  hgvsp: ENSP00000376480.2:p.Asn755Lys
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000261740
  ensembl transcript: ENST00000261740
  gene symbol: TRPV4
  hgvsc: ENST00000261740.2:c.2406T>G
  hgvsp: ENSP00000261740.2:p.Asn802Lys
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000443611
  ensembl transcript: ENST00000544971
  gene symbol: TRPV4
  hgvsc: ENST00000544971.1:c.2085T>G
  hgvsp: ENSP00000443611.1:p.Asn695Lys
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000442167
  ensembl transcript: ENST00000541794
  gene symbol: TRPV4
  hgvsc: ENST00000541794.1:c.2265T>G
  hgvsp: ENSP00000442167.1:p.Asn755Lys
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000444336
  ensembl transcript: ENST00000536838
  gene symbol: TRPV4
  hgvsc: ENST00000536838.1:c.2304T>G
  hgvsp: ENSP00000444336.1:p.Asn768Lys
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000406191
  ensembl transcript: ENST00000418703
  gene symbol: TRPV4
  hgvsc: ENST00000418703.2:c.2406T>G
  hgvsp: ENSP00000406191.2:p.Asn802Lys
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000437449
  ensembl transcript: ENST00000538125
  gene symbol: TRPV4
  hgvsc: ENST00000538125.1:c.*789T>G
  variant of: http://identifiers.org/hgnc/18083
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1157
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5065
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 739
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5397
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7257
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3682
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7439
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2207
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2523
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1055
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3001
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2286
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6874
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1688
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6316
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3978
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2168
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1485
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Asn802Lys
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
reference allele: A
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: DP

12-110222182-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 110222182
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 110222182
    reference: chr 12
allele count: 1
allele frequency: 8.237503706876667e-6
allele num: 121396
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000443611
  ensembl transcript: ENST00000544971
  gene symbol: TRPV4
  hgvsc: ENST00000544971.1:c.2076G>A
  hgvsp: ENST00000544971.1:c.2076G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000319003
  ensembl transcript: ENST00000346520
  gene symbol: TRPV4
  hgvsc: ENST00000346520.2:c.2217G>A
  hgvsp: ENST00000346520.2:c.2217G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000261740
  ensembl transcript: ENST00000261740
  gene symbol: TRPV4
  hgvsc: ENST00000261740.2:c.2397G>A
  hgvsp: ENST00000261740.2:c.2397G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000442167
  ensembl transcript: ENST00000541794
  gene symbol: TRPV4
  hgvsc: ENST00000541794.1:c.2256G>A
  hgvsp: ENST00000541794.1:c.2256G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000442738
  ensembl transcript: ENST00000537083
  gene symbol: TRPV4
  hgvsc: ENST00000537083.1:c.2217G>A
  hgvsp: ENST00000537083.1:c.2217G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000444336
  ensembl transcript: ENST00000536838
  gene symbol: TRPV4
  hgvsc: ENST00000536838.1:c.2295G>A
  hgvsp: ENST00000536838.1:c.2295G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000376480
  ensembl transcript: ENST00000392719
  gene symbol: TRPV4
  hgvsc: ENST00000392719.2:c.2256G>A
  hgvsp: ENST00000392719.2:c.2256G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000406191
  ensembl transcript: ENST00000418703
  gene symbol: TRPV4
  hgvsc: ENST00000418703.2:c.2397G>A
  hgvsp: ENST00000418703.2:c.2397G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000437449
  ensembl transcript: ENST00000538125
  gene symbol: TRPV4
  hgvsc: ENST00000538125.1:c.*780G>A
  variant of: http://identifiers.org/hgnc/18083
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2207
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6316
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7439
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3004
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3980
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1156
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2523
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1049
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5065
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1688
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3682
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5397
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 738
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6875
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2286
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7258
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1483
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Pro799Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: Other
population: East Asian
population: African
population: South Asian
population: European (Finnish)
reference allele: C
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD

12-110222188-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 110222188
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 110222188
    reference: chr 12
allele count: 1
allele frequency: 8.237639422047218e-6
allele num: 121394
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000376480
  ensembl transcript: ENST00000392719
  gene symbol: TRPV4
  hgvsc: ENST00000392719.2:c.2250G>A
  hgvsp: ENST00000392719.2:c.2250G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000442167
  ensembl transcript: ENST00000541794
  gene symbol: TRPV4
  hgvsc: ENST00000541794.1:c.2250G>A
  hgvsp: ENST00000541794.1:c.2250G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000444336
  ensembl transcript: ENST00000536838
  gene symbol: TRPV4
  hgvsc: ENST00000536838.1:c.2289G>A
  hgvsp: ENST00000536838.1:c.2289G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000442738
  ensembl transcript: ENST00000537083
  gene symbol: TRPV4
  hgvsc: ENST00000537083.1:c.2211G>A
  hgvsp: ENST00000537083.1:c.2211G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000437449
  ensembl transcript: ENST00000538125
  gene symbol: TRPV4
  hgvsc: ENST00000538125.1:c.*774G>A
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000319003
  ensembl transcript: ENST00000346520
  gene symbol: TRPV4
  hgvsc: ENST00000346520.2:c.2211G>A
  hgvsp: ENST00000346520.2:c.2211G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000406191
  ensembl transcript: ENST00000418703
  gene symbol: TRPV4
  hgvsc: ENST00000418703.2:c.2391G>A
  hgvsp: ENST00000418703.2:c.2391G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000261740
  ensembl transcript: ENST00000261740
  gene symbol: TRPV4
  hgvsc: ENST00000261740.2:c.2391G>A
  hgvsp: ENST00000261740.2:c.2391G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000443611
  ensembl transcript: ENST00000544971
  gene symbol: TRPV4
  hgvsc: ENST00000544971.1:c.2070G>A
  hgvsp: ENST00000544971.1:c.2070G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5396
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3980
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1688
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2206
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6874
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1156
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6316
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1047
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7257
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2288
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 738
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5064
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2524
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7438
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3007
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3682
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2431
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1656
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Glu797Glu
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: Other
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: QD

12-110222191-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 110222191
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 110222191
    reference: chr 12
allele count: 29
allele frequency: 2.388876074994234e-4
allele num: 121396
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000376480
  ensembl transcript: ENST00000392719
  gene symbol: TRPV4
  hgvsc: ENST00000392719.2:c.2247C>T
  hgvsp: ENST00000392719.2:c.2247C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000442167
  ensembl transcript: ENST00000541794
  gene symbol: TRPV4
  hgvsc: ENST00000541794.1:c.2247C>T
  hgvsp: ENST00000541794.1:c.2247C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000437449
  ensembl transcript: ENST00000538125
  gene symbol: TRPV4
  hgvsc: ENST00000538125.1:c.*771C>T
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000261740
  ensembl transcript: ENST00000261740
  gene symbol: TRPV4
  hgvsc: ENST00000261740.2:c.2388C>T
  hgvsp: ENST00000261740.2:c.2388C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000442738
  ensembl transcript: ENST00000537083
  gene symbol: TRPV4
  hgvsc: ENST00000537083.1:c.2208C>T
  hgvsp: ENST00000537083.1:c.2208C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000444336
  ensembl transcript: ENST00000536838
  gene symbol: TRPV4
  hgvsc: ENST00000536838.1:c.2286C>T
  hgvsp: ENST00000536838.1:c.2286C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000406191
  ensembl transcript: ENST00000418703
  gene symbol: TRPV4
  hgvsc: ENST00000418703.2:c.2388C>T
  hgvsp: ENST00000418703.2:c.2388C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000319003
  ensembl transcript: ENST00000346520
  gene symbol: TRPV4
  hgvsc: ENST00000346520.2:c.2208C>T
  hgvsp: ENST00000346520.2:c.2208C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000443611
  ensembl transcript: ENST00000544971
  gene symbol: TRPV4
  hgvsc: ENST00000544971.1:c.2067C>T
  hgvsp: ENST00000544971.1:c.2067C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3680
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7258
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6316
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5397
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7439
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 736
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1050
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6873
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2284
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2523
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2212
  bin: 9.75e1
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 1156
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1687
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5064
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3009
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3978
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1482
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Asn796Asn
num of homozygotes: 0
population: East Asian
population: South Asian
population: Other
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff

12-110222194-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 110222194
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 110222194
    reference: chr 12
allele count: 1
allele frequency: 8.237503706876667e-6
allele num: 121396
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000261740
  ensembl transcript: ENST00000261740
  gene symbol: TRPV4
  hgvsc: ENST00000261740.2:c.2385C>T
  hgvsp: ENST00000261740.2:c.2385C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000406191
  ensembl transcript: ENST00000418703
  gene symbol: TRPV4
  hgvsc: ENST00000418703.2:c.2385C>T
  hgvsp: ENST00000418703.2:c.2385C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000442738
  ensembl transcript: ENST00000537083
  gene symbol: TRPV4
  hgvsc: ENST00000537083.1:c.2205C>T
  hgvsp: ENST00000537083.1:c.2205C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000443611
  ensembl transcript: ENST00000544971
  gene symbol: TRPV4
  hgvsc: ENST00000544971.1:c.2064C>T
  hgvsp: ENST00000544971.1:c.2064C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000442167
  ensembl transcript: ENST00000541794
  gene symbol: TRPV4
  hgvsc: ENST00000541794.1:c.2244C>T
  hgvsp: ENST00000541794.1:c.2244C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000376480
  ensembl transcript: ENST00000392719
  gene symbol: TRPV4
  hgvsc: ENST00000392719.2:c.2244C>T
  hgvsp: ENST00000392719.2:c.2244C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000437449
  ensembl transcript: ENST00000538125
  gene symbol: TRPV4
  hgvsc: ENST00000538125.1:c.*768C>T
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000319003
  ensembl transcript: ENST00000346520
  gene symbol: TRPV4
  hgvsc: ENST00000346520.2:c.2205C>T
  hgvsp: ENST00000346520.2:c.2205C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000444336
  ensembl transcript: ENST00000536838
  gene symbol: TRPV4
  hgvsc: ENST00000536838.1:c.2283C>T
  hgvsp: ENST00000536838.1:c.2283C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6878
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3011
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7260
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1687
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7443
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3979
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5401
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3682
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1156
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2286
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 735
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2522
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5068
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1046
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6319
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2187
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2429
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1507
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Ile795Ile
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: MQ

12-110222230-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 110222230
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 110222230
    reference: chr 12
allele count: 2
allele frequency: 1.647609318878308e-5
allele num: 121388
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000437449
  ensembl transcript: ENST00000538125
  gene symbol: TRPV4
  hgvsc: ENST00000538125.1:c.*732G>A
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000406191
  ensembl transcript: ENST00000418703
  gene symbol: TRPV4
  hgvsc: ENST00000418703.2:c.2349G>A
  hgvsp: ENST00000418703.2:c.2349G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000376480
  ensembl transcript: ENST00000392719
  gene symbol: TRPV4
  hgvsc: ENST00000392719.2:c.2208G>A
  hgvsp: ENST00000392719.2:c.2208G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000444336
  ensembl transcript: ENST00000536838
  gene symbol: TRPV4
  hgvsc: ENST00000536838.1:c.2247G>A
  hgvsp: ENST00000536838.1:c.2247G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000261740
  ensembl transcript: ENST00000261740
  gene symbol: TRPV4
  hgvsc: ENST00000261740.2:c.2349G>A
  hgvsp: ENST00000261740.2:c.2349G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000319003
  ensembl transcript: ENST00000346520
  gene symbol: TRPV4
  hgvsc: ENST00000346520.2:c.2169G>A
  hgvsp: ENST00000346520.2:c.2169G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000442167
  ensembl transcript: ENST00000541794
  gene symbol: TRPV4
  hgvsc: ENST00000541794.1:c.2208G>A
  hgvsp: ENST00000541794.1:c.2208G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000443611
  ensembl transcript: ENST00000544971
  gene symbol: TRPV4
  hgvsc: ENST00000544971.1:c.2028G>A
  hgvsp: ENST00000544971.1:c.2028G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000442738
  ensembl transcript: ENST00000537083
  gene symbol: TRPV4
  hgvsc: ENST00000537083.1:c.2169G>A
  hgvsp: ENST00000537083.1:c.2169G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6877
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7260
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1027
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2186
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2284
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3005
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1687
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3978
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6319
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7442
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 735
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2522
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1156
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5068
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3683
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5399
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 964
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Val783Val
num of homozygotes: 0
population: South Asian
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
population: Latino
reference allele: C
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

12-110222245-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 110222245
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 110222245
    reference: chr 12
allele count: 1
allele frequency: 8.238996819747227e-6
allele num: 121374
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000376480
  ensembl transcript: ENST00000392719
  gene symbol: TRPV4
  hgvsc: ENST00000392719.2:c.2196-3C>T
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000442738
  ensembl transcript: ENST00000537083
  gene symbol: TRPV4
  hgvsc: ENST00000537083.1:c.2157-3C>T
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000444336
  ensembl transcript: ENST00000536838
  gene symbol: TRPV4
  hgvsc: ENST00000536838.1:c.2235-3C>T
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000437449
  ensembl transcript: ENST00000538125
  gene symbol: TRPV4
  hgvsc: ENST00000538125.1:c.*720-3C>T
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000443611
  ensembl transcript: ENST00000544971
  gene symbol: TRPV4
  hgvsc: ENST00000544971.1:c.2016-3C>T
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000319003
  ensembl transcript: ENST00000346520
  gene symbol: TRPV4
  hgvsc: ENST00000346520.2:c.2157-3C>T
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000406191
  ensembl transcript: ENST00000418703
  gene symbol: TRPV4
  hgvsc: ENST00000418703.2:c.2337-3C>T
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000261740
  ensembl transcript: ENST00000261740
  gene symbol: TRPV4
  hgvsc: ENST00000261740.2:c.2337-3C>T
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000442167
  ensembl transcript: ENST00000541794
  gene symbol: TRPV4
  hgvsc: ENST00000541794.1:c.2196-3C>T
  variant of: http://identifiers.org/hgnc/18083
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5400
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3979
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1686
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6873
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7260
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1032
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1156
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3007
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3683
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7442
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5068
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6319
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 735
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2185
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2522
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2277
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 967
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
hgvs: c.2337-3C>T
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD

12-110222246-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 110222246
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 110222246
    reference: chr 12
allele count: 1
allele frequency: 8.238182327451271e-6
allele num: 121386
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000437449
  ensembl transcript: ENST00000538125
  gene symbol: TRPV4
  hgvsc: ENST00000538125.1:c.*720-4C>A
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000406191
  ensembl transcript: ENST00000418703
  gene symbol: TRPV4
  hgvsc: ENST00000418703.2:c.2337-4C>A
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000444336
  ensembl transcript: ENST00000536838
  gene symbol: TRPV4
  hgvsc: ENST00000536838.1:c.2235-4C>A
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000319003
  ensembl transcript: ENST00000346520
  gene symbol: TRPV4
  hgvsc: ENST00000346520.2:c.2157-4C>A
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000442167
  ensembl transcript: ENST00000541794
  gene symbol: TRPV4
  hgvsc: ENST00000541794.1:c.2196-4C>A
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000443611
  ensembl transcript: ENST00000544971
  gene symbol: TRPV4
  hgvsc: ENST00000544971.1:c.2016-4C>A
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000261740
  ensembl transcript: ENST00000261740
  gene symbol: TRPV4
  hgvsc: ENST00000261740.2:c.2337-4C>A
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000376480
  ensembl transcript: ENST00000392719
  gene symbol: TRPV4
  hgvsc: ENST00000392719.2:c.2196-4C>A
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000442738
  ensembl transcript: ENST00000537083
  gene symbol: TRPV4
  hgvsc: ENST00000537083.1:c.2157-4C>A
  variant of: http://identifiers.org/hgnc/18083
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7260
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1155
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6873
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6319
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1035
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3006
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3682
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5399
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3979
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7442
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5068
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2278
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 735
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1686
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2186
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2522
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
hgvs: c.2337-4C>A
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
population: African
reference allele: G
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff

12-110222248-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 110222248
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 110222248
    reference: chr 12
allele count: 1
allele frequency: 8.238453806989504e-6
allele num: 121382
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000444336
  ensembl transcript: ENST00000536838
  gene symbol: TRPV4
  hgvsc: ENST00000536838.1:c.2235-6T>C
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000261740
  ensembl transcript: ENST00000261740
  gene symbol: TRPV4
  hgvsc: ENST00000261740.2:c.2337-6T>C
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000443611
  ensembl transcript: ENST00000544971
  gene symbol: TRPV4
  hgvsc: ENST00000544971.1:c.2016-6T>C
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000442738
  ensembl transcript: ENST00000537083
  gene symbol: TRPV4
  hgvsc: ENST00000537083.1:c.2157-6T>C
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000376480
  ensembl transcript: ENST00000392719
  gene symbol: TRPV4
  hgvsc: ENST00000392719.2:c.2196-6T>C
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000319003
  ensembl transcript: ENST00000346520
  gene symbol: TRPV4
  hgvsc: ENST00000346520.2:c.2157-6T>C
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000442167
  ensembl transcript: ENST00000541794
  gene symbol: TRPV4
  hgvsc: ENST00000541794.1:c.2196-6T>C
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000437449
  ensembl transcript: ENST00000538125
  gene symbol: TRPV4
  hgvsc: ENST00000538125.1:c.*720-6T>C
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000406191
  ensembl transcript: ENST00000418703
  gene symbol: TRPV4
  hgvsc: ENST00000418703.2:c.2337-6T>C
  variant of: http://identifiers.org/hgnc/18083
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3682
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 735
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1034
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3004
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6319
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7261
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5399
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7442
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2185
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3979
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2275
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1686
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2522
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1155
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5068
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6874
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1474
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1515
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
hgvs: c.2337-6T>C
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: East Asian
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: A
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD

