10-103588561-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103588561
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103588561
    reference: chr 10
allele count: 1
allele frequency: 1.801477211313277e-5
allele num: 55510
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000350733
  ensembl transcript: ENST00000358038
  gene symbol: KCNIP2
  hgvsc: ENST00000358038.3:c.295-108G>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000341624
  ensembl transcript: ENST00000353068
  gene symbol: KCNIP2
  hgvsc: ENST00000353068.3:c.199-87G>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000349055
  ensembl transcript: ENST00000356640
  gene symbol: KCNIP2
  hgvsc: ENST00000356640.2:c.349-108G>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000359063
  ensembl transcript: ENST00000370046
  gene symbol: KCNIP2
  hgvsc: ENST00000370046.1:c.199-108G>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000483385
  gene symbol: KCNIP2
  hgvsc: ENST00000483385.1:n.474-108G>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000344169
  ensembl transcript: ENST00000343195
  gene symbol: KCNIP2
  hgvsc: ENST00000343195.4:c.199-108G>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000355657
  gene symbol: KCNIP2
  hgvsc: ENST00000355657.2:n.773+15G>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000420040
  ensembl transcript: ENST00000461105
  gene symbol: KCNIP2
  hgvsc: ENST00000461105.1:c.394-108G>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000411679
  ensembl transcript: ENST00000434163
  gene symbol: KCNIP2
  hgvsc: ENST00000434163.1:c.141-108G>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000239118
  ensembl transcript: ENST00000348850
  gene symbol: KCNIP2
  hgvsc: ENST00000348850.5:c.214-108G>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000472764
  gene symbol: KCNIP2
  hgvsc: ENST00000472764.1:n.325+15G>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000239117
  ensembl transcript: ENST00000239117
  gene symbol: KCNIP2
  hgvsc: ENST00000239117.3:c.199-108G>A
  variant of: http://identifiers.org/hgnc/15522
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15526
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1987
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5680
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24345
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7344
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4315
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
population: South Asian
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: ReadPosRankSum

10-103588585-CAT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103588585
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103588583
    reference: chr 10
allele count: 1
allele frequency: 2.531132935101752e-5
allele num: 39508
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000420040
  ensembl transcript: ENST00000461105
  gene symbol: KCNIP2
  hgvsc: ENST00000461105.1:c.394-134_394-133delAT
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000411679
  ensembl transcript: ENST00000434163
  gene symbol: KCNIP2
  hgvsc: ENST00000434163.1:c.141-134_141-133delAT
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000341624
  ensembl transcript: ENST00000353068
  gene symbol: KCNIP2
  hgvsc: ENST00000353068.3:c.199-113_199-112delAT
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000355657
  gene symbol: KCNIP2
  hgvsc: ENST00000355657.2:n.762_763delAT
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000349055
  ensembl transcript: ENST00000356640
  gene symbol: KCNIP2
  hgvsc: ENST00000356640.2:c.349-134_349-133delAT
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000344169
  ensembl transcript: ENST00000343195
  gene symbol: KCNIP2
  hgvsc: ENST00000343195.4:c.199-134_199-133delAT
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000472764
  gene symbol: KCNIP2
  hgvsc: ENST00000472764.1:n.314_315delAT
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000350733
  ensembl transcript: ENST00000358038
  gene symbol: KCNIP2
  hgvsc: ENST00000358038.3:c.295-134_295-133delAT
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000239118
  ensembl transcript: ENST00000348850
  gene symbol: KCNIP2
  hgvsc: ENST00000348850.5:c.214-134_214-133delAT
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000359063
  ensembl transcript: ENST00000370046
  gene symbol: KCNIP2
  hgvsc: ENST00000370046.1:c.199-134_199-133delAT
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000239117
  ensembl transcript: ENST00000239117
  gene symbol: KCNIP2
  hgvsc: ENST00000239117.3:c.199-134_199-133delAT
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000483385
  gene symbol: KCNIP2
  hgvsc: ENST00000483385.1:n.474-134_474-133delAT
  variant of: http://identifiers.org/hgnc/15522
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16347
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10300
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 797
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23152
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3503
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 697
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4398
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: Other
population: East Asian
reference allele: CAT
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ

10-103588586-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103588586
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103588586
    reference: chr 10
allele count: 1
allele frequency: 2.615062761506276e-5
allele num: 38240
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000239117
  ensembl transcript: ENST00000239117
  gene symbol: KCNIP2
  hgvsc: ENST00000239117.3:c.199-133T>C
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000472764
  gene symbol: KCNIP2
  hgvsc: ENST00000472764.1:n.315T>C
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000420040
  ensembl transcript: ENST00000461105
  gene symbol: KCNIP2
  hgvsc: ENST00000461105.1:c.394-133T>C
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000341624
  ensembl transcript: ENST00000353068
  gene symbol: KCNIP2
  hgvsc: ENST00000353068.3:c.199-112T>C
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000411679
  ensembl transcript: ENST00000434163
  gene symbol: KCNIP2
  hgvsc: ENST00000434163.1:c.141-133T>C
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000359063
  ensembl transcript: ENST00000370046
  gene symbol: KCNIP2
  hgvsc: ENST00000370046.1:c.199-133T>C
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000344169
  ensembl transcript: ENST00000343195
  gene symbol: KCNIP2
  hgvsc: ENST00000343195.4:c.199-133T>C
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000349055
  ensembl transcript: ENST00000356640
  gene symbol: KCNIP2
  hgvsc: ENST00000356640.2:c.349-133T>C
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000355657
  gene symbol: KCNIP2
  hgvsc: ENST00000355657.2:n.763T>C
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000239118
  ensembl transcript: ENST00000348850
  gene symbol: KCNIP2
  hgvsc: ENST00000348850.5:c.214-133T>C
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000350733
  ensembl transcript: ENST00000358038
  gene symbol: KCNIP2
  hgvsc: ENST00000358038.3:c.295-133T>C
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000483385
  gene symbol: KCNIP2
  hgvsc: ENST00000483385.1:n.474-133T>C
  variant of: http://identifiers.org/hgnc/15522
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 808
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22694
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 688
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3420
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4272
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17317
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
reference allele: A
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum

10-103588594-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103588594
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103588594
    reference: chr 10
allele count: 1
allele frequency: 3.049710277523635e-5
allele num: 32790
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000355657
  gene symbol: KCNIP2
  hgvsc: ENST00000355657.2:n.755C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000350733
  ensembl transcript: ENST00000358038
  gene symbol: KCNIP2
  hgvsc: ENST00000358038.3:c.295-141C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000411679
  ensembl transcript: ENST00000434163
  gene symbol: KCNIP2
  hgvsc: ENST00000434163.1:c.141-141C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000472764
  gene symbol: KCNIP2
  hgvsc: ENST00000472764.1:n.307C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000420040
  ensembl transcript: ENST00000461105
  gene symbol: KCNIP2
  hgvsc: ENST00000461105.1:c.394-141C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000349055
  ensembl transcript: ENST00000356640
  gene symbol: KCNIP2
  hgvsc: ENST00000356640.2:c.349-141C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000483385
  gene symbol: KCNIP2
  hgvsc: ENST00000483385.1:n.474-141C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000344169
  ensembl transcript: ENST00000343195
  gene symbol: KCNIP2
  hgvsc: ENST00000343195.4:c.199-141C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000359063
  ensembl transcript: ENST00000370046
  gene symbol: KCNIP2
  hgvsc: ENST00000370046.1:c.199-141C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000239117
  ensembl transcript: ENST00000239117
  gene symbol: KCNIP2
  hgvsc: ENST00000239117.3:c.199-141C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000341624
  ensembl transcript: ENST00000353068
  gene symbol: KCNIP2
  hgvsc: ENST00000353068.3:c.199-120C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000239118
  ensembl transcript: ENST00000348850
  gene symbol: KCNIP2
  hgvsc: ENST00000348850.5:c.214-141C>T
  variant of: http://identifiers.org/hgnc/15522
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21462
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3184
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4000
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20613
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7831
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 731
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
reference allele: G
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD

