18-34539297-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34539297
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 34539297
    reference: chr 18
allele count: 1
allele frequency: 1.532144389287247e-5
allele num: 65268
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000280020
  ensembl transcript: ENST00000280020
  gene symbol: KIAA1328
  hgvsc: ENST00000280020.5:c.475C>T
  hgvsp: ENSP00000280020.5:p.Gln159Ter
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000466355
  ensembl transcript: ENST00000587139
  gene symbol: KIAA1328
  hgvsc: ENST00000587139.1:c.438C>T
  hgvsp: ENSP00000466355.1:p.Gln147Ter
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000468653
  ensembl transcript: ENST00000592611
  gene symbol: KIAA1328
  hgvsc: ENST00000592611.1:c.*134C>T
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000465550
  ensembl transcript: ENST00000591619
  gene symbol: KIAA1328
  hgvsc: ENST00000591619.1:c.463C>T
  hgvsp: ENSP00000465550.1:p.Gln155Ter
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000470002
  ensembl transcript: ENST00000591911
  gene symbol: KIAA1328
  hgvsc: ENST00000591911.1:c.-277+34292C>T
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000441359
  ensembl transcript: ENST00000543923
  gene symbol: KIAA1328
  hgvsc: ENST00000543923.1:c.151C>T
  hgvsp: ENSP00000441359.1:p.Gln51Ter
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000467507
  ensembl transcript: ENST00000586135
  gene symbol: KIAA1328
  hgvsc: ENST00000586135.1:c.-277+12817C>T
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000467248
  ensembl transcript: ENST00000590617
  gene symbol: KIAA1328
  hgvsc: ENST00000590617.1:c.*134C>T
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000390515
  ensembl transcript: ENST00000435985
  gene symbol: KIAA1328
  hgvsc: ENST00000435985.2:c.-378C>T
  variant of: http://identifiers.org/hgnc/29248
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2750
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1290
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2995
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6614
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1272
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14357
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26143
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1976
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 261
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 523
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2317
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4571
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Gln159Ter
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
population: African
population: European (Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum

18-34539298-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34539298
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 34539298
    reference: chr 18
allele count: 7
allele frequency: 1.066000670057564e-4
allele num: 65666
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000468653
  ensembl transcript: ENST00000592611
  gene symbol: KIAA1328
  hgvsc: ENST00000592611.1:c.*135A>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000467507
  ensembl transcript: ENST00000586135
  gene symbol: KIAA1328
  hgvsc: ENST00000586135.1:c.-277+12818A>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000470002
  ensembl transcript: ENST00000591911
  gene symbol: KIAA1328
  hgvsc: ENST00000591911.1:c.-277+34293A>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000467248
  ensembl transcript: ENST00000590617
  gene symbol: KIAA1328
  hgvsc: ENST00000590617.1:c.*135A>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000465550
  ensembl transcript: ENST00000591619
  gene symbol: KIAA1328
  hgvsc: ENST00000591619.1:c.464A>G
  hgvsp: ENSP00000465550.1:p.Gln155Arg
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000466355
  ensembl transcript: ENST00000587139
  gene symbol: KIAA1328
  hgvsc: ENST00000587139.1:c.439A>G
  hgvsp: ENSP00000466355.1:p.Gln147Arg
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000441359
  ensembl transcript: ENST00000543923
  gene symbol: KIAA1328
  hgvsc: ENST00000543923.1:c.152A>G
  hgvsp: ENSP00000441359.1:p.Gln51Arg
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000390515
  ensembl transcript: ENST00000435985
  gene symbol: KIAA1328
  hgvsc: ENST00000435985.2:c.-377A>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000280020
  ensembl transcript: ENST00000280020
  gene symbol: KIAA1328
  hgvsc: ENST00000280020.5:c.476A>G
  hgvsp: ENSP00000280020.5:p.Gln159Arg
  variant of: http://identifiers.org/hgnc/29248
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26070
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6741
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1289
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3026
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3039
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13988
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1976
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1266
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2373
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1351
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1383
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 534
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Gln159Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: Other
population: East Asian
reference allele: A
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum

18-34539302-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34539302
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 34539302
    reference: chr 18
allele count: 1
allele frequency: 1.497274959573576e-5
allele num: 66788
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000465550
  ensembl transcript: ENST00000591619
  gene symbol: KIAA1328
  hgvsc: ENST00000591619.1:c.468A>G
  hgvsp: ENST00000591619.1:c.468A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000467248
  ensembl transcript: ENST00000590617
  gene symbol: KIAA1328
  hgvsc: ENST00000590617.1:c.*139A>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000470002
  ensembl transcript: ENST00000591911
  gene symbol: KIAA1328
  hgvsc: ENST00000591911.1:c.-277+34297A>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000280020
  ensembl transcript: ENST00000280020
  gene symbol: KIAA1328
  hgvsc: ENST00000280020.5:c.480A>G
  hgvsp: ENST00000280020.5:c.480A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000468653
  ensembl transcript: ENST00000592611
  gene symbol: KIAA1328
  hgvsc: ENST00000592611.1:c.*139A>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000466355
  ensembl transcript: ENST00000587139
  gene symbol: KIAA1328
  hgvsc: ENST00000587139.1:c.443A>G
  hgvsp: ENST00000587139.1:c.443A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000390515
  ensembl transcript: ENST00000435985
  gene symbol: KIAA1328
  hgvsc: ENST00000435985.2:c.-373A>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000441359
  ensembl transcript: ENST00000543923
  gene symbol: KIAA1328
  hgvsc: ENST00000543923.1:c.156A>G
  hgvsp: ENST00000543923.1:c.156A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000467507
  ensembl transcript: ENST00000586135
  gene symbol: KIAA1328
  hgvsc: ENST00000586135.1:c.-277+12822A>G
  variant of: http://identifiers.org/hgnc/29248
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14387
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1205
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3060
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1976
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25633
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6800
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1271
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3066
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 631
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 607
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1261
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 853
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Glu160Glu
num of homozygotes: 0
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
population: African
reference allele: A
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum

18-34539303-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34539303
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 34539303
    reference: chr 18
allele count: 8
allele frequency: 1.196565855993299e-4
allele num: 66858
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000468653
  ensembl transcript: ENST00000592611
  gene symbol: KIAA1328
  hgvsc: ENST00000592611.1:c.*140C>T
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000441359
  ensembl transcript: ENST00000543923
  gene symbol: KIAA1328
  hgvsc: ENST00000543923.1:c.157C>T
  hgvsp: ENSP00000441359.1:p.Leu53Phe
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000467507
  ensembl transcript: ENST00000586135
  gene symbol: KIAA1328
  hgvsc: ENST00000586135.1:c.-277+12823C>T
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000280020
  ensembl transcript: ENST00000280020
  gene symbol: KIAA1328
  hgvsc: ENST00000280020.5:c.481C>T
  hgvsp: ENSP00000280020.5:p.Leu161Phe
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000467248
  ensembl transcript: ENST00000590617
  gene symbol: KIAA1328
  hgvsc: ENST00000590617.1:c.*140C>T
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000466355
  ensembl transcript: ENST00000587139
  gene symbol: KIAA1328
  hgvsc: ENST00000587139.1:c.444C>T
  hgvsp: ENSP00000466355.1:p.Leu149Phe
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000465550
  ensembl transcript: ENST00000591619
  gene symbol: KIAA1328
  hgvsc: ENST00000591619.1:c.469C>T
  hgvsp: ENSP00000465550.1:p.Leu157Phe
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000390515
  ensembl transcript: ENST00000435985
  gene symbol: KIAA1328
  hgvsc: ENST00000435985.2:c.-372C>T
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000470002
  ensembl transcript: ENST00000591911
  gene symbol: KIAA1328
  hgvsc: ENST00000591911.1:c.-277+34298C>T
  variant of: http://identifiers.org/hgnc/29248
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3106
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6833
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1190
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3265
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25516
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14232
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1976
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1283
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 645
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 260
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 471
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 119
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Leu161Phe
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: Other
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD

18-34539309-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34539309
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 34539309
    reference: chr 18
allele count: 3
allele frequency: 4.391743522178305e-5
allele num: 68310
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000441359
  ensembl transcript: ENST00000543923
  gene symbol: KIAA1328
  hgvsc: ENST00000543923.1:c.163A>G
  hgvsp: ENSP00000441359.1:p.Ser55Gly
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000467248
  ensembl transcript: ENST00000590617
  gene symbol: KIAA1328
  hgvsc: ENST00000590617.1:c.*146A>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000390515
  ensembl transcript: ENST00000435985
  gene symbol: KIAA1328
  hgvsc: ENST00000435985.2:c.-366A>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000467507
  ensembl transcript: ENST00000586135
  gene symbol: KIAA1328
  hgvsc: ENST00000586135.1:c.-277+12829A>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000470002
  ensembl transcript: ENST00000591911
  gene symbol: KIAA1328
  hgvsc: ENST00000591911.1:c.-277+34304A>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000466355
  ensembl transcript: ENST00000587139
  gene symbol: KIAA1328
  hgvsc: ENST00000587139.1:c.450A>G
  hgvsp: ENSP00000466355.1:p.Ser151Gly
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000468653
  ensembl transcript: ENST00000592611
  gene symbol: KIAA1328
  hgvsc: ENST00000592611.1:c.*146A>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000465550
  ensembl transcript: ENST00000591619
  gene symbol: KIAA1328
  hgvsc: ENST00000591619.1:c.475A>G
  hgvsp: ENSP00000465550.1:p.Ser159Gly
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000280020
  ensembl transcript: ENST00000280020
  gene symbol: KIAA1328
  hgvsc: ENST00000280020.5:c.487A>G
  hgvsp: ENSP00000280020.5:p.Ser163Gly
  variant of: http://identifiers.org/hgnc/29248
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1086
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3616
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1976
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24914
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14313
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7001
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3221
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1273
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25849
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4574
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 208
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 721
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Ser163Gly
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
population: Latino
population: European (Finnish)
population: African
reference allele: A
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD

18-34539312-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34539312
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 34539312
    reference: chr 18
allele count: 1
allele frequency: 1.441545336600836e-5
allele num: 69370
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000466355
  ensembl transcript: ENST00000587139
  gene symbol: KIAA1328
  hgvsc: ENST00000587139.1:c.453C>G
  hgvsp: ENSP00000466355.1:p.Leu152Val
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000467248
  ensembl transcript: ENST00000590617
  gene symbol: KIAA1328
  hgvsc: ENST00000590617.1:c.*149C>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000468653
  ensembl transcript: ENST00000592611
  gene symbol: KIAA1328
  hgvsc: ENST00000592611.1:c.*149C>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000467507
  ensembl transcript: ENST00000586135
  gene symbol: KIAA1328
  hgvsc: ENST00000586135.1:c.-277+12832C>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000390515
  ensembl transcript: ENST00000435985
  gene symbol: KIAA1328
  hgvsc: ENST00000435985.2:c.-363C>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000441359
  ensembl transcript: ENST00000543923
  gene symbol: KIAA1328
  hgvsc: ENST00000543923.1:c.166C>G
  hgvsp: ENSP00000441359.1:p.Leu56Val
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000280020
  ensembl transcript: ENST00000280020
  gene symbol: KIAA1328
  hgvsc: ENST00000280020.5:c.490C>G
  hgvsp: ENSP00000280020.5:p.Leu164Val
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000465550
  ensembl transcript: ENST00000591619
  gene symbol: KIAA1328
  hgvsc: ENST00000591619.1:c.478C>G
  hgvsp: ENSP00000465550.1:p.Leu160Val
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000470002
  ensembl transcript: ENST00000591911
  gene symbol: KIAA1328
  hgvsc: ENST00000591911.1:c.-277+34307C>G
  variant of: http://identifiers.org/hgnc/29248
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3345
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24417
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7047
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1976
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1280
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14706
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1001
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3630
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1641
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 260
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 209
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1147
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Leu164Val
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Latino
population: African
population: Other
reference allele: C
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD

18-34539319-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34539319
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 34539319
    reference: chr 18
allele count: 5
allele frequency: 6.997117187718659e-5
allele num: 71458
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000470002
  ensembl transcript: ENST00000591911
  gene symbol: KIAA1328
  hgvsc: ENST00000591911.1:c.-277+34314A>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000465550
  ensembl transcript: ENST00000591619
  gene symbol: KIAA1328
  hgvsc: ENST00000591619.1:c.485A>G
  hgvsp: ENSP00000465550.1:p.Gln162Arg
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000441359
  ensembl transcript: ENST00000543923
  gene symbol: KIAA1328
  hgvsc: ENST00000543923.1:c.173A>G
  hgvsp: ENSP00000441359.1:p.Gln58Arg
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000467507
  ensembl transcript: ENST00000586135
  gene symbol: KIAA1328
  hgvsc: ENST00000586135.1:c.-277+12839A>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000468653
  ensembl transcript: ENST00000592611
  gene symbol: KIAA1328
  hgvsc: ENST00000592611.1:c.*156A>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000390515
  ensembl transcript: ENST00000435985
  gene symbol: KIAA1328
  hgvsc: ENST00000435985.2:c.-356A>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000467248
  ensembl transcript: ENST00000590617
  gene symbol: KIAA1328
  hgvsc: ENST00000590617.1:c.*156A>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000466355
  ensembl transcript: ENST00000587139
  gene symbol: KIAA1328
  hgvsc: ENST00000587139.1:c.460A>G
  hgvsp: ENSP00000466355.1:p.Gln154Arg
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000280020
  ensembl transcript: ENST00000280020
  gene symbol: KIAA1328
  hgvsc: ENST00000280020.5:c.497A>G
  hgvsp: ENSP00000280020.5:p.Gln166Arg
  variant of: http://identifiers.org/hgnc/29248
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23525
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3500
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7244
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3961
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1976
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1276
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 890
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15032
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 466
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 929
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2432
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24959
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Gln166Arg
num of homozygotes: 0
population: African
population: Other
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD

http://identifiers.org/exac.variant/18-34539323-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34539323
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 34539323
    reference: chr 18
allele count: 1
allele frequency: 1.375705048837529e-5
allele num: 72690
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000465550
  ensembl transcript: ENST00000591619
  gene symbol: KIAA1328
  hgvsc: ENST00000591619.1:c.489A>C
  hgvsp: ENSP00000465550.1:p.Lys163Asn
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000390515
  ensembl transcript: ENST00000435985
  gene symbol: KIAA1328
  hgvsc: ENST00000435985.2:c.-352A>C
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000466355
  ensembl transcript: ENST00000587139
  gene symbol: KIAA1328
  hgvsc: ENST00000587139.1:c.464A>C
  hgvsp: ENSP00000466355.1:p.Lys155Asn
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000280020
  ensembl transcript: ENST00000280020
  gene symbol: KIAA1328
  hgvsc: ENST00000280020.5:c.501A>C
  hgvsp: ENSP00000280020.5:p.Lys167Asn
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000467248
  ensembl transcript: ENST00000590617
  gene symbol: KIAA1328
  hgvsc: ENST00000590617.1:c.*160A>C
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000441359
  ensembl transcript: ENST00000543923
  gene symbol: KIAA1328
  hgvsc: ENST00000543923.1:c.177A>C
  hgvsp: ENSP00000441359.1:p.Lys59Asn
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000470002
  ensembl transcript: ENST00000591911
  gene symbol: KIAA1328
  hgvsc: ENST00000591911.1:c.-277+34318A>C
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000468653
  ensembl transcript: ENST00000592611
  gene symbol: KIAA1328
  hgvsc: ENST00000592611.1:c.*160A>C
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000467507
  ensembl transcript: ENST00000586135
  gene symbol: KIAA1328
  hgvsc: ENST00000586135.1:c.-277+12843A>C
  variant of: http://identifiers.org/hgnc/29248
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3985
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7264
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3665
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15371
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1273
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23060
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 815
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1976
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24667
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 854
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1179
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2395
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Lys167Asn
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
reference allele: A
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: FS
site quality: VQSLOD

18-34539336-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34539336
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 34539336
    reference: chr 18
allele count: 1
allele frequency: 1.295605306799337e-5
allele num: 77184
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000468653
  ensembl transcript: ENST00000592611
  gene symbol: KIAA1328
  hgvsc: ENST00000592611.1:c.*173C>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000466355
  ensembl transcript: ENST00000587139
  gene symbol: KIAA1328
  hgvsc: ENST00000587139.1:c.477C>G
  hgvsp: ENSP00000466355.1:p.Gln160Glu
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000390515
  ensembl transcript: ENST00000435985
  gene symbol: KIAA1328
  hgvsc: ENST00000435985.2:c.-339C>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000280020
  ensembl transcript: ENST00000280020
  gene symbol: KIAA1328
  hgvsc: ENST00000280020.5:c.514C>G
  hgvsp: ENSP00000280020.5:p.Gln172Glu
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000441359
  ensembl transcript: ENST00000543923
  gene symbol: KIAA1328
  hgvsc: ENST00000543923.1:c.190C>G
  hgvsp: ENSP00000441359.1:p.Gln64Glu
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000465550
  ensembl transcript: ENST00000591619
  gene symbol: KIAA1328
  hgvsc: ENST00000591619.1:c.502C>G
  hgvsp: ENSP00000465550.1:p.Gln168Glu
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000470002
  ensembl transcript: ENST00000591911
  gene symbol: KIAA1328
  hgvsc: ENST00000591911.1:c.-277+34331C>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000467507
  ensembl transcript: ENST00000586135
  gene symbol: KIAA1328
  hgvsc: ENST00000586135.1:c.-277+12856C>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000467248
  ensembl transcript: ENST00000590617
  gene symbol: KIAA1328
  hgvsc: ENST00000590617.1:c.*173C>G
  variant of: http://identifiers.org/hgnc/29248
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17812
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3723
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1302
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7032
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20905
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4063
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1976
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 360
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 581
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 722
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1704
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Gln172Glu
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum

18-34539338-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34539338
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 34539338
    reference: chr 18
allele count: 1
allele frequency: 1.281065846784525e-5
allele num: 78060
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000465550
  ensembl transcript: ENST00000591619
  gene symbol: KIAA1328
  hgvsc: ENST00000591619.1:c.504A>G
  hgvsp: ENST00000591619.1:c.504A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000280020
  ensembl transcript: ENST00000280020
  gene symbol: KIAA1328
  hgvsc: ENST00000280020.5:c.516A>G
  hgvsp: ENST00000280020.5:c.516A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000390515
  ensembl transcript: ENST00000435985
  gene symbol: KIAA1328
  hgvsc: ENST00000435985.2:c.-337A>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000441359
  ensembl transcript: ENST00000543923
  gene symbol: KIAA1328
  hgvsc: ENST00000543923.1:c.192A>G
  hgvsp: ENST00000543923.1:c.192A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000467248
  ensembl transcript: ENST00000590617
  gene symbol: KIAA1328
  hgvsc: ENST00000590617.1:c.*175A>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000466355
  ensembl transcript: ENST00000587139
  gene symbol: KIAA1328
  hgvsc: ENST00000587139.1:c.479A>G
  hgvsp: ENST00000587139.1:c.479A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000468653
  ensembl transcript: ENST00000592611
  gene symbol: KIAA1328
  hgvsc: ENST00000592611.1:c.*175A>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000467507
  ensembl transcript: ENST00000586135
  gene symbol: KIAA1328
  hgvsc: ENST00000586135.1:c.-277+12858A>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000470002
  ensembl transcript: ENST00000591911
  gene symbol: KIAA1328
  hgvsc: ENST00000591911.1:c.-277+34333A>G
  variant of: http://identifiers.org/hgnc/29248
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18416
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3596
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4039
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6949
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1293
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20578
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1976
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2155
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 512
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1082
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 962
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Gln172Gln
num of homozygotes: 0
population: Other
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
reference allele: A
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum

18-34539352-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34539352
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 34539352
    reference: chr 18
allele count: 9
allele frequency: 1.0791625698458e-4
allele num: 83398
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000470002
  ensembl transcript: ENST00000591911
  gene symbol: KIAA1328
  hgvsc: ENST00000591911.1:c.-277+34347C>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000466355
  ensembl transcript: ENST00000587139
  gene symbol: KIAA1328
  hgvsc: ENST00000587139.1:c.493C>G
  hgvsp: ENSP00000466355.1:p.Thr165Ser
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000390515
  ensembl transcript: ENST00000435985
  gene symbol: KIAA1328
  hgvsc: ENST00000435985.2:c.-323C>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000467248
  ensembl transcript: ENST00000590617
  gene symbol: KIAA1328
  hgvsc: ENST00000590617.1:c.*189C>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000280020
  ensembl transcript: ENST00000280020
  gene symbol: KIAA1328
  hgvsc: ENST00000280020.5:c.530C>G
  hgvsp: ENSP00000280020.5:p.Thr177Ser
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000467507
  ensembl transcript: ENST00000586135
  gene symbol: KIAA1328
  hgvsc: ENST00000586135.1:c.-277+12872C>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000465550
  ensembl transcript: ENST00000591619
  gene symbol: KIAA1328
  hgvsc: ENST00000591619.1:c.518C>G
  hgvsp: ENSP00000465550.1:p.Thr173Ser
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000468653
  ensembl transcript: ENST00000592611
  gene symbol: KIAA1328
  hgvsc: ENST00000592611.1:c.*189C>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000441359
  ensembl transcript: ENST00000543923
  gene symbol: KIAA1328
  hgvsc: ENST00000543923.1:c.206C>G
  hgvsp: ENSP00000441359.1:p.Thr69Ser
  variant of: http://identifiers.org/hgnc/29248
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21497
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18085
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6632
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4431
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1336
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1976
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3056
  bin: 1.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20757
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1900
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4583
  bin: 9.75e1
  variant carriers: 9
genotype quality: GenotypeQuality
  all individuals: 558
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Thr177Ser
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
reference allele: C
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: VQSLOD