12-110222258-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 110222258
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 110222258
    reference: chr 12
allele count: 32
allele frequency: 2.636305218236641e-4
allele num: 121382
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000442738
  ensembl transcript: ENST00000537083
  gene symbol: TRPV4
  hgvsc: ENST00000537083.1:c.2157-16G>A
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000261740
  ensembl transcript: ENST00000261740
  gene symbol: TRPV4
  hgvsc: ENST00000261740.2:c.2337-16G>A
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000319003
  ensembl transcript: ENST00000346520
  gene symbol: TRPV4
  hgvsc: ENST00000346520.2:c.2157-16G>A
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000443611
  ensembl transcript: ENST00000544971
  gene symbol: TRPV4
  hgvsc: ENST00000544971.1:c.2016-16G>A
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000444336
  ensembl transcript: ENST00000536838
  gene symbol: TRPV4
  hgvsc: ENST00000536838.1:c.2235-16G>A
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000437449
  ensembl transcript: ENST00000538125
  gene symbol: TRPV4
  hgvsc: ENST00000538125.1:c.*720-16G>A
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000376480
  ensembl transcript: ENST00000392719
  gene symbol: TRPV4
  hgvsc: ENST00000392719.2:c.2196-16G>A
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000442167
  ensembl transcript: ENST00000541794
  gene symbol: TRPV4
  hgvsc: ENST00000541794.1:c.2196-16G>A
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000406191
  ensembl transcript: ENST00000418703
  gene symbol: TRPV4
  hgvsc: ENST00000418703.2:c.2337-16G>A
  variant of: http://identifiers.org/hgnc/18083
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3681
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 6315
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2258
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5069
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1157
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1687
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5399
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2992
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2518
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1036
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3979
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7260
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 735
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6869
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2197
  bin: 9.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 7440
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1649
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1512
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1469
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
population: Other
population: East Asian
reference allele: C
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD

http://identifiers.org/exac.variant/12-110222275-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 110222275
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 110222275
    reference: chr 12
allele count: 5
allele frequency: 4.119566292060772e-5
allele num: 121372
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000444336
  ensembl transcript: ENST00000536838
  gene symbol: TRPV4
  hgvsc: ENST00000536838.1:c.2235-33G>T
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000261740
  ensembl transcript: ENST00000261740
  gene symbol: TRPV4
  hgvsc: ENST00000261740.2:c.2337-33G>T
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000437449
  ensembl transcript: ENST00000538125
  gene symbol: TRPV4
  hgvsc: ENST00000538125.1:c.*720-33G>T
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000376480
  ensembl transcript: ENST00000392719
  gene symbol: TRPV4
  hgvsc: ENST00000392719.2:c.2196-33G>T
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000442167
  ensembl transcript: ENST00000541794
  gene symbol: TRPV4
  hgvsc: ENST00000541794.1:c.2196-33G>T
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000406191
  ensembl transcript: ENST00000418703
  gene symbol: TRPV4
  hgvsc: ENST00000418703.2:c.2337-33G>T
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000443611
  ensembl transcript: ENST00000544971
  gene symbol: TRPV4
  hgvsc: ENST00000544971.1:c.2016-33G>T
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000319003
  ensembl transcript: ENST00000346520
  gene symbol: TRPV4
  hgvsc: ENST00000346520.2:c.2157-33G>T
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000442738
  ensembl transcript: ENST00000537083
  gene symbol: TRPV4
  hgvsc: ENST00000537083.1:c.2157-33G>T
  variant of: http://identifiers.org/hgnc/18083
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2172
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3967
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7260
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6870
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3681
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1155
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5068
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7438
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6316
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2964
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1689
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 735
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1015
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2183
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2519
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5388
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2168
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1445
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum

12-110222279-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 110222279
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 110222279
    reference: chr 12
allele count: 1
allele frequency: 8.239675686364985e-6
allele num: 121364
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000443611
  ensembl transcript: ENST00000544971
  gene symbol: TRPV4
  hgvsc: ENST00000544971.1:c.2016-37A>G
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000376480
  ensembl transcript: ENST00000392719
  gene symbol: TRPV4
  hgvsc: ENST00000392719.2:c.2196-37A>G
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000444336
  ensembl transcript: ENST00000536838
  gene symbol: TRPV4
  hgvsc: ENST00000536838.1:c.2235-37A>G
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000442738
  ensembl transcript: ENST00000537083
  gene symbol: TRPV4
  hgvsc: ENST00000537083.1:c.2157-37A>G
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000261740
  ensembl transcript: ENST00000261740
  gene symbol: TRPV4
  hgvsc: ENST00000261740.2:c.2337-37A>G
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000442167
  ensembl transcript: ENST00000541794
  gene symbol: TRPV4
  hgvsc: ENST00000541794.1:c.2196-37A>G
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000437449
  ensembl transcript: ENST00000538125
  gene symbol: TRPV4
  hgvsc: ENST00000538125.1:c.*720-37A>G
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000319003
  ensembl transcript: ENST00000346520
  gene symbol: TRPV4
  hgvsc: ENST00000346520.2:c.2157-37A>G
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000406191
  ensembl transcript: ENST00000418703
  gene symbol: TRPV4
  hgvsc: ENST00000418703.2:c.2337-37A>G
  variant of: http://identifiers.org/hgnc/18083
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6314
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5383
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2183
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7261
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5067
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6868
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7435
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2519
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2109
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1688
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3682
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1010
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 735
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2936
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3967
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1156
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1400
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1647
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2100
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1158
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: T
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP

12-110222286-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 110222286
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 110222286
    reference: chr 12
allele count: 29
allele frequency: 2.389939180168449e-4
allele num: 121342
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000437449
  ensembl transcript: ENST00000538125
  gene symbol: TRPV4
  hgvsc: ENST00000538125.1:c.*720-44G>A
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000444336
  ensembl transcript: ENST00000536838
  gene symbol: TRPV4
  hgvsc: ENST00000536838.1:c.2235-44G>A
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000406191
  ensembl transcript: ENST00000418703
  gene symbol: TRPV4
  hgvsc: ENST00000418703.2:c.2337-44G>A
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000261740
  ensembl transcript: ENST00000261740
  gene symbol: TRPV4
  hgvsc: ENST00000261740.2:c.2337-44G>A
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000376480
  ensembl transcript: ENST00000392719
  gene symbol: TRPV4
  hgvsc: ENST00000392719.2:c.2196-44G>A
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000442167
  ensembl transcript: ENST00000541794
  gene symbol: TRPV4
  hgvsc: ENST00000541794.1:c.2196-44G>A
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000319003
  ensembl transcript: ENST00000346520
  gene symbol: TRPV4
  hgvsc: ENST00000346520.2:c.2157-44G>A
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000442738
  ensembl transcript: ENST00000537083
  gene symbol: TRPV4
  hgvsc: ENST00000537083.1:c.2157-44G>A
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000443611
  ensembl transcript: ENST00000544971
  gene symbol: TRPV4
  hgvsc: ENST00000544971.1:c.2016-44G>A
  variant of: http://identifiers.org/hgnc/18083
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7433
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6312
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1116
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 737
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3949
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5383
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3685
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 7261
  bin: 5.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 5066
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2907
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2519
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1153
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2007
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6864
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1689
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2186
  bin: 9.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 946
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1951
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1642
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1158
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: Other
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
reference allele: C
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP

12-110222287-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 110222287
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 110222287
    reference: chr 12
allele count: 3
allele frequency: 2.472147142197904e-5
allele num: 121352
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000261740
  ensembl transcript: ENST00000261740
  gene symbol: TRPV4
  hgvsc: ENST00000261740.2:c.2337-45C>T
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000442167
  ensembl transcript: ENST00000541794
  gene symbol: TRPV4
  hgvsc: ENST00000541794.1:c.2196-45C>T
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000406191
  ensembl transcript: ENST00000418703
  gene symbol: TRPV4
  hgvsc: ENST00000418703.2:c.2337-45C>T
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000444336
  ensembl transcript: ENST00000536838
  gene symbol: TRPV4
  hgvsc: ENST00000536838.1:c.2235-45C>T
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000376480
  ensembl transcript: ENST00000392719
  gene symbol: TRPV4
  hgvsc: ENST00000392719.2:c.2196-45C>T
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000437449
  ensembl transcript: ENST00000538125
  gene symbol: TRPV4
  hgvsc: ENST00000538125.1:c.*720-45C>T
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000442738
  ensembl transcript: ENST00000537083
  gene symbol: TRPV4
  hgvsc: ENST00000537083.1:c.2157-45C>T
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000443611
  ensembl transcript: ENST00000544971
  gene symbol: TRPV4
  hgvsc: ENST00000544971.1:c.2016-45C>T
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000319003
  ensembl transcript: ENST00000346520
  gene symbol: TRPV4
  hgvsc: ENST00000346520.2:c.2157-45C>T
  variant of: http://identifiers.org/hgnc/18083
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2886
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7260
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1169
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1982
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2521
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7433
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2186
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5386
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6862
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3683
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3945
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6310
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1688
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 735
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5068
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1153
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1372
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 944
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2171
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP

12-110222287-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 110222287
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 110222287
    reference: chr 12
allele count: 1
allele frequency: 8.240490473993011e-6
allele num: 121352
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000261740
  ensembl transcript: ENST00000261740
  gene symbol: TRPV4
  hgvsc: ENST00000261740.2:c.2337-45C>A
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000443611
  ensembl transcript: ENST00000544971
  gene symbol: TRPV4
  hgvsc: ENST00000544971.1:c.2016-45C>A
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000444336
  ensembl transcript: ENST00000536838
  gene symbol: TRPV4
  hgvsc: ENST00000536838.1:c.2235-45C>A
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000319003
  ensembl transcript: ENST00000346520
  gene symbol: TRPV4
  hgvsc: ENST00000346520.2:c.2157-45C>A
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000442738
  ensembl transcript: ENST00000537083
  gene symbol: TRPV4
  hgvsc: ENST00000537083.1:c.2157-45C>A
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000442167
  ensembl transcript: ENST00000541794
  gene symbol: TRPV4
  hgvsc: ENST00000541794.1:c.2196-45C>A
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000376480
  ensembl transcript: ENST00000392719
  gene symbol: TRPV4
  hgvsc: ENST00000392719.2:c.2196-45C>A
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000437449
  ensembl transcript: ENST00000538125
  gene symbol: TRPV4
  hgvsc: ENST00000538125.1:c.*720-45C>A
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000406191
  ensembl transcript: ENST00000418703
  gene symbol: TRPV4
  hgvsc: ENST00000418703.2:c.2337-45C>A
  variant of: http://identifiers.org/hgnc/18083
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5386
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1688
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1982
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6862
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2186
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3945
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2886
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1169
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5068
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6310
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7433
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3683
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2521
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7260
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1153
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 735
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49228
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 198
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2171
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 126
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1632
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
population: Other
population: African
reference allele: G
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum

12-110222294-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 110222294
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 110222294
    reference: chr 12
allele count: 1
allele frequency: 8.240626287597857e-6
allele num: 121350
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000437449
  ensembl transcript: ENST00000538125
  gene symbol: TRPV4
  hgvsc: ENST00000538125.1:c.*720-52T>C
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000444336
  ensembl transcript: ENST00000536838
  gene symbol: TRPV4
  hgvsc: ENST00000536838.1:c.2235-52T>C
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000319003
  ensembl transcript: ENST00000346520
  gene symbol: TRPV4
  hgvsc: ENST00000346520.2:c.2157-52T>C
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000443611
  ensembl transcript: ENST00000544971
  gene symbol: TRPV4
  hgvsc: ENST00000544971.1:c.2016-52T>C
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000442167
  ensembl transcript: ENST00000541794
  gene symbol: TRPV4
  hgvsc: ENST00000541794.1:c.2196-52T>C
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000442738
  ensembl transcript: ENST00000537083
  gene symbol: TRPV4
  hgvsc: ENST00000537083.1:c.2157-52T>C
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000406191
  ensembl transcript: ENST00000418703
  gene symbol: TRPV4
  hgvsc: ENST00000418703.2:c.2337-52T>C
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000376480
  ensembl transcript: ENST00000392719
  gene symbol: TRPV4
  hgvsc: ENST00000392719.2:c.2196-52T>C
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000261740
  ensembl transcript: ENST00000261740
  gene symbol: TRPV4
  hgvsc: ENST00000261740.2:c.2337-52T>C
  variant of: http://identifiers.org/hgnc/18083
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1687
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 735
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3944
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5068
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6309
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1153
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2186
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2800
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1257
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5381
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2522
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1988
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6857
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7260
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3683
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7434
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2176
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 157
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1315
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 945
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: A
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD

12-110224466-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 110224466
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 110224466
    reference: chr 12
allele count: 6
allele frequency: 5.209237714881056e-5
allele num: 115180
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000376480
  ensembl transcript: ENST00000392719
  gene symbol: TRPV4
  hgvsc: ENST00000392719.2:c.2195+49C>A
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000443611
  ensembl transcript: ENST00000544971
  gene symbol: TRPV4
  hgvsc: ENST00000544971.1:c.2015+49C>A
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000444336
  ensembl transcript: ENST00000536838
  gene symbol: TRPV4
  hgvsc: ENST00000536838.1:c.2234+49C>A
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000261740
  ensembl transcript: ENST00000261740
  gene symbol: TRPV4
  hgvsc: ENST00000261740.2:c.2336+49C>A
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000406191
  ensembl transcript: ENST00000418703
  gene symbol: TRPV4
  hgvsc: ENST00000418703.2:c.2336+49C>A
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000442167
  ensembl transcript: ENST00000541794
  gene symbol: TRPV4
  hgvsc: ENST00000541794.1:c.2195+49C>A
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000437449
  ensembl transcript: ENST00000538125
  gene symbol: TRPV4
  hgvsc: ENST00000538125.1:c.*719+49C>A
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000442738
  ensembl transcript: ENST00000537083
  gene symbol: TRPV4
  hgvsc: ENST00000537083.1:c.2156+49C>A
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000319003
  ensembl transcript: ENST00000346520
  gene symbol: TRPV4
  hgvsc: ENST00000346520.2:c.2156+49C>A
  variant of: http://identifiers.org/hgnc/18083
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 927
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13793
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2034
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5160
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8459
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2316
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13536
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3496
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 622
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7456
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1327
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18056
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2409
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1392
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 472
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2231
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2777
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum

12-110224467-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 110224467
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 110224467
    reference: chr 12
allele count: 1
allele frequency: 8.693686644758577e-6
allele num: 115026
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000437449
  ensembl transcript: ENST00000538125
  gene symbol: TRPV4
  hgvsc: ENST00000538125.1:c.*719+48A>G
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000444336
  ensembl transcript: ENST00000536838
  gene symbol: TRPV4
  hgvsc: ENST00000536838.1:c.2234+48A>G
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000319003
  ensembl transcript: ENST00000346520
  gene symbol: TRPV4
  hgvsc: ENST00000346520.2:c.2156+48A>G
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000406191
  ensembl transcript: ENST00000418703
  gene symbol: TRPV4
  hgvsc: ENST00000418703.2:c.2336+48A>G
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000443611
  ensembl transcript: ENST00000544971
  gene symbol: TRPV4
  hgvsc: ENST00000544971.1:c.2015+48A>G
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000376480
  ensembl transcript: ENST00000392719
  gene symbol: TRPV4
  hgvsc: ENST00000392719.2:c.2195+48A>G
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000442738
  ensembl transcript: ENST00000537083
  gene symbol: TRPV4
  hgvsc: ENST00000537083.1:c.2156+48A>G
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000442167
  ensembl transcript: ENST00000541794
  gene symbol: TRPV4
  hgvsc: ENST00000541794.1:c.2195+48A>G
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000261740
  ensembl transcript: ENST00000261740
  gene symbol: TRPV4
  hgvsc: ENST00000261740.2:c.2336+48A>G
  variant of: http://identifiers.org/hgnc/18083
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2305
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1327
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7470
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3501
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 926
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7934
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 623
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13596
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2035
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14261
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5151
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1390
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2493
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3376
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 505
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5310
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 681
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum

12-110224479-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 110224479
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 110224479
    reference: chr 12
allele count: 39
allele frequency: 3.371893966903564e-4
allele num: 115662
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000376480
  ensembl transcript: ENST00000392719
  gene symbol: TRPV4
  hgvsc: ENST00000392719.2:c.2195+36G>C
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000437449
  ensembl transcript: ENST00000538125
  gene symbol: TRPV4
  hgvsc: ENST00000538125.1:c.*719+36G>C
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000444336
  ensembl transcript: ENST00000536838
  gene symbol: TRPV4
  hgvsc: ENST00000536838.1:c.2234+36G>C
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000319003
  ensembl transcript: ENST00000346520
  gene symbol: TRPV4
  hgvsc: ENST00000346520.2:c.2156+36G>C
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000442167
  ensembl transcript: ENST00000541794
  gene symbol: TRPV4
  hgvsc: ENST00000541794.1:c.2195+36G>C
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000261740
  ensembl transcript: ENST00000261740
  gene symbol: TRPV4
  hgvsc: ENST00000261740.2:c.2336+36G>C
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000443611
  ensembl transcript: ENST00000544971
  gene symbol: TRPV4
  hgvsc: ENST00000544971.1:c.2015+36G>C
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000442738
  ensembl transcript: ENST00000537083
  gene symbol: TRPV4
  hgvsc: ENST00000537083.1:c.2156+36G>C
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000406191
  ensembl transcript: ENST00000418703
  gene symbol: TRPV4
  hgvsc: ENST00000418703.2:c.2336+36G>C
  variant of: http://identifiers.org/hgnc/18083
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4264
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14862
  bin: 2.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1329
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 622
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18647
  bin: 2.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 3560
  bin: 3.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 2763
  bin: 1.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 925
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2202
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8008
  bin: 3.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 2047
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 8.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 377
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1395
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1066
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 5352
  bin: 9.75e1
  variant carriers: 39
genotype quality: GenotypeQuality
  all individuals: 2401
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2518
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
population: Other
reference allele: C
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: ClippingRankSum

12-110224479-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 110224479
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 110224479
    reference: chr 12
allele count: 2
allele frequency: 1.729176393283879e-5
allele num: 115662
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000261740
  ensembl transcript: ENST00000261740
  gene symbol: TRPV4
  hgvsc: ENST00000261740.2:c.2336+36G>A
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000442738
  ensembl transcript: ENST00000537083
  gene symbol: TRPV4
  hgvsc: ENST00000537083.1:c.2156+36G>A
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000442167
  ensembl transcript: ENST00000541794
  gene symbol: TRPV4
  hgvsc: ENST00000541794.1:c.2195+36G>A
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000406191
  ensembl transcript: ENST00000418703
  gene symbol: TRPV4
  hgvsc: ENST00000418703.2:c.2336+36G>A
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000437449
  ensembl transcript: ENST00000538125
  gene symbol: TRPV4
  hgvsc: ENST00000538125.1:c.*719+36G>A
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000443611
  ensembl transcript: ENST00000544971
  gene symbol: TRPV4
  hgvsc: ENST00000544971.1:c.2015+36G>A
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000376480
  ensembl transcript: ENST00000392719
  gene symbol: TRPV4
  hgvsc: ENST00000392719.2:c.2195+36G>A
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000319003
  ensembl transcript: ENST00000346520
  gene symbol: TRPV4
  hgvsc: ENST00000346520.2:c.2156+36G>A
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000444336
  ensembl transcript: ENST00000536838
  gene symbol: TRPV4
  hgvsc: ENST00000536838.1:c.2234+36G>A
  variant of: http://identifiers.org/hgnc/18083
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2763
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8008
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2047
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4264
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14862
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18647
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3560
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1329
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 622
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2202
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 925
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 570
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 377
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1791
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5352
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 7889
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: East Asian
population: African
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: QD

12-110224480-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 110224480
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 110224480
    reference: chr 12
allele count: 3
allele frequency: 2.593002350988798e-5
allele num: 115696
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000444336
  ensembl transcript: ENST00000536838
  gene symbol: TRPV4
  hgvsc: ENST00000536838.1:c.2234+35C>T
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000376480
  ensembl transcript: ENST00000392719
  gene symbol: TRPV4
  hgvsc: ENST00000392719.2:c.2195+35C>T
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000442738
  ensembl transcript: ENST00000537083
  gene symbol: TRPV4
  hgvsc: ENST00000537083.1:c.2156+35C>T
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000261740
  ensembl transcript: ENST00000261740
  gene symbol: TRPV4
  hgvsc: ENST00000261740.2:c.2336+35C>T
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000406191
  ensembl transcript: ENST00000418703
  gene symbol: TRPV4
  hgvsc: ENST00000418703.2:c.2336+35C>T
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000319003
  ensembl transcript: ENST00000346520
  gene symbol: TRPV4
  hgvsc: ENST00000346520.2:c.2156+35C>T
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000443611
  ensembl transcript: ENST00000544971
  gene symbol: TRPV4
  hgvsc: ENST00000544971.1:c.2015+35C>T
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000437449
  ensembl transcript: ENST00000538125
  gene symbol: TRPV4
  hgvsc: ENST00000538125.1:c.*719+35C>T
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000442167
  ensembl transcript: ENST00000541794
  gene symbol: TRPV4
  hgvsc: ENST00000541794.1:c.2195+35C>T
  variant of: http://identifiers.org/hgnc/18083
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2285
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 926
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19102
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2053
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15051
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8135
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1331
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 622
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3984
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2178
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3581
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1069
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3352
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2488
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 166
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1717
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
reference allele: G
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: QD
site quality: ReadPosRankSum

12-110224483-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 110224483
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 110224483
    reference: chr 12
allele count: 1
allele frequency: 8.615045315138358e-6
allele num: 116076
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000376480
  ensembl transcript: ENST00000392719
  gene symbol: TRPV4
  hgvsc: ENST00000392719.2:c.2195+32G>C
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000319003
  ensembl transcript: ENST00000346520
  gene symbol: TRPV4
  hgvsc: ENST00000346520.2:c.2156+32G>C
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000406191
  ensembl transcript: ENST00000418703
  gene symbol: TRPV4
  hgvsc: ENST00000418703.2:c.2336+32G>C
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000437449
  ensembl transcript: ENST00000538125
  gene symbol: TRPV4
  hgvsc: ENST00000538125.1:c.*719+32G>C
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000444336
  ensembl transcript: ENST00000536838
  gene symbol: TRPV4
  hgvsc: ENST00000536838.1:c.2234+32G>C
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000442167
  ensembl transcript: ENST00000541794
  gene symbol: TRPV4
  hgvsc: ENST00000541794.1:c.2195+32G>C
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000261740
  ensembl transcript: ENST00000261740
  gene symbol: TRPV4
  hgvsc: ENST00000261740.2:c.2336+32G>C
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000443611
  ensembl transcript: ENST00000544971
  gene symbol: TRPV4
  hgvsc: ENST00000544971.1:c.2015+32G>C
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000442738
  ensembl transcript: ENST00000537083
  gene symbol: TRPV4
  hgvsc: ENST00000537083.1:c.2156+32G>C
  variant of: http://identifiers.org/hgnc/18083
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19903
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8296
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3425
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1330
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15404
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2129
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2050
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3582
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 622
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 925
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1627
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 550
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2812
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1019
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 395
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1233
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5324
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: South Asian
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD

12-110224487-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 110224487
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 110224487
    reference: chr 12
allele count: 1
allele frequency: 8.589736982253604e-6
allele num: 116418
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000376480
  ensembl transcript: ENST00000392719
  gene symbol: TRPV4
  hgvsc: ENST00000392719.2:c.2195+28G>A
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000443611
  ensembl transcript: ENST00000544971
  gene symbol: TRPV4
  hgvsc: ENST00000544971.1:c.2015+28G>A
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000406191
  ensembl transcript: ENST00000418703
  gene symbol: TRPV4
  hgvsc: ENST00000418703.2:c.2336+28G>A
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000444336
  ensembl transcript: ENST00000536838
  gene symbol: TRPV4
  hgvsc: ENST00000536838.1:c.2234+28G>A
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000319003
  ensembl transcript: ENST00000346520
  gene symbol: TRPV4
  hgvsc: ENST00000346520.2:c.2156+28G>A
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000437449
  ensembl transcript: ENST00000538125
  gene symbol: TRPV4
  hgvsc: ENST00000538125.1:c.*719+28G>A
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000261740
  ensembl transcript: ENST00000261740
  gene symbol: TRPV4
  hgvsc: ENST00000261740.2:c.2336+28G>A
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000442738
  ensembl transcript: ENST00000537083
  gene symbol: TRPV4
  hgvsc: ENST00000537083.1:c.2156+28G>A
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000442167
  ensembl transcript: ENST00000541794
  gene symbol: TRPV4
  hgvsc: ENST00000541794.1:c.2195+28G>A
  variant of: http://identifiers.org/hgnc/18083
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15898
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2061
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20560
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1094
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1329
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8469
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2764
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 925
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2012
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3603
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 622
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 875
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 358
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 368
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1409
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 392
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1080
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
population: Other
population: Latino
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

12-110224490-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 110224490
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 110224490
    reference: chr 12
allele count: 2
allele frequency: 1.714324898854831e-5
allele num: 116664
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000443611
  ensembl transcript: ENST00000544971
  gene symbol: TRPV4
  hgvsc: ENST00000544971.1:c.2015+25G>A
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000444336
  ensembl transcript: ENST00000536838
  gene symbol: TRPV4
  hgvsc: ENST00000536838.1:c.2234+25G>A
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000406191
  ensembl transcript: ENST00000418703
  gene symbol: TRPV4
  hgvsc: ENST00000418703.2:c.2336+25G>A
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000442167
  ensembl transcript: ENST00000541794
  gene symbol: TRPV4
  hgvsc: ENST00000541794.1:c.2195+25G>A
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000319003
  ensembl transcript: ENST00000346520
  gene symbol: TRPV4
  hgvsc: ENST00000346520.2:c.2156+25G>A
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000261740
  ensembl transcript: ENST00000261740
  gene symbol: TRPV4
  hgvsc: ENST00000261740.2:c.2336+25G>A
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000442738
  ensembl transcript: ENST00000537083
  gene symbol: TRPV4
  hgvsc: ENST00000537083.1:c.2156+25G>A
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000376480
  ensembl transcript: ENST00000392719
  gene symbol: TRPV4
  hgvsc: ENST00000392719.2:c.2195+25G>A
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000437449
  ensembl transcript: ENST00000538125
  gene symbol: TRPV4
  hgvsc: ENST00000538125.1:c.*719+25G>A
  variant of: http://identifiers.org/hgnc/18083
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 925
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16111
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21030
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1915
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2060
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8539
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1331
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 844
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2371
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 622
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3611
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2865
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29486
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 298
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2455
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 979
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP

12-110224493-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 110224493
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 110224493
    reference: chr 12
allele count: 2
allele frequency: 1.710893257369673e-5
allele num: 116898
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000442167
  ensembl transcript: ENST00000541794
  gene symbol: TRPV4
  hgvsc: ENST00000541794.1:c.2195+22C>A
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000406191
  ensembl transcript: ENST00000418703
  gene symbol: TRPV4
  hgvsc: ENST00000418703.2:c.2336+22C>A
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000376480
  ensembl transcript: ENST00000392719
  gene symbol: TRPV4
  hgvsc: ENST00000392719.2:c.2195+22C>A
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000442738
  ensembl transcript: ENST00000537083
  gene symbol: TRPV4
  hgvsc: ENST00000537083.1:c.2156+22C>A
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000319003
  ensembl transcript: ENST00000346520
  gene symbol: TRPV4
  hgvsc: ENST00000346520.2:c.2156+22C>A
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000437449
  ensembl transcript: ENST00000538125
  gene symbol: TRPV4
  hgvsc: ENST00000538125.1:c.*719+22C>A
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000443611
  ensembl transcript: ENST00000544971
  gene symbol: TRPV4
  hgvsc: ENST00000544971.1:c.2015+22C>A
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000444336
  ensembl transcript: ENST00000536838
  gene symbol: TRPV4
  hgvsc: ENST00000536838.1:c.2234+22C>A
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000261740
  ensembl transcript: ENST00000261740
  gene symbol: TRPV4
  hgvsc: ENST00000261740.2:c.2336+22C>A
  variant of: http://identifiers.org/hgnc/18083
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 622
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2066
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1330
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2077
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8592
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1833
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3622
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21291
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16358
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 925
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 234
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2078
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8449
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2460
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 323
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
population: Latino
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: DP
site quality: QD
site quality: BaseQRankSum

12-110224497-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 110224497
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 110224497
    reference: chr 12
allele count: 1
allele frequency: 8.529075618784437e-6
allele num: 117246
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000442738
  ensembl transcript: ENST00000537083
  gene symbol: TRPV4
  hgvsc: ENST00000537083.1:c.2156+18G>C
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000443611
  ensembl transcript: ENST00000544971
  gene symbol: TRPV4
  hgvsc: ENST00000544971.1:c.2015+18G>C
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000261740
  ensembl transcript: ENST00000261740
  gene symbol: TRPV4
  hgvsc: ENST00000261740.2:c.2336+18G>C
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000444336
  ensembl transcript: ENST00000536838
  gene symbol: TRPV4
  hgvsc: ENST00000536838.1:c.2234+18G>C
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000376480
  ensembl transcript: ENST00000392719
  gene symbol: TRPV4
  hgvsc: ENST00000392719.2:c.2195+18G>C
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000319003
  ensembl transcript: ENST00000346520
  gene symbol: TRPV4
  hgvsc: ENST00000346520.2:c.2156+18G>C
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000406191
  ensembl transcript: ENST00000418703
  gene symbol: TRPV4
  hgvsc: ENST00000418703.2:c.2336+18G>C
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000437449
  ensembl transcript: ENST00000538125
  gene symbol: TRPV4
  hgvsc: ENST00000538125.1:c.*719+18G>C
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000442167
  ensembl transcript: ENST00000541794
  gene symbol: TRPV4
  hgvsc: ENST00000541794.1:c.2195+18G>C
  variant of: http://identifiers.org/hgnc/18083
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 606
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1331
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16787
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 622
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1693
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8686
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2065
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1777
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 925
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3623
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21302
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8599
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 170
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1406
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2925
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 229
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: ReadPosRankSum

12-110224505-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 110224505
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 110224505
    reference: chr 12
allele count: 1
allele frequency: 8.467830711128423e-6
allele num: 118094
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000437449
  ensembl transcript: ENST00000538125
  gene symbol: TRPV4
  hgvsc: ENST00000538125.1:c.*719+10G>A
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000442738
  ensembl transcript: ENST00000537083
  gene symbol: TRPV4
  hgvsc: ENST00000537083.1:c.2156+10G>A
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000443611
  ensembl transcript: ENST00000544971
  gene symbol: TRPV4
  hgvsc: ENST00000544971.1:c.2015+10G>A
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000442167
  ensembl transcript: ENST00000541794
  gene symbol: TRPV4
  hgvsc: ENST00000541794.1:c.2195+10G>A
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000376480
  ensembl transcript: ENST00000392719
  gene symbol: TRPV4
  hgvsc: ENST00000392719.2:c.2195+10G>A
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000319003
  ensembl transcript: ENST00000346520
  gene symbol: TRPV4
  hgvsc: ENST00000346520.2:c.2156+10G>A
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000444336
  ensembl transcript: ENST00000536838
  gene symbol: TRPV4
  hgvsc: ENST00000536838.1:c.2234+10G>A
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000406191
  ensembl transcript: ENST00000418703
  gene symbol: TRPV4
  hgvsc: ENST00000418703.2:c.2336+10G>A
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000261740
  ensembl transcript: ENST00000261740
  gene symbol: TRPV4
  hgvsc: ENST00000261740.2:c.2336+10G>A
  variant of: http://identifiers.org/hgnc/18083
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17419
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1368
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1329
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3640
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 925
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1197
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21680
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2062
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 622
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8817
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2469
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5337
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 8768
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 243
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1562
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: European (Finnish)
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum

12-110224514-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 110224514
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 110224514
    reference: chr 12
allele count: 1
allele frequency: 8.423038695439767e-6
allele num: 118722
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000442167
  ensembl transcript: ENST00000541794
  gene symbol: TRPV4
  hgvsc: ENST00000541794.1:c.2195+1G>A
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000444336
  ensembl transcript: ENST00000536838
  gene symbol: TRPV4
  hgvsc: ENST00000536838.1:c.2234+1G>A
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: true
  consequence: splice_donor_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000406191
  ensembl transcript: ENST00000418703
  gene symbol: TRPV4
  hgvsc: ENST00000418703.2:c.2336+1G>A
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000443611
  ensembl transcript: ENST00000544971
  gene symbol: TRPV4
  hgvsc: ENST00000544971.1:c.2015+1G>A
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000261740
  ensembl transcript: ENST00000261740
  gene symbol: TRPV4
  hgvsc: ENST00000261740.2:c.2336+1G>A
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000376480
  ensembl transcript: ENST00000392719
  gene symbol: TRPV4
  hgvsc: ENST00000392719.2:c.2195+1G>A
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000319003
  ensembl transcript: ENST00000346520
  gene symbol: TRPV4
  hgvsc: ENST00000346520.2:c.2156+1G>A
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000437449
  ensembl transcript: ENST00000538125
  gene symbol: TRPV4
  hgvsc: ENST00000538125.1:c.*719+1G>A
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000442738
  ensembl transcript: ENST00000537083
  gene symbol: TRPV4
  hgvsc: ENST00000537083.1:c.2156+1G>A
  variant of: http://identifiers.org/hgnc/18083
canonical: true
consequence: splice donor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 796
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1128
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 925
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22097
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8881
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17752
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2060
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3640
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1332
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 622
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1272
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 140
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1407
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 281
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2472
  bin: 8.25e1
  variant carriers: 0
hgvs: c.2336+1G>A
num of homozygotes: 0
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: C
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: MQRankSum