10-103588632-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103588632
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103588632
    reference: chr 10
allele count: 0
allele frequency: 0.0e0
allele num: 19770
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000483385
  gene symbol: KCNIP2
  hgvsc: ENST00000483385.1:n.474-179T>C
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000341624
  ensembl transcript: ENST00000353068
  gene symbol: KCNIP2
  hgvsc: ENST00000353068.3:c.199-158T>C
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000239117
  ensembl transcript: ENST00000239117
  gene symbol: KCNIP2
  hgvsc: ENST00000239117.3:c.199-179T>C
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000355657
  gene symbol: KCNIP2
  hgvsc: ENST00000355657.2:n.746-29T>C
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000344169
  ensembl transcript: ENST00000343195
  gene symbol: KCNIP2
  hgvsc: ENST00000343195.4:c.199-179T>C
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000359063
  ensembl transcript: ENST00000370046
  gene symbol: KCNIP2
  hgvsc: ENST00000370046.1:c.199-179T>C
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000350733
  ensembl transcript: ENST00000358038
  gene symbol: KCNIP2
  hgvsc: ENST00000358038.3:c.295-179T>C
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000349055
  ensembl transcript: ENST00000356640
  gene symbol: KCNIP2
  hgvsc: ENST00000356640.2:c.349-179T>C
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000239118
  ensembl transcript: ENST00000348850
  gene symbol: KCNIP2
  hgvsc: ENST00000348850.5:c.214-179T>C
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000411679
  ensembl transcript: ENST00000434163
  gene symbol: KCNIP2
  hgvsc: ENST00000434163.1:c.141-179T>C
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000420040
  ensembl transcript: ENST00000461105
  gene symbol: KCNIP2
  hgvsc: ENST00000461105.1:c.394-179T>C
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000472764
  gene symbol: KCNIP2
  hgvsc: ENST00000472764.1:n.295-26T>C
  variant of: http://identifiers.org/hgnc/15522
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15285
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4862
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1664
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29729
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1048
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1687
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: South Asian
reference allele: A
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff

10-103588634-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103588634
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103588634
    reference: chr 10
allele count: 0
allele frequency: 0.0e0
allele num: 19574
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000355657
  gene symbol: KCNIP2
  hgvsc: ENST00000355657.2:n.746-31C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000239117
  ensembl transcript: ENST00000239117
  gene symbol: KCNIP2
  hgvsc: ENST00000239117.3:c.199-181C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000344169
  ensembl transcript: ENST00000343195
  gene symbol: KCNIP2
  hgvsc: ENST00000343195.4:c.199-181C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000483385
  gene symbol: KCNIP2
  hgvsc: ENST00000483385.1:n.474-181C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000359063
  ensembl transcript: ENST00000370046
  gene symbol: KCNIP2
  hgvsc: ENST00000370046.1:c.199-181C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000350733
  ensembl transcript: ENST00000358038
  gene symbol: KCNIP2
  hgvsc: ENST00000358038.3:c.295-181C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000349055
  ensembl transcript: ENST00000356640
  gene symbol: KCNIP2
  hgvsc: ENST00000356640.2:c.349-181C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000341624
  ensembl transcript: ENST00000353068
  gene symbol: KCNIP2
  hgvsc: ENST00000353068.3:c.199-160C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000420040
  ensembl transcript: ENST00000461105
  gene symbol: KCNIP2
  hgvsc: ENST00000461105.1:c.394-181C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000472764
  gene symbol: KCNIP2
  hgvsc: ENST00000472764.1:n.295-28C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000239118
  ensembl transcript: ENST00000348850
  gene symbol: KCNIP2
  hgvsc: ENST00000348850.5:c.214-181C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000411679
  ensembl transcript: ENST00000434163
  gene symbol: KCNIP2
  hgvsc: ENST00000434163.1:c.141-181C>T
  variant of: http://identifiers.org/hgnc/15522
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4899
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1074
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15320
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29787
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1587
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1626
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ

10-103588638-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103588638
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103588638
    reference: chr 10
allele count: 0
allele frequency: 0.0e0
allele num: 18704
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000344169
  ensembl transcript: ENST00000343195
  gene symbol: KCNIP2
  hgvsc: ENST00000343195.4:c.199-185G>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000411679
  ensembl transcript: ENST00000434163
  gene symbol: KCNIP2
  hgvsc: ENST00000434163.1:c.141-185G>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000472764
  gene symbol: KCNIP2
  hgvsc: ENST00000472764.1:n.295-32G>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000420040
  ensembl transcript: ENST00000461105
  gene symbol: KCNIP2
  hgvsc: ENST00000461105.1:c.394-185G>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000341624
  ensembl transcript: ENST00000353068
  gene symbol: KCNIP2
  hgvsc: ENST00000353068.3:c.199-164G>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000239118
  ensembl transcript: ENST00000348850
  gene symbol: KCNIP2
  hgvsc: ENST00000348850.5:c.214-185G>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000359063
  ensembl transcript: ENST00000370046
  gene symbol: KCNIP2
  hgvsc: ENST00000370046.1:c.199-185G>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000350733
  ensembl transcript: ENST00000358038
  gene symbol: KCNIP2
  hgvsc: ENST00000358038.3:c.295-185G>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000483385
  gene symbol: KCNIP2
  hgvsc: ENST00000483385.1:n.474-185G>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000355657
  gene symbol: KCNIP2
  hgvsc: ENST00000355657.2:n.746-35G>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000349055
  ensembl transcript: ENST00000356640
  gene symbol: KCNIP2
  hgvsc: ENST00000356640.2:c.349-185G>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000239117
  ensembl transcript: ENST00000239117
  gene symbol: KCNIP2
  hgvsc: ENST00000239117.3:c.199-185G>A
  variant of: http://identifiers.org/hgnc/15522
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1315
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15429
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30002
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1176
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4993
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1424
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum

10-103588639-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103588639
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103588639
    reference: chr 10
allele count: 1
allele frequency: 5.425935973955508e-5
allele num: 18430
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000344169
  ensembl transcript: ENST00000343195
  gene symbol: KCNIP2
  hgvsc: ENST00000343195.4:c.199-186C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000355657
  gene symbol: KCNIP2
  hgvsc: ENST00000355657.2:n.746-36C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000341624
  ensembl transcript: ENST00000353068
  gene symbol: KCNIP2
  hgvsc: ENST00000353068.3:c.199-165C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000359063
  ensembl transcript: ENST00000370046
  gene symbol: KCNIP2
  hgvsc: ENST00000370046.1:c.199-186C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000483385
  gene symbol: KCNIP2
  hgvsc: ENST00000483385.1:n.474-186C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000349055
  ensembl transcript: ENST00000356640
  gene symbol: KCNIP2
  hgvsc: ENST00000356640.2:c.349-186C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000411679
  ensembl transcript: ENST00000434163
  gene symbol: KCNIP2
  hgvsc: ENST00000434163.1:c.141-186C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000350733
  ensembl transcript: ENST00000358038
  gene symbol: KCNIP2
  hgvsc: ENST00000358038.3:c.295-186C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000420040
  ensembl transcript: ENST00000461105
  gene symbol: KCNIP2
  hgvsc: ENST00000461105.1:c.394-186C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000239117
  ensembl transcript: ENST00000239117
  gene symbol: KCNIP2
  hgvsc: ENST00000239117.3:c.199-186C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000472764
  gene symbol: KCNIP2
  hgvsc: ENST00000472764.1:n.295-33C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000239118
  ensembl transcript: ENST00000348850
  gene symbol: KCNIP2
  hgvsc: ENST00000348850.5:c.214-186C>T
  variant of: http://identifiers.org/hgnc/15522
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1172
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15613
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1342
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30026
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5120
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1156
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: DP

10-103588640-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103588640
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103588640
    reference: chr 10
allele count: 0
allele frequency: 0.0e0
allele num: 18582
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000349055
  ensembl transcript: ENST00000356640
  gene symbol: KCNIP2
  hgvsc: ENST00000356640.2:c.349-187T>C
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000239118
  ensembl transcript: ENST00000348850
  gene symbol: KCNIP2
  hgvsc: ENST00000348850.5:c.214-187T>C
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000483385
  gene symbol: KCNIP2
  hgvsc: ENST00000483385.1:n.474-187T>C
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000350733
  ensembl transcript: ENST00000358038
  gene symbol: KCNIP2
  hgvsc: ENST00000358038.3:c.295-187T>C
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000420040
  ensembl transcript: ENST00000461105
  gene symbol: KCNIP2
  hgvsc: ENST00000461105.1:c.394-187T>C
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000355657
  gene symbol: KCNIP2
  hgvsc: ENST00000355657.2:n.746-37T>C
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000341624
  ensembl transcript: ENST00000353068
  gene symbol: KCNIP2
  hgvsc: ENST00000353068.3:c.199-166T>C
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000344169
  ensembl transcript: ENST00000343195
  gene symbol: KCNIP2
  hgvsc: ENST00000343195.4:c.199-187T>C
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000411679
  ensembl transcript: ENST00000434163
  gene symbol: KCNIP2
  hgvsc: ENST00000434163.1:c.141-187T>C
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000239117
  ensembl transcript: ENST00000239117
  gene symbol: KCNIP2
  hgvsc: ENST00000239117.3:c.199-187T>C
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000359063
  ensembl transcript: ENST00000370046
  gene symbol: KCNIP2
  hgvsc: ENST00000370046.1:c.199-187T>C
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000472764
  gene symbol: KCNIP2
  hgvsc: ENST00000472764.1:n.295-34T>C
  variant of: http://identifiers.org/hgnc/15522
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5114
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15705
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1147
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30073
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1138
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1373
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
population: African
population: East Asian
population: South Asian
reference allele: A
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: MQ