18-34539354-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34539354
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 34539354
    reference: chr 18
allele count: 1
allele frequency: 1.185901997058963e-5
allele num: 84324
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000465550
  ensembl transcript: ENST00000591619
  gene symbol: KIAA1328
  hgvsc: ENST00000591619.1:c.520A>G
  hgvsp: ENSP00000465550.1:p.Met174Val
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000280020
  ensembl transcript: ENST00000280020
  gene symbol: KIAA1328
  hgvsc: ENST00000280020.5:c.532A>G
  hgvsp: ENSP00000280020.5:p.Met178Val
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000441359
  ensembl transcript: ENST00000543923
  gene symbol: KIAA1328
  hgvsc: ENST00000543923.1:c.208A>G
  hgvsp: ENSP00000441359.1:p.Met70Val
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000467248
  ensembl transcript: ENST00000590617
  gene symbol: KIAA1328
  hgvsc: ENST00000590617.1:c.*191A>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000467507
  ensembl transcript: ENST00000586135
  gene symbol: KIAA1328
  hgvsc: ENST00000586135.1:c.-277+12874A>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000390515
  ensembl transcript: ENST00000435985
  gene symbol: KIAA1328
  hgvsc: ENST00000435985.2:c.-321A>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000466355
  ensembl transcript: ENST00000587139
  gene symbol: KIAA1328
  hgvsc: ENST00000587139.1:c.495A>G
  hgvsp: ENSP00000466355.1:p.Met166Val
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000468653
  ensembl transcript: ENST00000592611
  gene symbol: KIAA1328
  hgvsc: ENST00000592611.1:c.*191A>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000470002
  ensembl transcript: ENST00000591911
  gene symbol: KIAA1328
  hgvsc: ENST00000591911.1:c.-277+34349A>G
  variant of: http://identifiers.org/hgnc/29248
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1976
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4469
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17744
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1334
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2883
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6541
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22095
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1197
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 210
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1921
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 444
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Met178Val
num of homozygotes: 0
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
reference allele: A
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ

18-34539360-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34539360
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 34539360
    reference: chr 18
allele count: 2
allele frequency: 2.332089552238806e-5
allele num: 85760
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000280020
  ensembl transcript: ENST00000280020
  gene symbol: KIAA1328
  hgvsc: ENST00000280020.5:c.538C>G
  hgvsp: ENSP00000280020.5:p.Leu180Val
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000467507
  ensembl transcript: ENST00000586135
  gene symbol: KIAA1328
  hgvsc: ENST00000586135.1:c.-277+12880C>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000468653
  ensembl transcript: ENST00000592611
  gene symbol: KIAA1328
  hgvsc: ENST00000592611.1:c.*197C>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000465550
  ensembl transcript: ENST00000591619
  gene symbol: KIAA1328
  hgvsc: ENST00000591619.1:c.526C>G
  hgvsp: ENSP00000465550.1:p.Leu176Val
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000466355
  ensembl transcript: ENST00000587139
  gene symbol: KIAA1328
  hgvsc: ENST00000587139.1:c.501C>G
  hgvsp: ENSP00000466355.1:p.Leu168Val
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000390515
  ensembl transcript: ENST00000435985
  gene symbol: KIAA1328
  hgvsc: ENST00000435985.2:c.-315C>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000441359
  ensembl transcript: ENST00000543923
  gene symbol: KIAA1328
  hgvsc: ENST00000543923.1:c.214C>G
  hgvsp: ENSP00000441359.1:p.Leu72Val
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000470002
  ensembl transcript: ENST00000591911
  gene symbol: KIAA1328
  hgvsc: ENST00000591911.1:c.-277+34355C>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000467248
  ensembl transcript: ENST00000590617
  gene symbol: KIAA1328
  hgvsc: ENST00000590617.1:c.*197C>G
  variant of: http://identifiers.org/hgnc/29248
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1976
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1347
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6491
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2822
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17005
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22737
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4671
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 392
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 162
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1086
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 261
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Leu180Val
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum

18-34539363-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34539363
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 34539363
    reference: chr 18
allele count: 1
allele frequency: 1.157193112386595e-5
allele num: 86416
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000465550
  ensembl transcript: ENST00000591619
  gene symbol: KIAA1328
  hgvsc: ENST00000591619.1:c.529T>G
  hgvsp: ENSP00000465550.1:p.Ser177Ala
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000470002
  ensembl transcript: ENST00000591911
  gene symbol: KIAA1328
  hgvsc: ENST00000591911.1:c.-277+34358T>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000467248
  ensembl transcript: ENST00000590617
  gene symbol: KIAA1328
  hgvsc: ENST00000590617.1:c.*200T>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000390515
  ensembl transcript: ENST00000435985
  gene symbol: KIAA1328
  hgvsc: ENST00000435985.2:c.-312T>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000466355
  ensembl transcript: ENST00000587139
  gene symbol: KIAA1328
  hgvsc: ENST00000587139.1:c.504T>G
  hgvsp: ENSP00000466355.1:p.Ser169Ala
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000280020
  ensembl transcript: ENST00000280020
  gene symbol: KIAA1328
  hgvsc: ENST00000280020.5:c.541T>G
  hgvsp: ENSP00000280020.5:p.Ser181Ala
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000468653
  ensembl transcript: ENST00000592611
  gene symbol: KIAA1328
  hgvsc: ENST00000592611.1:c.*200T>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000441359
  ensembl transcript: ENST00000543923
  gene symbol: KIAA1328
  hgvsc: ENST00000543923.1:c.217T>G
  hgvsp: ENSP00000441359.1:p.Ser73Ala
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000467507
  ensembl transcript: ENST00000586135
  gene symbol: KIAA1328
  hgvsc: ENST00000586135.1:c.-277+12883T>G
  variant of: http://identifiers.org/hgnc/29248
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6535
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2712
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4715
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1350
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16701
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23079
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1976
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 302
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 411
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 147
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 433
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Ser181Ala
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
reference allele: T
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum

18-34539368-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34539368
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 34539368
    reference: chr 18
allele count: 1
allele frequency: 1.14544913060411e-5
allele num: 87302
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000466355
  ensembl transcript: ENST00000587139
  gene symbol: KIAA1328
  hgvsc: ENST00000587139.1:c.509A>G
  hgvsp: ENST00000587139.1:c.509A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000467248
  ensembl transcript: ENST00000590617
  gene symbol: KIAA1328
  hgvsc: ENST00000590617.1:c.*205A>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000467507
  ensembl transcript: ENST00000586135
  gene symbol: KIAA1328
  hgvsc: ENST00000586135.1:c.-277+12888A>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000441359
  ensembl transcript: ENST00000543923
  gene symbol: KIAA1328
  hgvsc: ENST00000543923.1:c.222A>G
  hgvsp: ENST00000543923.1:c.222A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000465550
  ensembl transcript: ENST00000591619
  gene symbol: KIAA1328
  hgvsc: ENST00000591619.1:c.534A>G
  hgvsp: ENST00000591619.1:c.534A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000390515
  ensembl transcript: ENST00000435985
  gene symbol: KIAA1328
  hgvsc: ENST00000435985.2:c.-307A>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000280020
  ensembl transcript: ENST00000280020
  gene symbol: KIAA1328
  hgvsc: ENST00000280020.5:c.546A>G
  hgvsp: ENST00000280020.5:c.546A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000470002
  ensembl transcript: ENST00000591911
  gene symbol: KIAA1328
  hgvsc: ENST00000591911.1:c.-277+34363A>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000468653
  ensembl transcript: ENST00000592611
  gene symbol: KIAA1328
  hgvsc: ENST00000592611.1:c.*205A>G
  variant of: http://identifiers.org/hgnc/29248
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1354
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23384
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2573
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16304
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4843
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6637
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1976
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1845
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 260
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 430
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 368
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Glu182Glu
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: A
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD

18-34539379-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34539379
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 34539379
    reference: chr 18
allele count: 33
allele frequency: 3.73244056371163e-4
allele num: 88414
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000390515
  ensembl transcript: ENST00000435985
  gene symbol: KIAA1328
  hgvsc: ENST00000435985.2:c.-296C>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000465550
  ensembl transcript: ENST00000591619
  gene symbol: KIAA1328
  hgvsc: ENST00000591619.1:c.545C>G
  hgvsp: ENSP00000465550.1:p.Ala182Gly
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000470002
  ensembl transcript: ENST00000591911
  gene symbol: KIAA1328
  hgvsc: ENST00000591911.1:c.-277+34374C>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000468653
  ensembl transcript: ENST00000592611
  gene symbol: KIAA1328
  hgvsc: ENST00000592611.1:c.*216C>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000441359
  ensembl transcript: ENST00000543923
  gene symbol: KIAA1328
  hgvsc: ENST00000543923.1:c.233C>G
  hgvsp: ENSP00000441359.1:p.Ala78Gly
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000467248
  ensembl transcript: ENST00000590617
  gene symbol: KIAA1328
  hgvsc: ENST00000590617.1:c.*216C>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000280020
  ensembl transcript: ENST00000280020
  gene symbol: KIAA1328
  hgvsc: ENST00000280020.5:c.557C>G
  hgvsp: ENSP00000280020.5:p.Ala186Gly
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000467507
  ensembl transcript: ENST00000586135
  gene symbol: KIAA1328
  hgvsc: ENST00000586135.1:c.-277+12899C>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000466355
  ensembl transcript: ENST00000587139
  gene symbol: KIAA1328
  hgvsc: ENST00000587139.1:c.520C>G
  hgvsp: ENSP00000466355.1:p.Ala174Gly
  variant of: http://identifiers.org/hgnc/29248
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2129
  bin: 1.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5230
  bin: 2.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23443
  bin: 2.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 1980
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7257
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1370
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15619
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1004
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 328
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1972
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 418
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Ala186Gly
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: C
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum

http://identifiers.org/exac.variant/18-34539392-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34539392
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 34539392
    reference: chr 18
allele count: 1
allele frequency: 1.128744610244486e-5
allele num: 88594
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000467248
  ensembl transcript: ENST00000590617
  gene symbol: KIAA1328
  hgvsc: ENST00000590617.1:c.*229A>C
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000466355
  ensembl transcript: ENST00000587139
  gene symbol: KIAA1328
  hgvsc: ENST00000587139.1:c.533A>C
  hgvsp: ENSP00000466355.1:p.Glu178Asp
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000390515
  ensembl transcript: ENST00000435985
  gene symbol: KIAA1328
  hgvsc: ENST00000435985.2:c.-283A>C
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000470002
  ensembl transcript: ENST00000591911
  gene symbol: KIAA1328
  hgvsc: ENST00000591911.1:c.-277+34387A>C
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000468653
  ensembl transcript: ENST00000592611
  gene symbol: KIAA1328
  hgvsc: ENST00000592611.1:c.*229A>C
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000465550
  ensembl transcript: ENST00000591619
  gene symbol: KIAA1328
  hgvsc: ENST00000591619.1:c.558A>C
  hgvsp: ENSP00000465550.1:p.Glu186Asp
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000280020
  ensembl transcript: ENST00000280020
  gene symbol: KIAA1328
  hgvsc: ENST00000280020.5:c.570A>C
  hgvsp: ENSP00000280020.5:p.Glu190Asp
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000441359
  ensembl transcript: ENST00000543923
  gene symbol: KIAA1328
  hgvsc: ENST00000543923.1:c.246A>C
  hgvsp: ENSP00000441359.1:p.Glu82Asp
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000467507
  ensembl transcript: ENST00000586135
  gene symbol: KIAA1328
  hgvsc: ENST00000586135.1:c.-277+12912A>C
  variant of: http://identifiers.org/hgnc/29248
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1332
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20409
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5541
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10074
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15457
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2079
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1979
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 629
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 158
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20615
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 448
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Glu190Asp
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
reference allele: A
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: DP

18-34539393-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34539393
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 34539393
    reference: chr 18
allele count: 1
allele frequency: 1.129024974032426e-5
allele num: 88572
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000467507
  ensembl transcript: ENST00000586135
  gene symbol: KIAA1328
  hgvsc: ENST00000586135.1:c.-277+12913C>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000466355
  ensembl transcript: ENST00000587139
  gene symbol: KIAA1328
  hgvsc: ENST00000587139.1:c.534C>G
  hgvsp: ENSP00000466355.1:p.Gln179Glu
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000468653
  ensembl transcript: ENST00000592611
  gene symbol: KIAA1328
  hgvsc: ENST00000592611.1:c.*230C>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000470002
  ensembl transcript: ENST00000591911
  gene symbol: KIAA1328
  hgvsc: ENST00000591911.1:c.-277+34388C>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000465550
  ensembl transcript: ENST00000591619
  gene symbol: KIAA1328
  hgvsc: ENST00000591619.1:c.559C>G
  hgvsp: ENSP00000465550.1:p.Gln187Glu
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000390515
  ensembl transcript: ENST00000435985
  gene symbol: KIAA1328
  hgvsc: ENST00000435985.2:c.-282C>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000441359
  ensembl transcript: ENST00000543923
  gene symbol: KIAA1328
  hgvsc: ENST00000543923.1:c.247C>G
  hgvsp: ENSP00000441359.1:p.Gln83Glu
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000280020
  ensembl transcript: ENST00000280020
  gene symbol: KIAA1328
  hgvsc: ENST00000280020.5:c.571C>G
  hgvsp: ENSP00000280020.5:p.Gln191Glu
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000467248
  ensembl transcript: ENST00000590617
  gene symbol: KIAA1328
  hgvsc: ENST00000590617.1:c.*230C>G
  variant of: http://identifiers.org/hgnc/29248
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2026
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20428
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10093
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1347
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1979
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15409
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5586
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 570
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 276
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20606
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Gln191Glu
num of homozygotes: 0
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
reference allele: C
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum

18-34539398-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34539398
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 34539398
    reference: chr 18
allele count: 2
allele frequency: 2.272623971637653e-5
allele num: 88004
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000280020
  ensembl transcript: ENST00000280020
  gene symbol: KIAA1328
  hgvsc: ENST00000280020.5:c.576G>C
  hgvsp: ENSP00000280020.5:p.Gln192His
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000441359
  ensembl transcript: ENST00000543923
  gene symbol: KIAA1328
  hgvsc: ENST00000543923.1:c.252G>C
  hgvsp: ENSP00000441359.1:p.Gln84His
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000470002
  ensembl transcript: ENST00000591911
  gene symbol: KIAA1328
  hgvsc: ENST00000591911.1:c.-277+34393G>C
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000390515
  ensembl transcript: ENST00000435985
  gene symbol: KIAA1328
  hgvsc: ENST00000435985.2:c.-277G>C
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000468653
  ensembl transcript: ENST00000592611
  gene symbol: KIAA1328
  hgvsc: ENST00000592611.1:c.*235G>C
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000467507
  ensembl transcript: ENST00000586135
  gene symbol: KIAA1328
  hgvsc: ENST00000586135.1:c.-277+12918G>C
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000465550
  ensembl transcript: ENST00000591619
  gene symbol: KIAA1328
  hgvsc: ENST00000591619.1:c.564G>C
  hgvsp: ENSP00000465550.1:p.Gln188His
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000466355
  ensembl transcript: ENST00000587139
  gene symbol: KIAA1328
  hgvsc: ENST00000587139.1:c.539G>C
  hgvsp: ENSP00000466355.1:p.Gln180His
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000467248
  ensembl transcript: ENST00000590617
  gene symbol: KIAA1328
  hgvsc: ENST00000590617.1:c.*235G>C
  variant of: http://identifiers.org/hgnc/29248
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5267
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11729
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1346
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15540
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2429
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18459
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1979
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2851
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 584
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 335
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Gln192His
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
population: East Asian
reference allele: G
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff

18-34539410-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34539410
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 34539410
    reference: chr 18
allele count: 3
allele frequency: 3.47214184856832e-5
allele num: 86402
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000390515
  ensembl transcript: ENST00000435985
  gene symbol: KIAA1328
  hgvsc: ENST00000435985.2:c.-277+12T>C
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000280020
  ensembl transcript: ENST00000280020
  gene symbol: KIAA1328
  hgvsc: ENST00000280020.5:c.576+12T>C
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000468653
  ensembl transcript: ENST00000592611
  gene symbol: KIAA1328
  hgvsc: ENST00000592611.1:c.*235+12T>C
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000466355
  ensembl transcript: ENST00000587139
  gene symbol: KIAA1328
  hgvsc: ENST00000587139.1:c.539+12T>C
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000470002
  ensembl transcript: ENST00000591911
  gene symbol: KIAA1328
  hgvsc: ENST00000591911.1:c.-277+34405T>C
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000465550
  ensembl transcript: ENST00000591619
  gene symbol: KIAA1328
  hgvsc: ENST00000591619.1:c.564+12T>C
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000441359
  ensembl transcript: ENST00000543923
  gene symbol: KIAA1328
  hgvsc: ENST00000543923.1:c.252+12T>C
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000467507
  ensembl transcript: ENST00000586135
  gene symbol: KIAA1328
  hgvsc: ENST00000586135.1:c.-277+12930T>C
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000467248
  ensembl transcript: ENST00000590617
  gene symbol: KIAA1328
  hgvsc: ENST00000590617.1:c.*235+12T>C
  variant of: http://identifiers.org/hgnc/29248
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13631
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 15360
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4114
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4087
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1979
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15770
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1190
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1280
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 525
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 462
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 511
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1284
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4026
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
reference allele: T
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/18-34539411-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34539411
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 34539411
    reference: chr 18
allele count: 1
allele frequency: 1.156470452179947e-5
allele num: 86470
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000390515
  ensembl transcript: ENST00000435985
  gene symbol: KIAA1328
  hgvsc: ENST00000435985.2:c.-277+13A>C
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000468653
  ensembl transcript: ENST00000592611
  gene symbol: KIAA1328
  hgvsc: ENST00000592611.1:c.*235+13A>C
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000467507
  ensembl transcript: ENST00000586135
  gene symbol: KIAA1328
  hgvsc: ENST00000586135.1:c.-277+12931A>C
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000441359
  ensembl transcript: ENST00000543923
  gene symbol: KIAA1328
  hgvsc: ENST00000543923.1:c.252+13A>C
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000280020
  ensembl transcript: ENST00000280020
  gene symbol: KIAA1328
  hgvsc: ENST00000280020.5:c.576+13A>C
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000466355
  ensembl transcript: ENST00000587139
  gene symbol: KIAA1328
  hgvsc: ENST00000587139.1:c.539+13A>C
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000470002
  ensembl transcript: ENST00000591911
  gene symbol: KIAA1328
  hgvsc: ENST00000591911.1:c.-277+34406A>C
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000465550
  ensembl transcript: ENST00000591619
  gene symbol: KIAA1328
  hgvsc: ENST00000591619.1:c.564+13A>C
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000467248
  ensembl transcript: ENST00000590617
  gene symbol: KIAA1328
  hgvsc: ENST00000590617.1:c.*235+13A>C
  variant of: http://identifiers.org/hgnc/29248
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13656
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15790
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4032
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1979
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1196
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1275
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15377
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4107
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 610
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4024
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 207
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22687
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 321
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: African
population: Latino
population: South Asian
population: East Asian
reference allele: A
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: VQSLOD

18-34539412-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34539412
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 34539412
    reference: chr 18
allele count: 1
allele frequency: 1.157594980668164e-5
allele num: 86386
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000470002
  ensembl transcript: ENST00000591911
  gene symbol: KIAA1328
  hgvsc: ENST00000591911.1:c.-277+34407A>T
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000467248
  ensembl transcript: ENST00000590617
  gene symbol: KIAA1328
  hgvsc: ENST00000590617.1:c.*235+14A>T
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000441359
  ensembl transcript: ENST00000543923
  gene symbol: KIAA1328
  hgvsc: ENST00000543923.1:c.252+14A>T
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000465550
  ensembl transcript: ENST00000591619
  gene symbol: KIAA1328
  hgvsc: ENST00000591619.1:c.564+14A>T
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000280020
  ensembl transcript: ENST00000280020
  gene symbol: KIAA1328
  hgvsc: ENST00000280020.5:c.576+14A>T
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000390515
  ensembl transcript: ENST00000435985
  gene symbol: KIAA1328
  hgvsc: ENST00000435985.2:c.-277+14A>T
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000467507
  ensembl transcript: ENST00000586135
  gene symbol: KIAA1328
  hgvsc: ENST00000586135.1:c.-277+12932A>T
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000468653
  ensembl transcript: ENST00000592611
  gene symbol: KIAA1328
  hgvsc: ENST00000592611.1:c.*235+14A>T
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000466355
  ensembl transcript: ENST00000587139
  gene symbol: KIAA1328
  hgvsc: ENST00000587139.1:c.539+14A>T
  variant of: http://identifiers.org/hgnc/29248
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1980
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13349
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1273
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4208
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1247
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4014
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15570
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15770
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 414
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22704
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 590
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 487
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2209
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
reference allele: A
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

18-34539422-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34539422
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 34539422
    reference: chr 18
allele count: 1
allele frequency: 1.174646431424141e-5
allele num: 85132
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000441359
  ensembl transcript: ENST00000543923
  gene symbol: KIAA1328
  hgvsc: ENST00000543923.1:c.252+24T>C
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000390515
  ensembl transcript: ENST00000435985
  gene symbol: KIAA1328
  hgvsc: ENST00000435985.2:c.-277+24T>C
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000467507
  ensembl transcript: ENST00000586135
  gene symbol: KIAA1328
  hgvsc: ENST00000586135.1:c.-277+12942T>C
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000468653
  ensembl transcript: ENST00000592611
  gene symbol: KIAA1328
  hgvsc: ENST00000592611.1:c.*235+24T>C
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000280020
  ensembl transcript: ENST00000280020
  gene symbol: KIAA1328
  hgvsc: ENST00000280020.5:c.576+24T>C
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000467248
  ensembl transcript: ENST00000590617
  gene symbol: KIAA1328
  hgvsc: ENST00000590617.1:c.*235+24T>C
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000465550
  ensembl transcript: ENST00000591619
  gene symbol: KIAA1328
  hgvsc: ENST00000591619.1:c.564+24T>C
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000466355
  ensembl transcript: ENST00000587139
  gene symbol: KIAA1328
  hgvsc: ENST00000587139.1:c.539+24T>C
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000470002
  ensembl transcript: ENST00000591911
  gene symbol: KIAA1328
  hgvsc: ENST00000591911.1:c.-277+34417T>C
  variant of: http://identifiers.org/hgnc/29248
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3206
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1239
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15860
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1774
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16698
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6189
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10453
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1979
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 591
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3032
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 967
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 639
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 164
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
reference allele: T
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ

18-34539426-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34539426
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 34539426
    reference: chr 18
allele count: 2
allele frequency: 2.377047231928499e-5
allele num: 84138
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000390515
  ensembl transcript: ENST00000435985
  gene symbol: KIAA1328
  hgvsc: ENST00000435985.2:c.-277+28G>T
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000280020
  ensembl transcript: ENST00000280020
  gene symbol: KIAA1328
  hgvsc: ENST00000280020.5:c.576+28G>T
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000470002
  ensembl transcript: ENST00000591911
  gene symbol: KIAA1328
  hgvsc: ENST00000591911.1:c.-277+34421G>T
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000441359
  ensembl transcript: ENST00000543923
  gene symbol: KIAA1328
  hgvsc: ENST00000543923.1:c.252+28G>T
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000466355
  ensembl transcript: ENST00000587139
  gene symbol: KIAA1328
  hgvsc: ENST00000587139.1:c.539+28G>T
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000467507
  ensembl transcript: ENST00000586135
  gene symbol: KIAA1328
  hgvsc: ENST00000586135.1:c.-277+12946G>T
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000468653
  ensembl transcript: ENST00000592611
  gene symbol: KIAA1328
  hgvsc: ENST00000592611.1:c.*235+28G>T
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000467248
  ensembl transcript: ENST00000590617
  gene symbol: KIAA1328
  hgvsc: ENST00000590617.1:c.*235+28G>T
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000465550
  ensembl transcript: ENST00000591619
  gene symbol: KIAA1328
  hgvsc: ENST00000591619.1:c.564+28G>T
  variant of: http://identifiers.org/hgnc/29248
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16032
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1979
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7262
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16677
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9373
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1226
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1979
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2870
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 380
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1149
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2334
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4576
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 594
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Latino
population: African
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: QD

18-34539430-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34539430
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 34539430
    reference: chr 18
allele count: 3
allele frequency: 3.592298112846058e-5
allele num: 83512
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000467248
  ensembl transcript: ENST00000590617
  gene symbol: KIAA1328
  hgvsc: ENST00000590617.1:c.*235+32T>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000390515
  ensembl transcript: ENST00000435985
  gene symbol: KIAA1328
  hgvsc: ENST00000435985.2:c.-277+32T>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000467507
  ensembl transcript: ENST00000586135
  gene symbol: KIAA1328
  hgvsc: ENST00000586135.1:c.-277+12950T>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000465550
  ensembl transcript: ENST00000591619
  gene symbol: KIAA1328
  hgvsc: ENST00000591619.1:c.564+32T>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000466355
  ensembl transcript: ENST00000587139
  gene symbol: KIAA1328
  hgvsc: ENST00000587139.1:c.539+32T>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000470002
  ensembl transcript: ENST00000591911
  gene symbol: KIAA1328
  hgvsc: ENST00000591911.1:c.-277+34425T>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000441359
  ensembl transcript: ENST00000543923
  gene symbol: KIAA1328
  hgvsc: ENST00000543923.1:c.252+32T>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000280020
  ensembl transcript: ENST00000280020
  gene symbol: KIAA1328
  hgvsc: ENST00000280020.5:c.576+32T>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000468653
  ensembl transcript: ENST00000592611
  gene symbol: KIAA1328
  hgvsc: ENST00000592611.1:c.*235+32T>G
  variant of: http://identifiers.org/hgnc/29248
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1205
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8141
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16223
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2148
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2658
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16583
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8457
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1980
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 909
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 256
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1854
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1074
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 206
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
population: African
population: European (Finnish)
reference allele: T
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum

18-34539431-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34539431
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 34539431
    reference: chr 18
allele count: 1
allele frequency: 1.200768491834774e-5
allele num: 83280
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000280020
  ensembl transcript: ENST00000280020
  gene symbol: KIAA1328
  hgvsc: ENST00000280020.5:c.576+33C>T
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000465550
  ensembl transcript: ENST00000591619
  gene symbol: KIAA1328
  hgvsc: ENST00000591619.1:c.564+33C>T
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000441359
  ensembl transcript: ENST00000543923
  gene symbol: KIAA1328
  hgvsc: ENST00000543923.1:c.252+33C>T
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000390515
  ensembl transcript: ENST00000435985
  gene symbol: KIAA1328
  hgvsc: ENST00000435985.2:c.-277+33C>T
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000470002
  ensembl transcript: ENST00000591911
  gene symbol: KIAA1328
  hgvsc: ENST00000591911.1:c.-277+34426C>T
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000468653
  ensembl transcript: ENST00000592611
  gene symbol: KIAA1328
  hgvsc: ENST00000592611.1:c.*235+33C>T
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000467248
  ensembl transcript: ENST00000590617
  gene symbol: KIAA1328
  hgvsc: ENST00000590617.1:c.*235+33C>T
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000466355
  ensembl transcript: ENST00000587139
  gene symbol: KIAA1328
  hgvsc: ENST00000587139.1:c.539+33C>T
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000467507
  ensembl transcript: ENST00000586135
  gene symbol: KIAA1328
  hgvsc: ENST00000586135.1:c.-277+12951C>T
  variant of: http://identifiers.org/hgnc/29248
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2146
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2661
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8119
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16230
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16592
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1979
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8454
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1211
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 254
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 256
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 885
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 488
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4819
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
population: Latino
population: South Asian
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum

18-34539434-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34539434
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 34539434
    reference: chr 18
allele count: 1
allele frequency: 1.201172344207947e-5
allele num: 83252
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000280020
  ensembl transcript: ENST00000280020
  gene symbol: KIAA1328
  hgvsc: ENST00000280020.5:c.576+36T>A
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000470002
  ensembl transcript: ENST00000591911
  gene symbol: KIAA1328
  hgvsc: ENST00000591911.1:c.-277+34429T>A
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000468653
  ensembl transcript: ENST00000592611
  gene symbol: KIAA1328
  hgvsc: ENST00000592611.1:c.*235+36T>A
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000465550
  ensembl transcript: ENST00000591619
  gene symbol: KIAA1328
  hgvsc: ENST00000591619.1:c.564+36T>A
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000466355
  ensembl transcript: ENST00000587139
  gene symbol: KIAA1328
  hgvsc: ENST00000587139.1:c.539+36T>A
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000441359
  ensembl transcript: ENST00000543923
  gene symbol: KIAA1328
  hgvsc: ENST00000543923.1:c.252+36T>A
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000390515
  ensembl transcript: ENST00000435985
  gene symbol: KIAA1328
  hgvsc: ENST00000435985.2:c.-277+36T>A
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000467248
  ensembl transcript: ENST00000590617
  gene symbol: KIAA1328
  hgvsc: ENST00000590617.1:c.*235+36T>A
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000467507
  ensembl transcript: ENST00000586135
  gene symbol: KIAA1328
  hgvsc: ENST00000586135.1:c.-277+12954T>A
  variant of: http://identifiers.org/hgnc/29248
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1194
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2599
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1979
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16347
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8117
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8405
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2169
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16582
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 580
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2785
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 410
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4868
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1681
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
population: Other
population: East Asian
population: Latino
reference allele: T
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum

18-34539436-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34539436
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 34539436
    reference: chr 18
allele count: 2
allele frequency: 2.425241917881309e-5
allele num: 82466
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000390515
  ensembl transcript: ENST00000435985
  gene symbol: KIAA1328
  hgvsc: ENST00000435985.2:c.-277+38G>T
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000465550
  ensembl transcript: ENST00000591619
  gene symbol: KIAA1328
  hgvsc: ENST00000591619.1:c.564+38G>T
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000466355
  ensembl transcript: ENST00000587139
  gene symbol: KIAA1328
  hgvsc: ENST00000587139.1:c.539+38G>T
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000280020
  ensembl transcript: ENST00000280020
  gene symbol: KIAA1328
  hgvsc: ENST00000280020.5:c.576+38G>T
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000467248
  ensembl transcript: ENST00000590617
  gene symbol: KIAA1328
  hgvsc: ENST00000590617.1:c.*235+38G>T
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000467507
  ensembl transcript: ENST00000586135
  gene symbol: KIAA1328
  hgvsc: ENST00000586135.1:c.-277+12956G>T
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000468653
  ensembl transcript: ENST00000592611
  gene symbol: KIAA1328
  hgvsc: ENST00000592611.1:c.*235+38G>T
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000441359
  ensembl transcript: ENST00000543923
  gene symbol: KIAA1328
  hgvsc: ENST00000543923.1:c.252+38G>T
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000470002
  ensembl transcript: ENST00000591911
  gene symbol: KIAA1328
  hgvsc: ENST00000591911.1:c.-277+34431G>T
  variant of: http://identifiers.org/hgnc/29248
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7695
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16595
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2514
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1184
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8862
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16373
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2178
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1979
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2369
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 575
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 246
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1391
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 409
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff

18-34539441-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34539441
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 34539441
    reference: chr 18
allele count: 0
allele frequency: 0.0e0
allele num: 81870
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000390515
  ensembl transcript: ENST00000435985
  gene symbol: KIAA1328
  hgvsc: ENST00000435985.2:c.-277+43G>A
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000280020
  ensembl transcript: ENST00000280020
  gene symbol: KIAA1328
  hgvsc: ENST00000280020.5:c.576+43G>A
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000468653
  ensembl transcript: ENST00000592611
  gene symbol: KIAA1328
  hgvsc: ENST00000592611.1:c.*235+43G>A
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000465550
  ensembl transcript: ENST00000591619
  gene symbol: KIAA1328
  hgvsc: ENST00000591619.1:c.564+43G>A
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000470002
  ensembl transcript: ENST00000591911
  gene symbol: KIAA1328
  hgvsc: ENST00000591911.1:c.-277+34436G>A
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000467248
  ensembl transcript: ENST00000590617
  gene symbol: KIAA1328
  hgvsc: ENST00000590617.1:c.*235+43G>A
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000466355
  ensembl transcript: ENST00000587139
  gene symbol: KIAA1328
  hgvsc: ENST00000587139.1:c.539+43G>A
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000467507
  ensembl transcript: ENST00000586135
  gene symbol: KIAA1328
  hgvsc: ENST00000586135.1:c.-277+12961G>A
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000441359
  ensembl transcript: ENST00000543923
  gene symbol: KIAA1328
  hgvsc: ENST00000543923.1:c.252+43G>A
  variant of: http://identifiers.org/hgnc/29248
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 2426
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7824
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16811
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8711
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16261
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1181
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2183
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1979
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1354
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 353
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 409
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6200
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2543
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
reference allele: G
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD

18-34646803-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34646803
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 34646803
    reference: chr 18
allele count: 0
allele frequency: 0.0e0
allele num: 30484
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000465550
  ensembl transcript: ENST00000591619
  gene symbol: KIAA1328
  hgvsc: ENST00000591619.1:c.565-50C>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000467507
  ensembl transcript: ENST00000586135
  gene symbol: KIAA1328
  hgvsc: ENST00000586135.1:c.-276-50C>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000441359
  ensembl transcript: ENST00000543923
  gene symbol: KIAA1328
  hgvsc: ENST00000543923.1:c.253-50C>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000280020
  ensembl transcript: ENST00000280020
  gene symbol: KIAA1328
  hgvsc: ENST00000280020.5:c.577-50C>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000470002
  ensembl transcript: ENST00000591911
  gene symbol: KIAA1328
  hgvsc: ENST00000591911.1:c.-276-50C>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000390515
  ensembl transcript: ENST00000435985
  gene symbol: KIAA1328
  hgvsc: ENST00000435985.2:c.-276-50C>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000468653
  ensembl transcript: ENST00000592611
  gene symbol: KIAA1328
  hgvsc: ENST00000592611.1:c.*236-50C>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000467248
  ensembl transcript: ENST00000590617
  gene symbol: KIAA1328
  hgvsc: ENST00000590617.1:c.*236-50C>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000466355
  ensembl transcript: ENST00000587139
  gene symbol: KIAA1328
  hgvsc: ENST00000587139.1:c.540-50C>G
  variant of: http://identifiers.org/hgnc/29248
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 1145
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 719
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16741
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7673
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1805
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 945
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27653
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11384
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 246
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 112
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3036
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 517
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: ReadPosRankSum

18-34646806-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34646806
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 34646806
    reference: chr 18
allele count: 1
allele frequency: 3.27847354271851e-5
allele num: 30502
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000465550
  ensembl transcript: ENST00000591619
  gene symbol: KIAA1328
  hgvsc: ENST00000591619.1:c.565-47G>A
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000470002
  ensembl transcript: ENST00000591911
  gene symbol: KIAA1328
  hgvsc: ENST00000591911.1:c.-276-47G>A
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000441359
  ensembl transcript: ENST00000543923
  gene symbol: KIAA1328
  hgvsc: ENST00000543923.1:c.253-47G>A
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000468653
  ensembl transcript: ENST00000592611
  gene symbol: KIAA1328
  hgvsc: ENST00000592611.1:c.*236-47G>A
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000466355
  ensembl transcript: ENST00000587139
  gene symbol: KIAA1328
  hgvsc: ENST00000587139.1:c.540-47G>A
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000467248
  ensembl transcript: ENST00000590617
  gene symbol: KIAA1328
  hgvsc: ENST00000590617.1:c.*236-47G>A
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000390515
  ensembl transcript: ENST00000435985
  gene symbol: KIAA1328
  hgvsc: ENST00000435985.2:c.-276-47G>A
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000280020
  ensembl transcript: ENST00000280020
  gene symbol: KIAA1328
  hgvsc: ENST00000280020.5:c.577-47G>A
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000467507
  ensembl transcript: ENST00000586135
  gene symbol: KIAA1328
  hgvsc: ENST00000586135.1:c.-276-47G>A
  variant of: http://identifiers.org/hgnc/29248
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16683
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1150
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27689
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1687
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1075
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7676
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 184
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11640
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9801
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3135
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1687
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
population: Latino
population: Other
population: European (Finnish)
reference allele: G
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: DP

18-34646822-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34646822
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 34646822
    reference: chr 18
allele count: 15
allele frequency: 4.64482566421007e-4
allele num: 32294
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000467248
  ensembl transcript: ENST00000590617
  gene symbol: KIAA1328
  hgvsc: ENST00000590617.1:c.*236-31A>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000441359
  ensembl transcript: ENST00000543923
  gene symbol: KIAA1328
  hgvsc: ENST00000543923.1:c.253-31A>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000467507
  ensembl transcript: ENST00000586135
  gene symbol: KIAA1328
  hgvsc: ENST00000586135.1:c.-276-31A>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000465550
  ensembl transcript: ENST00000591619
  gene symbol: KIAA1328
  hgvsc: ENST00000591619.1:c.565-31A>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000466355
  ensembl transcript: ENST00000587139
  gene symbol: KIAA1328
  hgvsc: ENST00000587139.1:c.540-31A>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000468653
  ensembl transcript: ENST00000592611
  gene symbol: KIAA1328
  hgvsc: ENST00000592611.1:c.*236-31A>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000280020
  ensembl transcript: ENST00000280020
  gene symbol: KIAA1328
  hgvsc: ENST00000280020.5:c.577-31A>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000390515
  ensembl transcript: ENST00000435985
  gene symbol: KIAA1328
  hgvsc: ENST00000435985.2:c.-276-31A>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000470002
  ensembl transcript: ENST00000591911
  gene symbol: KIAA1328
  hgvsc: ENST00000591911.1:c.-276-31A>G
  variant of: http://identifiers.org/hgnc/29248
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12081
  bin: 2.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 743
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31563
  bin: 7.5e0
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 817
  bin: 1.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1265
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7840
  bin: 1.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 2709
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3156
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 190
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 642
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2477
  bin: 9.75e1
  variant carriers: 19
genotype quality: GenotypeQuality
  all individuals: 257
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
population: European (Finnish)
reference allele: A
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

18-34646839-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34646839
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 34646839
    reference: chr 18
allele count: 1
allele frequency: 2.639497439687483e-5
allele num: 37886
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000465550
  ensembl transcript: ENST00000591619
  gene symbol: KIAA1328
  hgvsc: ENST00000591619.1:c.565-14G>C
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000467507
  ensembl transcript: ENST00000586135
  gene symbol: KIAA1328
  hgvsc: ENST00000586135.1:c.-276-14G>C
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000467248
  ensembl transcript: ENST00000590617
  gene symbol: KIAA1328
  hgvsc: ENST00000590617.1:c.*236-14G>C
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000470002
  ensembl transcript: ENST00000591911
  gene symbol: KIAA1328
  hgvsc: ENST00000591911.1:c.-276-14G>C
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000441359
  ensembl transcript: ENST00000543923
  gene symbol: KIAA1328
  hgvsc: ENST00000543923.1:c.253-14G>C
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000280020
  ensembl transcript: ENST00000280020
  gene symbol: KIAA1328
  hgvsc: ENST00000280020.5:c.577-14G>C
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000390515
  ensembl transcript: ENST00000435985
  gene symbol: KIAA1328
  hgvsc: ENST00000435985.2:c.-276-14G>C
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000468653
  ensembl transcript: ENST00000592611
  gene symbol: KIAA1328
  hgvsc: ENST00000592611.1:c.*236-14G>C
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000470371
  ensembl transcript: ENST00000586501
  gene symbol: KIAA1328
  hgvsc: ENST00000586501.1:c.-290G>C
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000466355
  ensembl transcript: ENST00000587139
  gene symbol: KIAA1328
  hgvsc: ENST00000587139.1:c.540-14G>C
  variant of: http://identifiers.org/hgnc/29248
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1467
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 914
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6276
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7684
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 34786
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5258
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 779
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1305
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2997
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 259
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Latino
reference allele: G
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: QD

18-34646856-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34646856
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 34646856
    reference: chr 18
allele count: 1
allele frequency: 2.133378845415369e-5
allele num: 46874
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000441359
  ensembl transcript: ENST00000543923
  gene symbol: KIAA1328
  hgvsc: ENST00000543923.1:c.256T>A
  hgvsp: ENSP00000441359.1:p.Ser86Thr
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000466355
  ensembl transcript: ENST00000587139
  gene symbol: KIAA1328
  hgvsc: ENST00000587139.1:c.543T>A
  hgvsp: ENSP00000466355.1:p.Ser182Thr
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000468653
  ensembl transcript: ENST00000592611
  gene symbol: KIAA1328
  hgvsc: ENST00000592611.1:c.*239T>A
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000467507
  ensembl transcript: ENST00000586135
  gene symbol: KIAA1328
  hgvsc: ENST00000586135.1:c.-273T>A
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000390515
  ensembl transcript: ENST00000435985
  gene symbol: KIAA1328
  hgvsc: ENST00000435985.2:c.-273T>A
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000467248
  ensembl transcript: ENST00000590617
  gene symbol: KIAA1328
  hgvsc: ENST00000590617.1:c.*239T>A
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000280020
  ensembl transcript: ENST00000280020
  gene symbol: KIAA1328
  hgvsc: ENST00000280020.5:c.580T>A
  hgvsp: ENSP00000280020.5:p.Ser194Thr
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000470002
  ensembl transcript: ENST00000591911
  gene symbol: KIAA1328
  hgvsc: ENST00000591911.1:c.-273T>A
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000465550
  ensembl transcript: ENST00000591619
  gene symbol: KIAA1328
  hgvsc: ENST00000591619.1:c.568T>A
  hgvsp: ENSP00000465550.1:p.Ser190Thr
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000470371
  ensembl transcript: ENST00000586501
  gene symbol: KIAA1328
  hgvsc: ENST00000586501.1:c.-273T>A
  variant of: http://identifiers.org/hgnc/29248
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9086
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7424
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33634
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 812
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1333
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3095
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1836
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 969
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 327
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Ser194Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
population: Other
population: East Asian
population: European (Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: DP

18-34646856-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34646856
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 34646856
    reference: chr 18
allele count: 2
allele frequency: 4.266757690830738e-5
allele num: 46874
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000466355
  ensembl transcript: ENST00000587139
  gene symbol: KIAA1328
  hgvsc: ENST00000587139.1:c.543T>C
  hgvsp: ENSP00000466355.1:p.Ser182Pro
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000470371
  ensembl transcript: ENST00000586501
  gene symbol: KIAA1328
  hgvsc: ENST00000586501.1:c.-273T>C
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000470002
  ensembl transcript: ENST00000591911
  gene symbol: KIAA1328
  hgvsc: ENST00000591911.1:c.-273T>C
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000468653
  ensembl transcript: ENST00000592611
  gene symbol: KIAA1328
  hgvsc: ENST00000592611.1:c.*239T>C
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000280020
  ensembl transcript: ENST00000280020
  gene symbol: KIAA1328
  hgvsc: ENST00000280020.5:c.580T>C
  hgvsp: ENSP00000280020.5:p.Ser194Pro
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000467248
  ensembl transcript: ENST00000590617
  gene symbol: KIAA1328
  hgvsc: ENST00000590617.1:c.*239T>C
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000441359
  ensembl transcript: ENST00000543923
  gene symbol: KIAA1328
  hgvsc: ENST00000543923.1:c.256T>C
  hgvsp: ENSP00000441359.1:p.Ser86Pro
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000465550
  ensembl transcript: ENST00000591619
  gene symbol: KIAA1328
  hgvsc: ENST00000591619.1:c.568T>C
  hgvsp: ENSP00000465550.1:p.Ser190Pro
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000390515
  ensembl transcript: ENST00000435985
  gene symbol: KIAA1328
  hgvsc: ENST00000435985.2:c.-273T>C
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000467507
  ensembl transcript: ENST00000586135
  gene symbol: KIAA1328
  hgvsc: ENST00000586135.1:c.-273T>C
  variant of: http://identifiers.org/hgnc/29248
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3095
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9086
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33634
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1333
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1836
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 812
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7424
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 147
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33018
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Ser194Pro
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum

18-34646880-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34646880
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 34646880
    reference: chr 18
allele count: 1
allele frequency: 1.575051189163648e-5
allele num: 63490
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000466355
  ensembl transcript: ENST00000587139
  gene symbol: KIAA1328
  hgvsc: ENST00000587139.1:c.567T>A
  hgvsp: ENSP00000466355.1:p.Cys190Ser
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000470002
  ensembl transcript: ENST00000591911
  gene symbol: KIAA1328
  hgvsc: ENST00000591911.1:c.-249T>A
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000467248
  ensembl transcript: ENST00000590617
  gene symbol: KIAA1328
  hgvsc: ENST00000590617.1:c.*263T>A
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000280020
  ensembl transcript: ENST00000280020
  gene symbol: KIAA1328
  hgvsc: ENST00000280020.5:c.604T>A
  hgvsp: ENSP00000280020.5:p.Cys202Ser
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000467507
  ensembl transcript: ENST00000586135
  gene symbol: KIAA1328
  hgvsc: ENST00000586135.1:c.-249T>A
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000441359
  ensembl transcript: ENST00000543923
  gene symbol: KIAA1328
  hgvsc: ENST00000543923.1:c.280T>A
  hgvsp: ENSP00000441359.1:p.Cys94Ser
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000390515
  ensembl transcript: ENST00000435985
  gene symbol: KIAA1328
  hgvsc: ENST00000435985.2:c.-249T>A
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000470371
  ensembl transcript: ENST00000586501
  gene symbol: KIAA1328
  hgvsc: ENST00000586501.1:c.-249T>A
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000465550
  ensembl transcript: ENST00000591619
  gene symbol: KIAA1328
  hgvsc: ENST00000591619.1:c.592T>A
  hgvsp: ENSP00000465550.1:p.Cys198Ser
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000468653
  ensembl transcript: ENST00000592611
  gene symbol: KIAA1328
  hgvsc: ENST00000592611.1:c.*263T>A
  variant of: http://identifiers.org/hgnc/29248
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14847
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27104
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1234
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3133
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7160
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2786
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 976
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2472
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 14497
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Cys202Ser
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: T
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum

18-34646910-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34646910
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 34646910
    reference: chr 18
allele count: 1
allele frequency: 1.187056337693787e-5
allele num: 84242
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000465550
  ensembl transcript: ENST00000591619
  gene symbol: KIAA1328
  hgvsc: ENST00000591619.1:c.622T>C
  hgvsp: ENST00000591619.1:c.622T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000390515
  ensembl transcript: ENST00000435985
  gene symbol: KIAA1328
  hgvsc: ENST00000435985.2:c.-219T>C
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000466355
  ensembl transcript: ENST00000587139
  gene symbol: KIAA1328
  hgvsc: ENST00000587139.1:c.597T>C
  hgvsp: ENST00000587139.1:c.597T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000441359
  ensembl transcript: ENST00000543923
  gene symbol: KIAA1328
  hgvsc: ENST00000543923.1:c.310T>C
  hgvsp: ENST00000543923.1:c.310T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000280020
  ensembl transcript: ENST00000280020
  gene symbol: KIAA1328
  hgvsc: ENST00000280020.5:c.634T>C
  hgvsp: ENST00000280020.5:c.634T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000467248
  ensembl transcript: ENST00000590617
  gene symbol: KIAA1328
  hgvsc: ENST00000590617.1:c.*293T>C
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000467507
  ensembl transcript: ENST00000586135
  gene symbol: KIAA1328
  hgvsc: ENST00000586135.1:c.-219T>C
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000470371
  ensembl transcript: ENST00000586501
  gene symbol: KIAA1328
  hgvsc: ENST00000586501.1:c.-219T>C
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000470002
  ensembl transcript: ENST00000591911
  gene symbol: KIAA1328
  hgvsc: ENST00000591911.1:c.-219T>C
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000468653
  ensembl transcript: ENST00000592611
  gene symbol: KIAA1328
  hgvsc: ENST00000592611.1:c.*293T>C
  variant of: http://identifiers.org/hgnc/29248
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17728
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23589
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5738
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5139
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1356
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3297
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 972
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 180
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Leu212Leu
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: T
site quality: FS
site quality: DP
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum

18-34646914-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34646914
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 34646914
    reference: chr 18
allele count: 1
allele frequency: 1.152711176687569e-5
allele num: 86752
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000467507
  ensembl transcript: ENST00000586135
  gene symbol: KIAA1328
  hgvsc: ENST00000586135.1:c.-215G>C
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000280020
  ensembl transcript: ENST00000280020
  gene symbol: KIAA1328
  hgvsc: ENST00000280020.5:c.638G>C
  hgvsp: ENSP00000280020.5:p.Ser213Thr
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000470002
  ensembl transcript: ENST00000591911
  gene symbol: KIAA1328
  hgvsc: ENST00000591911.1:c.-215G>C
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000470371
  ensembl transcript: ENST00000586501
  gene symbol: KIAA1328
  hgvsc: ENST00000586501.1:c.-215G>C
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000441359
  ensembl transcript: ENST00000543923
  gene symbol: KIAA1328
  hgvsc: ENST00000543923.1:c.314G>C
  hgvsp: ENSP00000441359.1:p.Ser105Thr
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000468653
  ensembl transcript: ENST00000592611
  gene symbol: KIAA1328
  hgvsc: ENST00000592611.1:c.*297G>C
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000465550
  ensembl transcript: ENST00000591619
  gene symbol: KIAA1328
  hgvsc: ENST00000591619.1:c.626G>C
  hgvsp: ENSP00000465550.1:p.Ser209Thr
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000466355
  ensembl transcript: ENST00000587139
  gene symbol: KIAA1328
  hgvsc: ENST00000587139.1:c.601G>C
  hgvsp: ENSP00000466355.1:p.Ser201Thr
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000467248
  ensembl transcript: ENST00000590617
  gene symbol: KIAA1328
  hgvsc: ENST00000590617.1:c.*297G>C
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000390515
  ensembl transcript: ENST00000435985
  gene symbol: KIAA1328
  hgvsc: ENST00000435985.2:c.-215G>C
  variant of: http://identifiers.org/hgnc/29248
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5479
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5412
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24938
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16375
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3240
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1452
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 188
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25755
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Ser213Thr
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum

18-34646924-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34646924
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 34646924
    reference: chr 18
allele count: 1
allele frequency: 1.045565755630372e-5
allele num: 95642
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000280020
  ensembl transcript: ENST00000280020
  gene symbol: KIAA1328
  hgvsc: ENST00000280020.5:c.648A>G
  hgvsp: ENST00000280020.5:c.648A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000466355
  ensembl transcript: ENST00000587139
  gene symbol: KIAA1328
  hgvsc: ENST00000587139.1:c.611A>G
  hgvsp: ENST00000587139.1:c.611A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000467248
  ensembl transcript: ENST00000590617
  gene symbol: KIAA1328
  hgvsc: ENST00000590617.1:c.*307A>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000470371
  ensembl transcript: ENST00000586501
  gene symbol: KIAA1328
  hgvsc: ENST00000586501.1:c.-205A>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000467507
  ensembl transcript: ENST00000586135
  gene symbol: KIAA1328
  hgvsc: ENST00000586135.1:c.-205A>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000390515
  ensembl transcript: ENST00000435985
  gene symbol: KIAA1328
  hgvsc: ENST00000435985.2:c.-205A>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000441359
  ensembl transcript: ENST00000543923
  gene symbol: KIAA1328
  hgvsc: ENST00000543923.1:c.324A>G
  hgvsp: ENST00000543923.1:c.324A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000465550
  ensembl transcript: ENST00000591619
  gene symbol: KIAA1328
  hgvsc: ENST00000591619.1:c.636A>G
  hgvsp: ENST00000591619.1:c.636A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000468653
  ensembl transcript: ENST00000592611
  gene symbol: KIAA1328
  hgvsc: ENST00000592611.1:c.*307A>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000470002
  ensembl transcript: ENST00000591911
  gene symbol: KIAA1328
  hgvsc: ENST00000591911.1:c.-205A>G
  variant of: http://identifiers.org/hgnc/29248
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 586
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2690
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1673
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12284
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4311
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6840
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29187
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 209
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13284
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Arg216Arg
num of homozygotes: 0
population: African
population: South Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: A
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP

18-34646931-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34646931
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 34646931
    reference: chr 18
allele count: 1
allele frequency: 9.912178102016138e-6
allele num: 100886
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000468653
  ensembl transcript: ENST00000592611
  gene symbol: KIAA1328
  hgvsc: ENST00000592611.1:c.*314A>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000390515
  ensembl transcript: ENST00000435985
  gene symbol: KIAA1328
  hgvsc: ENST00000435985.2:c.-198A>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000280020
  ensembl transcript: ENST00000280020
  gene symbol: KIAA1328
  hgvsc: ENST00000280020.5:c.655A>G
  hgvsp: ENSP00000280020.5:p.Thr219Ala
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000467248
  ensembl transcript: ENST00000590617
  gene symbol: KIAA1328
  hgvsc: ENST00000590617.1:c.*314A>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000465550
  ensembl transcript: ENST00000591619
  gene symbol: KIAA1328
  hgvsc: ENST00000591619.1:c.643A>G
  hgvsp: ENSP00000465550.1:p.Thr215Ala
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000466355
  ensembl transcript: ENST00000587139
  gene symbol: KIAA1328
  hgvsc: ENST00000587139.1:c.618A>G
  hgvsp: ENSP00000466355.1:p.Thr207Ala
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000470002
  ensembl transcript: ENST00000591911
  gene symbol: KIAA1328
  hgvsc: ENST00000591911.1:c.-198A>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000470371
  ensembl transcript: ENST00000586501
  gene symbol: KIAA1328
  hgvsc: ENST00000586501.1:c.-198A>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000441359
  ensembl transcript: ENST00000543923
  gene symbol: KIAA1328
  hgvsc: ENST00000543923.1:c.331A>G
  hgvsp: ENSP00000441359.1:p.Thr111Ala
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000467507
  ensembl transcript: ENST00000586135
  gene symbol: KIAA1328
  hgvsc: ENST00000586135.1:c.-198A>G
  variant of: http://identifiers.org/hgnc/29248
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9758
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 586
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7546
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1832
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3542
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2361
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31990
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 828
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 539
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Thr219Ala
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: Other
reference allele: A
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD

18-34646939-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34646939
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 34646939
    reference: chr 18
allele count: 1
allele frequency: 9.494512171964605e-6
allele num: 105324
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000466355
  ensembl transcript: ENST00000587139
  gene symbol: KIAA1328
  hgvsc: ENST00000587139.1:c.626T>C
  hgvsp: ENST00000587139.1:c.626T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000441359
  ensembl transcript: ENST00000543923
  gene symbol: KIAA1328
  hgvsc: ENST00000543923.1:c.339T>C
  hgvsp: ENST00000543923.1:c.339T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000467507
  ensembl transcript: ENST00000586135
  gene symbol: KIAA1328
  hgvsc: ENST00000586135.1:c.-190T>C
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000467248
  ensembl transcript: ENST00000590617
  gene symbol: KIAA1328
  hgvsc: ENST00000590617.1:c.*322T>C
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000470002
  ensembl transcript: ENST00000591911
  gene symbol: KIAA1328
  hgvsc: ENST00000591911.1:c.-190T>C
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000280020
  ensembl transcript: ENST00000280020
  gene symbol: KIAA1328
  hgvsc: ENST00000280020.5:c.663T>C
  hgvsp: ENST00000280020.5:c.663T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000390515
  ensembl transcript: ENST00000435985
  gene symbol: KIAA1328
  hgvsc: ENST00000435985.2:c.-190T>C
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000465550
  ensembl transcript: ENST00000591619
  gene symbol: KIAA1328
  hgvsc: ENST00000591619.1:c.651T>C
  hgvsp: ENST00000591619.1:c.651T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000468653
  ensembl transcript: ENST00000592611
  gene symbol: KIAA1328
  hgvsc: ENST00000592611.1:c.*322T>C
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000470371
  ensembl transcript: ENST00000586501
  gene symbol: KIAA1328
  hgvsc: ENST00000586501.1:c.-190T>C
  variant of: http://identifiers.org/hgnc/29248
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1993
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 606
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7568
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8317
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2822
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1983
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34351
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 224
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36779
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Tyr221Tyr
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
population: Other
reference allele: T
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD

18-34646950-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34646950
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 34646950
    reference: chr 18
allele count: 1
allele frequency: 9.072763563781527e-6
allele num: 110220
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000468653
  ensembl transcript: ENST00000592611
  gene symbol: KIAA1328
  hgvsc: ENST00000592611.1:c.*333A>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000470002
  ensembl transcript: ENST00000591911
  gene symbol: KIAA1328
  hgvsc: ENST00000591911.1:c.-179A>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000441359
  ensembl transcript: ENST00000543923
  gene symbol: KIAA1328
  hgvsc: ENST00000543923.1:c.350A>G
  hgvsp: ENSP00000441359.1:p.Gln117Arg
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000467507
  ensembl transcript: ENST00000586135
  gene symbol: KIAA1328
  hgvsc: ENST00000586135.1:c.-179A>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000470371
  ensembl transcript: ENST00000586501
  gene symbol: KIAA1328
  hgvsc: ENST00000586501.1:c.-179A>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000466355
  ensembl transcript: ENST00000587139
  gene symbol: KIAA1328
  hgvsc: ENST00000587139.1:c.637A>G
  hgvsp: ENSP00000466355.1:p.Gln213Arg
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000465550
  ensembl transcript: ENST00000591619
  gene symbol: KIAA1328
  hgvsc: ENST00000591619.1:c.662A>G
  hgvsp: ENSP00000465550.1:p.Gln221Arg
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000280020
  ensembl transcript: ENST00000280020
  gene symbol: KIAA1328
  hgvsc: ENST00000280020.5:c.674A>G
  hgvsp: ENSP00000280020.5:p.Gln225Arg
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000467248
  ensembl transcript: ENST00000590617
  gene symbol: KIAA1328
  hgvsc: ENST00000590617.1:c.*333A>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000390515
  ensembl transcript: ENST00000435985
  gene symbol: KIAA1328
  hgvsc: ENST00000435985.2:c.-179A>G
  variant of: http://identifiers.org/hgnc/29248
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2008
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2265
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5181
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9538
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1597
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 621
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36459
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1283
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 689
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Gln225Arg
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
reference allele: A
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD

18-34646955-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34646955
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 34646955
    reference: chr 18
allele count: 2
allele frequency: 1.790638541703971e-5
allele num: 111692
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000470371
  ensembl transcript: ENST00000586501
  gene symbol: KIAA1328
  hgvsc: ENST00000586501.1:c.-174C>T
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000467507
  ensembl transcript: ENST00000586135
  gene symbol: KIAA1328
  hgvsc: ENST00000586135.1:c.-174C>T
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000466355
  ensembl transcript: ENST00000587139
  gene symbol: KIAA1328
  hgvsc: ENST00000587139.1:c.642C>T
  hgvsp: ENSP00000466355.1:p.Pro215Ser
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000467248
  ensembl transcript: ENST00000590617
  gene symbol: KIAA1328
  hgvsc: ENST00000590617.1:c.*338C>T
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000390515
  ensembl transcript: ENST00000435985
  gene symbol: KIAA1328
  hgvsc: ENST00000435985.2:c.-174C>T
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000468653
  ensembl transcript: ENST00000592611
  gene symbol: KIAA1328
  hgvsc: ENST00000592611.1:c.*338C>T
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000441359
  ensembl transcript: ENST00000543923
  gene symbol: KIAA1328
  hgvsc: ENST00000543923.1:c.355C>T
  hgvsp: ENSP00000441359.1:p.Pro119Ser
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000280020
  ensembl transcript: ENST00000280020
  gene symbol: KIAA1328
  hgvsc: ENST00000280020.5:c.679C>T
  hgvsp: ENSP00000280020.5:p.Pro227Ser
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000465550
  ensembl transcript: ENST00000591619
  gene symbol: KIAA1328
  hgvsc: ENST00000591619.1:c.667C>T
  hgvsp: ENSP00000465550.1:p.Pro223Ser
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000470002
  ensembl transcript: ENST00000591911
  gene symbol: KIAA1328
  hgvsc: ENST00000591911.1:c.-174C>T
  variant of: http://identifiers.org/hgnc/29248
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 632
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1532
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2372
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4442
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37062
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1776
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9865
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 255
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1229
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Pro227Ser
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
population: Latino
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: QD

18-34646976-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34646976
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 34646976
    reference: chr 18
allele count: 1
allele frequency: 8.576917798819816e-6
allele num: 116592
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000390515
  ensembl transcript: ENST00000435985
  gene symbol: KIAA1328
  hgvsc: ENST00000435985.2:c.-153T>A
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000470002
  ensembl transcript: ENST00000591911
  gene symbol: KIAA1328
  hgvsc: ENST00000591911.1:c.-153T>A
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000466355
  ensembl transcript: ENST00000587139
  gene symbol: KIAA1328
  hgvsc: ENST00000587139.1:c.663T>A
  hgvsp: ENSP00000466355.1:p.Ser222Thr
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000441359
  ensembl transcript: ENST00000543923
  gene symbol: KIAA1328
  hgvsc: ENST00000543923.1:c.376T>A
  hgvsp: ENSP00000441359.1:p.Ser126Thr
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000280020
  ensembl transcript: ENST00000280020
  gene symbol: KIAA1328
  hgvsc: ENST00000280020.5:c.700T>A
  hgvsp: ENSP00000280020.5:p.Ser234Thr
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000467507
  ensembl transcript: ENST00000586135
  gene symbol: KIAA1328
  hgvsc: ENST00000586135.1:c.-153T>A
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000470371
  ensembl transcript: ENST00000586501
  gene symbol: KIAA1328
  hgvsc: ENST00000586501.1:c.-153T>A
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000467248
  ensembl transcript: ENST00000590617
  gene symbol: KIAA1328
  hgvsc: ENST00000590617.1:c.*359T>A
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000468653
  ensembl transcript: ENST00000592611
  gene symbol: KIAA1328
  hgvsc: ENST00000592611.1:c.*359T>A
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000465550
  ensembl transcript: ENST00000591619
  gene symbol: KIAA1328
  hgvsc: ENST00000591619.1:c.688T>A
  hgvsp: ENSP00000465550.1:p.Ser230Thr
  variant of: http://identifiers.org/hgnc/29248
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2039
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 969
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2832
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38904
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 979
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 656
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11296
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43675
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 416
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Ser234Thr
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
reference allele: T
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: BaseQRankSum

18-34646976-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34646976
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 34646976
    reference: chr 18
allele count: 1
allele frequency: 8.576917798819816e-6
allele num: 116592
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000466355
  ensembl transcript: ENST00000587139
  gene symbol: KIAA1328
  hgvsc: ENST00000587139.1:c.663T>G
  hgvsp: ENSP00000466355.1:p.Ser222Ala
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000280020
  ensembl transcript: ENST00000280020
  gene symbol: KIAA1328
  hgvsc: ENST00000280020.5:c.700T>G
  hgvsp: ENSP00000280020.5:p.Ser234Ala
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000468653
  ensembl transcript: ENST00000592611
  gene symbol: KIAA1328
  hgvsc: ENST00000592611.1:c.*359T>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000465550
  ensembl transcript: ENST00000591619
  gene symbol: KIAA1328
  hgvsc: ENST00000591619.1:c.688T>G
  hgvsp: ENSP00000465550.1:p.Ser230Ala
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000470371
  ensembl transcript: ENST00000586501
  gene symbol: KIAA1328
  hgvsc: ENST00000586501.1:c.-153T>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000470002
  ensembl transcript: ENST00000591911
  gene symbol: KIAA1328
  hgvsc: ENST00000591911.1:c.-153T>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000441359
  ensembl transcript: ENST00000543923
  gene symbol: KIAA1328
  hgvsc: ENST00000543923.1:c.376T>G
  hgvsp: ENSP00000441359.1:p.Ser126Ala
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000390515
  ensembl transcript: ENST00000435985
  gene symbol: KIAA1328
  hgvsc: ENST00000435985.2:c.-153T>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000467248
  ensembl transcript: ENST00000590617
  gene symbol: KIAA1328
  hgvsc: ENST00000590617.1:c.*359T>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000467507
  ensembl transcript: ENST00000586135
  gene symbol: KIAA1328
  hgvsc: ENST00000586135.1:c.-153T>G
  variant of: http://identifiers.org/hgnc/29248
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 969
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38904
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11296
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 979
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2039
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 656
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2832
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 854
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 476
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Ser234Ala
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Latino
population: Other
population: African
population: European (Finnish)
reference allele: T
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum

18-34646988-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34646988
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 34646988
    reference: chr 18
allele count: 2
allele frequency: 1.694829076487636e-5
allele num: 118006
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000470371
  ensembl transcript: ENST00000586501
  gene symbol: KIAA1328
  hgvsc: ENST00000586501.1:c.-141T>C
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000465550
  ensembl transcript: ENST00000591619
  gene symbol: KIAA1328
  hgvsc: ENST00000591619.1:c.700T>C
  hgvsp: ENSP00000465550.1:p.Ser234Pro
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000441359
  ensembl transcript: ENST00000543923
  gene symbol: KIAA1328
  hgvsc: ENST00000543923.1:c.388T>C
  hgvsp: ENSP00000441359.1:p.Ser130Pro
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000467248
  ensembl transcript: ENST00000590617
  gene symbol: KIAA1328
  hgvsc: ENST00000590617.1:c.*371T>C
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000280020
  ensembl transcript: ENST00000280020
  gene symbol: KIAA1328
  hgvsc: ENST00000280020.5:c.712T>C
  hgvsp: ENSP00000280020.5:p.Ser238Pro
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000390515
  ensembl transcript: ENST00000435985
  gene symbol: KIAA1328
  hgvsc: ENST00000435985.2:c.-141T>C
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000466355
  ensembl transcript: ENST00000587139
  gene symbol: KIAA1328
  hgvsc: ENST00000587139.1:c.675T>C
  hgvsp: ENSP00000466355.1:p.Ser226Pro
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000467507
  ensembl transcript: ENST00000586135
  gene symbol: KIAA1328
  hgvsc: ENST00000586135.1:c.-141T>C
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000470002
  ensembl transcript: ENST00000591911
  gene symbol: KIAA1328
  hgvsc: ENST00000591911.1:c.-141T>C
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000468653
  ensembl transcript: ENST00000592611
  gene symbol: KIAA1328
  hgvsc: ENST00000592611.1:c.*371T>C
  variant of: http://identifiers.org/hgnc/29248
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 926
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1332
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12054
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38913
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 691
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3049
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 496
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2571
  bin: 9.75e1
  variant carriers: 2
hgvs: p.Ser238Pro
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
population: Latino
reference allele: T
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum

18-34646991-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34646991
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 34646991
    reference: chr 18
allele count: 1
allele frequency: 8.45851942076059e-6
allele num: 118224
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000390515
  ensembl transcript: ENST00000435985
  gene symbol: KIAA1328
  hgvsc: ENST00000435985.2:c.-138C>T
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000441359
  ensembl transcript: ENST00000543923
  gene symbol: KIAA1328
  hgvsc: ENST00000543923.1:c.391C>T
  hgvsp: ENSP00000441359.1:p.Leu131Phe
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000467248
  ensembl transcript: ENST00000590617
  gene symbol: KIAA1328
  hgvsc: ENST00000590617.1:c.*374C>T
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000466355
  ensembl transcript: ENST00000587139
  gene symbol: KIAA1328
  hgvsc: ENST00000587139.1:c.678C>T
  hgvsp: ENSP00000466355.1:p.Leu227Phe
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000468653
  ensembl transcript: ENST00000592611
  gene symbol: KIAA1328
  hgvsc: ENST00000592611.1:c.*374C>T
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000467507
  ensembl transcript: ENST00000586135
  gene symbol: KIAA1328
  hgvsc: ENST00000586135.1:c.-138C>T
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000280020
  ensembl transcript: ENST00000280020
  gene symbol: KIAA1328
  hgvsc: ENST00000280020.5:c.715C>T
  hgvsp: ENSP00000280020.5:p.Leu239Phe
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000465550
  ensembl transcript: ENST00000591619
  gene symbol: KIAA1328
  hgvsc: ENST00000591619.1:c.703C>T
  hgvsp: ENSP00000465550.1:p.Leu235Phe
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000470371
  ensembl transcript: ENST00000586501
  gene symbol: KIAA1328
  hgvsc: ENST00000586501.1:c.-138C>T
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000470002
  ensembl transcript: ENST00000591911
  gene symbol: KIAA1328
  hgvsc: ENST00000591911.1:c.-138C>T
  variant of: http://identifiers.org/hgnc/29248
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1218
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3157
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12253
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 892
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 645
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38800
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 898
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Leu239Phe
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum

18-34646994-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34646994
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 34646994
    reference: chr 18
allele count: 1
allele frequency: 8.439388313135065e-6
allele num: 118492
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000280020
  ensembl transcript: ENST00000280020
  gene symbol: KIAA1328
  hgvsc: ENST00000280020.5:c.718A>T
  hgvsp: ENSP00000280020.5:p.Ile240Leu
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000467248
  ensembl transcript: ENST00000590617
  gene symbol: KIAA1328
  hgvsc: ENST00000590617.1:c.*377A>T
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000390515
  ensembl transcript: ENST00000435985
  gene symbol: KIAA1328
  hgvsc: ENST00000435985.2:c.-135A>T
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000468653
  ensembl transcript: ENST00000592611
  gene symbol: KIAA1328
  hgvsc: ENST00000592611.1:c.*377A>T
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000466355
  ensembl transcript: ENST00000587139
  gene symbol: KIAA1328
  hgvsc: ENST00000587139.1:c.681A>T
  hgvsp: ENSP00000466355.1:p.Ile228Leu
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000441359
  ensembl transcript: ENST00000543923
  gene symbol: KIAA1328
  hgvsc: ENST00000543923.1:c.394A>T
  hgvsp: ENSP00000441359.1:p.Ile132Leu
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000470371
  ensembl transcript: ENST00000586501
  gene symbol: KIAA1328
  hgvsc: ENST00000586501.1:c.-135A>T
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000465550
  ensembl transcript: ENST00000591619
  gene symbol: KIAA1328
  hgvsc: ENST00000591619.1:c.706A>T
  hgvsp: ENSP00000465550.1:p.Ile236Leu
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000467507
  ensembl transcript: ENST00000586135
  gene symbol: KIAA1328
  hgvsc: ENST00000586135.1:c.-135A>T
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000470002
  ensembl transcript: ENST00000591911
  gene symbol: KIAA1328
  hgvsc: ENST00000591911.1:c.-135A>T
  variant of: http://identifiers.org/hgnc/29248
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 586
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38830
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 865
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12405
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1094
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3189
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 298
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 145
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Ile240Leu
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum

18-34646999-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34646999
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 34646999
    reference: chr 18
allele count: 540
allele frequency: 4.542242858584839e-3
allele num: 118884
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000468653
  ensembl transcript: ENST00000592611
  gene symbol: KIAA1328
  hgvsc: ENST00000592611.1:c.*382A>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000390515
  ensembl transcript: ENST00000435985
  gene symbol: KIAA1328
  hgvsc: ENST00000435985.2:c.-130A>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000470371
  ensembl transcript: ENST00000586501
  gene symbol: KIAA1328
  hgvsc: ENST00000586501.1:c.-130A>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000467507
  ensembl transcript: ENST00000586135
  gene symbol: KIAA1328
  hgvsc: ENST00000586135.1:c.-130A>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000466355
  ensembl transcript: ENST00000587139
  gene symbol: KIAA1328
  hgvsc: ENST00000587139.1:c.686A>G
  hgvsp: ENST00000587139.1:c.686A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000441359
  ensembl transcript: ENST00000543923
  gene symbol: KIAA1328
  hgvsc: ENST00000543923.1:c.399A>G
  hgvsp: ENST00000543923.1:c.399A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000470002
  ensembl transcript: ENST00000591911
  gene symbol: KIAA1328
  hgvsc: ENST00000591911.1:c.-130A>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000280020
  ensembl transcript: ENST00000280020
  gene symbol: KIAA1328
  hgvsc: ENST00000280020.5:c.723A>G
  hgvsp: ENST00000280020.5:c.723A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000465550
  ensembl transcript: ENST00000591619
  gene symbol: KIAA1328
  hgvsc: ENST00000591619.1:c.711A>G
  hgvsp: ENST00000591619.1:c.711A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000467248
  ensembl transcript: ENST00000590617
  gene symbol: KIAA1328
  hgvsc: ENST00000590617.1:c.*382A>G
  variant of: http://identifiers.org/hgnc/29248
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 4.75e1
  variant carriers: 45
genotype depth: GenotypeDepth
  all individuals: 38545
  bin: 2.25e1
  variant carriers: 48
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 5.25e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 12603
  bin: 2.75e1
  variant carriers: 69
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 6.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 1.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 900
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 813
  bin: 1.75e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 811
  bin: 3.75e1
  variant carriers: 101
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 5.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3322
  bin: 3.25e1
  variant carriers: 105
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 4.25e1
  variant carriers: 76
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 253
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Ala241Ala
num of homozygotes: 19
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: Latino
population: South Asian
population: East Asian
population: African
reference allele: A
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum

18-34647006-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34647006
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 34647006
    reference: chr 18
allele count: 1
allele frequency: 8.384619254439656e-6
allele num: 119266
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000465550
  ensembl transcript: ENST00000591619
  gene symbol: KIAA1328
  hgvsc: ENST00000591619.1:c.718A>G
  hgvsp: ENSP00000465550.1:p.Asn240Asp
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000466355
  ensembl transcript: ENST00000587139
  gene symbol: KIAA1328
  hgvsc: ENST00000587139.1:c.693A>G
  hgvsp: ENSP00000466355.1:p.Asn232Asp
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000441359
  ensembl transcript: ENST00000543923
  gene symbol: KIAA1328
  hgvsc: ENST00000543923.1:c.406A>G
  hgvsp: ENSP00000441359.1:p.Asn136Asp
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000470371
  ensembl transcript: ENST00000586501
  gene symbol: KIAA1328
  hgvsc: ENST00000586501.1:c.-123A>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000467248
  ensembl transcript: ENST00000590617
  gene symbol: KIAA1328
  hgvsc: ENST00000590617.1:c.*389A>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000470002
  ensembl transcript: ENST00000591911
  gene symbol: KIAA1328
  hgvsc: ENST00000591911.1:c.-123A>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000280020
  ensembl transcript: ENST00000280020
  gene symbol: KIAA1328
  hgvsc: ENST00000280020.5:c.730A>G
  hgvsp: ENSP00000280020.5:p.Asn244Asp
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000390515
  ensembl transcript: ENST00000435985
  gene symbol: KIAA1328
  hgvsc: ENST00000435985.2:c.-123A>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000467507
  ensembl transcript: ENST00000586135
  gene symbol: KIAA1328
  hgvsc: ENST00000586135.1:c.-123A>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000468653
  ensembl transcript: ENST00000592611
  gene symbol: KIAA1328
  hgvsc: ENST00000592611.1:c.*389A>G
  variant of: http://identifiers.org/hgnc/29248
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3386
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 720
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12865
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 701
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38626
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 820
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 251
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Asn244Asp
num of homozygotes: 0
population: Other
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: A
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD

18-34647019-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34647019
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 34647019
    reference: chr 18
allele count: 1
allele frequency: 8.353381448810478e-6
allele num: 119712
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000466355
  ensembl transcript: ENST00000587139
  gene symbol: KIAA1328
  hgvsc: ENST00000587139.1:c.706A>G
  hgvsp: ENSP00000466355.1:p.Lys236Arg
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000470002
  ensembl transcript: ENST00000591911
  gene symbol: KIAA1328
  hgvsc: ENST00000591911.1:c.-110A>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000280020
  ensembl transcript: ENST00000280020
  gene symbol: KIAA1328
  hgvsc: ENST00000280020.5:c.743A>G
  hgvsp: ENSP00000280020.5:p.Lys248Arg
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000467248
  ensembl transcript: ENST00000590617
  gene symbol: KIAA1328
  hgvsc: ENST00000590617.1:c.*402A>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000465550
  ensembl transcript: ENST00000591619
  gene symbol: KIAA1328
  hgvsc: ENST00000591619.1:c.731A>G
  hgvsp: ENSP00000465550.1:p.Lys244Arg
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000441359
  ensembl transcript: ENST00000543923
  gene symbol: KIAA1328
  hgvsc: ENST00000543923.1:c.419A>G
  hgvsp: ENSP00000441359.1:p.Lys140Arg
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000470371
  ensembl transcript: ENST00000586501
  gene symbol: KIAA1328
  hgvsc: ENST00000586501.1:c.-110A>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000467507
  ensembl transcript: ENST00000586135
  gene symbol: KIAA1328
  hgvsc: ENST00000586135.1:c.-110A>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000390515
  ensembl transcript: ENST00000435985
  gene symbol: KIAA1328
  hgvsc: ENST00000435985.2:c.-110A>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000468653
  ensembl transcript: ENST00000592611
  gene symbol: KIAA1328
  hgvsc: ENST00000592611.1:c.*402A>G
  variant of: http://identifiers.org/hgnc/29248
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 836
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13219
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38596
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3483
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 581
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 126
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Lys248Arg
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
population: African
population: European (Finnish)
reference allele: A
site quality: MQ
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum

18-34647026-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34647026
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 34647026
    reference: chr 18
allele count: 1
allele frequency: 8.338336335134414e-6
allele num: 119928
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000467248
  ensembl transcript: ENST00000590617
  gene symbol: KIAA1328
  hgvsc: ENST00000590617.1:c.*409A>T
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000468653
  ensembl transcript: ENST00000592611
  gene symbol: KIAA1328
  hgvsc: ENST00000592611.1:c.*409A>T
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000470371
  ensembl transcript: ENST00000586501
  gene symbol: KIAA1328
  hgvsc: ENST00000586501.1:c.-103A>T
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000441359
  ensembl transcript: ENST00000543923
  gene symbol: KIAA1328
  hgvsc: ENST00000543923.1:c.426A>T
  hgvsp: ENST00000543923.1:c.426A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000465550
  ensembl transcript: ENST00000591619
  gene symbol: KIAA1328
  hgvsc: ENST00000591619.1:c.738A>T
  hgvsp: ENST00000591619.1:c.738A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000280020
  ensembl transcript: ENST00000280020
  gene symbol: KIAA1328
  hgvsc: ENST00000280020.5:c.750A>T
  hgvsp: ENST00000280020.5:c.750A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000467507
  ensembl transcript: ENST00000586135
  gene symbol: KIAA1328
  hgvsc: ENST00000586135.1:c.-103A>T
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000390515
  ensembl transcript: ENST00000435985
  gene symbol: KIAA1328
  hgvsc: ENST00000435985.2:c.-103A>T
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000470002
  ensembl transcript: ENST00000591911
  gene symbol: KIAA1328
  hgvsc: ENST00000591911.1:c.-103A>T
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000466355
  ensembl transcript: ENST00000587139
  gene symbol: KIAA1328
  hgvsc: ENST00000587139.1:c.713A>T
  hgvsp: ENST00000587139.1:c.713A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29248
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 498
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38578
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13407
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3537
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 845
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 361
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 172
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Val250Val
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: South Asian
population: East Asian
population: European (Finnish)
population: African
population: Latino
reference allele: A
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/18-34647027-A-AC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34647027
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 34647028
    reference: chr 18
allele count: 1
allele frequency: 8.335973058135075e-6
allele num: 119962
alternate allele: AC
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000470371
  ensembl transcript: ENST00000586501
  gene symbol: KIAA1328
  hgvsc: ENST00000586501.1:c.-99dupC
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000466355
  ensembl transcript: ENST00000587139
  gene symbol: KIAA1328
  hgvsc: ENST00000587139.1:c.717dupC
  hgvsp: ENSP00000466355.1:p.Leu240ProfsTer7
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000467507
  ensembl transcript: ENST00000586135
  gene symbol: KIAA1328
  hgvsc: ENST00000586135.1:c.-99dupC
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000441359
  ensembl transcript: ENST00000543923
  gene symbol: KIAA1328
  hgvsc: ENST00000543923.1:c.430dupC
  hgvsp: ENSP00000441359.1:p.Leu144ProfsTer7
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000390515
  ensembl transcript: ENST00000435985
  gene symbol: KIAA1328
  hgvsc: ENST00000435985.2:c.-99dupC
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000465550
  ensembl transcript: ENST00000591619
  gene symbol: KIAA1328
  hgvsc: ENST00000591619.1:c.742dupC
  hgvsp: ENSP00000465550.1:p.Leu248ProfsTer7
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000467248
  ensembl transcript: ENST00000590617
  gene symbol: KIAA1328
  hgvsc: ENST00000590617.1:c.*413dupC
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000470002
  ensembl transcript: ENST00000591911
  gene symbol: KIAA1328
  hgvsc: ENST00000591911.1:c.-99dupC
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000280020
  ensembl transcript: ENST00000280020
  gene symbol: KIAA1328
  hgvsc: ENST00000280020.5:c.754dupC
  hgvsp: ENSP00000280020.5:p.Leu252ProfsTer7
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000468653
  ensembl transcript: ENST00000592611
  gene symbol: KIAA1328
  hgvsc: ENST00000592611.1:c.*413dupC
  variant of: http://identifiers.org/hgnc/29248
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 843
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38572
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13439
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3537
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1031
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Leu252ProfsTer7
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
population: African
population: Latino
population: Other
reference allele: A
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: DP

18-34647028-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34647028
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 34647028
    reference: chr 18
allele count: 3
allele frequency: 2.500500100020004e-5
allele num: 119976
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000280020
  ensembl transcript: ENST00000280020
  gene symbol: KIAA1328
  hgvsc: ENST00000280020.5:c.752C>T
  hgvsp: ENSP00000280020.5:p.Thr251Ile
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000470002
  ensembl transcript: ENST00000591911
  gene symbol: KIAA1328
  hgvsc: ENST00000591911.1:c.-101C>T
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000466355
  ensembl transcript: ENST00000587139
  gene symbol: KIAA1328
  hgvsc: ENST00000587139.1:c.715C>T
  hgvsp: ENSP00000466355.1:p.Thr239Ile
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000465550
  ensembl transcript: ENST00000591619
  gene symbol: KIAA1328
  hgvsc: ENST00000591619.1:c.740C>T
  hgvsp: ENSP00000465550.1:p.Thr247Ile
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000470371
  ensembl transcript: ENST00000586501
  gene symbol: KIAA1328
  hgvsc: ENST00000586501.1:c.-101C>T
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000468653
  ensembl transcript: ENST00000592611
  gene symbol: KIAA1328
  hgvsc: ENST00000592611.1:c.*411C>T
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000441359
  ensembl transcript: ENST00000543923
  gene symbol: KIAA1328
  hgvsc: ENST00000543923.1:c.428C>T
  hgvsp: ENSP00000441359.1:p.Thr143Ile
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000467507
  ensembl transcript: ENST00000586135
  gene symbol: KIAA1328
  hgvsc: ENST00000586135.1:c.-101C>T
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000467248
  ensembl transcript: ENST00000590617
  gene symbol: KIAA1328
  hgvsc: ENST00000590617.1:c.*411C>T
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000390515
  ensembl transcript: ENST00000435985
  gene symbol: KIAA1328
  hgvsc: ENST00000435985.2:c.-101C>T
  variant of: http://identifiers.org/hgnc/29248
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 850
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3548
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38561
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13467
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 384
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Thr251Ile
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum

18-34647029-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34647029
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 34647029
    reference: chr 18
allele count: 1
allele frequency: 8.332777814812346e-6
allele num: 120008
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000467507
  ensembl transcript: ENST00000586135
  gene symbol: KIAA1328
  hgvsc: ENST00000586135.1:c.-100C>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000466355
  ensembl transcript: ENST00000587139
  gene symbol: KIAA1328
  hgvsc: ENST00000587139.1:c.716C>G
  hgvsp: ENST00000587139.1:c.716C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000441359
  ensembl transcript: ENST00000543923
  gene symbol: KIAA1328
  hgvsc: ENST00000543923.1:c.429C>G
  hgvsp: ENST00000543923.1:c.429C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000467248
  ensembl transcript: ENST00000590617
  gene symbol: KIAA1328
  hgvsc: ENST00000590617.1:c.*412C>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000468653
  ensembl transcript: ENST00000592611
  gene symbol: KIAA1328
  hgvsc: ENST00000592611.1:c.*412C>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000390515
  ensembl transcript: ENST00000435985
  gene symbol: KIAA1328
  hgvsc: ENST00000435985.2:c.-100C>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000280020
  ensembl transcript: ENST00000280020
  gene symbol: KIAA1328
  hgvsc: ENST00000280020.5:c.753C>G
  hgvsp: ENST00000280020.5:c.753C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000465550
  ensembl transcript: ENST00000591619
  gene symbol: KIAA1328
  hgvsc: ENST00000591619.1:c.741C>G
  hgvsp: ENST00000591619.1:c.741C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000470371
  ensembl transcript: ENST00000586501
  gene symbol: KIAA1328
  hgvsc: ENST00000586501.1:c.-100C>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000470002
  ensembl transcript: ENST00000591911
  gene symbol: KIAA1328
  hgvsc: ENST00000591911.1:c.-100C>G
  variant of: http://identifiers.org/hgnc/29248
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13494
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3573
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38525
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 847
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 463
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 115
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Thr251Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: Other
population: South Asian
population: European (Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ

18-34647034-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34647034
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 34647034
    reference: chr 18
allele count: 2
allele frequency: 1.665057111458923e-5
allele num: 120116
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000390515
  ensembl transcript: ENST00000435985
  gene symbol: KIAA1328
  hgvsc: ENST00000435985.2:c.-95A>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000466355
  ensembl transcript: ENST00000587139
  gene symbol: KIAA1328
  hgvsc: ENST00000587139.1:c.721A>G
  hgvsp: ENSP00000466355.1:p.His241Arg
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000441359
  ensembl transcript: ENST00000543923
  gene symbol: KIAA1328
  hgvsc: ENST00000543923.1:c.434A>G
  hgvsp: ENSP00000441359.1:p.His145Arg
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000467507
  ensembl transcript: ENST00000586135
  gene symbol: KIAA1328
  hgvsc: ENST00000586135.1:c.-95A>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000470002
  ensembl transcript: ENST00000591911
  gene symbol: KIAA1328
  hgvsc: ENST00000591911.1:c.-95A>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000470371
  ensembl transcript: ENST00000586501
  gene symbol: KIAA1328
  hgvsc: ENST00000586501.1:c.-95A>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000468653
  ensembl transcript: ENST00000592611
  gene symbol: KIAA1328
  hgvsc: ENST00000592611.1:c.*417A>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000467248
  ensembl transcript: ENST00000590617
  gene symbol: KIAA1328
  hgvsc: ENST00000590617.1:c.*417A>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000465550
  ensembl transcript: ENST00000591619
  gene symbol: KIAA1328
  hgvsc: ENST00000591619.1:c.746A>G
  hgvsp: ENSP00000465550.1:p.His249Arg
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000280020
  ensembl transcript: ENST00000280020
  gene symbol: KIAA1328
  hgvsc: ENST00000280020.5:c.758A>G
  hgvsp: ENSP00000280020.5:p.His253Arg
  variant of: http://identifiers.org/hgnc/29248
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 38464
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13623
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 853
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3616
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1831
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 164
  bin: 5.75e1
  variant carriers: 0
hgvs: p.His253Arg
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
reference allele: A
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum

18-34647053-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34647053
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 34647053
    reference: chr 18
allele count: 57
allele frequency: 4.73555655251483e-4
allele num: 120366
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000470371
  ensembl transcript: ENST00000586501
  gene symbol: KIAA1328
  hgvsc: ENST00000586501.1:c.-76A>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000467507
  ensembl transcript: ENST00000586135
  gene symbol: KIAA1328
  hgvsc: ENST00000586135.1:c.-76A>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000280020
  ensembl transcript: ENST00000280020
  gene symbol: KIAA1328
  hgvsc: ENST00000280020.5:c.777A>G
  hgvsp: ENST00000280020.5:c.777A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000390515
  ensembl transcript: ENST00000435985
  gene symbol: KIAA1328
  hgvsc: ENST00000435985.2:c.-76A>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000465550
  ensembl transcript: ENST00000591619
  gene symbol: KIAA1328
  hgvsc: ENST00000591619.1:c.765A>G
  hgvsp: ENST00000591619.1:c.765A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000441359
  ensembl transcript: ENST00000543923
  gene symbol: KIAA1328
  hgvsc: ENST00000543923.1:c.453A>G
  hgvsp: ENST00000543923.1:c.453A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000470002
  ensembl transcript: ENST00000591911
  gene symbol: KIAA1328
  hgvsc: ENST00000591911.1:c.-76A>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000466355
  ensembl transcript: ENST00000587139
  gene symbol: KIAA1328
  hgvsc: ENST00000587139.1:c.740A>G
  hgvsp: ENST00000587139.1:c.740A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000467248
  ensembl transcript: ENST00000590617
  gene symbol: KIAA1328
  hgvsc: ENST00000590617.1:c.*436A>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000468653
  ensembl transcript: ENST00000592611
  gene symbol: KIAA1328
  hgvsc: ENST00000592611.1:c.*436A>G
  variant of: http://identifiers.org/hgnc/29248
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 495
  bin: 4.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 9.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 5.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 869
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 4.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 38131
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 5.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 14013
  bin: 2.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3766
  bin: 3.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 148
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Leu259Leu
num of homozygotes: 1
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: Latino
reference allele: A
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: FS
site quality: VQSLOD

http://identifiers.org/exac.variant/18-34647063-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34647063
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 34647063
    reference: chr 18
allele count: 1
allele frequency: 8.302889405513118e-6
allele num: 120440
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000441359
  ensembl transcript: ENST00000543923
  gene symbol: KIAA1328
  hgvsc: ENST00000543923.1:c.463C>A
  hgvsp: ENSP00000441359.1:p.Pro155Thr
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000470371
  ensembl transcript: ENST00000586501
  gene symbol: KIAA1328
  hgvsc: ENST00000586501.1:c.-66C>A
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000466355
  ensembl transcript: ENST00000587139
  gene symbol: KIAA1328
  hgvsc: ENST00000587139.1:c.750C>A
  hgvsp: ENSP00000466355.1:p.Pro251Thr
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000468653
  ensembl transcript: ENST00000592611
  gene symbol: KIAA1328
  hgvsc: ENST00000592611.1:c.*446C>A
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000470002
  ensembl transcript: ENST00000591911
  gene symbol: KIAA1328
  hgvsc: ENST00000591911.1:c.-66C>A
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000467507
  ensembl transcript: ENST00000586135
  gene symbol: KIAA1328
  hgvsc: ENST00000586135.1:c.-66C>A
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000467248
  ensembl transcript: ENST00000590617
  gene symbol: KIAA1328
  hgvsc: ENST00000590617.1:c.*446C>A
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000465550
  ensembl transcript: ENST00000591619
  gene symbol: KIAA1328
  hgvsc: ENST00000591619.1:c.775C>A
  hgvsp: ENSP00000465550.1:p.Pro259Thr
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000280020
  ensembl transcript: ENST00000280020
  gene symbol: KIAA1328
  hgvsc: ENST00000280020.5:c.787C>A
  hgvsp: ENSP00000280020.5:p.Pro263Thr
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000390515
  ensembl transcript: ENST00000435985
  gene symbol: KIAA1328
  hgvsc: ENST00000435985.2:c.-66C>A
  variant of: http://identifiers.org/hgnc/29248
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14194
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3826
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37961
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 495
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 878
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 126
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1772
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Pro263Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
population: South Asian
population: African
population: European (Finnish)
reference allele: C
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum

18-34647065-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34647065
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 34647065
    reference: chr 18
allele count: 1
allele frequency: 8.301510874979247e-6
allele num: 120460
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000466355
  ensembl transcript: ENST00000587139
  gene symbol: KIAA1328
  hgvsc: ENST00000587139.1:c.752A>G
  hgvsp: ENST00000587139.1:c.752A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000468653
  ensembl transcript: ENST00000592611
  gene symbol: KIAA1328
  hgvsc: ENST00000592611.1:c.*448A>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000465550
  ensembl transcript: ENST00000591619
  gene symbol: KIAA1328
  hgvsc: ENST00000591619.1:c.777A>G
  hgvsp: ENST00000591619.1:c.777A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000390515
  ensembl transcript: ENST00000435985
  gene symbol: KIAA1328
  hgvsc: ENST00000435985.2:c.-64A>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000467507
  ensembl transcript: ENST00000586135
  gene symbol: KIAA1328
  hgvsc: ENST00000586135.1:c.-64A>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000470002
  ensembl transcript: ENST00000591911
  gene symbol: KIAA1328
  hgvsc: ENST00000591911.1:c.-64A>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000470371
  ensembl transcript: ENST00000586501
  gene symbol: KIAA1328
  hgvsc: ENST00000586501.1:c.-64A>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000441359
  ensembl transcript: ENST00000543923
  gene symbol: KIAA1328
  hgvsc: ENST00000543923.1:c.465A>G
  hgvsp: ENST00000543923.1:c.465A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000280020
  ensembl transcript: ENST00000280020
  gene symbol: KIAA1328
  hgvsc: ENST00000280020.5:c.789A>G
  hgvsp: ENST00000280020.5:c.789A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000467248
  ensembl transcript: ENST00000590617
  gene symbol: KIAA1328
  hgvsc: ENST00000590617.1:c.*448A>G
  variant of: http://identifiers.org/hgnc/29248
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3830
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 880
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14262
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37915
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 121
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 176
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Pro263Pro
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
reference allele: A
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: QD

18-34647066-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34647066
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 34647066
    reference: chr 18
allele count: 2
allele frequency: 1.660164356271271e-5
allele num: 120470
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000465550
  ensembl transcript: ENST00000591619
  gene symbol: KIAA1328
  hgvsc: ENST00000591619.1:c.778T>A
  hgvsp: ENSP00000465550.1:p.Ser260Thr
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000470002
  ensembl transcript: ENST00000591911
  gene symbol: KIAA1328
  hgvsc: ENST00000591911.1:c.-63T>A
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000467507
  ensembl transcript: ENST00000586135
  gene symbol: KIAA1328
  hgvsc: ENST00000586135.1:c.-63T>A
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000390515
  ensembl transcript: ENST00000435985
  gene symbol: KIAA1328
  hgvsc: ENST00000435985.2:c.-63T>A
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000468653
  ensembl transcript: ENST00000592611
  gene symbol: KIAA1328
  hgvsc: ENST00000592611.1:c.*449T>A
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000467248
  ensembl transcript: ENST00000590617
  gene symbol: KIAA1328
  hgvsc: ENST00000590617.1:c.*449T>A
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000441359
  ensembl transcript: ENST00000543923
  gene symbol: KIAA1328
  hgvsc: ENST00000543923.1:c.466T>A
  hgvsp: ENSP00000441359.1:p.Ser156Thr
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000280020
  ensembl transcript: ENST00000280020
  gene symbol: KIAA1328
  hgvsc: ENST00000280020.5:c.790T>A
  hgvsp: ENSP00000280020.5:p.Ser264Thr
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000470371
  ensembl transcript: ENST00000586501
  gene symbol: KIAA1328
  hgvsc: ENST00000586501.1:c.-63T>A
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000466355
  ensembl transcript: ENST00000587139
  gene symbol: KIAA1328
  hgvsc: ENST00000587139.1:c.753T>A
  hgvsp: ENSP00000466355.1:p.Ser252Thr
  variant of: http://identifiers.org/hgnc/29248
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14279
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37907
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 883
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3835
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45602
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 146
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Ser264Thr
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
reference allele: T
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD

18-34647072-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34647072
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 34647072
    reference: chr 18
allele count: 2
allele frequency: 1.659833684664797e-5
allele num: 120494
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000467507
  ensembl transcript: ENST00000586135
  gene symbol: KIAA1328
  hgvsc: ENST00000586135.1:c.-57A>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000280020
  ensembl transcript: ENST00000280020
  gene symbol: KIAA1328
  hgvsc: ENST00000280020.5:c.796A>G
  hgvsp: ENSP00000280020.5:p.Thr266Ala
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000470371
  ensembl transcript: ENST00000586501
  gene symbol: KIAA1328
  hgvsc: ENST00000586501.1:c.-57A>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000470002
  ensembl transcript: ENST00000591911
  gene symbol: KIAA1328
  hgvsc: ENST00000591911.1:c.-57A>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000390515
  ensembl transcript: ENST00000435985
  gene symbol: KIAA1328
  hgvsc: ENST00000435985.2:c.-57A>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000465550
  ensembl transcript: ENST00000591619
  gene symbol: KIAA1328
  hgvsc: ENST00000591619.1:c.784A>G
  hgvsp: ENSP00000465550.1:p.Thr262Ala
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000441359
  ensembl transcript: ENST00000543923
  gene symbol: KIAA1328
  hgvsc: ENST00000543923.1:c.472A>G
  hgvsp: ENSP00000441359.1:p.Thr158Ala
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000467248
  ensembl transcript: ENST00000590617
  gene symbol: KIAA1328
  hgvsc: ENST00000590617.1:c.*455A>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000468653
  ensembl transcript: ENST00000592611
  gene symbol: KIAA1328
  hgvsc: ENST00000592611.1:c.*455A>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000466355
  ensembl transcript: ENST00000587139
  gene symbol: KIAA1328
  hgvsc: ENST00000587139.1:c.759A>G
  hgvsp: ENSP00000466355.1:p.Thr254Ala
  variant of: http://identifiers.org/hgnc/29248
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14329
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3859
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 884
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37893
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 495
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1792
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45670
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Thr266Ala
num of homozygotes: 0
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
population: South Asian
reference allele: A
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ

18-34647080-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34647080
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 34647080
    reference: chr 18
allele count: 3
allele frequency: 2.488759104710391e-5
allele num: 120542
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000468653
  ensembl transcript: ENST00000592611
  gene symbol: KIAA1328
  hgvsc: ENST00000592611.1:c.*463A>T
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000280020
  ensembl transcript: ENST00000280020
  gene symbol: KIAA1328
  hgvsc: ENST00000280020.5:c.804A>T
  hgvsp: ENST00000280020.5:c.804A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000470371
  ensembl transcript: ENST00000586501
  gene symbol: KIAA1328
  hgvsc: ENST00000586501.1:c.-49A>T
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000470002
  ensembl transcript: ENST00000591911
  gene symbol: KIAA1328
  hgvsc: ENST00000591911.1:c.-49A>T
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000467248
  ensembl transcript: ENST00000590617
  gene symbol: KIAA1328
  hgvsc: ENST00000590617.1:c.*463A>T
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000441359
  ensembl transcript: ENST00000543923
  gene symbol: KIAA1328
  hgvsc: ENST00000543923.1:c.480A>T
  hgvsp: ENST00000543923.1:c.480A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000467507
  ensembl transcript: ENST00000586135
  gene symbol: KIAA1328
  hgvsc: ENST00000586135.1:c.-49A>T
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000465550
  ensembl transcript: ENST00000591619
  gene symbol: KIAA1328
  hgvsc: ENST00000591619.1:c.792A>T
  hgvsp: ENST00000591619.1:c.792A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000466355
  ensembl transcript: ENST00000587139
  gene symbol: KIAA1328
  hgvsc: ENST00000587139.1:c.767A>T
  hgvsp: ENST00000587139.1:c.767A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000390515
  ensembl transcript: ENST00000435985
  gene symbol: KIAA1328
  hgvsc: ENST00000435985.2:c.-49A>T
  variant of: http://identifiers.org/hgnc/29248
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14383
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37833
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 892
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3913
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Thr268Thr
num of homozygotes: 0
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
population: Latino
reference allele: A
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD

18-34647081-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34647081
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 34647081
    reference: chr 18
allele count: 1
allele frequency: 8.296276631047985e-6
allele num: 120536
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000467507
  ensembl transcript: ENST00000586135
  gene symbol: KIAA1328
  hgvsc: ENST00000586135.1:c.-48T>C
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000280020
  ensembl transcript: ENST00000280020
  gene symbol: KIAA1328
  hgvsc: ENST00000280020.5:c.805T>C
  hgvsp: ENSP00000280020.5:p.Cys269Arg
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000465550
  ensembl transcript: ENST00000591619
  gene symbol: KIAA1328
  hgvsc: ENST00000591619.1:c.793T>C
  hgvsp: ENSP00000465550.1:p.Cys265Arg
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000470371
  ensembl transcript: ENST00000586501
  gene symbol: KIAA1328
  hgvsc: ENST00000586501.1:c.-48T>C
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000467248
  ensembl transcript: ENST00000590617
  gene symbol: KIAA1328
  hgvsc: ENST00000590617.1:c.*464T>C
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000441359
  ensembl transcript: ENST00000543923
  gene symbol: KIAA1328
  hgvsc: ENST00000543923.1:c.481T>C
  hgvsp: ENSP00000441359.1:p.Cys161Arg
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000470002
  ensembl transcript: ENST00000591911
  gene symbol: KIAA1328
  hgvsc: ENST00000591911.1:c.-48T>C
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000468653
  ensembl transcript: ENST00000592611
  gene symbol: KIAA1328
  hgvsc: ENST00000592611.1:c.*464T>C
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000466355
  ensembl transcript: ENST00000587139
  gene symbol: KIAA1328
  hgvsc: ENST00000587139.1:c.768T>C
  hgvsp: ENSP00000466355.1:p.Cys257Arg
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000390515
  ensembl transcript: ENST00000435985
  gene symbol: KIAA1328
  hgvsc: ENST00000435985.2:c.-48T>C
  variant of: http://identifiers.org/hgnc/29248
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 892
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3913
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14396
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37827
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Cys269Arg
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
population: Other
reference allele: T
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP

18-34647083-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34647083
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 34647083
    reference: chr 18
allele count: 1
allele frequency: 8.296001327360212e-6
allele num: 120540
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000470371
  ensembl transcript: ENST00000586501
  gene symbol: KIAA1328
  hgvsc: ENST00000586501.1:c.-46T>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000466355
  ensembl transcript: ENST00000587139
  gene symbol: KIAA1328
  hgvsc: ENST00000587139.1:c.770T>G
  hgvsp: ENSP00000466355.1:p.Cys257Trp
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000467248
  ensembl transcript: ENST00000590617
  gene symbol: KIAA1328
  hgvsc: ENST00000590617.1:c.*466T>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000470002
  ensembl transcript: ENST00000591911
  gene symbol: KIAA1328
  hgvsc: ENST00000591911.1:c.-46T>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000465550
  ensembl transcript: ENST00000591619
  gene symbol: KIAA1328
  hgvsc: ENST00000591619.1:c.795T>G
  hgvsp: ENSP00000465550.1:p.Cys265Trp
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000441359
  ensembl transcript: ENST00000543923
  gene symbol: KIAA1328
  hgvsc: ENST00000543923.1:c.483T>G
  hgvsp: ENSP00000441359.1:p.Cys161Trp
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000468653
  ensembl transcript: ENST00000592611
  gene symbol: KIAA1328
  hgvsc: ENST00000592611.1:c.*466T>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000390515
  ensembl transcript: ENST00000435985
  gene symbol: KIAA1328
  hgvsc: ENST00000435985.2:c.-46T>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000280020
  ensembl transcript: ENST00000280020
  gene symbol: KIAA1328
  hgvsc: ENST00000280020.5:c.807T>G
  hgvsp: ENSP00000280020.5:p.Cys269Trp
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000467507
  ensembl transcript: ENST00000586135
  gene symbol: KIAA1328
  hgvsc: ENST00000586135.1:c.-46T>G
  variant of: http://identifiers.org/hgnc/29248
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37765
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 899
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14426
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3940
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Cys269Trp
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: African
population: South Asian
population: Other
population: Latino
reference allele: T
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum

18-34647086-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34647086
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 34647086
    reference: chr 18
allele count: 2
allele frequency: 1.658842459731599e-5
allele num: 120566
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000468653
  ensembl transcript: ENST00000592611
  gene symbol: KIAA1328
  hgvsc: ENST00000592611.1:c.*469T>C
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000441359
  ensembl transcript: ENST00000543923
  gene symbol: KIAA1328
  hgvsc: ENST00000543923.1:c.486T>C
  hgvsp: ENST00000543923.1:c.486T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000467507
  ensembl transcript: ENST00000586135
  gene symbol: KIAA1328
  hgvsc: ENST00000586135.1:c.-43T>C
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000467248
  ensembl transcript: ENST00000590617
  gene symbol: KIAA1328
  hgvsc: ENST00000590617.1:c.*469T>C
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000390515
  ensembl transcript: ENST00000435985
  gene symbol: KIAA1328
  hgvsc: ENST00000435985.2:c.-43T>C
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000280020
  ensembl transcript: ENST00000280020
  gene symbol: KIAA1328
  hgvsc: ENST00000280020.5:c.810T>C
  hgvsp: ENST00000280020.5:c.810T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000466355
  ensembl transcript: ENST00000587139
  gene symbol: KIAA1328
  hgvsc: ENST00000587139.1:c.773T>C
  hgvsp: ENST00000587139.1:c.773T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000470002
  ensembl transcript: ENST00000591911
  gene symbol: KIAA1328
  hgvsc: ENST00000591911.1:c.-43T>C
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000470371
  ensembl transcript: ENST00000586501
  gene symbol: KIAA1328
  hgvsc: ENST00000586501.1:c.-43T>C
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000465550
  ensembl transcript: ENST00000591619
  gene symbol: KIAA1328
  hgvsc: ENST00000591619.1:c.798T>C
  hgvsp: ENST00000591619.1:c.798T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29248
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3934
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 897
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37758
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14465
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Asn270Asn
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
reference allele: T
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: VQSLOD

18-34647086-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34647086
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 34647086
    reference: chr 18
allele count: 1
allele frequency: 8.294212298657997e-6
allele num: 120566
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000467248
  ensembl transcript: ENST00000590617
  gene symbol: KIAA1328
  hgvsc: ENST00000590617.1:c.*469T>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000465550
  ensembl transcript: ENST00000591619
  gene symbol: KIAA1328
  hgvsc: ENST00000591619.1:c.798T>G
  hgvsp: ENSP00000465550.1:p.Asn266Lys
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000466355
  ensembl transcript: ENST00000587139
  gene symbol: KIAA1328
  hgvsc: ENST00000587139.1:c.773T>G
  hgvsp: ENSP00000466355.1:p.Asn258Lys
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000468653
  ensembl transcript: ENST00000592611
  gene symbol: KIAA1328
  hgvsc: ENST00000592611.1:c.*469T>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000470371
  ensembl transcript: ENST00000586501
  gene symbol: KIAA1328
  hgvsc: ENST00000586501.1:c.-43T>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000390515
  ensembl transcript: ENST00000435985
  gene symbol: KIAA1328
  hgvsc: ENST00000435985.2:c.-43T>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000280020
  ensembl transcript: ENST00000280020
  gene symbol: KIAA1328
  hgvsc: ENST00000280020.5:c.810T>G
  hgvsp: ENSP00000280020.5:p.Asn270Lys
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000441359
  ensembl transcript: ENST00000543923
  gene symbol: KIAA1328
  hgvsc: ENST00000543923.1:c.486T>G
  hgvsp: ENSP00000441359.1:p.Asn162Lys
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000467507
  ensembl transcript: ENST00000586135
  gene symbol: KIAA1328
  hgvsc: ENST00000586135.1:c.-43T>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000470002
  ensembl transcript: ENST00000591911
  gene symbol: KIAA1328
  hgvsc: ENST00000591911.1:c.-43T>G
  variant of: http://identifiers.org/hgnc/29248
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37758
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3934
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 897
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14465
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1108
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Asn270Lys
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
population: Latino
population: Other
population: East Asian
reference allele: T
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum

18-34647099-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34647099
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 34647099
    reference: chr 18
allele count: 1
allele frequency: 8.294074713025015e-6
allele num: 120568
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000468653
  ensembl transcript: ENST00000592611
  gene symbol: KIAA1328
  hgvsc: ENST00000592611.1:c.*482G>A
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000466355
  ensembl transcript: ENST00000587139
  gene symbol: KIAA1328
  hgvsc: ENST00000587139.1:c.786G>A
  hgvsp: ENSP00000466355.1:p.Gly263Arg
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000390515
  ensembl transcript: ENST00000435985
  gene symbol: KIAA1328
  hgvsc: ENST00000435985.2:c.-30G>A
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000467507
  ensembl transcript: ENST00000586135
  gene symbol: KIAA1328
  hgvsc: ENST00000586135.1:c.-30G>A
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000441359
  ensembl transcript: ENST00000543923
  gene symbol: KIAA1328
  hgvsc: ENST00000543923.1:c.499G>A
  hgvsp: ENSP00000441359.1:p.Gly167Arg
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000470371
  ensembl transcript: ENST00000586501
  gene symbol: KIAA1328
  hgvsc: ENST00000586501.1:c.-30G>A
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000467248
  ensembl transcript: ENST00000590617
  gene symbol: KIAA1328
  hgvsc: ENST00000590617.1:c.*482G>A
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000465550
  ensembl transcript: ENST00000591619
  gene symbol: KIAA1328
  hgvsc: ENST00000591619.1:c.811G>A
  hgvsp: ENSP00000465550.1:p.Gly271Arg
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000280020
  ensembl transcript: ENST00000280020
  gene symbol: KIAA1328
  hgvsc: ENST00000280020.5:c.823G>A
  hgvsp: ENSP00000280020.5:p.Gly275Arg
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000470002
  ensembl transcript: ENST00000591911
  gene symbol: KIAA1328
  hgvsc: ENST00000591911.1:c.-30G>A
  variant of: http://identifiers.org/hgnc/29248
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14594
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3993
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37599
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 918
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 45660
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Gly275Arg
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: DP

18-34647107-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34647107
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 34647107
    reference: chr 18
allele count: 5
allele frequency: 4.145799475970946e-5
allele num: 120604
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000466355
  ensembl transcript: ENST00000587139
  gene symbol: KIAA1328
  hgvsc: ENST00000587139.1:c.794A>G
  hgvsp: ENST00000587139.1:c.794A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000465550
  ensembl transcript: ENST00000591619
  gene symbol: KIAA1328
  hgvsc: ENST00000591619.1:c.819A>G
  hgvsp: ENST00000591619.1:c.819A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000390515
  ensembl transcript: ENST00000435985
  gene symbol: KIAA1328
  hgvsc: ENST00000435985.2:c.-22A>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000441359
  ensembl transcript: ENST00000543923
  gene symbol: KIAA1328
  hgvsc: ENST00000543923.1:c.507A>G
  hgvsp: ENST00000543923.1:c.507A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000467507
  ensembl transcript: ENST00000586135
  gene symbol: KIAA1328
  hgvsc: ENST00000586135.1:c.-22A>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000467248
  ensembl transcript: ENST00000590617
  gene symbol: KIAA1328
  hgvsc: ENST00000590617.1:c.*490A>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000280020
  ensembl transcript: ENST00000280020
  gene symbol: KIAA1328
  hgvsc: ENST00000280020.5:c.831A>G
  hgvsp: ENST00000280020.5:c.831A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000470371
  ensembl transcript: ENST00000586501
  gene symbol: KIAA1328
  hgvsc: ENST00000586501.1:c.-22A>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000468653
  ensembl transcript: ENST00000592611
  gene symbol: KIAA1328
  hgvsc: ENST00000592611.1:c.*490A>G
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000470002
  ensembl transcript: ENST00000591911
  gene symbol: KIAA1328
  hgvsc: ENST00000591911.1:c.-22A>G
  variant of: http://identifiers.org/hgnc/29248
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 927
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4020
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37559
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14623
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1833
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 118
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Lys277Lys
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
population: Other
reference allele: A
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: QD

18-34647109-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34647109
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 34647109
    reference: chr 18
allele count: 3
allele frequency: 2.487273450843186e-5
allele num: 120614
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000466355
  ensembl transcript: ENST00000587139
  gene symbol: KIAA1328
  hgvsc: ENST00000587139.1:c.796C>T
  hgvsp: ENSP00000466355.1:p.Pro266Leu
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000467507
  ensembl transcript: ENST00000586135
  gene symbol: KIAA1328
  hgvsc: ENST00000586135.1:c.-20C>T
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000468653
  ensembl transcript: ENST00000592611
  gene symbol: KIAA1328
  hgvsc: ENST00000592611.1:c.*492C>T
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000465550
  ensembl transcript: ENST00000591619
  gene symbol: KIAA1328
  hgvsc: ENST00000591619.1:c.821C>T
  hgvsp: ENSP00000465550.1:p.Pro274Leu
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000390515
  ensembl transcript: ENST00000435985
  gene symbol: KIAA1328
  hgvsc: ENST00000435985.2:c.-20C>T
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000441359
  ensembl transcript: ENST00000543923
  gene symbol: KIAA1328
  hgvsc: ENST00000543923.1:c.509C>T
  hgvsp: ENSP00000441359.1:p.Pro170Leu
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000470002
  ensembl transcript: ENST00000591911
  gene symbol: KIAA1328
  hgvsc: ENST00000591911.1:c.-20C>T
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000470371
  ensembl transcript: ENST00000586501
  gene symbol: KIAA1328
  hgvsc: ENST00000586501.1:c.-20C>T
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000467248
  ensembl transcript: ENST00000590617
  gene symbol: KIAA1328
  hgvsc: ENST00000590617.1:c.*492C>T
  variant of: http://identifiers.org/hgnc/29248
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000150477
  ensembl protein: ENSP00000280020
  ensembl transcript: ENST00000280020
  gene symbol: KIAA1328
  hgvsc: ENST00000280020.5:c.833C>T
  hgvsp: ENSP00000280020.5:p.Pro278Leu
  variant of: http://identifiers.org/hgnc/29248
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37545
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4021
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 931
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14634
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Pro278Leu
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: FS

GenotypeQuality
all individuals: 164
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 799
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 743
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1363
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 624
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 239
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14207
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1283
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27120
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2192
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1561
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 786
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 461
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 532
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 424
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 207
bin: 8.75e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 9.509319132750095e-5
allele num: 10516
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 34586
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4028
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4828
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 534
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6578
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4198
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.324e0

QD
type: SiteQuality
SIO_000300: 8.449999999999999e0

VQSLOD
type: SiteQuality
SIO_000300: -1.711e0

MQRankSum
type: SiteQuality
SIO_000300: 2.25e0

DP
type: SiteQuality
SIO_000300: 1.203556e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.24e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.17e0

GenotypeQuality
all individuals: 1208
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 626
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 596
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 76
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 424
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2262
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 458
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 862
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26696
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 932
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 207
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12866
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1554
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1125
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 261
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4579
bin: 9.75e1
variant carriers: 8

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 34818
num of homozygotes: 0

Latino
type: Population
allele count: 7
allele frequency: 1.711491442542787e-3
allele num: 4090
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6610
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10532
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4218
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 536
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4862
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.65e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 4.81e0

VQSLOD
type: SiteQuality
SIO_000300: 8.179999999999999e-1

QD
type: SiteQuality
SIO_000300: 1.216e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.8e-3

DP
type: SiteQuality
SIO_000300: 1.202526e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -1.71e-1

GenotypeQuality
all individuals: 1418
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 839
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 260
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 424
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2248
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2374
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 935
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 534
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 26693
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 311
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 441
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1565
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 207
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14120
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4572
bin: 9.75e1
variant carriers: 1

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 544
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4936
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 35506
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10614
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 2.370791844476055e-4
allele num: 4218
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4262
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6708
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 5.88e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.5e-2

DP
type: SiteQuality
SIO_000300: 1.210252e6

FS
type: SiteQuality
SIO_000300: 2.447e0

VQSLOD
type: SiteQuality
SIO_000300: -2.098e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.42e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.5e-3

QD
type: SiteQuality
SIO_000300: 4.11e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.96e-1

GenotypeQuality
all individuals: 930
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 628
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1573
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 537
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2373
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 549
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1261
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1030
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1465
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2278
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26475
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 424
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13583
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 208
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 993
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4578
bin: 9.75e1
variant carriers: 8

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4270
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4928
num of homozygotes: 0

African
type: Population
allele count: 8
allele frequency: 1.193317422434368e-3
allele num: 6704
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 544
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4230
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 35558
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10624
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 3.72e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.7e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -2.67e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.3e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.346e0

DP
type: SiteQuality
SIO_000300: 1.211622e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.05e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 4.1e0

QD
type: SiteQuality
SIO_000300: 1.375e1

GenotypeQuality
all individuals: 1618
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1110
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 106
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2377
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2419
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1181
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 499
bin: 1.25e1
variant carriers: 1

GenotypeQuality
all individuals: 538
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 261
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13232
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1180
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1120
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1584
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 757
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 628
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 422
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 36464
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5006
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 2.797463632972771e-4
allele num: 10724
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 550
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4422
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4342
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6802
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.079e0

VQSLOD
type: SiteQuality
SIO_000300: 7.25e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.67e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.3e-3

DP
type: SiteQuality
SIO_000300: 1.220244e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.4e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 4.67e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.12e-1

QD
type: SiteQuality
SIO_000300: 1.273e1

GenotypeQuality
all individuals: 1592
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 836
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2344
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 466
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 627
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2414
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 311
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 538
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1126
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 25776
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 138
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 823
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 421
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4574
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 14412
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 732
bin: 4.25e1
variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.970831690973591e-4
allele num: 5074
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4380
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10812
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 37112
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4580
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6860
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 552
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -5.53e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.9e-2

FS
type: SiteQuality
SIO_000300: 3.862e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.61e-1

DP
type: SiteQuality
SIO_000300: 1.229546e6

VQSLOD
type: SiteQuality
SIO_000300: -1.073e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.3e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -1.893e0

QD
type: SiteQuality
SIO_000300: 6.27e0

GenotypeQuality
all individuals: 1008
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 812
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1595
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1815
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 546
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1374
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 421
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14242
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 517
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 117
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2428
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 206
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4576
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 1058
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 260
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 627
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 5
allele frequency: 7.140816909454442e-4
allele num: 7002
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 566
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4818
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10976
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5220
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4512
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 38364
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.727e0

QD
type: SiteQuality
SIO_000300: 1.548e1

MQRankSum
type: SiteQuality
SIO_000300: 3.4e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.6e-1

FS
type: SiteQuality
SIO_000300: 1.142e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.24281e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.1e-2

VQSLOD
type: SiteQuality
SIO_000300: 2.31e0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
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GenotypeQuality
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GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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bin: 5.75e1
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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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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4962
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7082
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 39174
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5294
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 9.048136083966703e-5
allele num: 11052
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4552
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 574
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.74e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.344e0

MQRankSum
type: SiteQuality
SIO_000300: 9.6e-2

DP
type: SiteQuality
SIO_000300: 1.252139e6

ClippingRankSum
type: SiteQuality
SIO_000300: 2.03e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-3

QD
type: SiteQuality
SIO_000300: 1.2e1

MQ
type: SiteQuality
SIO_000300: 5.899e1

FS
type: SiteQuality
SIO_000300: 1.038e0

VQSLOD
type: SiteQuality
SIO_000300: -1.719e0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4736
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11352
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5636
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5590
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 590
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7344
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.384586035864174e-5
allele num: 41936
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.2e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.294758e6

MQRankSum
type: SiteQuality
SIO_000300: 6.5e-1

MQ
type: SiteQuality
SIO_000300: 5.875e1

QD
type: SiteQuality
SIO_000300: 3.293e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.46e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.61e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.09e0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.24e-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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 598
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7396
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5736
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.354048964218456e-5
allele num: 42480
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11404
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4776
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5670
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.29e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.4e-2

QD
type: SiteQuality
SIO_000300: 1.275e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.4e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.30116e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.93e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.34e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.44e0

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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bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6078
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5008
num of homozygotes: 0

Latino
type: Population
allele count: 9
allele frequency: 1.374885426214482e-3
allele num: 6546
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 45638
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7750
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11744
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 634
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.27e1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.66e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.06e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.8e-3

FS
type: SiteQuality
SIO_000300: 3.569e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.1e-2

DP
type: SiteQuality
SIO_000300: 1.347416e6

MQRankSum
type: SiteQuality
SIO_000300: 2.8e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.08e0

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: 11824
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7810
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 644
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 46202
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6660
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5042
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.62813415825464e-4
allele num: 6142
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.4e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -2.82e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.01e-1

QD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 1.18e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.354274e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.51e0

MQRankSum
type: SiteQuality
SIO_000300: -9.409999999999999e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 3

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: 6274
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5128
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6876
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11934
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.271940981938438e-4
allele num: 7862
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 640
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.125579220337542e-5
allele num: 47046
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.849e0

VQSLOD
type: SiteQuality
SIO_000300: 8.65e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.27e-1

MQRankSum
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InbreedingCoeff
type: SiteQuality
SIO_000300: -2.3e-3

DP
type: SiteQuality
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QD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.967e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.36e0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.7e-2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7882
num of homozygotes: 0

Other
type: Population
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allele frequency: 0.0e0
allele num: 640
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East Asian
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allele frequency: 0.0e0
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South Asian
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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
allele num: 5174
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European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.107748081949245e-5
allele num: 47444
num of homozygotes: 0

Latino
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allele num: 6952
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.93e-1

DP
type: SiteQuality
SIO_000300: 1.371257e6

VQSLOD
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.393e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.87e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.2e-3

MQRankSum
type: SiteQuality
SIO_000300: 1.08e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.55e-1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 3.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7064
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12042
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7936
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.084114876411988e-5
allele num: 47982
num of homozygotes: 0

East Asian
type: Population
allele count: 0
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Other
type: Population
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BaseQRankSum
type: SiteQuality
SIO_000300: 3.8e-1

FS
type: SiteQuality
SIO_000300: 1.848e0

DP
type: SiteQuality
SIO_000300: 1.377386e6

InbreedingCoeff
type: SiteQuality
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MQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
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SIO_000300: -1.747e0

VQSLOD
type: SiteQuality
SIO_000300: -7.276e-1

QD
type: SiteQuality
SIO_000300: 8.33e0

GenotypeQuality
all individuals: 658
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 313
bin: 1.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
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GenotypeQuality
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bin: 8.25e1
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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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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4599
bin: 9.75e1
variant carriers: 33

GenotypeQuality
all individuals: 208
bin: 8.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 662
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6492
num of homozygotes: 0

Latino
type: Population
allele count: 4
allele frequency: 5.532503457814661e-4
allele num: 7230
num of homozygotes: 0

African
type: Population
allele count: 29
allele frequency: 3.648716658278812e-3
allele num: 7948
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 48670
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5258
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12154
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.446e1

MQRankSum
type: SiteQuality
SIO_000300: -3.5e-2

FS
type: SiteQuality
SIO_000300: 2.472e0

MQ
type: SiteQuality
SIO_000300: 5.965e1

VQSLOD
type: SiteQuality
SIO_000300: 1.98e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.8e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.9e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.7e-3

DP
type: SiteQuality
SIO_000300: 1.385759e6

BaseQRankSum
type: SiteQuality
SIO_000300: -7.37e-1

GenotypeQuality
all individuals: 258
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
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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GenotypeQuality
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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: 2.5e0
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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: 4573
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 523
bin: 5.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.049180327868852e-5
allele num: 48800
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7254
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7908
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6514
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 664
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5258
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12196
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.7e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.19e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.76e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.91e0

VQSLOD
type: SiteQuality
SIO_000300: 6.899999999999999e-1

FS
type: SiteQuality
SIO_000300: 8.61e-1

QD
type: SiteQuality
SIO_000300: 1.363e1

MQRankSum
type: SiteQuality
SIO_000300: -7.37e-1

DP
type: SiteQuality
SIO_000300: 1.359496e6

GenotypeQuality
all individuals: 208
bin: 8.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
all individuals: 417
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7242
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 666
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 8.19672131147541e-5
allele num: 12200
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 48784
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7892
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5264
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6524
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.360791e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-3

FS
type: SiteQuality
SIO_000300: 9.24e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.659999999999999e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.82e-1

QD
type: SiteQuality
SIO_000300: 8.109999999999999e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.277e0

VQSLOD
type: SiteQuality
SIO_000300: -1.189e0

MQ
type: SiteQuality
SIO_000300: 5.886e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.82e-1

GenotypeQuality
all individuals: 334
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21383
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variant carriers: 0

GenotypeQuality
all individuals: 1942
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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
all individuals: 625
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 208
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variant carriers: 0

GenotypeQuality
all individuals: 1277
bin: 3.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7178
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5232
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 4.127455836222553e-5
allele num: 48456
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12152
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7856
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 668
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6462
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.032e0

DP
type: SiteQuality
SIO_000300: 1.336482e6

FS
type: SiteQuality
SIO_000300: 1.342e0

MQ
type: SiteQuality
SIO_000300: 5.878e1

VQSLOD
type: SiteQuality
SIO_000300: -9.54e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.1e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.76e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.28e0

QD
type: SiteQuality
SIO_000300: 7.11e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.4e-3

GenotypeQuality
all individuals: 1607
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variant carriers: 0

GenotypeQuality
all individuals: 511
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variant carriers: 0

GenotypeQuality
all individuals: 93
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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: 414
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GenotypeQuality
all individuals: 4576
bin: 9.75e1
variant carriers: 4

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 642
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7708
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 4.208931352329643e-5
allele num: 47518
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5194
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.439263097294185e-4
allele num: 6948
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12038
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6354
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 3.22e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.14e0

VQSLOD
type: SiteQuality
SIO_000300: 1.85e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.7e-3

DP
type: SiteQuality
SIO_000300: 1.271818e6

QD
type: SiteQuality
SIO_000300: 1.083e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.98e-1

FS
type: SiteQuality
SIO_000300: 3.201e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.11e-1

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: 6.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 414
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47562
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 648
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5192
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.298026998961578e-4
allele num: 7704
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6958
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12048
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6358
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.858e0

MQ
type: SiteQuality
SIO_000300: 5.964e1

MQRankSum
type: SiteQuality
SIO_000300: 1.65e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.17e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.28e0

FS
type: SiteQuality
SIO_000300: 1.382e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.6e-3

DP
type: SiteQuality
SIO_000300: 1.2715e6

QD
type: SiteQuality
SIO_000300: 1.015e1

VQSLOD
type: SiteQuality
SIO_000300: 2.7e-1

GenotypeQuality
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bin: 5.75e1
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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bin: 6.25e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 8.301510874979246e-5
allele num: 12046
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5196
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 646
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47500
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6348
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6946
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7704
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 3.7e-1

QD
type: SiteQuality
SIO_000300: 1.12e1

DP
type: SiteQuality
SIO_000300: 1.267459e6

ClippingRankSum
type: SiteQuality
SIO_000300: -7.29e-1

MQRankSum
type: SiteQuality
SIO_000300: -9.2e-1

FS
type: SiteQuality
SIO_000300: 3.86e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.79e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.2e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.76e-1

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 256
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GenotypeQuality
all individuals: 412
bin: 8.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6274
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6762
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11950
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 46716
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.311647429171039e-4
allele num: 7624
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5174
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 632
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.229153e6

QD
type: SiteQuality
SIO_000300: 7.98e0

VQSLOD
type: SiteQuality
SIO_000300: -3.084e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.31e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.37e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.1e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.37e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 9.61e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 411
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3440
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5793
bin: 3.25e1
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GenotypeQuality
all individuals: 498
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GenotypeQuality
all individuals: 168
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 929
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 256
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 750
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9624
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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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bin: 5.75e1
variant carriers: 0

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 620
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 46120
num of homozygotes: 0

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

East Asian
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allele frequency: 3.232062055591467e-4
allele num: 6188
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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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

ReadPosRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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VQSLOD
type: SiteQuality
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ClippingRankSum
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FS
type: SiteQuality
SIO_000300: 6.658e0

MQ
type: SiteQuality
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DP
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: -2.017e0

QD
type: SiteQuality
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GenotypeQuality
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bin: 7.75e1
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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variant carriers: 0

Latino
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allele frequency: 0.0e0
allele num: 6526
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
allele num: 616
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 45734
num of homozygotes: 0

South Asian
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allele frequency: 2.531645569620253e-4
allele num: 11850
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 7534
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5122
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -6.5e-1

FS
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -6.4e-3

MQ
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SIO_000300: 5.967e1

QD
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ReadPosRankSum
type: SiteQuality
SIO_000300: 1.4e-2

BaseQRankSum
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DP
type: SiteQuality
SIO_000300: 1.203287e6

VQSLOD
type: SiteQuality
SIO_000300: 7.1e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.3e-2

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

African
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allele frequency: 0.0e0
allele num: 7518
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 614
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 2.192982456140351e-5
allele num: 45600
num of homozygotes: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 11830
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5100
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 2.193367257413581e-5
allele num: 45592
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 7516
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5090
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11818
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 614
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6124
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6498
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.79e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.89e-1

VQSLOD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -5.73e-1

InbreedingCoeff
type: SiteQuality
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QD
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: 2.48e-1

DP
type: SiteQuality
SIO_000300: 1.19891e6

FS
type: SiteQuality
SIO_000300: 4.325e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.48e-1

GenotypeQuality
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variant carriers: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5070
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 6034
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 45094
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 11778
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 6396
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 2.672367717797969e-4
allele num: 7484
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: 9.379999999999999e-1

MQRankSum
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.4e1

DP
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.804e0

VQSLOD
type: SiteQuality
SIO_000300: -1.461e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.93e-1

FS
type: SiteQuality
SIO_000300: 8.878e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.9e-3

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 6334
num of homozygotes: 0

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

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

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

MQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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InbreedingCoeff
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BaseQRankSum
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FS
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QD
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MQ
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ReadPosRankSum
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DP
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VQSLOD
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GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

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

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

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

East Asian
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African
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South Asian
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Latino
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Other
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European (Finnish)
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FS
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ClippingRankSum
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VQSLOD
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BaseQRankSum
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MQRankSum
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InbreedingCoeff
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QD
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MQ
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ReadPosRankSum
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
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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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European (Non-Finnish)
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num of homozygotes: 0

South Asian
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allele frequency: 4.211332312404288e-3
allele num: 2612
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East Asian
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Other
type: Population
allele count: 3
allele frequency: 9.868421052631578e-3
allele num: 304
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2968
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.681e0

VQSLOD
type: SiteQuality
SIO_000300: 3.33e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.22e-1