12-110224517-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 110224517
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 110224517
    reference: chr 12
allele count: 1
allele frequency: 8.4088730428348e-6
allele num: 118922
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000443611
  ensembl transcript: ENST00000544971
  gene symbol: TRPV4
  hgvsc: ENST00000544971.1:c.2013C>T
  hgvsp: ENST00000544971.1:c.2013C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000319003
  ensembl transcript: ENST00000346520
  gene symbol: TRPV4
  hgvsc: ENST00000346520.2:c.2154C>T
  hgvsp: ENST00000346520.2:c.2154C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000444336
  ensembl transcript: ENST00000536838
  gene symbol: TRPV4
  hgvsc: ENST00000536838.1:c.2232C>T
  hgvsp: ENST00000536838.1:c.2232C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000437449
  ensembl transcript: ENST00000538125
  gene symbol: TRPV4
  hgvsc: ENST00000538125.1:c.*717C>T
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000442738
  ensembl transcript: ENST00000537083
  gene symbol: TRPV4
  hgvsc: ENST00000537083.1:c.2154C>T
  hgvsp: ENST00000537083.1:c.2154C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000406191
  ensembl transcript: ENST00000418703
  gene symbol: TRPV4
  hgvsc: ENST00000418703.2:c.2334C>T
  hgvsp: ENST00000418703.2:c.2334C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000442167
  ensembl transcript: ENST00000541794
  gene symbol: TRPV4
  hgvsc: ENST00000541794.1:c.2193C>T
  hgvsp: ENST00000541794.1:c.2193C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000376480
  ensembl transcript: ENST00000392719
  gene symbol: TRPV4
  hgvsc: ENST00000392719.2:c.2193C>T
  hgvsp: ENST00000392719.2:c.2193C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000261740
  ensembl transcript: ENST00000261740
  gene symbol: TRPV4
  hgvsc: ENST00000261740.2:c.2334C>T
  hgvsp: ENST00000261740.2:c.2334C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 22136
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1056
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8917
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 925
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3640
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17877
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 622
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2065
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1329
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3531
  bin: 7.75e1
  variant carriers: 0
hgvs: c.2334C>T
num of homozygotes: 0
population: Other
population: South Asian
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum

12-110224526-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 110224526
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 110224526
    reference: chr 12
allele count: 1
allele frequency: 8.390951198227832e-6
allele num: 119176
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000437449
  ensembl transcript: ENST00000538125
  gene symbol: TRPV4
  hgvsc: ENST00000538125.1:c.*708G>A
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000406191
  ensembl transcript: ENST00000418703
  gene symbol: TRPV4
  hgvsc: ENST00000418703.2:c.2325G>A
  hgvsp: ENST00000418703.2:c.2325G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000443611
  ensembl transcript: ENST00000544971
  gene symbol: TRPV4
  hgvsc: ENST00000544971.1:c.2004G>A
  hgvsp: ENST00000544971.1:c.2004G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000442738
  ensembl transcript: ENST00000537083
  gene symbol: TRPV4
  hgvsc: ENST00000537083.1:c.2145G>A
  hgvsp: ENST00000537083.1:c.2145G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000319003
  ensembl transcript: ENST00000346520
  gene symbol: TRPV4
  hgvsc: ENST00000346520.2:c.2145G>A
  hgvsp: ENST00000346520.2:c.2145G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000444336
  ensembl transcript: ENST00000536838
  gene symbol: TRPV4
  hgvsc: ENST00000536838.1:c.2223G>A
  hgvsp: ENST00000536838.1:c.2223G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000261740
  ensembl transcript: ENST00000261740
  gene symbol: TRPV4
  hgvsc: ENST00000261740.2:c.2325G>A
  hgvsp: ENST00000261740.2:c.2325G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000442167
  ensembl transcript: ENST00000541794
  gene symbol: TRPV4
  hgvsc: ENST00000541794.1:c.2184G>A
  hgvsp: ENST00000541794.1:c.2184G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000376480
  ensembl transcript: ENST00000392719
  gene symbol: TRPV4
  hgvsc: ENST00000392719.2:c.2184G>A
  hgvsp: ENST00000392719.2:c.2184G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 951
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18130
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1329
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 622
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22111
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8952
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 925
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2064
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3644
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 151
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1407
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Arg775Arg
num of homozygotes: 0
population: Latino
population: Other
population: South Asian
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: DP

12-110224530-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 110224530
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 110224530
    reference: chr 12
allele count: 1
allele frequency: 8.38321345338095e-6
allele num: 119286
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000319003
  ensembl transcript: ENST00000346520
  gene symbol: TRPV4
  hgvsc: ENST00000346520.2:c.2141G>A
  hgvsp: ENSP00000319003.2:p.Arg714His
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000444336
  ensembl transcript: ENST00000536838
  gene symbol: TRPV4
  hgvsc: ENST00000536838.1:c.2219G>A
  hgvsp: ENSP00000444336.1:p.Arg740His
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000443611
  ensembl transcript: ENST00000544971
  gene symbol: TRPV4
  hgvsc: ENST00000544971.1:c.2000G>A
  hgvsp: ENSP00000443611.1:p.Arg667His
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000442167
  ensembl transcript: ENST00000541794
  gene symbol: TRPV4
  hgvsc: ENST00000541794.1:c.2180G>A
  hgvsp: ENSP00000442167.1:p.Arg727His
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000406191
  ensembl transcript: ENST00000418703
  gene symbol: TRPV4
  hgvsc: ENST00000418703.2:c.2321G>A
  hgvsp: ENSP00000406191.2:p.Arg774His
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000437449
  ensembl transcript: ENST00000538125
  gene symbol: TRPV4
  hgvsc: ENST00000538125.1:c.*704G>A
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000376480
  ensembl transcript: ENST00000392719
  gene symbol: TRPV4
  hgvsc: ENST00000392719.2:c.2180G>A
  hgvsp: ENSP00000376480.2:p.Arg727His
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000261740
  ensembl transcript: ENST00000261740
  gene symbol: TRPV4
  hgvsc: ENST00000261740.2:c.2321G>A
  hgvsp: ENSP00000261740.2:p.Arg774His
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000442738
  ensembl transcript: ENST00000537083
  gene symbol: TRPV4
  hgvsc: ENST00000537083.1:c.2141G>A
  hgvsp: ENSP00000442738.1:p.Arg714His
  variant of: http://identifiers.org/hgnc/18083
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2064
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 896
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8984
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 622
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 925
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3654
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18228
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22081
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1330
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3005
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3543
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32696
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Arg774His
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
population: East Asian
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD

12-110224531-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 110224531
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 110224531
    reference: chr 12
allele count: 8
allele frequency: 6.70263748785147e-5
allele num: 119356
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000261740
  ensembl transcript: ENST00000261740
  gene symbol: TRPV4
  hgvsc: ENST00000261740.2:c.2320C>T
  hgvsp: ENSP00000261740.2:p.Arg774Cys
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000376480
  ensembl transcript: ENST00000392719
  gene symbol: TRPV4
  hgvsc: ENST00000392719.2:c.2179C>T
  hgvsp: ENSP00000376480.2:p.Arg727Cys
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000444336
  ensembl transcript: ENST00000536838
  gene symbol: TRPV4
  hgvsc: ENST00000536838.1:c.2218C>T
  hgvsp: ENSP00000444336.1:p.Arg740Cys
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000443611
  ensembl transcript: ENST00000544971
  gene symbol: TRPV4
  hgvsc: ENST00000544971.1:c.1999C>T
  hgvsp: ENSP00000443611.1:p.Arg667Cys
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000442738
  ensembl transcript: ENST00000537083
  gene symbol: TRPV4
  hgvsc: ENST00000537083.1:c.2140C>T
  hgvsp: ENSP00000442738.1:p.Arg714Cys
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000406191
  ensembl transcript: ENST00000418703
  gene symbol: TRPV4
  hgvsc: ENST00000418703.2:c.2320C>T
  hgvsp: ENSP00000406191.2:p.Arg774Cys
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000442167
  ensembl transcript: ENST00000541794
  gene symbol: TRPV4
  hgvsc: ENST00000541794.1:c.2179C>T
  hgvsp: ENSP00000442167.1:p.Arg727Cys
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000437449
  ensembl transcript: ENST00000538125
  gene symbol: TRPV4
  hgvsc: ENST00000538125.1:c.*703C>T
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000319003
  ensembl transcript: ENST00000346520
  gene symbol: TRPV4
  hgvsc: ENST00000346520.2:c.2140C>T
  hgvsp: ENSP00000319003.2:p.Arg714Cys
  variant of: http://identifiers.org/hgnc/18083
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 925
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 18300
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 865
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22068
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 501
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3651
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9006
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2070
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 623
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1332
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 157
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3544
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 977
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32740
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Arg774Cys
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
population: Latino
population: European (Finnish)
population: East Asian
reference allele: G
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: MQ

12-110224544-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 110224544
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 110224544
    reference: chr 12
allele count: 30
allele frequency: 2.507229177461681e-4
allele num: 119654
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000437449
  ensembl transcript: ENST00000538125
  gene symbol: TRPV4
  hgvsc: ENST00000538125.1:c.*690C>T
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000319003
  ensembl transcript: ENST00000346520
  gene symbol: TRPV4
  hgvsc: ENST00000346520.2:c.2127C>T
  hgvsp: ENST00000346520.2:c.2127C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000261740
  ensembl transcript: ENST00000261740
  gene symbol: TRPV4
  hgvsc: ENST00000261740.2:c.2307C>T
  hgvsp: ENST00000261740.2:c.2307C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000444336
  ensembl transcript: ENST00000536838
  gene symbol: TRPV4
  hgvsc: ENST00000536838.1:c.2205C>T
  hgvsp: ENST00000536838.1:c.2205C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000376480
  ensembl transcript: ENST00000392719
  gene symbol: TRPV4
  hgvsc: ENST00000392719.2:c.2166C>T
  hgvsp: ENST00000392719.2:c.2166C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000406191
  ensembl transcript: ENST00000418703
  gene symbol: TRPV4
  hgvsc: ENST00000418703.2:c.2307C>T
  hgvsp: ENST00000418703.2:c.2307C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000443611
  ensembl transcript: ENST00000544971
  gene symbol: TRPV4
  hgvsc: ENST00000544971.1:c.1986C>T
  hgvsp: ENST00000544971.1:c.1986C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000442167
  ensembl transcript: ENST00000541794
  gene symbol: TRPV4
  hgvsc: ENST00000541794.1:c.2166C>T
  hgvsp: ENST00000541794.1:c.2166C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000442738
  ensembl transcript: ENST00000537083
  gene symbol: TRPV4
  hgvsc: ENST00000537083.1:c.2127C>T
  hgvsp: ENST00000537083.1:c.2127C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3658
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 5.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1331
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 740
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22127
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18535
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 926
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2070
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 9038
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 6.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 138
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 135
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Asp769Asp
num of homozygotes: 1
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
population: Other
population: Latino
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: DP

12-110224547-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 110224547
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 110224547
    reference: chr 12
allele count: 55
allele frequency: 4.594743613306377e-4
allele num: 119702
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000261740
  ensembl transcript: ENST00000261740
  gene symbol: TRPV4
  hgvsc: ENST00000261740.2:c.2304G>C
  hgvsp: ENST00000261740.2:c.2304G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000443611
  ensembl transcript: ENST00000544971
  gene symbol: TRPV4
  hgvsc: ENST00000544971.1:c.1983G>C
  hgvsp: ENST00000544971.1:c.1983G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000442167
  ensembl transcript: ENST00000541794
  gene symbol: TRPV4
  hgvsc: ENST00000541794.1:c.2163G>C
  hgvsp: ENST00000541794.1:c.2163G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000406191
  ensembl transcript: ENST00000418703
  gene symbol: TRPV4
  hgvsc: ENST00000418703.2:c.2304G>C
  hgvsp: ENST00000418703.2:c.2304G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000376480
  ensembl transcript: ENST00000392719
  gene symbol: TRPV4
  hgvsc: ENST00000392719.2:c.2163G>C
  hgvsp: ENST00000392719.2:c.2163G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000444336
  ensembl transcript: ENST00000536838
  gene symbol: TRPV4
  hgvsc: ENST00000536838.1:c.2202G>C
  hgvsp: ENST00000536838.1:c.2202G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000319003
  ensembl transcript: ENST00000346520
  gene symbol: TRPV4
  hgvsc: ENST00000346520.2:c.2124G>C
  hgvsp: ENST00000346520.2:c.2124G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000442738
  ensembl transcript: ENST00000537083
  gene symbol: TRPV4
  hgvsc: ENST00000537083.1:c.2124G>C
  hgvsp: ENST00000537083.1:c.2124G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000437449
  ensembl transcript: ENST00000538125
  gene symbol: TRPV4
  hgvsc: ENST00000538125.1:c.*687G>C
  variant of: http://identifiers.org/hgnc/18083
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 6.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 18575
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 723
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 933
  bin: 5.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 1339
  bin: 4.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 22071
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3671
  bin: 3.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9043
  bin: 3.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2071
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 5.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 3545
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3028
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33082
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Ser768Ser
num of homozygotes: 0
population: African
population: South Asian
population: Other
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum

12-110224547-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 110224547
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 110224547
    reference: chr 12
allele count: 4
allele frequency: 3.341631718768275e-5
allele num: 119702
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000444336
  ensembl transcript: ENST00000536838
  gene symbol: TRPV4
  hgvsc: ENST00000536838.1:c.2202G>A
  hgvsp: ENST00000536838.1:c.2202G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000261740
  ensembl transcript: ENST00000261740
  gene symbol: TRPV4
  hgvsc: ENST00000261740.2:c.2304G>A
  hgvsp: ENST00000261740.2:c.2304G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000442738
  ensembl transcript: ENST00000537083
  gene symbol: TRPV4
  hgvsc: ENST00000537083.1:c.2124G>A
  hgvsp: ENST00000537083.1:c.2124G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000437449
  ensembl transcript: ENST00000538125
  gene symbol: TRPV4
  hgvsc: ENST00000538125.1:c.*687G>A
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000442167
  ensembl transcript: ENST00000541794
  gene symbol: TRPV4
  hgvsc: ENST00000541794.1:c.2163G>A
  hgvsp: ENST00000541794.1:c.2163G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000319003
  ensembl transcript: ENST00000346520
  gene symbol: TRPV4
  hgvsc: ENST00000346520.2:c.2124G>A
  hgvsp: ENST00000346520.2:c.2124G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000376480
  ensembl transcript: ENST00000392719
  gene symbol: TRPV4
  hgvsc: ENST00000392719.2:c.2163G>A
  hgvsp: ENST00000392719.2:c.2163G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000406191
  ensembl transcript: ENST00000418703
  gene symbol: TRPV4
  hgvsc: ENST00000418703.2:c.2304G>A
  hgvsp: ENST00000418703.2:c.2304G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000443611
  ensembl transcript: ENST00000544971
  gene symbol: TRPV4
  hgvsc: ENST00000544971.1:c.1983G>A
  hgvsp: ENST00000544971.1:c.1983G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 933
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 9043
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1339
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18575
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 723
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2071
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22071
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3671
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9022
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 820
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Ser768Ser
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff

12-110224548-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 110224548
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 110224548
    reference: chr 12
allele count: 1
allele frequency: 8.351288603831571e-6
allele num: 119742
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000376480
  ensembl transcript: ENST00000392719
  gene symbol: TRPV4
  hgvsc: ENST00000392719.2:c.2162C>T
  hgvsp: ENSP00000376480.2:p.Ser721Leu
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000444336
  ensembl transcript: ENST00000536838
  gene symbol: TRPV4
  hgvsc: ENST00000536838.1:c.2201C>T
  hgvsp: ENSP00000444336.1:p.Ser734Leu
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000443611
  ensembl transcript: ENST00000544971
  gene symbol: TRPV4
  hgvsc: ENST00000544971.1:c.1982C>T
  hgvsp: ENSP00000443611.1:p.Ser661Leu
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000442738
  ensembl transcript: ENST00000537083
  gene symbol: TRPV4
  hgvsc: ENST00000537083.1:c.2123C>T
  hgvsp: ENSP00000442738.1:p.Ser708Leu
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000261740
  ensembl transcript: ENST00000261740
  gene symbol: TRPV4
  hgvsc: ENST00000261740.2:c.2303C>T
  hgvsp: ENSP00000261740.2:p.Ser768Leu
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000442167
  ensembl transcript: ENST00000541794
  gene symbol: TRPV4
  hgvsc: ENST00000541794.1:c.2162C>T
  hgvsp: ENSP00000442167.1:p.Ser721Leu
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000319003
  ensembl transcript: ENST00000346520
  gene symbol: TRPV4
  hgvsc: ENST00000346520.2:c.2123C>T
  hgvsp: ENSP00000319003.2:p.Ser708Leu
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000437449
  ensembl transcript: ENST00000538125
  gene symbol: TRPV4
  hgvsc: ENST00000538125.1:c.*686C>T
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000406191
  ensembl transcript: ENST00000418703
  gene symbol: TRPV4
  hgvsc: ENST00000418703.2:c.2303C>T
  hgvsp: ENSP00000406191.2:p.Ser768Leu
  variant of: http://identifiers.org/hgnc/18083
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 924
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3671
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2068
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1334
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22096
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9058
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 622
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18625
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33205
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Ser768Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Other
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
reference allele: G
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD

12-110224555-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 110224555
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 110224555
    reference: chr 12
allele count: 1
allele frequency: 8.345155637152633e-6
allele num: 119830
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000437449
  ensembl transcript: ENST00000538125
  gene symbol: TRPV4
  hgvsc: ENST00000538125.1:c.*679A>C
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000442167
  ensembl transcript: ENST00000541794
  gene symbol: TRPV4
  hgvsc: ENST00000541794.1:c.2155A>C
  hgvsp: ENSP00000442167.1:p.Lys719Gln
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000442738
  ensembl transcript: ENST00000537083
  gene symbol: TRPV4
  hgvsc: ENST00000537083.1:c.2116A>C
  hgvsp: ENSP00000442738.1:p.Lys706Gln
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000444336
  ensembl transcript: ENST00000536838
  gene symbol: TRPV4
  hgvsc: ENST00000536838.1:c.2194A>C
  hgvsp: ENSP00000444336.1:p.Lys732Gln
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000319003
  ensembl transcript: ENST00000346520
  gene symbol: TRPV4
  hgvsc: ENST00000346520.2:c.2116A>C
  hgvsp: ENSP00000319003.2:p.Lys706Gln
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000406191
  ensembl transcript: ENST00000418703
  gene symbol: TRPV4
  hgvsc: ENST00000418703.2:c.2296A>C
  hgvsp: ENSP00000406191.2:p.Lys766Gln
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000376480
  ensembl transcript: ENST00000392719
  gene symbol: TRPV4
  hgvsc: ENST00000392719.2:c.2155A>C
  hgvsp: ENSP00000376480.2:p.Lys719Gln
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000261740
  ensembl transcript: ENST00000261740
  gene symbol: TRPV4
  hgvsc: ENST00000261740.2:c.2296A>C
  hgvsp: ENSP00000261740.2:p.Lys766Gln
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000443611
  ensembl transcript: ENST00000544971
  gene symbol: TRPV4
  hgvsc: ENST00000544971.1:c.1975A>C
  hgvsp: ENSP00000443611.1:p.Lys659Gln
  variant of: http://identifiers.org/hgnc/18083
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 924
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 681
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18681
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3670
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22092
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9048
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2068
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1334
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 622
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3035
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 775
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1079
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Lys766Gln
num of homozygotes: 0
population: South Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD

12-110224556-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 110224556
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 110224556
    reference: chr 12
allele count: 2
allele frequency: 1.669031127430527e-5
allele num: 119830
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000442167
  ensembl transcript: ENST00000541794
  gene symbol: TRPV4
  hgvsc: ENST00000541794.1:c.2154C>G
  hgvsp: ENST00000541794.1:c.2154C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000444336
  ensembl transcript: ENST00000536838
  gene symbol: TRPV4
  hgvsc: ENST00000536838.1:c.2193C>G
  hgvsp: ENST00000536838.1:c.2193C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000443611
  ensembl transcript: ENST00000544971
  gene symbol: TRPV4
  hgvsc: ENST00000544971.1:c.1974C>G
  hgvsp: ENST00000544971.1:c.1974C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000406191
  ensembl transcript: ENST00000418703
  gene symbol: TRPV4
  hgvsc: ENST00000418703.2:c.2295C>G
  hgvsp: ENST00000418703.2:c.2295C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000437449
  ensembl transcript: ENST00000538125
  gene symbol: TRPV4
  hgvsc: ENST00000538125.1:c.*678C>G
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000376480
  ensembl transcript: ENST00000392719
  gene symbol: TRPV4
  hgvsc: ENST00000392719.2:c.2154C>G
  hgvsp: ENST00000392719.2:c.2154C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000261740
  ensembl transcript: ENST00000261740
  gene symbol: TRPV4
  hgvsc: ENST00000261740.2:c.2295C>G
  hgvsp: ENST00000261740.2:c.2295C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000319003
  ensembl transcript: ENST00000346520
  gene symbol: TRPV4
  hgvsc: ENST00000346520.2:c.2115C>G
  hgvsp: ENST00000346520.2:c.2115C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000442738
  ensembl transcript: ENST00000537083
  gene symbol: TRPV4
  hgvsc: ENST00000537083.1:c.2115C>G
  hgvsp: ENST00000537083.1:c.2115C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 924
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 687
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22079
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2070
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9060
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1333
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3670
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 621
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18686
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 9066
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Gly765Gly
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
population: European (Finnish)
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP

12-110224562-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 110224562
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 110224562
    reference: chr 12
allele count: 62
allele frequency: 5.171838505171839e-4
allele num: 119880
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000444336
  ensembl transcript: ENST00000536838
  gene symbol: TRPV4
  hgvsc: ENST00000536838.1:c.2187C>T
  hgvsp: ENST00000536838.1:c.2187C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000437449
  ensembl transcript: ENST00000538125
  gene symbol: TRPV4
  hgvsc: ENST00000538125.1:c.*672C>T
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000376480
  ensembl transcript: ENST00000392719
  gene symbol: TRPV4
  hgvsc: ENST00000392719.2:c.2148C>T
  hgvsp: ENST00000392719.2:c.2148C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000261740
  ensembl transcript: ENST00000261740
  gene symbol: TRPV4
  hgvsc: ENST00000261740.2:c.2289C>T
  hgvsp: ENST00000261740.2:c.2289C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000319003
  ensembl transcript: ENST00000346520
  gene symbol: TRPV4
  hgvsc: ENST00000346520.2:c.2109C>T
  hgvsp: ENST00000346520.2:c.2109C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000442738
  ensembl transcript: ENST00000537083
  gene symbol: TRPV4
  hgvsc: ENST00000537083.1:c.2109C>T
  hgvsp: ENST00000537083.1:c.2109C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000406191
  ensembl transcript: ENST00000418703
  gene symbol: TRPV4
  hgvsc: ENST00000418703.2:c.2289C>T
  hgvsp: ENST00000418703.2:c.2289C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000443611
  ensembl transcript: ENST00000544971
  gene symbol: TRPV4
  hgvsc: ENST00000544971.1:c.1968C>T
  hgvsp: ENST00000544971.1:c.1968C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000442167
  ensembl transcript: ENST00000541794
  gene symbol: TRPV4
  hgvsc: ENST00000541794.1:c.2148C>T
  hgvsp: ENST00000541794.1:c.2148C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 3670
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 21978
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 18756
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 5.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 9079
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 6.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 929
  bin: 5.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2074
  bin: 4.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 655
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1346
  bin: 4.75e1
  variant carriers: 11
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 115
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Thr763Thr
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: VQSLOD

12-110224578-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 110224578
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 110224578
    reference: chr 12
allele count: 1
allele frequency: 8.338614455822021e-6
allele num: 119924
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000444336
  ensembl transcript: ENST00000536838
  gene symbol: TRPV4
  hgvsc: ENST00000536838.1:c.2171C>A
  hgvsp: ENSP00000444336.1:p.Ser724Tyr
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000442738
  ensembl transcript: ENST00000537083
  gene symbol: TRPV4
  hgvsc: ENST00000537083.1:c.2093C>A
  hgvsp: ENSP00000442738.1:p.Ser698Tyr
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000406191
  ensembl transcript: ENST00000418703
  gene symbol: TRPV4
  hgvsc: ENST00000418703.2:c.2273C>A
  hgvsp: ENSP00000406191.2:p.Ser758Tyr
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000261740
  ensembl transcript: ENST00000261740
  gene symbol: TRPV4
  hgvsc: ENST00000261740.2:c.2273C>A
  hgvsp: ENSP00000261740.2:p.Ser758Tyr
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000437449
  ensembl transcript: ENST00000538125
  gene symbol: TRPV4
  hgvsc: ENST00000538125.1:c.*656C>A
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000376480
  ensembl transcript: ENST00000392719
  gene symbol: TRPV4
  hgvsc: ENST00000392719.2:c.2132C>A
  hgvsp: ENSP00000376480.2:p.Ser711Tyr
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000319003
  ensembl transcript: ENST00000346520
  gene symbol: TRPV4
  hgvsc: ENST00000346520.2:c.2093C>A
  hgvsp: ENSP00000319003.2:p.Ser698Tyr
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000442167
  ensembl transcript: ENST00000541794
  gene symbol: TRPV4
  hgvsc: ENST00000541794.1:c.2132C>A
  hgvsp: ENSP00000442167.1:p.Ser711Tyr
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000443611
  ensembl transcript: ENST00000544971
  gene symbol: TRPV4
  hgvsc: ENST00000544971.1:c.1952C>A
  hgvsp: ENSP00000443611.1:p.Ser651Tyr
  variant of: http://identifiers.org/hgnc/18083
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 21778
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3675
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9104
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2071
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 620
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 928
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1339
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18930
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 771
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1076
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 117
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Ser758Tyr
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: G
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

12-110224581-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 110224581
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 110224581
    reference: chr 12
allele count: 2
allele frequency: 1.667583837777444e-5
allele num: 119934
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000376480
  ensembl transcript: ENST00000392719
  gene symbol: TRPV4
  hgvsc: ENST00000392719.2:c.2129G>A
  hgvsp: ENSP00000376480.2:p.Arg710His
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000442738
  ensembl transcript: ENST00000537083
  gene symbol: TRPV4
  hgvsc: ENST00000537083.1:c.2090G>A
  hgvsp: ENSP00000442738.1:p.Arg697His
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000442167
  ensembl transcript: ENST00000541794
  gene symbol: TRPV4
  hgvsc: ENST00000541794.1:c.2129G>A
  hgvsp: ENSP00000442167.1:p.Arg710His
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000319003
  ensembl transcript: ENST00000346520
  gene symbol: TRPV4
  hgvsc: ENST00000346520.2:c.2090G>A
  hgvsp: ENSP00000319003.2:p.Arg697His
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000437449
  ensembl transcript: ENST00000538125
  gene symbol: TRPV4
  hgvsc: ENST00000538125.1:c.*653G>A
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000406191
  ensembl transcript: ENST00000418703
  gene symbol: TRPV4
  hgvsc: ENST00000418703.2:c.2270G>A
  hgvsp: ENSP00000406191.2:p.Arg757His
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000443611
  ensembl transcript: ENST00000544971
  gene symbol: TRPV4
  hgvsc: ENST00000544971.1:c.1949G>A
  hgvsp: ENSP00000443611.1:p.Arg650His
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000261740
  ensembl transcript: ENST00000261740
  gene symbol: TRPV4
  hgvsc: ENST00000261740.2:c.2270G>A
  hgvsp: ENSP00000261740.2:p.Arg757His
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000444336
  ensembl transcript: ENST00000536838
  gene symbol: TRPV4
  hgvsc: ENST00000536838.1:c.2168G>A
  hgvsp: ENSP00000444336.1:p.Arg723His
  variant of: http://identifiers.org/hgnc/18083
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1336
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18942
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21757
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9115
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 928
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 624
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 620
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2072
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3678
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 765
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3026
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 126
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Arg757His
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
reference allele: C
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: DP

12-110224582-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 110224582
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 110224582
    reference: chr 12
allele count: 2
allele frequency: 1.667667267026883e-5
allele num: 119928
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000444336
  ensembl transcript: ENST00000536838
  gene symbol: TRPV4
  hgvsc: ENST00000536838.1:c.2167C>T
  hgvsp: ENSP00000444336.1:p.Arg723Cys
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000442167
  ensembl transcript: ENST00000541794
  gene symbol: TRPV4
  hgvsc: ENST00000541794.1:c.2128C>T
  hgvsp: ENSP00000442167.1:p.Arg710Cys
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000443611
  ensembl transcript: ENST00000544971
  gene symbol: TRPV4
  hgvsc: ENST00000544971.1:c.1948C>T
  hgvsp: ENSP00000443611.1:p.Arg650Cys
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000376480
  ensembl transcript: ENST00000392719
  gene symbol: TRPV4
  hgvsc: ENST00000392719.2:c.2128C>T
  hgvsp: ENSP00000376480.2:p.Arg710Cys
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000319003
  ensembl transcript: ENST00000346520
  gene symbol: TRPV4
  hgvsc: ENST00000346520.2:c.2089C>T
  hgvsp: ENSP00000319003.2:p.Arg697Cys
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000261740
  ensembl transcript: ENST00000261740
  gene symbol: TRPV4
  hgvsc: ENST00000261740.2:c.2269C>T
  hgvsp: ENSP00000261740.2:p.Arg757Cys
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000442738
  ensembl transcript: ENST00000537083
  gene symbol: TRPV4
  hgvsc: ENST00000537083.1:c.2089C>T
  hgvsp: ENSP00000442738.1:p.Arg697Cys
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000406191
  ensembl transcript: ENST00000418703
  gene symbol: TRPV4
  hgvsc: ENST00000418703.2:c.2269C>T
  hgvsp: ENSP00000406191.2:p.Arg757Cys
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000437449
  ensembl transcript: ENST00000538125
  gene symbol: TRPV4
  hgvsc: ENST00000538125.1:c.*652C>T
  variant of: http://identifiers.org/hgnc/18083
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3685
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 624
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1339
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21759
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 928
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18943
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9114
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2073
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 621
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1078
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 108
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Arg757Cys
num of homozygotes: 0
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
population: African
population: European (Finnish)
population: Latino
reference allele: G
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum

12-110224584-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 110224584
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 110224584
    reference: chr 12
allele count: 1
allele frequency: 8.336390009670212e-6
allele num: 119956
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000261740
  ensembl transcript: ENST00000261740
  gene symbol: TRPV4
  hgvsc: ENST00000261740.2:c.2267T>A
  hgvsp: ENSP00000261740.2:p.Phe756Tyr
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000444336
  ensembl transcript: ENST00000536838
  gene symbol: TRPV4
  hgvsc: ENST00000536838.1:c.2165T>A
  hgvsp: ENSP00000444336.1:p.Phe722Tyr
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000442167
  ensembl transcript: ENST00000541794
  gene symbol: TRPV4
  hgvsc: ENST00000541794.1:c.2126T>A
  hgvsp: ENSP00000442167.1:p.Phe709Tyr
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000442738
  ensembl transcript: ENST00000537083
  gene symbol: TRPV4
  hgvsc: ENST00000537083.1:c.2087T>A
  hgvsp: ENSP00000442738.1:p.Phe696Tyr
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000376480
  ensembl transcript: ENST00000392719
  gene symbol: TRPV4
  hgvsc: ENST00000392719.2:c.2126T>A
  hgvsp: ENSP00000376480.2:p.Phe709Tyr
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000437449
  ensembl transcript: ENST00000538125
  gene symbol: TRPV4
  hgvsc: ENST00000538125.1:c.*650T>A
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000319003
  ensembl transcript: ENST00000346520
  gene symbol: TRPV4
  hgvsc: ENST00000346520.2:c.2087T>A
  hgvsp: ENSP00000319003.2:p.Phe696Tyr
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000406191
  ensembl transcript: ENST00000418703
  gene symbol: TRPV4
  hgvsc: ENST00000418703.2:c.2267T>A
  hgvsp: ENSP00000406191.2:p.Phe756Tyr
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000443611
  ensembl transcript: ENST00000544971
  gene symbol: TRPV4
  hgvsc: ENST00000544971.1:c.1946T>A
  hgvsp: ENSP00000443611.1:p.Phe649Tyr
  variant of: http://identifiers.org/hgnc/18083
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 624
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9093
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2069
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21755
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18976
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1336
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 929
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 620
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3678
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3027
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5329
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Phe756Tyr
num of homozygotes: 0
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
reference allele: A
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP

12-110224587-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 110224587
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 110224587
    reference: chr 12
allele count: 1
allele frequency: 8.336807002917883e-6
allele num: 119950
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000444336
  ensembl transcript: ENST00000536838
  gene symbol: TRPV4
  hgvsc: ENST00000536838.1:c.2162C>T
  hgvsp: ENSP00000444336.1:p.Ala721Val
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000319003
  ensembl transcript: ENST00000346520
  gene symbol: TRPV4
  hgvsc: ENST00000346520.2:c.2084C>T
  hgvsp: ENSP00000319003.2:p.Ala695Val
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000437449
  ensembl transcript: ENST00000538125
  gene symbol: TRPV4
  hgvsc: ENST00000538125.1:c.*647C>T
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000442167
  ensembl transcript: ENST00000541794
  gene symbol: TRPV4
  hgvsc: ENST00000541794.1:c.2123C>T
  hgvsp: ENSP00000442167.1:p.Ala708Val
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000406191
  ensembl transcript: ENST00000418703
  gene symbol: TRPV4
  hgvsc: ENST00000418703.2:c.2264C>T
  hgvsp: ENSP00000406191.2:p.Ala755Val
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000261740
  ensembl transcript: ENST00000261740
  gene symbol: TRPV4
  hgvsc: ENST00000261740.2:c.2264C>T
  hgvsp: ENSP00000261740.2:p.Ala755Val
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000376480
  ensembl transcript: ENST00000392719
  gene symbol: TRPV4
  hgvsc: ENST00000392719.2:c.2123C>T
  hgvsp: ENSP00000376480.2:p.Ala708Val
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000442738
  ensembl transcript: ENST00000537083
  gene symbol: TRPV4
  hgvsc: ENST00000537083.1:c.2084C>T
  hgvsp: ENSP00000442738.1:p.Ala695Val
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000443611
  ensembl transcript: ENST00000544971
  gene symbol: TRPV4
  hgvsc: ENST00000544971.1:c.1943C>T
  hgvsp: ENSP00000443611.1:p.Ala648Val
  variant of: http://identifiers.org/hgnc/18083
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9110
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 618
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3683
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2071
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1336
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 620
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18981
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 928
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21721
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 123
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33156
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Ala755Val
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: ClippingRankSum