10-103588659-GCC-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103588659
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103588657
    reference: chr 10
allele count: 0
allele frequency: 0.0e0
allele num: 16038
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000350733
  ensembl transcript: ENST00000358038
  gene symbol: KCNIP2
  hgvsc: ENST00000358038.3:c.294+171_294+172delGG
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000355657
  gene symbol: KCNIP2
  hgvsc: ENST00000355657.2:n.746-58_746-57delGG
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000472764
  gene symbol: KCNIP2
  hgvsc: ENST00000472764.1:n.295-55_295-54delGG
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000411679
  ensembl transcript: ENST00000434163
  gene symbol: KCNIP2
  hgvsc: ENST00000434163.1:c.140+171_140+172delGG
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000420040
  ensembl transcript: ENST00000461105
  gene symbol: KCNIP2
  hgvsc: ENST00000461105.1:c.393+171_393+172delGG
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000359063
  ensembl transcript: ENST00000370046
  gene symbol: KCNIP2
  hgvsc: ENST00000370046.1:c.198+171_198+172delGG
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000344169
  ensembl transcript: ENST00000343195
  gene symbol: KCNIP2
  hgvsc: ENST00000343195.4:c.198+171_198+172delGG
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000341624
  ensembl transcript: ENST00000353068
  gene symbol: KCNIP2
  hgvsc: ENST00000353068.3:c.198+171_198+172delGG
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000239118
  ensembl transcript: ENST00000348850
  gene symbol: KCNIP2
  hgvsc: ENST00000348850.5:c.213+171_213+172delGG
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000349055
  ensembl transcript: ENST00000356640
  gene symbol: KCNIP2
  hgvsc: ENST00000356640.2:c.348+171_348+172delGG
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000483385
  gene symbol: KCNIP2
  hgvsc: ENST00000483385.1:n.473+171_473+172delGG
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000239117
  ensembl transcript: ENST00000239117
  gene symbol: KCNIP2
  hgvsc: ENST00000239117.3:c.198+171_198+172delGG
  variant of: http://identifiers.org/hgnc/15522
canonical: true
consequence: intron
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18496
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29490
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1113
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5422
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 882
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
population: African
population: Other
reference allele: GCC
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ

10-103599464-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103599464
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103599464
    reference: chr 10
allele count: 1
allele frequency: 8.265829062654984e-6
allele num: 120980
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000472764
  gene symbol: KCNIP2
  hgvsc: ENST00000472764.1:n.73+3789A>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000349055
  ensembl transcript: ENST00000356640
  gene symbol: KCNIP2
  hgvsc: ENST00000356640.2:c.73+3789A>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000344169
  ensembl transcript: ENST00000343195
  gene symbol: KCNIP2
  hgvsc: ENST00000343195.4:c.73+3789A>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000341624
  ensembl transcript: ENST00000353068
  gene symbol: KCNIP2
  hgvsc: ENST00000353068.3:c.73+3789A>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000350733
  ensembl transcript: ENST00000358038
  gene symbol: KCNIP2
  hgvsc: ENST00000358038.3:c.73+3789A>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000355657
  gene symbol: KCNIP2
  hgvsc: ENST00000355657.2:n.425+3789A>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000420040
  ensembl transcript: ENST00000461105
  gene symbol: KCNIP2
  hgvsc: ENST00000461105.1:c.73+3789A>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000239118
  ensembl transcript: ENST00000348850
  gene symbol: KCNIP2
  hgvsc: ENST00000348850.5:c.88+46A>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000359063
  ensembl transcript: ENST00000370046
  gene symbol: KCNIP2
  hgvsc: ENST00000370046.1:c.73+3789A>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000239117
  ensembl transcript: ENST00000239117
  gene symbol: KCNIP2
  hgvsc: ENST00000239117.3:c.73+3789A>T
  variant of: http://identifiers.org/hgnc/15522
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2364
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9485
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3942
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6040
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1318
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15338
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3989
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 715
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15619
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 241
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 131
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 153
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
reference allele: T
site quality: QD
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff

10-103588679-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103588679
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103588679
    reference: chr 10
allele count: 0
allele frequency: 0.0e0
allele num: 15430
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000350733
  ensembl transcript: ENST00000358038
  gene symbol: KCNIP2
  hgvsc: ENST00000358038.3:c.294+153C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000483385
  gene symbol: KCNIP2
  hgvsc: ENST00000483385.1:n.473+153C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000239118
  ensembl transcript: ENST00000348850
  gene symbol: KCNIP2
  hgvsc: ENST00000348850.5:c.213+153C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000239117
  ensembl transcript: ENST00000239117
  gene symbol: KCNIP2
  hgvsc: ENST00000239117.3:c.198+153C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000411679
  ensembl transcript: ENST00000434163
  gene symbol: KCNIP2
  hgvsc: ENST00000434163.1:c.140+153C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000359063
  ensembl transcript: ENST00000370046
  gene symbol: KCNIP2
  hgvsc: ENST00000370046.1:c.198+153C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000341624
  ensembl transcript: ENST00000353068
  gene symbol: KCNIP2
  hgvsc: ENST00000353068.3:c.198+153C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000344169
  ensembl transcript: ENST00000343195
  gene symbol: KCNIP2
  hgvsc: ENST00000343195.4:c.198+153C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000472764
  gene symbol: KCNIP2
  hgvsc: ENST00000472764.1:n.295-73C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000349055
  ensembl transcript: ENST00000356640
  gene symbol: KCNIP2
  hgvsc: ENST00000356640.2:c.348+153C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000420040
  ensembl transcript: ENST00000461105
  gene symbol: KCNIP2
  hgvsc: ENST00000461105.1:c.393+153C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000355657
  gene symbol: KCNIP2
  hgvsc: ENST00000355657.2:n.746-76C>T
  variant of: http://identifiers.org/hgnc/15522
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 988
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1162
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25483
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5016
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24744
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: African
population: European (Finnish)
population: Other
population: East Asian
population: Latino
reference allele: G
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD

10-103588683-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103588683
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103588683
    reference: chr 10
allele count: 0
allele frequency: 0.0e0
allele num: 16442
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000349055
  ensembl transcript: ENST00000356640
  gene symbol: KCNIP2
  hgvsc: ENST00000356640.2:c.348+149G>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000472764
  gene symbol: KCNIP2
  hgvsc: ENST00000472764.1:n.295-77G>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000344169
  ensembl transcript: ENST00000343195
  gene symbol: KCNIP2
  hgvsc: ENST00000343195.4:c.198+149G>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000239118
  ensembl transcript: ENST00000348850
  gene symbol: KCNIP2
  hgvsc: ENST00000348850.5:c.213+149G>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000411679
  ensembl transcript: ENST00000434163
  gene symbol: KCNIP2
  hgvsc: ENST00000434163.1:c.140+149G>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000341624
  ensembl transcript: ENST00000353068
  gene symbol: KCNIP2
  hgvsc: ENST00000353068.3:c.198+149G>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000355657
  gene symbol: KCNIP2
  hgvsc: ENST00000355657.2:n.746-80G>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000420040
  ensembl transcript: ENST00000461105
  gene symbol: KCNIP2
  hgvsc: ENST00000461105.1:c.393+149G>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000483385
  gene symbol: KCNIP2
  hgvsc: ENST00000483385.1:n.473+149G>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000239117
  ensembl transcript: ENST00000239117
  gene symbol: KCNIP2
  hgvsc: ENST00000239117.3:c.198+149G>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000350733
  ensembl transcript: ENST00000358038
  gene symbol: KCNIP2
  hgvsc: ENST00000358038.3:c.294+149G>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000359063
  ensembl transcript: ENST00000370046
  gene symbol: KCNIP2
  hgvsc: ENST00000370046.1:c.198+149G>A
  variant of: http://identifiers.org/hgnc/15522
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23113
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1282
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 986
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27076
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5334
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
population: African
population: East Asian
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: DP
site quality: QD