QD
type: SiteQuality
SIO_000300: 1.443e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.77e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 6.89819e5

MQRankSum
type: SiteQuality
SIO_000300: 4.4e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.84e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.43e-1

GenotypeQuality
all individuals: 281
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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
all individuals: 258
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 340
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4660
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3234
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 4.690871563936579e-5
allele num: 21318
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 2986
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3586
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 1762
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MQRankSum
type: SiteQuality
SIO_000300: 2.12e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.06e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.485e0

VQSLOD
type: SiteQuality
SIO_000300: -9.819e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.22e-2

MQ
type: SiteQuality
SIO_000300: 5.866e1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.202e0

DP
type: SiteQuality
SIO_000300: 7.60265e5

QD
type: SiteQuality
SIO_000300: 1.492e1

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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bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.868172675228222e-5
allele num: 25852
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2440
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5430
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5358
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 410
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3700
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3684
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.02e0

BaseQRankSum
type: SiteQuality
SIO_000300: 8.67e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.2e-3

MQRankSum
type: SiteQuality
SIO_000300: -5.659999999999999e-1

FS
type: SiteQuality
SIO_000300: 2.468e0

QD
type: SiteQuality
SIO_000300: 6.49e0

VQSLOD
type: SiteQuality
SIO_000300: -9.816e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.06e-1

DP
type: SiteQuality
SIO_000300: 8.41162e5

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 2

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3700
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5430
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3684
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2440
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 410
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 3.732736095558044e-4
allele num: 5358
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 25852
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -5.659999999999999e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.06e-1

QD
type: SiteQuality
SIO_000300: 6.49e0

VQSLOD
type: SiteQuality
SIO_000300: -9.816e-1

FS
type: SiteQuality
SIO_000300: 2.468e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.02e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.2e-3

DP
type: SiteQuality
SIO_000300: 8.41162e5

BaseQRankSum
type: SiteQuality
SIO_000300: 8.67e-1

GenotypeQuality
all individuals: 133
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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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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: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.070663811563169e-4
allele num: 9340
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6428
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4340
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4718
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 34302
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3834
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 528
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.62e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.1e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 9.78081e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.16e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.11e0

QD
type: SiteQuality
SIO_000300: 1.443e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -2.499e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.59e-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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GenotypeQuality
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variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 662
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6232
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6008
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12304
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5234
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7594
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.164127423822715e-5
allele num: 46208
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.87e-1

DP
type: SiteQuality
SIO_000300: 1.158066e6

QD
type: SiteQuality
SIO_000300: 8.58e0

MQ
type: SiteQuality
SIO_000300: 5.897e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.9e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -1.434e0

VQSLOD
type: SiteQuality
SIO_000300: -9.716e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.45e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.739e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.91e0

GenotypeQuality
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variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7732
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.09669979452342e-5
allele num: 47694
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 6166
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12570
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5350
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 680
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.42e0

ReadPosRankSum
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MQ
type: SiteQuality
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BaseQRankSum
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InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-3

FS
type: SiteQuality
SIO_000300: 5.73e-1

DP
type: SiteQuality
SIO_000300: 1.185003e6

MQRankSum
type: SiteQuality
SIO_000300: -1.89e-1

QD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8204
num of homozygotes: 0

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

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

Latino
type: Population
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: 1.88771850341677e-5
allele num: 52974
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 6760
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5780
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.842e0

MQ
type: SiteQuality
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VQSLOD
type: SiteQuality
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QD
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ClippingRankSum
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MQRankSum
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SIO_000300: 2.5e-1

BaseQRankSum
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SIO_000300: 3.09e0

ReadPosRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

DP
type: SiteQuality
SIO_000300: 1.270748e6

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.782848992690319e-5
allele num: 56090
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7148
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6026
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13842
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8522
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 776
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 2.14e-1

ClippingRankSum
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SIO_000300: -5.570000000000001e-1

FS
type: SiteQuality
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QD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.322251e6

MQ
type: SiteQuality
SIO_000300: 5.806e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.0e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.36e0

VQSLOD
type: SiteQuality
SIO_000300: -3.875e-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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GenotypeQuality
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bin: 5.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9210
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7464
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.705320600272851e-5
allele num: 58640
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 8696
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6196
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14310
num of homozygotes: 0

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

FS
type: SiteQuality
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DP
type: SiteQuality
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VQSLOD
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MQ
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BaseQRankSum
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SIO_000300: 2.85e0

MQRankSum
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SIO_000300: 1.32e0

ClippingRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

ReadPosRankSum
type: SiteQuality
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QD
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SIO_000300: 1.337e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 6.71591672263264e-5
allele num: 14890
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6384
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8948
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61344
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10024
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7796
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.5e-3

MQRankSum
type: SiteQuality
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FS
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SIO_000300: 8.787000000000001e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.14e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
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SIO_000300: -5.83e-1

DP
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SIO_000300: 1.424581e6

VQSLOD
type: SiteQuality
SIO_000300: -1.051e0

ReadPosRankSum
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 8.390000000000001e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 1
allele frequency: 1.108647450110865e-4
allele num: 9020
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7916
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62146
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15110
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6430
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 9.771350400625366e-5
allele num: 10234
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -4.44e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.39e0

ReadPosRankSum
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SIO_000300: -5.17e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.108e0

DP
type: SiteQuality
SIO_000300: 1.440921e6

ClippingRankSum
type: SiteQuality
SIO_000300: 9.66e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.3e-3

FS
type: SiteQuality
SIO_000300: 1.002e0

QD
type: SiteQuality
SIO_000300: 1.521e1

GenotypeQuality
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variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8268
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10960
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6556
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 64762
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9382
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.333122229259025e-5
allele num: 15790
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 1.03e0

DP
type: SiteQuality
SIO_000300: 1.499677e6

MQRankSum
type: SiteQuality
SIO_000300: 6.46e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.99e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.2e-2

MQ
type: SiteQuality
SIO_000300: 5.917e1

QD
type: SiteQuality
SIO_000300: 1.139e1

BaseQRankSum
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SIO_000300: 2.07e0

GenotypeQuality
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bin: 9.75e1
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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 4.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64762
num of homozygotes: 0

South Asian
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allele count: 1
allele frequency: 6.333122229259025e-5
allele num: 15790
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8268
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 10960
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9382
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6556
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.499677e6

QD
type: SiteQuality
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BaseQRankSum
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SIO_000300: 2.07e0

MQ
type: SiteQuality
SIO_000300: 5.917e1

FS
type: SiteQuality
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MQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 5.99e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.2e-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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bin: 5.75e1
variant carriers: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6572
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
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 882
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65450
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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Latino
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allele count: 2
allele frequency: 1.793400286944046e-4
allele num: 11152
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.520274e6

QD
type: SiteQuality
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ReadPosRankSum
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SIO_000300: 1.16e-1

ClippingRankSum
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FS
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VQSLOD
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MQ
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BaseQRankSum
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InbreedingCoeff
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MQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 8420
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16066
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6584
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11176
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9546
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.525553012967201e-5
allele num: 65550
num of homozygotes: 0

Other
type: Population
allele count: 0
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allele num: 882
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.07e-1

MQ
type: SiteQuality
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FS
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BaseQRankSum
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ReadPosRankSum
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InbreedingCoeff
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DP
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VQSLOD
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QD
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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bin: 2.25e1
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GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 211
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1683
bin: 7.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11210
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16132
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9566
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8430
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6586
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.522440777053773e-5
allele num: 65684
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.381e1

MQ
type: SiteQuality
SIO_000300: 5.959e1

VQSLOD
type: SiteQuality
SIO_000300: 1.17e0

DP
type: SiteQuality
SIO_000300: 1.529192e6

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.3e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -5.35e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.08e0

MQRankSum
type: SiteQuality
SIO_000300: -1.422e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.98e-1

GenotypeQuality
all individuals: 5015
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 18
bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 509

GenotypeQuality
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bin: 8.75e1
variant carriers: 2

GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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bin: 8.25e1
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GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 1.25e1
variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 2

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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bin: 6.25e1
variant carriers: 2

GenotypeQuality
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bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 358
bin: 4.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 8
allele frequency: 1.214956109710537e-4
allele num: 65846
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6594
num of homozygotes: 0

Other
type: Population
allele count: 2
allele frequency: 2.262443438914027e-3
allele num: 884
num of homozygotes: 0

Latino
type: Population
allele count: 524
allele frequency: 4.637168141592921e-2
allele num: 11300
num of homozygotes: 19

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16196
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8446
num of homozygotes: 0

African
type: Population
allele count: 6
allele frequency: 6.238303181534623e-4
allele num: 9618
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.94e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.42e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.349e1

DP
type: SiteQuality
SIO_000300: 1.542479e6

VQSLOD
type: SiteQuality
SIO_000300: 6.18e0

MQRankSum
type: SiteQuality
SIO_000300: 2.2e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.8e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.55e-1

GenotypeQuality
all individuals: 368
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1606
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
all individuals: 161
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variant carriers: 0

GenotypeQuality
all individuals: 5161
bin: 6.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8474
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6594
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9654
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.515013786625458e-5
allele num: 66006
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11370
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16282
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.72e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.08e-1

DP
type: SiteQuality
SIO_000300: 1.547326e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.4e-3

FS
type: SiteQuality
SIO_000300: 1.903e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.4e0

MQ
type: SiteQuality
SIO_000300: 5.919e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.144e0

VQSLOD
type: SiteQuality
SIO_000300: 7.7e-2

QD
type: SiteQuality
SIO_000300: 1.24e1

GenotypeQuality
all individuals: 624
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
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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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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bin: 3.75e1
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 379
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variant carriers: 0

GenotypeQuality
all individuals: 1013
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 8.745845723281441e-5
allele num: 11434
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66222
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8506
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16360
num of homozygotes: 0

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6600
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.991e1

DP
type: SiteQuality
SIO_000300: 1.555582e6

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.572e0

VQSLOD
type: SiteQuality
SIO_000300: -1.759e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.68e0

QD
type: SiteQuality
SIO_000300: 1.638e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.3e-3

MQRankSum
type: SiteQuality
SIO_000300: -1.884e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.06e0

GenotypeQuality
all individuals: 116
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 501
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
all individuals: 10
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 8
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GenotypeQuality
all individuals: 1813
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 3
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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

GenotypeQuality
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45456
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 384
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.507567991316408e-5
allele num: 66332
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 890
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16406
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8516
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9730
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11452
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 7.906e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.6e-3

MQRankSum
type: SiteQuality
SIO_000300: 2.0e-2

MQ
type: SiteQuality
SIO_000300: 5.934e1

BaseQRankSum
type: SiteQuality
SIO_000300: -9.54e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.75e-1

QD
type: SiteQuality
SIO_000300: 1.277e1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.860000000000001e-1

DP
type: SiteQuality
SIO_000300: 1.559708e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.19e-1

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 176
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 361
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 177
bin: 3.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.507022725902707e-5
allele num: 66356
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8518
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16410
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9732
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11454
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 890
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.4e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.6e-3

MQRankSum
type: SiteQuality
SIO_000300: -1.535e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.56e0

FS
type: SiteQuality
SIO_000300: 1.078e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.32e-1

MQ
type: SiteQuality
SIO_000300: 5.944e1

QD
type: SiteQuality
SIO_000300: 1.314e1

VQSLOD
type: SiteQuality
SIO_000300: 2.43e0

DP
type: SiteQuality
SIO_000300: 1.560087e6

GenotypeQuality
all individuals: 1815
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
all individuals: 9
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GenotypeQuality
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variant carriers: 3

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 200
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GenotypeQuality
all individuals: 45480
bin: 6.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9730
num of homozygotes: 0

East Asian
type: Population
allele count: 3
allele frequency: 3.52112676056338e-4
allele num: 8520
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11458
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16410
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66366
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 890
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.612e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.45e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -3.28e-1

DP
type: SiteQuality
SIO_000300: 1.560901e6

MQRankSum
type: SiteQuality
SIO_000300: 2.58e-1

QD
type: SiteQuality
SIO_000300: 9.98e0

FS
type: SiteQuality
SIO_000300: 1.2709e1

MQ
type: SiteQuality
SIO_000300: 5.967e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.293e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.16e-1

GenotypeQuality
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bin: 7.75e1
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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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
all individuals: 1668
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2748
bin: 9.75e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66378
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: 0
allele frequency: 0.0e0
allele num: 9734
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11466
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 890
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.090875867949811e-5
allele num: 16418
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: 4.09e-1

FS
type: SiteQuality
SIO_000300: 3.247e0

VQSLOD
type: SiteQuality
SIO_000300: -4.436e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.37e-1

QD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.56155e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.599999999999999e-3

MQRankSum
type: SiteQuality
SIO_000300: 1.11e0

MQ
type: SiteQuality
SIO_000300: 5.943e1

GenotypeQuality
all individuals: 173
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
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variant carriers: 0

GenotypeQuality
all individuals: 45413
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 366
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 386
bin: 8.75e1
variant carriers: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.710801393728223e-5
allele num: 11480
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9744
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66434
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.17343346632246e-4
allele num: 8522
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 892
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16440
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.399e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.07e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.5e-3

DP
type: SiteQuality
SIO_000300: 1.564e6

MQ
type: SiteQuality
SIO_000300: 5.917e1

VQSLOD
type: SiteQuality
SIO_000300: 5.69e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 3.5e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 8.080000000000001e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.639999999999999e-1

GenotypeQuality
all individuals: 262
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 45571
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 122
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1075
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2805
bin: 9.75e1
variant carriers: 56

GenotypeQuality
all individuals: 5435
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 50
allele frequency: 7.511793515819837e-4
allele num: 66562
num of homozygotes: 1

Other
type: Population
allele count: 1
allele frequency: 1.118568232662192e-3
allele num: 894
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8558
num of homozygotes: 0

African
type: Population
allele count: 3
allele frequency: 3.068112088361628e-4
allele num: 9778
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16460
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 2.60778859527121e-4
allele num: 11504
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.42e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.24e-1

DP
type: SiteQuality
SIO_000300: 1.572675e6

BaseQRankSum
type: SiteQuality
SIO_000300: 3.37e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.48e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.54e-1

MQ
type: SiteQuality
SIO_000300: 5.986e1

QD
type: SiteQuality
SIO_000300: 1.594e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 6.14e0

GenotypeQuality
all individuals: 131
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35
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variant carriers: 0

GenotypeQuality
all individuals: 215
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 1915
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GenotypeQuality
all individuals: 86
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 2766
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variant carriers: 1

GenotypeQuality
all individuals: 127
bin: 5.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501681883709755e-5
allele num: 66592
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8564
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16478
num of homozygotes: 0

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

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

MQ
type: SiteQuality
SIO_000300: 5.982e1

FS
type: SiteQuality
SIO_000300: 3.788e0

VQSLOD
type: SiteQuality
SIO_000300: 1.72e0

MQRankSum
type: SiteQuality
SIO_000300: -3.27e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.54e-1

QD
type: SiteQuality
SIO_000300: 1.515e1

DP
type: SiteQuality
SIO_000300: 1.573632e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -2.721e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.1e-1

GenotypeQuality
all individuals: 1081
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45539
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variant carriers: 0

GenotypeQuality
all individuals: 116
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variant carriers: 0

GenotypeQuality
all individuals: 36
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GenotypeQuality
all individuals: 152
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variant carriers: 0

GenotypeQuality
all individuals: 3
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GenotypeQuality
all individuals: 8
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variant carriers: 0

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

GenotypeQuality
all individuals: 87
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variant carriers: 0

GenotypeQuality
all individuals: 207
bin: 2.25e1
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GenotypeQuality
all individuals: 401
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GenotypeQuality
all individuals: 81
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1928
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GenotypeQuality
all individuals: 2767
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 50
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1781
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 380
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5492
bin: 6.75e1
variant carriers: 0

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16482
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501321162623108e-5
allele num: 66608
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11516
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.31e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -3.31e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.23e-1

VQSLOD
type: SiteQuality
SIO_000300: -7.453e-1

DP
type: SiteQuality
SIO_000300: 1.574125e6

FS
type: SiteQuality
SIO_000300: 1.0685e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.063e0

QD
type: SiteQuality
SIO_000300: 1.201e1

GenotypeQuality
all individuals: 403
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 74
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2769
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 116
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36
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variant carriers: 0

GenotypeQuality
all individuals: 3
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GenotypeQuality
all individuals: 83
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variant carriers: 0

GenotypeQuality
all individuals: 5489
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variant carriers: 0

GenotypeQuality
all individuals: 35
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variant carriers: 0

GenotypeQuality
all individuals: 380
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1934
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GenotypeQuality
all individuals: 210
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1782
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 116
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1082
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 146
bin: 4.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11518
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8560
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66614
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.213297743266198e-4
allele num: 16484
num of homozygotes: 0

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: -1.79e-1

FS
type: SiteQuality
SIO_000300: 1.568e0

VQSLOD
type: SiteQuality
SIO_000300: 1.49e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.93e-1

DP
type: SiteQuality
SIO_000300: 1.574405e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

MQ
type: SiteQuality
SIO_000300: 5.972e1

MQRankSum
type: SiteQuality
SIO_000300: 2.22e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.05e0

QD
type: SiteQuality
SIO_000300: 1.059e1

GenotypeQuality
all individuals: 65
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 382
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 400
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5516
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37
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GenotypeQuality
all individuals: 5
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variant carriers: 0

GenotypeQuality
all individuals: 109
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GenotypeQuality
all individuals: 1089
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 190
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GenotypeQuality
all individuals: 1937
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variant carriers: 0

GenotypeQuality
all individuals: 101
bin: 3.25e1
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GenotypeQuality
all individuals: 2770
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 79
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variant carriers: 0

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

GenotypeQuality
all individuals: 100
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 100
bin: 3.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11516
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66624
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: 9788
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.335357309668379e-4
allele num: 8564
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.325e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.07e0

FS
type: SiteQuality
SIO_000300: 5.217e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.13e-1

DP
type: SiteQuality
SIO_000300: 1.575656e6

VQSLOD
type: SiteQuality
SIO_000300: 6.34e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -6.840000000000001e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.02e-1

MQ
type: SiteQuality
SIO_000300: 5.95e1

GenotypeQuality
all individuals: 71
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 7.5e0
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GenotypeQuality
all individuals: 92
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variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1948
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variant carriers: 0

GenotypeQuality
all individuals: 1100
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GenotypeQuality
all individuals: 2777
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 48
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 163
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GenotypeQuality
all individuals: 7
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GenotypeQuality
all individuals: 45721
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GenotypeQuality
all individuals: 79
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 389
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GenotypeQuality
all individuals: 1810
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5544
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 404
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9792
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500645277469312e-5
allele num: 66638
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8574
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: 896
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.73460537727667e-4
allele num: 11530
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.52e-1

DP
type: SiteQuality
SIO_000300: 1.577432e6

MQRankSum
type: SiteQuality
SIO_000300: 1.16e0

MQ
type: SiteQuality
SIO_000300: 5.967e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.73e0

QD
type: SiteQuality
SIO_000300: 1.419e1

FS
type: SiteQuality
SIO_000300: 1.739e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.02e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.3e-1

GenotypeQuality
all individuals: 8
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1103
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 70
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GenotypeQuality
all individuals: 54
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GenotypeQuality
all individuals: 91
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GenotypeQuality
all individuals: 163
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1947
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variant carriers: 0

GenotypeQuality
all individuals: 4
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GenotypeQuality
all individuals: 1809
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 7.5e0
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GenotypeQuality
all individuals: 80
bin: 3.25e1
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 403
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 91
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 387
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 4.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11528
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66638
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9792
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8570
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 1.0631e1

VQSLOD
type: SiteQuality
SIO_000300: -1.149e0

MQRankSum
type: SiteQuality
SIO_000300: -1.062e0

MQ
type: SiteQuality
SIO_000300: 5.965e1

InbreedingCoeff
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QD
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ClippingRankSum
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BaseQRankSum
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ReadPosRankSum
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

East Asian
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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African
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South Asian
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Other
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Latino
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DP
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MQ
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BaseQRankSum
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QD
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VQSLOD
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MQRankSum
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ClippingRankSum
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InbreedingCoeff
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SIO_000300: -1.0e-4

FS
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SIO_000300: 1.302e0

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

Latino
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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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African
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 3.000930288389401e-5
allele num: 66646
num of homozygotes: 0

East Asian
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Other
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num of homozygotes: 0

South Asian
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BaseQRankSum
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SIO_000300: 2.81e0

ClippingRankSum
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MQRankSum
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ReadPosRankSum
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QD
type: SiteQuality
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DP
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InbreedingCoeff
type: SiteQuality
SIO_000300: 5.2e-3

FS
type: SiteQuality
SIO_000300: 8.709e0

MQ
type: SiteQuality
SIO_000300: 5.961e1

VQSLOD
type: SiteQuality
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GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66646
num of homozygotes: 0

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

African
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allele frequency: 0.0e0
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South Asian
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allele num: 16502
num of homozygotes: 0

Latino
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Other
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East Asian
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DP
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SIO_000300: 1.57846e6

MQ
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ClippingRankSum
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MQRankSum
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InbreedingCoeff
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VQSLOD
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FS
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BaseQRankSum
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QD
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ReadPosRankSum
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SIO_000300: 1.02e0

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

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

European (Finnish)
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allele frequency: 0.0e0
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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 frequency: 0.0e0
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African
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allele num: 9800
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Latino
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South Asian
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InbreedingCoeff
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SIO_000300: 4.8e-3

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

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

European (Finnish)
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allele frequency: 0.0e0
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South Asian
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allele num: 16506
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Latino
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European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 66666
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African
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Other
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BaseQRankSum
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SIO_000300: 1.5e0

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

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

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

African
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66672
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Latino
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allele num: 11544
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South Asian
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allele num: 16506
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Other
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ReadPosRankSum
type: SiteQuality
SIO_000300: 3.18e-1

MQ
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DP
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BaseQRankSum
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FS
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