12-110224598-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 110224598
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 110224598
    reference: chr 12
allele count: 1
allele frequency: 8.337224037884346e-6
allele num: 119944
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000319003
  ensembl transcript: ENST00000346520
  gene symbol: TRPV4
  hgvsc: ENST00000346520.2:c.2073C>T
  hgvsp: ENST00000346520.2:c.2073C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000442738
  ensembl transcript: ENST00000537083
  gene symbol: TRPV4
  hgvsc: ENST00000537083.1:c.2073C>T
  hgvsp: ENST00000537083.1:c.2073C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000406191
  ensembl transcript: ENST00000418703
  gene symbol: TRPV4
  hgvsc: ENST00000418703.2:c.2253C>T
  hgvsp: ENST00000418703.2:c.2253C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000437449
  ensembl transcript: ENST00000538125
  gene symbol: TRPV4
  hgvsc: ENST00000538125.1:c.*636C>T
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000444336
  ensembl transcript: ENST00000536838
  gene symbol: TRPV4
  hgvsc: ENST00000536838.1:c.2151C>T
  hgvsp: ENST00000536838.1:c.2151C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000443611
  ensembl transcript: ENST00000544971
  gene symbol: TRPV4
  hgvsc: ENST00000544971.1:c.1932C>T
  hgvsp: ENST00000544971.1:c.1932C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000261740
  ensembl transcript: ENST00000261740
  gene symbol: TRPV4
  hgvsc: ENST00000261740.2:c.2253C>T
  hgvsp: ENST00000261740.2:c.2253C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000376480
  ensembl transcript: ENST00000392719
  gene symbol: TRPV4
  hgvsc: ENST00000392719.2:c.2112C>T
  hgvsp: ENST00000392719.2:c.2112C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000442167
  ensembl transcript: ENST00000541794
  gene symbol: TRPV4
  hgvsc: ENST00000541794.1:c.2112C>T
  hgvsp: ENST00000541794.1:c.2112C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9139
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19075
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3680
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1337
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21537
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 928
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2067
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 620
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 95
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 804
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 112
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Phe751Phe
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
population: Latino
population: African
population: European (Finnish)
reference allele: G
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum

12-110224603-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 110224603
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 110224603
    reference: chr 12
allele count: 93
allele frequency: 7.756463719766472e-4
allele num: 119900
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000319003
  ensembl transcript: ENST00000346520
  gene symbol: TRPV4
  hgvsc: ENST00000346520.2:c.2068G>A
  hgvsp: ENSP00000319003.2:p.Val690Ile
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000444336
  ensembl transcript: ENST00000536838
  gene symbol: TRPV4
  hgvsc: ENST00000536838.1:c.2146G>A
  hgvsp: ENSP00000444336.1:p.Val716Ile
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000261740
  ensembl transcript: ENST00000261740
  gene symbol: TRPV4
  hgvsc: ENST00000261740.2:c.2248G>A
  hgvsp: ENSP00000261740.2:p.Val750Ile
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000442167
  ensembl transcript: ENST00000541794
  gene symbol: TRPV4
  hgvsc: ENST00000541794.1:c.2107G>A
  hgvsp: ENSP00000442167.1:p.Val703Ile
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000443611
  ensembl transcript: ENST00000544971
  gene symbol: TRPV4
  hgvsc: ENST00000544971.1:c.1927G>A
  hgvsp: ENSP00000443611.1:p.Val643Ile
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000406191
  ensembl transcript: ENST00000418703
  gene symbol: TRPV4
  hgvsc: ENST00000418703.2:c.2248G>A
  hgvsp: ENSP00000406191.2:p.Val750Ile
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000376480
  ensembl transcript: ENST00000392719
  gene symbol: TRPV4
  hgvsc: ENST00000392719.2:c.2107G>A
  hgvsp: ENSP00000376480.2:p.Val703Ile
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000442738
  ensembl transcript: ENST00000537083
  gene symbol: TRPV4
  hgvsc: ENST00000537083.1:c.2068G>A
  hgvsp: ENSP00000442738.1:p.Val690Ile
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000437449
  ensembl transcript: ENST00000538125
  gene symbol: TRPV4
  hgvsc: ENST00000538125.1:c.*631G>A
  variant of: http://identifiers.org/hgnc/18083
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 21429
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2083
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 6.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 3689
  bin: 3.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 19061
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 617
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9144
  bin: 3.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 5.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 938
  bin: 5.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 9.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 6.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1354
  bin: 4.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 832
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Val750Ile
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: East Asian
population: African
population: South Asian
population: Latino
reference allele: C
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum

12-110224604-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 110224604
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 110224604
    reference: chr 12
allele count: 6
allele frequency: 5.004253615573237e-5
allele num: 119898
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000376480
  ensembl transcript: ENST00000392719
  gene symbol: TRPV4
  hgvsc: ENST00000392719.2:c.2106C>T
  hgvsp: ENST00000392719.2:c.2106C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000437449
  ensembl transcript: ENST00000538125
  gene symbol: TRPV4
  hgvsc: ENST00000538125.1:c.*630C>T
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000319003
  ensembl transcript: ENST00000346520
  gene symbol: TRPV4
  hgvsc: ENST00000346520.2:c.2067C>T
  hgvsp: ENST00000346520.2:c.2067C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000442738
  ensembl transcript: ENST00000537083
  gene symbol: TRPV4
  hgvsc: ENST00000537083.1:c.2067C>T
  hgvsp: ENST00000537083.1:c.2067C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000443611
  ensembl transcript: ENST00000544971
  gene symbol: TRPV4
  hgvsc: ENST00000544971.1:c.1926C>T
  hgvsp: ENST00000544971.1:c.1926C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000444336
  ensembl transcript: ENST00000536838
  gene symbol: TRPV4
  hgvsc: ENST00000536838.1:c.2145C>T
  hgvsp: ENST00000536838.1:c.2145C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000261740
  ensembl transcript: ENST00000261740
  gene symbol: TRPV4
  hgvsc: ENST00000261740.2:c.2247C>T
  hgvsp: ENST00000261740.2:c.2247C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000442167
  ensembl transcript: ENST00000541794
  gene symbol: TRPV4
  hgvsc: ENST00000541794.1:c.2106C>T
  hgvsp: ENST00000541794.1:c.2106C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000406191
  ensembl transcript: ENST00000418703
  gene symbol: TRPV4
  hgvsc: ENST00000418703.2:c.2247C>T
  hgvsp: ENST00000418703.2:c.2247C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9155
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2081
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 932
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 622
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19117
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3691
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21426
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 618
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1343
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1402
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 118
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Pro749Pro
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum

12-110224613-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 110224613
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 110224613
    reference: chr 12
allele count: 2
allele frequency: 1.668752607425949e-5
allele num: 119850
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000444336
  ensembl transcript: ENST00000536838
  gene symbol: TRPV4
  hgvsc: ENST00000536838.1:c.2136C>T
  hgvsp: ENST00000536838.1:c.2136C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000437449
  ensembl transcript: ENST00000538125
  gene symbol: TRPV4
  hgvsc: ENST00000538125.1:c.*621C>T
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000319003
  ensembl transcript: ENST00000346520
  gene symbol: TRPV4
  hgvsc: ENST00000346520.2:c.2058C>T
  hgvsp: ENST00000346520.2:c.2058C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000376480
  ensembl transcript: ENST00000392719
  gene symbol: TRPV4
  hgvsc: ENST00000392719.2:c.2097C>T
  hgvsp: ENST00000392719.2:c.2097C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000406191
  ensembl transcript: ENST00000418703
  gene symbol: TRPV4
  hgvsc: ENST00000418703.2:c.2238C>T
  hgvsp: ENST00000418703.2:c.2238C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000261740
  ensembl transcript: ENST00000261740
  gene symbol: TRPV4
  hgvsc: ENST00000261740.2:c.2238C>T
  hgvsp: ENST00000261740.2:c.2238C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000442738
  ensembl transcript: ENST00000537083
  gene symbol: TRPV4
  hgvsc: ENST00000537083.1:c.2058C>T
  hgvsp: ENST00000537083.1:c.2058C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000443611
  ensembl transcript: ENST00000544971
  gene symbol: TRPV4
  hgvsc: ENST00000544971.1:c.1917C>T
  hgvsp: ENST00000544971.1:c.1917C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000442167
  ensembl transcript: ENST00000541794
  gene symbol: TRPV4
  hgvsc: ENST00000541794.1:c.2097C>T
  hgvsp: ENST00000541794.1:c.2097C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18083
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19157
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 645
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2073
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1339
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9128
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3683
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 931
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21337
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 617
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 139
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 121
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Arg746Arg
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: Other
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum

12-110224621-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 110224621
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 110224621
    reference: chr 12
allele count: 1
allele frequency: 8.348778573694668e-6
allele num: 119778
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000442167
  ensembl transcript: ENST00000541794
  gene symbol: TRPV4
  hgvsc: ENST00000541794.1:c.2089A>G
  hgvsp: ENSP00000442167.1:p.Ile697Val
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000261740
  ensembl transcript: ENST00000261740
  gene symbol: TRPV4
  hgvsc: ENST00000261740.2:c.2230A>G
  hgvsp: ENSP00000261740.2:p.Ile744Val
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000437449
  ensembl transcript: ENST00000538125
  gene symbol: TRPV4
  hgvsc: ENST00000538125.1:c.*613A>G
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000376480
  ensembl transcript: ENST00000392719
  gene symbol: TRPV4
  hgvsc: ENST00000392719.2:c.2089A>G
  hgvsp: ENSP00000376480.2:p.Ile697Val
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000319003
  ensembl transcript: ENST00000346520
  gene symbol: TRPV4
  hgvsc: ENST00000346520.2:c.2050A>G
  hgvsp: ENSP00000319003.2:p.Ile684Val
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000442738
  ensembl transcript: ENST00000537083
  gene symbol: TRPV4
  hgvsc: ENST00000537083.1:c.2050A>G
  hgvsp: ENSP00000442738.1:p.Ile684Val
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000406191
  ensembl transcript: ENST00000418703
  gene symbol: TRPV4
  hgvsc: ENST00000418703.2:c.2230A>G
  hgvsp: ENSP00000406191.2:p.Ile744Val
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000444336
  ensembl transcript: ENST00000536838
  gene symbol: TRPV4
  hgvsc: ENST00000536838.1:c.2128A>G
  hgvsp: ENSP00000444336.1:p.Ile710Val
  variant of: http://identifiers.org/hgnc/18083
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111199
  ensembl protein: ENSP00000443611
  ensembl transcript: ENST00000544971
  gene symbol: TRPV4
  hgvsc: ENST00000544971.1:c.1909A>G
  hgvsp: ENSP00000443611.1:p.Ile637Val
  variant of: http://identifiers.org/hgnc/18083
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3675
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 931
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1340
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21214
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 617
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9118
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 606
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2071
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Ile744Val
num of homozygotes: 0
reference allele: T

GenotypeQuality
all individuals: 1475
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2174
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 967
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1418
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1150
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2093
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1608
bin: 8.25e1
variant carriers: 0

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

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66682
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.31107002542177e-4
allele num: 8654
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.586e0

MQRankSum
type: SiteQuality
SIO_000300: -1.49e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.44e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

QD
type: SiteQuality
SIO_000300: 1.029e1

FS
type: SiteQuality
SIO_000300: 1.1617e1

DP
type: SiteQuality
SIO_000300: 3.472886e6

VQSLOD
type: SiteQuality
SIO_000300: -1.575e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.580000000000001e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 24
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1606
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 1466
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1417
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 49465
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 966
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2208
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2093
bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.31107002542177e-4
allele num: 8654
num of homozygotes: 0

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

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

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

African
type: Population
allele count: 1
allele frequency: 9.617234083477592e-5
allele num: 10398
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499790029395885e-5
allele num: 66676
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 6.31e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.81e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.28e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.02e0

VQSLOD
type: SiteQuality
SIO_000300: 1.96e0

QD
type: SiteQuality
SIO_000300: 1.222e1

DP
type: SiteQuality
SIO_000300: 3.473152e6

MQ
type: SiteQuality
SIO_000300: 5.967e1

GenotypeQuality
all individuals: 24
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1150
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2089
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1411
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1611
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 26
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 49445
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 46
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 967
bin: 7.25e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.056935190793458e-5
allele num: 16510
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499790029395885e-5
allele num: 66676
num of homozygotes: 0

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6602
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.94e-1

DP
type: SiteQuality
SIO_000300: 3.473052e6

FS
type: SiteQuality
SIO_000300: 5.993e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.16e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.0e0

MQ
type: SiteQuality
SIO_000300: 5.935e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -2.233e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.25e-1

QD
type: SiteQuality
SIO_000300: 1.125e1

GenotypeQuality
all individuals: 23
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 9
bin: 4.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 2257
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1615
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 24
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1152
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 978
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 49450
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 2093
bin: 9.25e1
variant carriers: 0

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

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

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

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

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

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.59e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.55e-1

QD
type: SiteQuality
SIO_000300: 1.103e1

FS
type: SiteQuality
SIO_000300: 7.734e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.66e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.68e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.9e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 7.99e-1

DP
type: SiteQuality
SIO_000300: 3.473157e6

MQ
type: SiteQuality
SIO_000300: 5.98e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

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

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

Other
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allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.7e-3

ClippingRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 5.012e0

QD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.982e1

MQRankSum
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SIO_000300: -1.109e0

BaseQRankSum
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SIO_000300: -1.043e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.82e-1

VQSLOD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 3.473124e6

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.499655079331754e-5
allele num: 66682
num of homozygotes: 0

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

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

Other
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allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

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

South Asian
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VQSLOD
type: SiteQuality
SIO_000300: -9.073e-1

MQ
type: SiteQuality
SIO_000300: 5.926e1

MQRankSum
type: SiteQuality
SIO_000300: -9.370000000000001e-1

DP
type: SiteQuality
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InbreedingCoeff
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SIO_000300: 6.0e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -6.14e-1

FS
type: SiteQuality
SIO_000300: 6.549e0

ClippingRankSum
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SIO_000300: 1.03e0

QD
type: SiteQuality
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ReadPosRankSum
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SIO_000300: -6.39e-1

GenotypeQuality
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variant carriers: 0

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

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

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

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

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.499430216517723e-5
allele num: 66692
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

ClippingRankSum
type: SiteQuality
SIO_000300: 5.86e-1

DP
type: SiteQuality
SIO_000300: 3.472405e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 4.2e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.07e0

MQRankSum
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SIO_000300: 2.26e0

ReadPosRankSum
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SIO_000300: 1.31e0

QD
type: SiteQuality
SIO_000300: 1.237e1

MQ
type: SiteQuality
SIO_000300: 5.979e1

VQSLOD
type: SiteQuality
SIO_000300: -6.691e-1

GenotypeQuality
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variant carriers: 0

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

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

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

Other
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allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499385252046661e-5
allele num: 66694
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 3.472502e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.0e-3

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 4.985e0

ReadPosRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.984e1

VQSLOD
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.146e1

GenotypeQuality
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variant carriers: 0

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

European (Non-Finnish)
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allele frequency: 1.499430216517723e-5
allele num: 66692
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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South Asian
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allele frequency: 0.0e0
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African
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Other
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QD
type: SiteQuality
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ReadPosRankSum
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FS
type: SiteQuality
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BaseQRankSum
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InbreedingCoeff
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MQ
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MQRankSum
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VQSLOD
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DP
type: SiteQuality
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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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

Latino
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num of homozygotes: 0

Other
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele num: 66692
num of homozygotes: 0

South Asian
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European (Finnish)
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InbreedingCoeff
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MQ
type: SiteQuality
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MQRankSum
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FS
type: SiteQuality
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VQSLOD
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QD
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ReadPosRankSum
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BaseQRankSum
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DP
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

Other
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num of homozygotes: 0

European (Non-Finnish)
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allele num: 66686
num of homozygotes: 0

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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South Asian
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Latino
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BaseQRankSum
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ClippingRankSum
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MQRankSum
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InbreedingCoeff
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QD
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FS
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MQ
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DP
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ReadPosRankSum
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.75e1
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African
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
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Latino
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East Asian
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European (Finnish)
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European (Non-Finnish)
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allele frequency: 1.499565126113427e-5
allele num: 66686
num of homozygotes: 0

South Asian
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BaseQRankSum
type: SiteQuality
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MQ
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ClippingRankSum
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QD
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FS
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VQSLOD
type: SiteQuality
SIO_000300: 6.879999999999999e-1

MQRankSum
type: SiteQuality
SIO_000300: -6.37e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.26e0

DP
type: SiteQuality
SIO_000300: 3.472664e6

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

GenotypeQuality
all individuals: 2095
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 49432
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1492
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1153
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1465
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1608
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 985
bin: 7.25e1
variant carriers: 0

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

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

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

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

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

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: -1.536e0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -2.852e0

MQRankSum
type: SiteQuality
SIO_000300: 2.61e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.8e-2

MQ
type: SiteQuality
SIO_000300: 5.943e1

QD
type: SiteQuality
SIO_000300: 1.9e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 3.472764e6

ClippingRankSum
type: SiteQuality
SIO_000300: -2.61e-1

GenotypeQuality
all individuals: 21
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2255
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variant carriers: 0