10-103588783-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103588783
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103588783
    reference: chr 10
allele count: 390
allele frequency: 3.833903503597971e-3
allele num: 101724
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000420040
  ensembl transcript: ENST00000461105
  gene symbol: KCNIP2
  hgvsc: ENST00000461105.1:c.393+49C>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000344169
  ensembl transcript: ENST00000343195
  gene symbol: KCNIP2
  hgvsc: ENST00000343195.4:c.198+49C>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000355657
  gene symbol: KCNIP2
  hgvsc: ENST00000355657.2:n.745+49C>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000350733
  ensembl transcript: ENST00000358038
  gene symbol: KCNIP2
  hgvsc: ENST00000358038.3:c.294+49C>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000341624
  ensembl transcript: ENST00000353068
  gene symbol: KCNIP2
  hgvsc: ENST00000353068.3:c.198+49C>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000472764
  gene symbol: KCNIP2
  hgvsc: ENST00000472764.1:n.294+49C>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000349055
  ensembl transcript: ENST00000356640
  gene symbol: KCNIP2
  hgvsc: ENST00000356640.2:c.348+49C>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000483385
  gene symbol: KCNIP2
  hgvsc: ENST00000483385.1:n.473+49C>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000411679
  ensembl transcript: ENST00000434163
  gene symbol: KCNIP2
  hgvsc: ENST00000434163.1:c.140+49C>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000359063
  ensembl transcript: ENST00000370046
  gene symbol: KCNIP2
  hgvsc: ENST00000370046.1:c.198+49C>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000239117
  ensembl transcript: ENST00000239117
  gene symbol: KCNIP2
  hgvsc: ENST00000239117.3:c.198+49C>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000239118
  ensembl transcript: ENST00000348850
  gene symbol: KCNIP2
  hgvsc: ENST00000348850.5:c.213+49C>A
  variant of: http://identifiers.org/hgnc/15522
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 14623
  bin: 2.25e1
  variant carriers: 109
genotype depth: GenotypeDepth
  all individuals: 19918
  bin: 2.75e1
  variant carriers: 84
genotype depth: GenotypeDepth
  all individuals: 1756
  bin: 3.75e1
  variant carriers: 33
genotype depth: GenotypeDepth
  all individuals: 8045
  bin: 1.75e1
  variant carriers: 85
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 5.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 6.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 5435
  bin: 1.25e1
  variant carriers: 35
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2195
  bin: 7.5e0
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 4.25e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 6.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 6984
  bin: 3.25e1
  variant carriers: 53
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Other
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
reference allele: G
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD

10-103588787-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103588787
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103588787
    reference: chr 10
allele count: 2
allele frequency: 1.739856635813209e-5
allele num: 114952
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000239117
  ensembl transcript: ENST00000239117
  gene symbol: KCNIP2
  hgvsc: ENST00000239117.3:c.198+45G>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000483385
  gene symbol: KCNIP2
  hgvsc: ENST00000483385.1:n.473+45G>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000359063
  ensembl transcript: ENST00000370046
  gene symbol: KCNIP2
  hgvsc: ENST00000370046.1:c.198+45G>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000420040
  ensembl transcript: ENST00000461105
  gene symbol: KCNIP2
  hgvsc: ENST00000461105.1:c.393+45G>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000349055
  ensembl transcript: ENST00000356640
  gene symbol: KCNIP2
  hgvsc: ENST00000356640.2:c.348+45G>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000341624
  ensembl transcript: ENST00000353068
  gene symbol: KCNIP2
  hgvsc: ENST00000353068.3:c.198+45G>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000350733
  ensembl transcript: ENST00000358038
  gene symbol: KCNIP2
  hgvsc: ENST00000358038.3:c.294+45G>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000239118
  ensembl transcript: ENST00000348850
  gene symbol: KCNIP2
  hgvsc: ENST00000348850.5:c.213+45G>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000344169
  ensembl transcript: ENST00000343195
  gene symbol: KCNIP2
  hgvsc: ENST00000343195.4:c.198+45G>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000472764
  gene symbol: KCNIP2
  hgvsc: ENST00000472764.1:n.294+45G>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000355657
  gene symbol: KCNIP2
  hgvsc: ENST00000355657.2:n.745+45G>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000411679
  ensembl transcript: ENST00000434163
  gene symbol: KCNIP2
  hgvsc: ENST00000434163.1:c.140+45G>A
  variant of: http://identifiers.org/hgnc/15522
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6020
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17107
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20269
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 866
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2438
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7661
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP

10-103588788-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103588788
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103588788
    reference: chr 10
allele count: 1
allele frequency: 8.657558914688415e-6
allele num: 115506
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000472764
  gene symbol: KCNIP2
  hgvsc: ENST00000472764.1:n.294+44G>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000483385
  gene symbol: KCNIP2
  hgvsc: ENST00000483385.1:n.473+44G>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000359063
  ensembl transcript: ENST00000370046
  gene symbol: KCNIP2
  hgvsc: ENST00000370046.1:c.198+44G>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000349055
  ensembl transcript: ENST00000356640
  gene symbol: KCNIP2
  hgvsc: ENST00000356640.2:c.348+44G>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000341624
  ensembl transcript: ENST00000353068
  gene symbol: KCNIP2
  hgvsc: ENST00000353068.3:c.198+44G>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000355657
  gene symbol: KCNIP2
  hgvsc: ENST00000355657.2:n.745+44G>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000239117
  ensembl transcript: ENST00000239117
  gene symbol: KCNIP2
  hgvsc: ENST00000239117.3:c.198+44G>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000420040
  ensembl transcript: ENST00000461105
  gene symbol: KCNIP2
  hgvsc: ENST00000461105.1:c.393+44G>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000350733
  ensembl transcript: ENST00000358038
  gene symbol: KCNIP2
  hgvsc: ENST00000358038.3:c.294+44G>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000344169
  ensembl transcript: ENST00000343195
  gene symbol: KCNIP2
  hgvsc: ENST00000343195.4:c.198+44G>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000239118
  ensembl transcript: ENST00000348850
  gene symbol: KCNIP2
  hgvsc: ENST00000348850.5:c.213+44G>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000411679
  ensembl transcript: ENST00000434163
  gene symbol: KCNIP2
  hgvsc: ENST00000434163.1:c.140+44G>A
  variant of: http://identifiers.org/hgnc/15522
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 850
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17968
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20579
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2442
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6588
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5350
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5971
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: Other
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
population: African
reference allele: C
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: MQ

10-103588789-TC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103588789
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103588788
    reference: chr 10
allele count: 2
allele frequency: 1.731122113353876e-5
allele num: 115532
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000355657
  gene symbol: KCNIP2
  hgvsc: ENST00000355657.2:n.745+42delG
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000420040
  ensembl transcript: ENST00000461105
  gene symbol: KCNIP2
  hgvsc: ENST00000461105.1:c.393+42delG
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000359063
  ensembl transcript: ENST00000370046
  gene symbol: KCNIP2
  hgvsc: ENST00000370046.1:c.198+42delG
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000239118
  ensembl transcript: ENST00000348850
  gene symbol: KCNIP2
  hgvsc: ENST00000348850.5:c.213+42delG
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000341624
  ensembl transcript: ENST00000353068
  gene symbol: KCNIP2
  hgvsc: ENST00000353068.3:c.198+42delG
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000350733
  ensembl transcript: ENST00000358038
  gene symbol: KCNIP2
  hgvsc: ENST00000358038.3:c.294+42delG
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000344169
  ensembl transcript: ENST00000343195
  gene symbol: KCNIP2
  hgvsc: ENST00000343195.4:c.198+42delG
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000411679
  ensembl transcript: ENST00000434163
  gene symbol: KCNIP2
  hgvsc: ENST00000434163.1:c.140+42delG
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000483385
  gene symbol: KCNIP2
  hgvsc: ENST00000483385.1:n.473+42delG
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000349055
  ensembl transcript: ENST00000356640
  gene symbol: KCNIP2
  hgvsc: ENST00000356640.2:c.348+42delG
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000472764
  gene symbol: KCNIP2
  hgvsc: ENST00000472764.1:n.294+42delG
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000239117
  ensembl transcript: ENST00000239117
  gene symbol: KCNIP2
  hgvsc: ENST00000239117.3:c.198+42delG
  variant of: http://identifiers.org/hgnc/15522
canonical: true
consequence: intron
filter: VQSRTrancheINDEL95.00to96.00
genotype depth: GenotypeDepth
  all individuals: 5937
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18432
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20645
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6097
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5356
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2440
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 851
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Latino
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: TC
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum

10-103588793-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103588793
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103588793
    reference: chr 10
allele count: 1
allele frequency: 8.639756704451203e-6
allele num: 115744
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000349055
  ensembl transcript: ENST00000356640
  gene symbol: KCNIP2
  hgvsc: ENST00000356640.2:c.348+39C>G
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000472764
  gene symbol: KCNIP2
  hgvsc: ENST00000472764.1:n.294+39C>G
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000341624
  ensembl transcript: ENST00000353068
  gene symbol: KCNIP2
  hgvsc: ENST00000353068.3:c.198+39C>G
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000344169
  ensembl transcript: ENST00000343195
  gene symbol: KCNIP2
  hgvsc: ENST00000343195.4:c.198+39C>G
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000239118
  ensembl transcript: ENST00000348850
  gene symbol: KCNIP2
  hgvsc: ENST00000348850.5:c.213+39C>G
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000483385
  gene symbol: KCNIP2
  hgvsc: ENST00000483385.1:n.473+39C>G
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000350733
  ensembl transcript: ENST00000358038
  gene symbol: KCNIP2
  hgvsc: ENST00000358038.3:c.294+39C>G
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000355657
  gene symbol: KCNIP2
  hgvsc: ENST00000355657.2:n.745+39C>G
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000239117
  ensembl transcript: ENST00000239117
  gene symbol: KCNIP2
  hgvsc: ENST00000239117.3:c.198+39C>G
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000359063
  ensembl transcript: ENST00000370046
  gene symbol: KCNIP2
  hgvsc: ENST00000370046.1:c.198+39C>G
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000420040
  ensembl transcript: ENST00000461105
  gene symbol: KCNIP2
  hgvsc: ENST00000461105.1:c.393+39C>G
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000411679
  ensembl transcript: ENST00000434163
  gene symbol: KCNIP2
  hgvsc: ENST00000434163.1:c.140+39C>G
  variant of: http://identifiers.org/hgnc/15522
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18702
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5718
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2396
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21635
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 850
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5094
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5407
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ

http://identifiers.org/exac.variant/10-103588795-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103588795
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103588795
    reference: chr 10
allele count: 3
allele frequency: 2.592150966872311e-5
allele num: 115734
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000411679
  ensembl transcript: ENST00000434163
  gene symbol: KCNIP2
  hgvsc: ENST00000434163.1:c.140+37G>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000344169
  ensembl transcript: ENST00000343195
  gene symbol: KCNIP2
  hgvsc: ENST00000343195.4:c.198+37G>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000349055
  ensembl transcript: ENST00000356640
  gene symbol: KCNIP2
  hgvsc: ENST00000356640.2:c.348+37G>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000350733
  ensembl transcript: ENST00000358038
  gene symbol: KCNIP2
  hgvsc: ENST00000358038.3:c.294+37G>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000355657
  gene symbol: KCNIP2
  hgvsc: ENST00000355657.2:n.745+37G>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000483385
  gene symbol: KCNIP2
  hgvsc: ENST00000483385.1:n.473+37G>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000420040
  ensembl transcript: ENST00000461105
  gene symbol: KCNIP2
  hgvsc: ENST00000461105.1:c.393+37G>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000341624
  ensembl transcript: ENST00000353068
  gene symbol: KCNIP2
  hgvsc: ENST00000353068.3:c.198+37G>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000239117
  ensembl transcript: ENST00000239117
  gene symbol: KCNIP2
  hgvsc: ENST00000239117.3:c.198+37G>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000239118
  ensembl transcript: ENST00000348850
  gene symbol: KCNIP2
  hgvsc: ENST00000348850.5:c.213+37G>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000472764
  gene symbol: KCNIP2
  hgvsc: ENST00000472764.1:n.294+37G>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000359063
  ensembl transcript: ENST00000370046
  gene symbol: KCNIP2
  hgvsc: ENST00000370046.1:c.198+37G>T
  variant of: http://identifiers.org/hgnc/15522
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4525
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22130
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5539
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5456
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2347
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 849
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18974
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: Other
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/10-103588798-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103588798
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103588798
    reference: chr 10
allele count: 1
allele frequency: 8.652465087303372e-6
allele num: 115574
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000344169
  ensembl transcript: ENST00000343195
  gene symbol: KCNIP2
  hgvsc: ENST00000343195.4:c.198+34T>G
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000411679
  ensembl transcript: ENST00000434163
  gene symbol: KCNIP2
  hgvsc: ENST00000434163.1:c.140+34T>G
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000239118
  ensembl transcript: ENST00000348850
  gene symbol: KCNIP2
  hgvsc: ENST00000348850.5:c.213+34T>G
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000349055
  ensembl transcript: ENST00000356640
  gene symbol: KCNIP2
  hgvsc: ENST00000356640.2:c.348+34T>G
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000239117
  ensembl transcript: ENST00000239117
  gene symbol: KCNIP2
  hgvsc: ENST00000239117.3:c.198+34T>G
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000350733
  ensembl transcript: ENST00000358038
  gene symbol: KCNIP2
  hgvsc: ENST00000358038.3:c.294+34T>G
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000483385
  gene symbol: KCNIP2
  hgvsc: ENST00000483385.1:n.473+34T>G
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000359063
  ensembl transcript: ENST00000370046
  gene symbol: KCNIP2
  hgvsc: ENST00000370046.1:c.198+34T>G
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000355657
  gene symbol: KCNIP2
  hgvsc: ENST00000355657.2:n.745+34T>G
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000472764
  gene symbol: KCNIP2
  hgvsc: ENST00000472764.1:n.294+34T>G
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000341624
  ensembl transcript: ENST00000353068
  gene symbol: KCNIP2
  hgvsc: ENST00000353068.3:c.198+34T>G
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000420040
  ensembl transcript: ENST00000461105
  gene symbol: KCNIP2
  hgvsc: ENST00000461105.1:c.393+34T>G
  variant of: http://identifiers.org/hgnc/15522
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5649
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2249
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22631
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 936
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19441
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5178
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
reference allele: A
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: DP

10-103588799-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103588799
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103588799
    reference: chr 10
allele count: 1
allele frequency: 8.598895901766214e-6
allele num: 116294
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000420040
  ensembl transcript: ENST00000461105
  gene symbol: KCNIP2
  hgvsc: ENST00000461105.1:c.393+33G>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000344169
  ensembl transcript: ENST00000343195
  gene symbol: KCNIP2
  hgvsc: ENST00000343195.4:c.198+33G>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000355657
  gene symbol: KCNIP2
  hgvsc: ENST00000355657.2:n.745+33G>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000349055
  ensembl transcript: ENST00000356640
  gene symbol: KCNIP2
  hgvsc: ENST00000356640.2:c.348+33G>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000359063
  ensembl transcript: ENST00000370046
  gene symbol: KCNIP2
  hgvsc: ENST00000370046.1:c.198+33G>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000350733
  ensembl transcript: ENST00000358038
  gene symbol: KCNIP2
  hgvsc: ENST00000358038.3:c.294+33G>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000341624
  ensembl transcript: ENST00000353068
  gene symbol: KCNIP2
  hgvsc: ENST00000353068.3:c.198+33G>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000483385
  gene symbol: KCNIP2
  hgvsc: ENST00000483385.1:n.473+33G>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000411679
  ensembl transcript: ENST00000434163
  gene symbol: KCNIP2
  hgvsc: ENST00000434163.1:c.140+33G>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000472764
  gene symbol: KCNIP2
  hgvsc: ENST00000472764.1:n.294+33G>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000239118
  ensembl transcript: ENST00000348850
  gene symbol: KCNIP2
  hgvsc: ENST00000348850.5:c.213+33G>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000239117
  ensembl transcript: ENST00000239117
  gene symbol: KCNIP2
  hgvsc: ENST00000239117.3:c.198+33G>A
  variant of: http://identifiers.org/hgnc/15522
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3285
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 847
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2228
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4929
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20181
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22944
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5463
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: C
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP

10-103588803-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103588803
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103588803
    reference: chr 10
allele count: 1
allele frequency: 8.582659594555161e-6
allele num: 116514
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000359063
  ensembl transcript: ENST00000370046
  gene symbol: KCNIP2
  hgvsc: ENST00000370046.1:c.198+29G>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000355657
  gene symbol: KCNIP2
  hgvsc: ENST00000355657.2:n.745+29G>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000239117
  ensembl transcript: ENST00000239117
  gene symbol: KCNIP2
  hgvsc: ENST00000239117.3:c.198+29G>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000349055
  ensembl transcript: ENST00000356640
  gene symbol: KCNIP2
  hgvsc: ENST00000356640.2:c.348+29G>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000341624
  ensembl transcript: ENST00000353068
  gene symbol: KCNIP2
  hgvsc: ENST00000353068.3:c.198+29G>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000411679
  ensembl transcript: ENST00000434163
  gene symbol: KCNIP2
  hgvsc: ENST00000434163.1:c.140+29G>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000344169
  ensembl transcript: ENST00000343195
  gene symbol: KCNIP2
  hgvsc: ENST00000343195.4:c.198+29G>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000483385
  gene symbol: KCNIP2
  hgvsc: ENST00000483385.1:n.473+29G>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000239118
  ensembl transcript: ENST00000348850
  gene symbol: KCNIP2
  hgvsc: ENST00000348850.5:c.213+29G>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000472764
  gene symbol: KCNIP2
  hgvsc: ENST00000472764.1:n.294+29G>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000350733
  ensembl transcript: ENST00000358038
  gene symbol: KCNIP2
  hgvsc: ENST00000358038.3:c.294+29G>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000420040
  ensembl transcript: ENST00000461105
  gene symbol: KCNIP2
  hgvsc: ENST00000461105.1:c.393+29G>A
  variant of: http://identifiers.org/hgnc/15522
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21664
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2460
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2162
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23044
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4266
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 836
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5483
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: C
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: QD

10-103588804-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103588804
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103588804
    reference: chr 10
allele count: 1
allele frequency: 8.595200440074262e-6
allele num: 116344
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000420040
  ensembl transcript: ENST00000461105
  gene symbol: KCNIP2
  hgvsc: ENST00000461105.1:c.393+28C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000239117
  ensembl transcript: ENST00000239117
  gene symbol: KCNIP2
  hgvsc: ENST00000239117.3:c.198+28C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000350733
  ensembl transcript: ENST00000358038
  gene symbol: KCNIP2
  hgvsc: ENST00000358038.3:c.294+28C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000239118
  ensembl transcript: ENST00000348850
  gene symbol: KCNIP2
  hgvsc: ENST00000348850.5:c.213+28C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000349055
  ensembl transcript: ENST00000356640
  gene symbol: KCNIP2
  hgvsc: ENST00000356640.2:c.348+28C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000411679
  ensembl transcript: ENST00000434163
  gene symbol: KCNIP2
  hgvsc: ENST00000434163.1:c.140+28C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000483385
  gene symbol: KCNIP2
  hgvsc: ENST00000483385.1:n.473+28C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000344169
  ensembl transcript: ENST00000343195
  gene symbol: KCNIP2
  hgvsc: ENST00000343195.4:c.198+28C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000472764
  gene symbol: KCNIP2
  hgvsc: ENST00000472764.1:n.294+28C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000341624
  ensembl transcript: ENST00000353068
  gene symbol: KCNIP2
  hgvsc: ENST00000353068.3:c.198+28C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000359063
  ensembl transcript: ENST00000370046
  gene symbol: KCNIP2
  hgvsc: ENST00000370046.1:c.198+28C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000355657
  gene symbol: KCNIP2
  hgvsc: ENST00000355657.2:n.745+28C>T
  variant of: http://identifiers.org/hgnc/15522
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4067
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2129
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2481
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21748
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5547
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23071
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 883
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
reference allele: G
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD

10-103588804-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103588804
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103588804
    reference: chr 10
allele count: 1
allele frequency: 8.595200440074262e-6
allele num: 116344
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000344169
  ensembl transcript: ENST00000343195
  gene symbol: KCNIP2
  hgvsc: ENST00000343195.4:c.198+28C>G
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000483385
  gene symbol: KCNIP2
  hgvsc: ENST00000483385.1:n.473+28C>G
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000355657
  gene symbol: KCNIP2
  hgvsc: ENST00000355657.2:n.745+28C>G
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000239118
  ensembl transcript: ENST00000348850
  gene symbol: KCNIP2
  hgvsc: ENST00000348850.5:c.213+28C>G
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000341624
  ensembl transcript: ENST00000353068
  gene symbol: KCNIP2
  hgvsc: ENST00000353068.3:c.198+28C>G
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000239117
  ensembl transcript: ENST00000239117
  gene symbol: KCNIP2
  hgvsc: ENST00000239117.3:c.198+28C>G
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000359063
  ensembl transcript: ENST00000370046
  gene symbol: KCNIP2
  hgvsc: ENST00000370046.1:c.198+28C>G
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000411679
  ensembl transcript: ENST00000434163
  gene symbol: KCNIP2
  hgvsc: ENST00000434163.1:c.140+28C>G
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000420040
  ensembl transcript: ENST00000461105
  gene symbol: KCNIP2
  hgvsc: ENST00000461105.1:c.393+28C>G
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000350733
  ensembl transcript: ENST00000358038
  gene symbol: KCNIP2
  hgvsc: ENST00000358038.3:c.294+28C>G
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000472764
  gene symbol: KCNIP2
  hgvsc: ENST00000472764.1:n.294+28C>G
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000349055
  ensembl transcript: ENST00000356640
  gene symbol: KCNIP2
  hgvsc: ENST00000356640.2:c.348+28C>G
  variant of: http://identifiers.org/hgnc/15522
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21748
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23071
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5547
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4067
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2481
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2129
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 883
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum

10-103588809-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103588809
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103588809
    reference: chr 10
allele count: 1
allele frequency: 8.527184664711099e-6
allele num: 117272
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000341624
  ensembl transcript: ENST00000353068
  gene symbol: KCNIP2
  hgvsc: ENST00000353068.3:c.198+23C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000239117
  ensembl transcript: ENST00000239117
  gene symbol: KCNIP2
  hgvsc: ENST00000239117.3:c.198+23C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000349055
  ensembl transcript: ENST00000356640
  gene symbol: KCNIP2
  hgvsc: ENST00000356640.2:c.348+23C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000411679
  ensembl transcript: ENST00000434163
  gene symbol: KCNIP2
  hgvsc: ENST00000434163.1:c.140+23C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000483385
  gene symbol: KCNIP2
  hgvsc: ENST00000483385.1:n.473+23C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000344169
  ensembl transcript: ENST00000343195
  gene symbol: KCNIP2
  hgvsc: ENST00000343195.4:c.198+23C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000355657
  gene symbol: KCNIP2
  hgvsc: ENST00000355657.2:n.745+23C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000472764
  gene symbol: KCNIP2
  hgvsc: ENST00000472764.1:n.294+23C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000239118
  ensembl transcript: ENST00000348850
  gene symbol: KCNIP2
  hgvsc: ENST00000348850.5:c.213+23C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000350733
  ensembl transcript: ENST00000358038
  gene symbol: KCNIP2
  hgvsc: ENST00000358038.3:c.294+23C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000420040
  ensembl transcript: ENST00000461105
  gene symbol: KCNIP2
  hgvsc: ENST00000461105.1:c.393+23C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000359063
  ensembl transcript: ENST00000370046
  gene symbol: KCNIP2
  hgvsc: ENST00000370046.1:c.198+23C>T
  variant of: http://identifiers.org/hgnc/15522
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1935
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23813
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3023
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1225
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 813
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23676
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5498
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
population: South Asian
reference allele: G
site quality: FS
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD

10-103588812-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103588812
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103588812
    reference: chr 10
allele count: 1
allele frequency: 8.511362669163334e-6
allele num: 117490
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000344169
  ensembl transcript: ENST00000343195
  gene symbol: KCNIP2
  hgvsc: ENST00000343195.4:c.198+20A>G
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000355657
  gene symbol: KCNIP2
  hgvsc: ENST00000355657.2:n.745+20A>G
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000349055
  ensembl transcript: ENST00000356640
  gene symbol: KCNIP2
  hgvsc: ENST00000356640.2:c.348+20A>G
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000341624
  ensembl transcript: ENST00000353068
  gene symbol: KCNIP2
  hgvsc: ENST00000353068.3:c.198+20A>G
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000239117
  ensembl transcript: ENST00000239117
  gene symbol: KCNIP2
  hgvsc: ENST00000239117.3:c.198+20A>G
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000239118
  ensembl transcript: ENST00000348850
  gene symbol: KCNIP2
  hgvsc: ENST00000348850.5:c.213+20A>G
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000350733
  ensembl transcript: ENST00000358038
  gene symbol: KCNIP2
  hgvsc: ENST00000358038.3:c.294+20A>G
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000420040
  ensembl transcript: ENST00000461105
  gene symbol: KCNIP2
  hgvsc: ENST00000461105.1:c.393+20A>G
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000411679
  ensembl transcript: ENST00000434163
  gene symbol: KCNIP2
  hgvsc: ENST00000434163.1:c.140+20A>G
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000483385
  gene symbol: KCNIP2
  hgvsc: ENST00000483385.1:n.473+20A>G
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000472764
  gene symbol: KCNIP2
  hgvsc: ENST00000472764.1:n.294+20A>G
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000359063
  ensembl transcript: ENST00000370046
  gene symbol: KCNIP2
  hgvsc: ENST00000370046.1:c.198+20A>G
  variant of: http://identifiers.org/hgnc/15522
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 988
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1844
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 808
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5495
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24332
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2707
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23816
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: QD

10-103588813-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103588813
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103588813
    reference: chr 10
allele count: 3
allele frequency: 2.55271353448716e-5
allele num: 117522
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000420040
  ensembl transcript: ENST00000461105
  gene symbol: KCNIP2
  hgvsc: ENST00000461105.1:c.393+19C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000359063
  ensembl transcript: ENST00000370046
  gene symbol: KCNIP2
  hgvsc: ENST00000370046.1:c.198+19C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000341624
  ensembl transcript: ENST00000353068
  gene symbol: KCNIP2
  hgvsc: ENST00000353068.3:c.198+19C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000483385
  gene symbol: KCNIP2
  hgvsc: ENST00000483385.1:n.473+19C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000350733
  ensembl transcript: ENST00000358038
  gene symbol: KCNIP2
  hgvsc: ENST00000358038.3:c.294+19C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000344169
  ensembl transcript: ENST00000343195
  gene symbol: KCNIP2
  hgvsc: ENST00000343195.4:c.198+19C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000411679
  ensembl transcript: ENST00000434163
  gene symbol: KCNIP2
  hgvsc: ENST00000434163.1:c.140+19C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000355657
  gene symbol: KCNIP2
  hgvsc: ENST00000355657.2:n.745+19C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000472764
  gene symbol: KCNIP2
  hgvsc: ENST00000472764.1:n.294+19C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000349055
  ensembl transcript: ENST00000356640
  gene symbol: KCNIP2
  hgvsc: ENST00000356640.2:c.348+19C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000239118
  ensembl transcript: ENST00000348850
  gene symbol: KCNIP2
  hgvsc: ENST00000348850.5:c.213+19C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000239117
  ensembl transcript: ENST00000239117
  gene symbol: KCNIP2
  hgvsc: ENST00000239117.3:c.198+19C>T
  variant of: http://identifiers.org/hgnc/15522
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1801
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 928
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5522
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 821
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2587
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24408
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23925
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
reference allele: G
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD

10-103588815-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103588815
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103588815
    reference: chr 10
allele count: 1
allele frequency: 8.502678343678259e-6
allele num: 117610
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000344169
  ensembl transcript: ENST00000343195
  gene symbol: KCNIP2
  hgvsc: ENST00000343195.4:c.198+17G>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000349055
  ensembl transcript: ENST00000356640
  gene symbol: KCNIP2
  hgvsc: ENST00000356640.2:c.348+17G>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000411679
  ensembl transcript: ENST00000434163
  gene symbol: KCNIP2
  hgvsc: ENST00000434163.1:c.140+17G>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000239117
  ensembl transcript: ENST00000239117
  gene symbol: KCNIP2
  hgvsc: ENST00000239117.3:c.198+17G>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000341624
  ensembl transcript: ENST00000353068
  gene symbol: KCNIP2
  hgvsc: ENST00000353068.3:c.198+17G>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000420040
  ensembl transcript: ENST00000461105
  gene symbol: KCNIP2
  hgvsc: ENST00000461105.1:c.393+17G>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000359063
  ensembl transcript: ENST00000370046
  gene symbol: KCNIP2
  hgvsc: ENST00000370046.1:c.198+17G>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000483385
  gene symbol: KCNIP2
  hgvsc: ENST00000483385.1:n.473+17G>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000472764
  gene symbol: KCNIP2
  hgvsc: ENST00000472764.1:n.294+17G>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000239118
  ensembl transcript: ENST00000348850
  gene symbol: KCNIP2
  hgvsc: ENST00000348850.5:c.213+17G>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000355657
  gene symbol: KCNIP2
  hgvsc: ENST00000355657.2:n.745+17G>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000350733
  ensembl transcript: ENST00000358038
  gene symbol: KCNIP2
  hgvsc: ENST00000358038.3:c.294+17G>A
  variant of: http://identifiers.org/hgnc/15522
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 875
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24132
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24528
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1702
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5573
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2375
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum

http://identifiers.org/exac.variant/10-103588830-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103588830
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103588830
    reference: chr 10
allele count: 1
allele frequency: 8.371283150281276e-6
allele num: 119456
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000344169
  ensembl transcript: ENST00000343195
  gene symbol: KCNIP2
  hgvsc: ENST00000343195.4:c.198+2T>G
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000349055
  ensembl transcript: ENST00000356640
  gene symbol: KCNIP2
  hgvsc: ENST00000356640.2:c.348+2T>G
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000359063
  ensembl transcript: ENST00000370046
  gene symbol: KCNIP2
  hgvsc: ENST00000370046.1:c.198+2T>G
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000411679
  ensembl transcript: ENST00000434163
  gene symbol: KCNIP2
  hgvsc: ENST00000434163.1:c.140+2T>G
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000483385
  gene symbol: KCNIP2
  hgvsc: ENST00000483385.1:n.473+2T>G
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000472764
  gene symbol: KCNIP2
  hgvsc: ENST00000472764.1:n.294+2T>G
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000239117
  ensembl transcript: ENST00000239117
  gene symbol: KCNIP2
  hgvsc: ENST00000239117.3:c.198+2T>G
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000239118
  ensembl transcript: ENST00000348850
  gene symbol: KCNIP2
  hgvsc: ENST00000348850.5:c.213+2T>G
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000350733
  ensembl transcript: ENST00000358038
  gene symbol: KCNIP2
  hgvsc: ENST00000358038.3:c.294+2T>G
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000341624
  ensembl transcript: ENST00000353068
  gene symbol: KCNIP2
  hgvsc: ENST00000353068.3:c.198+2T>G
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000355657
  gene symbol: KCNIP2
  hgvsc: ENST00000355657.2:n.745+2T>G
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: true
  consequence: splice_donor_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000420040
  ensembl transcript: ENST00000461105
  gene symbol: KCNIP2
  hgvsc: ENST00000461105.1:c.393+2T>G
  variant of: http://identifiers.org/hgnc/15522
canonical: true
consequence: splice donor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 942
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25099
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26453
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 801
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 812
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5663
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.393+2T>G
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Other
population: African
population: East Asian
population: Latino
reference allele: A
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: QD