GenotypeQuality
all individuals: 57
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GenotypeQuality
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GenotypeQuality
all individuals: 2
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GenotypeQuality
all individuals: 8
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variant carriers: 0

GenotypeQuality
all individuals: 23
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1591
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1145
bin: 8.75e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6602
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.49802087081684e-5
allele num: 66696
num of homozygotes: 0

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.2e-2

VQSLOD
type: SiteQuality
SIO_000300: 2.46e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.6e-1

MQ
type: SiteQuality
SIO_000300: 5.949e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.0e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.19e-1

QD
type: SiteQuality
SIO_000300: 1.214e1

FS
type: SiteQuality
SIO_000300: 5.27e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.87e0

DP
type: SiteQuality
SIO_000300: 3.549336e6

GenotypeQuality
all individuals: 1591
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 972
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
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variant carriers: 0

GenotypeQuality
all individuals: 2
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GenotypeQuality
all individuals: 6
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variant carriers: 0

GenotypeQuality
all individuals: 36
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GenotypeQuality
all individuals: 49508
bin: 9.75e1
variant carriers: 1199

GenotypeQuality
all individuals: 8
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variant carriers: 0

GenotypeQuality
all individuals: 27
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variant carriers: 0

GenotypeQuality
all individuals: 1477
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variant carriers: 1

GenotypeQuality
all individuals: 15
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 10
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GenotypeQuality
all individuals: 2089
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variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 5.25e1
variant carriers: 0

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

Other
type: Population
allele count: 4
allele frequency: 4.424778761061947e-3
allele num: 904
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 16
allele frequency: 2.423508027870342e-3
allele num: 6602
num of homozygotes: 0

South Asian
type: Population
allele count: 377
allele frequency: 2.283187984496124e-2
allele num: 16512
num of homozygotes: 4

African
type: Population
allele count: 12
allele frequency: 1.153846153846154e-3
allele num: 10400
num of homozygotes: 0

Latino
type: Population
allele count: 55
allele frequency: 4.750388668163759e-3
allele num: 11578
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 750
allele frequency: 1.12450521770421e-2
allele num: 66696
num of homozygotes: 8

MQRankSum
type: SiteQuality
SIO_000300: 1.19e-1

FS
type: SiteQuality
SIO_000300: 5.27e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.0e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 3.6e-1

DP
type: SiteQuality
SIO_000300: 3.549336e6

VQSLOD
type: SiteQuality
SIO_000300: 2.46e0

MQ
type: SiteQuality
SIO_000300: 5.949e1

QD
type: SiteQuality
SIO_000300: 1.214e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.87e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.2e-2

GenotypeQuality
all individuals: 21
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23
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variant carriers: 0

GenotypeQuality
all individuals: 20
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GenotypeQuality
all individuals: 1591
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GenotypeQuality
all individuals: 1
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GenotypeQuality
all individuals: 8
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variant carriers: 0

GenotypeQuality
all individuals: 6
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GenotypeQuality
all individuals: 1443
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variant carriers: 0

GenotypeQuality
all individuals: 10
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GenotypeQuality
all individuals: 2
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GenotypeQuality
all individuals: 972
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GenotypeQuality
all individuals: 36
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variant carriers: 0

GenotypeQuality
all individuals: 1477
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2089
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1145
bin: 8.75e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6602
num of homozygotes: 0

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

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

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

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

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

MQ
type: SiteQuality
SIO_000300: 5.949e1

DP
type: SiteQuality
SIO_000300: 3.549336e6

QD
type: SiteQuality
SIO_000300: 1.214e1

FS
type: SiteQuality
SIO_000300: 5.27e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.6e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.2e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.87e0

MQRankSum
type: SiteQuality
SIO_000300: 1.19e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.46e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.0e-2

GenotypeQuality
all individuals: 11
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 49312
bin: 9.75e1
variant carriers: 8

GenotypeQuality
all individuals: 25
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2296
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variant carriers: 0

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
all individuals: 13
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variant carriers: 0

GenotypeQuality
all individuals: 55
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variant carriers: 0

GenotypeQuality
all individuals: 6
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variant carriers: 0

GenotypeQuality
all individuals: 14
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GenotypeQuality
all individuals: 23
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GenotypeQuality
all individuals: 2135
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GenotypeQuality
all individuals: 992
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variant carriers: 0

GenotypeQuality
all individuals: 1469
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1169
bin: 8.75e1
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GenotypeQuality
all individuals: 23
bin: 2.75e1
variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.496926260233305e-5
allele num: 66694
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 3
allele frequency: 4.535833081342606e-4
allele num: 6614
num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
SIO_000300: -5.08e-1

FS
type: SiteQuality
SIO_000300: 4.6384e1

MQ
type: SiteQuality
SIO_000300: 5.948e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.87e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.117e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -1.732e0

DP
type: SiteQuality
SIO_000300: 3.4495e6

QD
type: SiteQuality
SIO_000300: 1.464e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.6e-2

GenotypeQuality
all individuals: 2067
bin: 9.25e1
variant carriers: 3

GenotypeQuality
all individuals: 1549
bin: 8.25e1
variant carriers: 2

GenotypeQuality
all individuals: 54
bin: 1.25e1
variant carriers: 5

GenotypeQuality
all individuals: 58
bin: 5.75e1
variant carriers: 3

GenotypeQuality
all individuals: 61
bin: 4.75e1
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GenotypeQuality
all individuals: 46892
bin: 9.75e1
variant carriers: 260

GenotypeQuality
all individuals: 53
bin: 7.5e0
variant carriers: 1

GenotypeQuality
all individuals: 55
bin: 1.75e1
variant carriers: 1

GenotypeQuality
all individuals: 85
bin: 2.25e1
variant carriers: 3

GenotypeQuality
all individuals: 72
bin: 2.75e1
variant carriers: 5

GenotypeQuality
all individuals: 1384
bin: 7.75e1
variant carriers: 2

GenotypeQuality
all individuals: 84
bin: 3.75e1
variant carriers: 4

GenotypeQuality
all individuals: 67
bin: 4.25e1
variant carriers: 1

GenotypeQuality
all individuals: 2735
bin: 2.5e0
variant carriers: 2

GenotypeQuality
all individuals: 1313
bin: 6.75e1
variant carriers: 5

GenotypeQuality
all individuals: 2077
bin: 6.25e1
variant carriers: 4

European (Non-Finnish)
type: Population
allele count: 178
allele frequency: 2.812272885265586e-3
allele num: 63294
num of homozygotes: 0

Latino
type: Population
allele count: 8
allele frequency: 7.005253940455342e-4
allele num: 11420
num of homozygotes: 0

Other
type: Population
allele count: 3
allele frequency: 3.658536585365854e-3
allele num: 820
num of homozygotes: 0

East Asian
type: Population
allele count: 7
allele frequency: 8.237232289950577e-4
allele num: 8498
num of homozygotes: 0

African
type: Population
allele count: 21
allele frequency: 2.19160926737633e-3
allele num: 9582
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 90
allele frequency: 1.638747268754552e-2
allele num: 5492
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.062075654704171e-5
allele num: 16496
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 3.546587e6

MQRankSum
type: SiteQuality
SIO_000300: 2.8e-2

FS
type: SiteQuality
SIO_000300: 2.58786e2

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.62e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 6.79e0

BaseQRankSum
type: SiteQuality
SIO_000300: -6.11e0

MQ
type: SiteQuality
SIO_000300: 5.915e1

QD
type: SiteQuality
SIO_000300: 1.58e0

VQSLOD
type: SiteQuality
SIO_000300: -3.303e2

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.523e0

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

GenotypeQuality
all individuals: 21
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variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 1490
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variant carriers: 0

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
all individuals: 1
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GenotypeQuality
all individuals: 1510
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GenotypeQuality
all individuals: 8
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 49293
bin: 9.75e1
variant carriers: 1

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66730
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 9.613535858488752e-5
allele num: 10402
num of homozygotes: 0

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

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

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

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

DP
type: SiteQuality
SIO_000300: 3.421461e6

ClippingRankSum
type: SiteQuality
SIO_000300: 2.38e-1

MQ
type: SiteQuality
SIO_000300: 5.909e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.132e0

MQRankSum
type: SiteQuality
SIO_000300: -6.870000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -1.415e0

QD
type: SiteQuality
SIO_000300: 2.44e1

FS
type: SiteQuality
SIO_000300: 9.77e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.39e-1

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

GenotypeQuality
all individuals: 25
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1508
bin: 7.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 0
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variant carriers: 0

GenotypeQuality
all individuals: 49275
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variant carriers: 0

GenotypeQuality
all individuals: 5
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variant carriers: 0

GenotypeQuality
all individuals: 965
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GenotypeQuality
all individuals: 1
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GenotypeQuality
all individuals: 13
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GenotypeQuality
all individuals: 0
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GenotypeQuality
all individuals: 11
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GenotypeQuality
all individuals: 2405
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GenotypeQuality
all individuals: 4
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variant carriers: 0

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

GenotypeQuality
all individuals: 1481
bin: 6.75e1
variant carriers: 0

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

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66730
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.628e1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.48e-1

QD
type: SiteQuality
SIO_000300: 1.0e-1

FS
type: SiteQuality
SIO_000300: 1.91951e2

BaseQRankSum
type: SiteQuality
SIO_000300: -3.861e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.03e-1

DP
type: SiteQuality
SIO_000300: 3.421175e6

MQRankSum
type: SiteQuality
SIO_000300: 8.92e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.692e2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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bin: 2.25e1
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

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

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498576352465158e-5
allele num: 66730
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

QD
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SIO_000300: 1.324e1

ClippingRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: 4.63e-1

InbreedingCoeff
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SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 3.420605e6

FS
type: SiteQuality
SIO_000300: 8.36e-1

MQ
type: SiteQuality
SIO_000300: 5.937e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.77e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.56e0

VQSLOD
type: SiteQuality
SIO_000300: 8.87e-1

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 2
allele frequency: 1.92270717169775e-4
allele num: 10402
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66730
num of homozygotes: 0

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

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

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

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

VQSLOD
type: SiteQuality
SIO_000300: 2.68e0

FS
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MQRankSum
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ReadPosRankSum
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BaseQRankSum
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SIO_000300: 5.81e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.86e-1

InbreedingCoeff
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SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.962e1

QD
type: SiteQuality
SIO_000300: 1.429e1

DP
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SIO_000300: 3.420609e6

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

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

GenotypeQuality
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bin: 4.75e1
variant carriers: 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: 904
num of homozygotes: 0

East 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: 10402
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
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MQRankSum
type: SiteQuality
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InbreedingCoeff
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ClippingRankSum
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MQ
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 2.08e-1

BaseQRankSum
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QD
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VQSLOD
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SIO_000300: 5.01e0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498576352465158e-5
allele num: 66730
num of homozygotes: 0

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

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

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

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

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

South Asian
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allele count: 0
allele frequency: 0.0e0
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MQRankSum
type: SiteQuality
SIO_000300: -1.564e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -1.247e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.7e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.809e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.48e-1

DP
type: SiteQuality
SIO_000300: 3.420441e6

FS
type: SiteQuality
SIO_000300: 9.606e0

MQ
type: SiteQuality
SIO_000300: 5.977e1

QD
type: SiteQuality
SIO_000300: 1.431e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 29

GenotypeQuality
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variant carriers: 0

East Asian
type: Population
allele count: 23
allele frequency: 2.657730529235036e-3
allele num: 8654
num of homozygotes: 0

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

Other
type: Population
allele count: 1
allele frequency: 1.106194690265487e-3
allele num: 904
num of homozygotes: 0

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

African
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allele count: 1
allele frequency: 9.613535858488752e-5
allele num: 10402
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 2.591121091725686e-4
allele num: 11578
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -1.78e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.62e-1

MQ
type: SiteQuality
SIO_000300: 5.973e1

QD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 3.421185e6

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.42e0

VQSLOD
type: SiteQuality
SIO_000300: 5.62e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.74e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

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

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

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

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16512
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: 1
allele frequency: 1.498531439189594e-5
allele num: 66732
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 3.418966e6

ClippingRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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BaseQRankSum
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ReadPosRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.346e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 2.28e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.997332374186974e-5
allele num: 66726
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10400
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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

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

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

QD
type: SiteQuality
SIO_000300: 1.403e1

ClippingRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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FS
type: SiteQuality
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MQ
type: SiteQuality
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InbreedingCoeff
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SIO_000300: -1.0e-4

DP
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SIO_000300: 3.41847e6

BaseQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 1.94e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

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

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

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

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: -6.45e-1

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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bin: 7.75e1
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

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

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

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

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

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

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

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

FS
type: SiteQuality
SIO_000300: 3.243e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.75e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.24e-1

BaseQRankSum
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SIO_000300: -2.401e0

MQ
type: SiteQuality
SIO_000300: 5.98e1

QD
type: SiteQuality
SIO_000300: 1.132e1

VQSLOD
type: SiteQuality
SIO_000300: 4.79e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.097e0

DP
type: SiteQuality
SIO_000300: 3.41817e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

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

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

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

African
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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

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

Latino
type: Population
allele count: 1
allele frequency: 8.638562543192812e-5
allele num: 11576
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66724
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 3.418115e6

MQ
type: SiteQuality
SIO_000300: 5.967e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.24e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -1.08e-1

FS
type: SiteQuality
SIO_000300: 5.159e0

BaseQRankSum
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SIO_000300: 1.8e0

VQSLOD
type: SiteQuality
SIO_000300: -1.076e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.22e0

QD
type: SiteQuality
SIO_000300: 1.116e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 32

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

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

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

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

South Asian
type: Population
allele count: 32
allele frequency: 1.937984496124031e-3
allele num: 16512
num of homozygotes: 0

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.24e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -4.358e0

DP
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 1.75e0

MQ
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SIO_000300: 5.969e1

QD
type: SiteQuality
SIO_000300: 1.174e1

MQRankSum
type: SiteQuality
SIO_000300: 1.52e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.59e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.2e0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1494
bin: 7.75e1
variant carriers: 0

Latino
type: Population
allele count: 4
allele frequency: 3.455425017277125e-4
allele num: 11576
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10394
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
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: 1.498845888665727e-5
allele num: 66718
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 3.414902e6

VQSLOD
type: SiteQuality
SIO_000300: 1.03e0

MQ
type: SiteQuality
SIO_000300: 5.983e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.06e-1

QD
type: SiteQuality
SIO_000300: 1.309e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.4e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -7.01e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.22e-1

FS
type: SiteQuality
SIO_000300: 4.062e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.12e0

GenotypeQuality
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variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10394
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 902
num of homozygotes: 0

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

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

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.7e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -1.069e0

MQRankSum
type: SiteQuality
SIO_000300: -2.185e0

FS
type: SiteQuality
SIO_000300: 4.575e0

QD
type: SiteQuality
SIO_000300: 1.457e1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.58e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.85e-1

MQ
type: SiteQuality
SIO_000300: 5.924e1

VQSLOD
type: SiteQuality
SIO_000300: -1.732e0

DP
type: SiteQuality
SIO_000300: 3.41341e6

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 29

Latino
type: Population
allele count: 4
allele frequency: 3.457216940363008e-4
allele num: 11570
num of homozygotes: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 20
allele frequency: 2.998320940273447e-4
allele num: 66704
num of homozygotes: 0

African
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allele count: 2
allele frequency: 1.923816852635629e-4
allele num: 10396
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 8.5e-1

QD
type: SiteQuality
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VQSLOD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 2.2e-1

MQ
type: SiteQuality
SIO_000300: 5.968e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.2e-3

BaseQRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: 3.26e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.6e-2

DP
type: SiteQuality
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GenotypeQuality
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variant carriers: 0

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

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

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

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

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

South Asian
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allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 902
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

QD
type: SiteQuality
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MQRankSum
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VQSLOD
type: SiteQuality
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FS
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.957e1

ReadPosRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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BaseQRankSum
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InbreedingCoeff
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 3.41154e6

GenotypeQuality
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variant carriers: 0

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

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

South Asian
type: Population
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Latino
type: Population
allele count: 1
allele frequency: 8.643042350907519e-5
allele num: 11570
num of homozygotes: 0

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

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 130
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GenotypeQuality
all individuals: 1591
bin: 6.25e1
variant carriers: 0

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

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

African
type: Population
allele count: 1
allele frequency: 9.619084263178146e-5
allele num: 10396
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6610
num of homozygotes: 0

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 902
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.484e1

MQRankSum
type: SiteQuality
SIO_000300: 3.79e-1

DP
type: SiteQuality
SIO_000300: 3.410445e6

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.7e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.1e-1

MQ
type: SiteQuality
SIO_000300: 5.932e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.13e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.516e0

VQSLOD
type: SiteQuality
SIO_000300: 2.77e0

GenotypeQuality
all individuals: 490
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1460
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
all individuals: 5315
bin: 9.75e1
variant carriers: 5

GenotypeQuality
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bin: 6.75e1
variant carriers: 1

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2970
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1665
bin: 4.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5888
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9580
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 828
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11244
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 9.52925481227368e-5
allele num: 62964
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8478
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16198
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.56e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 9.81e-1

QD
type: SiteQuality
SIO_000300: 1.307e1

DP
type: SiteQuality
SIO_000300: 1.559304e6

FS
type: SiteQuality
SIO_000300: 8.186999999999999e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.855e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 1.04e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.35e-1

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1682
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1446
bin: 2.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11242
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5864
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8478
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9554
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.590330788804071e-5
allele num: 62880
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 828
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -4.37e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.64e-1

DP
type: SiteQuality
SIO_000300: 1.562267e6

BaseQRankSum
type: SiteQuality
SIO_000300: 3.29e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 1.691e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.96e-1

QD
type: SiteQuality
SIO_000300: 1.317e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.09e-1

GenotypeQuality
all individuals: 570
bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 917
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variant carriers: 0

GenotypeQuality
all individuals: 7889
bin: 6.75e1
variant carriers: 1

African
type: Population
allele count: 37
allele frequency: 3.82785019656528e-3
allele num: 9666
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16232
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.581127660247289e-5
allele num: 63246
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5938
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.882572392965002e-5
allele num: 11258
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8490
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 832
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.0e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.48e-1

FS
type: SiteQuality
SIO_000300: 2.192e0

VQSLOD
type: SiteQuality
SIO_000300: 1.97e0

DP
type: SiteQuality
SIO_000300: 1.608913e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.738e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.5e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.126e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.3e-2

GenotypeQuality
all individuals: 2771
bin: 7.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1039
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variant carriers: 0

GenotypeQuality
all individuals: 457
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2518
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variant carriers: 0

GenotypeQuality
all individuals: 917
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variant carriers: 0

GenotypeQuality
all individuals: 25349
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 207
bin: 1.75e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 8.882572392965002e-5
allele num: 11258
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.581127660247289e-5
allele num: 63246
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5938
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 832
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8490
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9666
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16232
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.97e0

DP
type: SiteQuality
SIO_000300: 1.608913e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.48e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.0e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.5e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -4.3e-2

FS
type: SiteQuality
SIO_000300: 2.192e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.738e0

QD
type: SiteQuality
SIO_000300: 1.126e1

GenotypeQuality
all individuals: 443
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 498
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7987
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variant carriers: 0

GenotypeQuality
all individuals: 5324
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variant carriers: 3

GenotypeQuality
all individuals: 1393
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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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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 1147
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variant carriers: 0

GenotypeQuality
all individuals: 26162
bin: 6.25e1
variant carriers: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.231982259455464e-4
allele num: 16234
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5946
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 832
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11272
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8498
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63268
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.036699149906697e-4
allele num: 9646
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -4.13e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.33e0

VQSLOD
type: SiteQuality
SIO_000300: 8.46e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.0e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.3e-3

DP
type: SiteQuality
SIO_000300: 1.617351e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.529e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1463
bin: 3.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 126
bin: 1.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2423
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 281
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GenotypeQuality
all individuals: 1401
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 114
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 546
bin: 4.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11304
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63478
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9704
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.175088131609871e-4
allele num: 8510
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 836
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16264
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5980
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.564e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.61e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.630995e6

MQRankSum
type: SiteQuality
SIO_000300: -1.79e-1

MQ
type: SiteQuality
SIO_000300: 5.903e1

VQSLOD
type: SiteQuality
SIO_000300: 3.08e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.19e0

QD
type: SiteQuality
SIO_000300: 1.39e1

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 5330
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3430
bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63704
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8520
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.025430680885972e-4
allele num: 9752
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16274
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 842
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6002
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.1e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.06e-1

MQ
type: SiteQuality
SIO_000300: 5.942e1

MQRankSum
type: SiteQuality
SIO_000300: 5.15e-1

DP
type: SiteQuality
SIO_000300: 1.647657e6

QD
type: SiteQuality
SIO_000300: 1.121e1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.48e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.37e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.23e-1

GenotypeQuality
all individuals: 2154
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1406
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
all individuals: 342
bin: 7.5e0
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GenotypeQuality
all individuals: 5334
bin: 9.75e1
variant carriers: 2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 789
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GenotypeQuality
all individuals: 1088
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GenotypeQuality
all individuals: 679
bin: 3.75e1
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GenotypeQuality
all individuals: 219
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variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 284
bin: 4.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9786
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11334
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16296
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8536
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.132439543916802e-5
allele num: 63848
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6016
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.61e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.5e-1

QD
type: SiteQuality
SIO_000300: 1.132e1

FS
type: SiteQuality
SIO_000300: 9.27e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.1e-3

MQRankSum
type: SiteQuality
SIO_000300: -3.62e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.302e0

VQSLOD
type: SiteQuality
SIO_000300: 8.86e-1

DP
type: SiteQuality
SIO_000300: 1.656263e6

GenotypeQuality
all individuals: 125
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2893
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 235
bin: 4.25e1
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GenotypeQuality
all individuals: 77
bin: 1.25e1
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GenotypeQuality
all individuals: 1087
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GenotypeQuality
all individuals: 844
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variant carriers: 0

GenotypeQuality
all individuals: 703
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 235
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variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 2.5e0
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GenotypeQuality
all individuals: 30057
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

South Asian
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allele frequency: 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: 64010
num of homozygotes: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6038
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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allele frequency: 1.761493746697199e-4
allele num: 11354
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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MQRankSum
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VQSLOD
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ReadPosRankSum
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ClippingRankSum
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InbreedingCoeff
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MQ
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FS
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DP
type: SiteQuality
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QD
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele frequency: 0.0e0
allele num: 8548
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.557535356052582e-5
allele num: 64204
num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
allele num: 11374
num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 862
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6078
num of homozygotes: 0

BaseQRankSum
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VQSLOD
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DP
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ClippingRankSum
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InbreedingCoeff
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MQRankSum
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FS
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MQ
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QD
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele frequency: 0.0e0
allele num: 11416
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

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

South Asian
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allele frequency: 6.093102607847916e-5
allele num: 16412
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African
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allele frequency: 0.0e0
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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8580
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 64728
num of homozygotes: 0

MQRankSum
type: SiteQuality
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DP
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InbreedingCoeff
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ClippingRankSum
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VQSLOD
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MQ
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SIO_000300: 5.795e1

FS
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QD
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BaseQRankSum
type: SiteQuality
SIO_000300: 6.69e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.07e-1

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

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

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.535532215465881e-5
allele num: 65124
num of homozygotes: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16448
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
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SIO_000300: -1.19e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
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ReadPosRankSum
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ClippingRankSum
type: SiteQuality
SIO_000300: -2.88e-1

VQSLOD
type: SiteQuality
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DP
type: SiteQuality
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QD
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: 5.9e-2

GenotypeQuality
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variant carriers: 0

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

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

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
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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 (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
allele frequency: 1.532707988474036e-5
allele num: 65244
num of homozygotes: 0

QD
type: SiteQuality
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MQRankSum
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MQ
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ClippingRankSum
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FS
type: SiteQuality
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ReadPosRankSum
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DP
type: SiteQuality
SIO_000300: 1.705804e6

VQSLOD
type: SiteQuality
SIO_000300: -2.532e-1

InbreedingCoeff
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SIO_000300: -5.999999999999999e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -1.879e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11476
num of homozygotes: 0

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

South Asian
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allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
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African
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allele count: 0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.529332599253686e-5
allele num: 65388
num of homozygotes: 0

MQRankSum
type: SiteQuality
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FS
type: SiteQuality
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InbreedingCoeff
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BaseQRankSum
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ClippingRankSum
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MQ
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VQSLOD
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ReadPosRankSum
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QD
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 1.527650473571647e-5
allele num: 65460
num of homozygotes: 0

Latino
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Other
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East Asian
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South Asian
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MQRankSum
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ClippingRankSum
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DP
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FS
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MQ
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InbreedingCoeff
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ReadPosRankSum
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VQSLOD
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BaseQRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele num: 65494
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South Asian
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African
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Other
type: Population
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Latino
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allele num: 11478
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European (Finnish)
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East Asian
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VQSLOD
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ReadPosRankSum
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FS
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InbreedingCoeff
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MQRankSum
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BaseQRankSum
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QD
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ClippingRankSum
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DP
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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European (Finnish)
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allele num: 6310
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African
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European (Non-Finnish)
type: Population
allele count: 11
allele frequency: 1.675092891514893e-4
allele num: 65668
num of homozygotes: 0

South Asian
type: Population
allele count: 11
allele frequency: 6.671518680252305e-4
allele num: 16488
num of homozygotes: 1

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

Latino
type: Population
allele count: 2
allele frequency: 1.738828029907842e-4
allele num: 11502
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 3.81e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.43e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.62e-1

QD
type: SiteQuality
SIO_000300: 1.217e1

MQRankSum
type: SiteQuality
SIO_000300: 1.2e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.76e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.77e-1

FS
type: SiteQuality
SIO_000300: 1.112e0

MQ
type: SiteQuality
SIO_000300: 5.958e1

DP
type: SiteQuality
SIO_000300: 1.721979e6

GenotypeQuality
all individuals: 136
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 133
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 97
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 1.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 109
bin: 5.25e1
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GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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bin: 1.75e1
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GenotypeQuality
all individuals: 105
bin: 7.5e0
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GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
all individuals: 2474
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 9022
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5385
bin: 9.75e1
variant carriers: 55

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10198
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.063545961678389e-5
allele num: 16492
num of homozygotes: 0

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

Latino
type: Population
allele count: 3
allele frequency: 2.608695652173913e-4
allele num: 11500
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6312
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8618
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 51
allele frequency: 7.761848233038079e-4
allele num: 65706
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.723458e6

MQ
type: SiteQuality
SIO_000300: 5.961e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.7e-2

VQSLOD
type: SiteQuality
SIO_000300: 3.65e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.0e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -2.17e-1

QD
type: SiteQuality
SIO_000300: 1.084e1

MQRankSum
type: SiteQuality
SIO_000300: 1.18e-1

GenotypeQuality
all individuals: 133
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 8.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 4

GenotypeQuality
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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: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33082
bin: 6.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10198
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6312
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.160362032954282e-4
allele num: 8618
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.521931026085898e-5
allele num: 65706
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.141552511415525e-3
allele num: 876
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.063545961678389e-5
allele num: 16492
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 3.65e0

DP
type: SiteQuality
SIO_000300: 1.723458e6

MQRankSum
type: SiteQuality
SIO_000300: 1.18e-1

QD
type: SiteQuality
SIO_000300: 1.084e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.17e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.7e-2

MQ
type: SiteQuality
SIO_000300: 5.961e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.0e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
all individuals: 22
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 4.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
all individuals: 3551
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variant carriers: 0

GenotypeQuality
all individuals: 3034
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2477
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.521421616358325e-5
allele num: 65728
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10206
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6320
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8620
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11504
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16488
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.722693e6

MQ
type: SiteQuality
SIO_000300: 5.958e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 2.1e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -2.377e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.85e0

FS
type: SiteQuality
SIO_000300: 4.226e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.52e0

QD
type: SiteQuality
SIO_000300: 9.94e0

VQSLOD
type: SiteQuality
SIO_000300: 1.99e-1

GenotypeQuality
all individuals: 2477
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9071
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 108
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GenotypeQuality
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GenotypeQuality
all individuals: 14
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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
all individuals: 54
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variant carriers: 0

GenotypeQuality
all individuals: 1410
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5328
bin: 9.75e1
variant carriers: 1

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16492
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11508
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.519849230956289e-5
allele num: 65796
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8620
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10208
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6330
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.24e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.31e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

QD
type: SiteQuality
SIO_000300: 2.81e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.65e1

DP
type: SiteQuality
SIO_000300: 1.723598e6

ClippingRankSum
type: SiteQuality
SIO_000300: 4.6e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.25e0

VQSLOD
type: SiteQuality
SIO_000300: -1.534e0

GenotypeQuality
all individuals: 3545
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 110
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
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GenotypeQuality
all individuals: 785
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GenotypeQuality
all individuals: 1411
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GenotypeQuality
all individuals: 33251
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GenotypeQuality
all individuals: 117
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GenotypeQuality
all individuals: 3034
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GenotypeQuality
all individuals: 55
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GenotypeQuality
all individuals: 47
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GenotypeQuality
all individuals: 5328
bin: 9.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 2476
bin: 8.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8620
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10208
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.03960606705371e-5
allele num: 65798
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16492
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6328
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.211e0

MQ
type: SiteQuality
SIO_000300: 5.942e1

QD
type: SiteQuality
SIO_000300: 1.37e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.114e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 5.24e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.62e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.8e-1

DP
type: SiteQuality
SIO_000300: 1.724045e6

GenotypeQuality
all individuals: 108
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 98
bin: 5.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 69
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GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5384
bin: 9.75e1
variant carriers: 62

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11512
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 42
allele frequency: 6.38045756995716e-4
allele num: 65826
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10212
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.062810719049351e-5
allele num: 16494
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 18
allele frequency: 2.840012622278321e-3
allele num: 6338
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.141552511415525e-3
allele num: 876
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.727178e6

QD
type: SiteQuality
SIO_000300: 1.281e1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.51e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.9e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.62e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

MQRankSum
type: SiteQuality
SIO_000300: 2.45e-1

FS
type: SiteQuality
SIO_000300: 5.22e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.06e0

GenotypeQuality
all individuals: 3025
bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8620
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11514
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16496
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6338
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10222
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.518418415378542e-5
allele num: 65858
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.843e1

FS
type: SiteQuality
SIO_000300: 5.293e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.428e0

VQSLOD
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.054e1

MQRankSum
type: SiteQuality
SIO_000300: 1.89e0

DP
type: SiteQuality
SIO_000300: 1.726621e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.0e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 5.4e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
all individuals: 80
bin: 3.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8620
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 1.956181533646322e-4
allele num: 10224
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6336
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65866
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 878
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11512
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 1.249e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.24e0

MQRankSum
type: SiteQuality
SIO_000300: 1.32e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 6.42e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.55e0

MQ
type: SiteQuality
SIO_000300: 5.963e1

QD
type: SiteQuality
SIO_000300: 1.259e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.87e-1

DP
type: SiteQuality
SIO_000300: 1.727084e6

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
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bin: 7.25e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8620
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65860
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16500
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10224
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6336
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.737317581653926e-4
allele num: 11512
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 6.673e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.31e0

DP
type: SiteQuality
SIO_000300: 1.727257e6

MQRankSum
type: SiteQuality
SIO_000300: -7.78e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.22e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.98e-1

QD
type: SiteQuality
SIO_000300: 1.543e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.76e-1

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 5.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8620
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6346
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65882
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10224
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.686587908269631e-5
allele num: 11512
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 7.66e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 4.616e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.92e0

VQSLOD
type: SiteQuality
SIO_000300: 4.85e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.5e-3

QD
type: SiteQuality
SIO_000300: 1.302e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.025e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.38e-1

DP
type: SiteQuality
SIO_000300: 1.726924e6

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8620
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6340
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10226
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11514
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.518003521768171e-5
allele num: 65876
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16500
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.3e-3

QD
type: SiteQuality
SIO_000300: 1.287e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.77e0

MQRankSum
type: SiteQuality
SIO_000300: 6.65e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.97e-1

DP
type: SiteQuality
SIO_000300: 1.727089e6

VQSLOD
type: SiteQuality
SIO_000300: 2.65e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.983e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.56e-1

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65872
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.06134076857801e-5
allele num: 16498
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11514
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10228
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6336
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.727182e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 7.7e-2

VQSLOD
type: SiteQuality
SIO_000300: -2.547e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.74e-1

FS
type: SiteQuality
SIO_000300: 6.899999999999999e-1

MQ
type: SiteQuality
SIO_000300: 5.918e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.5e-2

QD
type: SiteQuality
SIO_000300: 1.038e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.458e0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 93

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.75e1
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GenotypeQuality
all individuals: 1400
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 65
allele frequency: 9.872417982989064e-4
allele num: 65840
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 2
allele frequency: 3.158559696778269e-4
allele num: 6332
num of homozygotes: 0

Other
type: Population
allele count: 2
allele frequency: 2.288329519450801e-3
allele num: 874
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8618
num of homozygotes: 0

African
type: Population
allele count: 5
allele frequency: 4.888541259288229e-4
allele num: 10228
num of homozygotes: 0

South Asian
type: Population
allele count: 5
allele frequency: 3.030670384289005e-4
allele num: 16498
num of homozygotes: 0

Latino
type: Population
allele count: 14
allele frequency: 1.216333622936577e-3
allele num: 11510
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.73087e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

VQSLOD
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.307e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.46e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.4e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.9e-1

MQ
type: SiteQuality
SIO_000300: 5.966e1

MQRankSum
type: SiteQuality
SIO_000300: 2.39e-1

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

Latino
type: Population
allele count: 3
allele frequency: 2.606429192006951e-4
allele num: 11510
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.06060606060606e-5
allele num: 16500
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10228
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8616
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6336
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.037851631326326e-5
allele num: 65836
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 872
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DP
type: SiteQuality
SIO_000300: 1.727791e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.000000000000001e-2

QD
type: SiteQuality
SIO_000300: 1.278e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 2.42e0

MQRankSum
type: SiteQuality
SIO_000300: 4.56e-1

MQ
type: SiteQuality
SIO_000300: 5.949e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.59e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.23e0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8612
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10218
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 870
num of homozygotes: 0

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

South Asian
type: Population
allele count: 2
allele frequency: 1.212415130940834e-4
allele num: 16496
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65836
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.09e0

VQSLOD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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FS
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.315e1

MQ
type: SiteQuality
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DP
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

MQRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: -2.29e0