10-103588836-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103588836
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103588836
    reference: chr 10
allele count: 2
allele frequency: 1.666361167119361e-5
allele num: 120022
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000341624
  ensembl transcript: ENST00000353068
  gene symbol: KCNIP2
  hgvsc: ENST00000353068.3:c.194A>T
  hgvsp: ENSP00000341624.3:p.Lys65Met
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000239117
  ensembl transcript: ENST00000239117
  gene symbol: KCNIP2
  hgvsc: ENST00000239117.3:c.194A>T
  hgvsp: ENSP00000239117.3:p.Lys65Met
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000411679
  ensembl transcript: ENST00000434163
  gene symbol: KCNIP2
  hgvsc: ENST00000434163.1:c.136A>T
  hgvsp: ENSP00000411679.1:p.Arg46Ter
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000350733
  ensembl transcript: ENST00000358038
  gene symbol: KCNIP2
  hgvsc: ENST00000358038.3:c.290A>T
  hgvsp: ENSP00000350733.3:p.Lys97Met
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000349055
  ensembl transcript: ENST00000356640
  gene symbol: KCNIP2
  hgvsc: ENST00000356640.2:c.344A>T
  hgvsp: ENSP00000349055.2:p.Lys115Met
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000420040
  ensembl transcript: ENST00000461105
  gene symbol: KCNIP2
  hgvsc: ENST00000461105.1:c.389A>T
  hgvsp: ENSP00000420040.1:p.Lys130Met
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000239118
  ensembl transcript: ENST00000348850
  gene symbol: KCNIP2
  hgvsc: ENST00000348850.5:c.209A>T
  hgvsp: ENSP00000239118.6:p.Lys70Met
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000483385
  gene symbol: KCNIP2
  hgvsc: ENST00000483385.1:n.469A>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000344169
  ensembl transcript: ENST00000343195
  gene symbol: KCNIP2
  hgvsc: ENST00000343195.4:c.194A>T
  hgvsp: ENSP00000344169.4:p.Lys65Met
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000472764
  gene symbol: KCNIP2
  hgvsc: ENST00000472764.1:n.290A>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000355657
  gene symbol: KCNIP2
  hgvsc: ENST00000355657.2:n.741A>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000359063
  ensembl transcript: ENST00000370046
  gene symbol: KCNIP2
  hgvsc: ENST00000370046.1:c.194A>T
  hgvsp: ENSP00000359063.1:p.Lys65Met
  variant of: http://identifiers.org/hgnc/15522
canonical: false
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 26797
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5712
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25355
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 810
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg46Ter
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
reference allele: T
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum

10-103588853-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103588853
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103588853
    reference: chr 10
allele count: 2
allele frequency: 1.654204989082247e-5
allele num: 120904
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000359063
  ensembl transcript: ENST00000370046
  gene symbol: KCNIP2
  hgvsc: ENST00000370046.1:c.177C>T
  hgvsp: ENST00000370046.1:c.177C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000411679
  ensembl transcript: ENST00000434163
  gene symbol: KCNIP2
  hgvsc: ENST00000434163.1:c.119C>T
  hgvsp: ENSP00000411679.1:p.Ser40Phe
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000472764
  gene symbol: KCNIP2
  hgvsc: ENST00000472764.1:n.273C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000420040
  ensembl transcript: ENST00000461105
  gene symbol: KCNIP2
  hgvsc: ENST00000461105.1:c.372C>T
  hgvsp: ENST00000461105.1:c.372C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000239118
  ensembl transcript: ENST00000348850
  gene symbol: KCNIP2
  hgvsc: ENST00000348850.5:c.192C>T
  hgvsp: ENST00000348850.5:c.192C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000349055
  ensembl transcript: ENST00000356640
  gene symbol: KCNIP2
  hgvsc: ENST00000356640.2:c.327C>T
  hgvsp: ENST00000356640.2:c.327C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000350733
  ensembl transcript: ENST00000358038
  gene symbol: KCNIP2
  hgvsc: ENST00000358038.3:c.273C>T
  hgvsp: ENST00000358038.3:c.273C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000344169
  ensembl transcript: ENST00000343195
  gene symbol: KCNIP2
  hgvsc: ENST00000343195.4:c.177C>T
  hgvsp: ENST00000343195.4:c.177C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000239117
  ensembl transcript: ENST00000239117
  gene symbol: KCNIP2
  hgvsc: ENST00000239117.3:c.177C>T
  hgvsp: ENST00000239117.3:c.177C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000355657
  gene symbol: KCNIP2
  hgvsc: ENST00000355657.2:n.724C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000341624
  ensembl transcript: ENST00000353068
  gene symbol: KCNIP2
  hgvsc: ENST00000353068.3:c.177C>T
  hgvsp: ENST00000353068.3:c.177C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000483385
  gene symbol: KCNIP2
  hgvsc: ENST00000483385.1:n.452C>T
  variant of: http://identifiers.org/hgnc/15522
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26009
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5835
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26863
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 817
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser40Phe
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: South Asian
population: Latino
population: African
population: East Asian
reference allele: G
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum

10-103588862-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103588862
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103588862
    reference: chr 10
allele count: 32
allele frequency: 2.644584387034925e-4
allele num: 121002
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000355657
  gene symbol: KCNIP2
  hgvsc: ENST00000355657.2:n.715G>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000420040
  ensembl transcript: ENST00000461105
  gene symbol: KCNIP2
  hgvsc: ENST00000461105.1:c.363G>A
  hgvsp: ENST00000461105.1:c.363G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000349055
  ensembl transcript: ENST00000356640
  gene symbol: KCNIP2
  hgvsc: ENST00000356640.2:c.318G>A
  hgvsp: ENST00000356640.2:c.318G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000344169
  ensembl transcript: ENST00000343195
  gene symbol: KCNIP2
  hgvsc: ENST00000343195.4:c.168G>A
  hgvsp: ENST00000343195.4:c.168G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000359063
  ensembl transcript: ENST00000370046
  gene symbol: KCNIP2
  hgvsc: ENST00000370046.1:c.168G>A
  hgvsp: ENST00000370046.1:c.168G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000341624
  ensembl transcript: ENST00000353068
  gene symbol: KCNIP2
  hgvsc: ENST00000353068.3:c.168G>A
  hgvsp: ENST00000353068.3:c.168G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000411679
  ensembl transcript: ENST00000434163
  gene symbol: KCNIP2
  hgvsc: ENST00000434163.1:c.110G>A
  hgvsp: ENSP00000411679.1:p.Ser37Asn
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000483385
  gene symbol: KCNIP2
  hgvsc: ENST00000483385.1:n.443G>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000472764
  gene symbol: KCNIP2
  hgvsc: ENST00000472764.1:n.264G>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000239118
  ensembl transcript: ENST00000348850
  gene symbol: KCNIP2
  hgvsc: ENST00000348850.5:c.183G>A
  hgvsp: ENST00000348850.5:c.183G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000239117
  ensembl transcript: ENST00000239117
  gene symbol: KCNIP2
  hgvsc: ENST00000239117.3:c.168G>A
  hgvsp: ENST00000239117.3:c.168G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000350733
  ensembl transcript: ENST00000358038
  gene symbol: KCNIP2
  hgvsc: ENST00000358038.3:c.264G>A
  hgvsp: ENST00000358038.3:c.264G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15522
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 26783
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 5.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 4.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 819
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 4.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26140
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 6.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
hgvs: p.Ser37Asn
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
population: Other
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: DP

10-103588865-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103588865
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103588865
    reference: chr 10
allele count: 1
allele frequency: 8.263916435277007e-6
allele num: 121008
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000239117
  ensembl transcript: ENST00000239117
  gene symbol: KCNIP2
  hgvsc: ENST00000239117.3:c.165G>A
  hgvsp: ENST00000239117.3:c.165G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000344169
  ensembl transcript: ENST00000343195
  gene symbol: KCNIP2
  hgvsc: ENST00000343195.4:c.165G>A
  hgvsp: ENST00000343195.4:c.165G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000355657
  gene symbol: KCNIP2
  hgvsc: ENST00000355657.2:n.712G>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000349055
  ensembl transcript: ENST00000356640
  gene symbol: KCNIP2
  hgvsc: ENST00000356640.2:c.315G>A
  hgvsp: ENST00000356640.2:c.315G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000239118
  ensembl transcript: ENST00000348850
  gene symbol: KCNIP2
  hgvsc: ENST00000348850.5:c.180G>A
  hgvsp: ENST00000348850.5:c.180G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000472764
  gene symbol: KCNIP2
  hgvsc: ENST00000472764.1:n.261G>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000411679
  ensembl transcript: ENST00000434163
  gene symbol: KCNIP2
  hgvsc: ENST00000434163.1:c.107G>A
  hgvsp: ENSP00000411679.1:p.Arg36Lys
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000359063
  ensembl transcript: ENST00000370046
  gene symbol: KCNIP2
  hgvsc: ENST00000370046.1:c.165G>A
  hgvsp: ENST00000370046.1:c.165G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000350733
  ensembl transcript: ENST00000358038
  gene symbol: KCNIP2
  hgvsc: ENST00000358038.3:c.261G>A
  hgvsp: ENST00000358038.3:c.261G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000341624
  ensembl transcript: ENST00000353068
  gene symbol: KCNIP2
  hgvsc: ENST00000353068.3:c.165G>A
  hgvsp: ENST00000353068.3:c.165G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000420040
  ensembl transcript: ENST00000461105
  gene symbol: KCNIP2
  hgvsc: ENST00000461105.1:c.360G>A
  hgvsp: ENST00000461105.1:c.360G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000483385
  gene symbol: KCNIP2
  hgvsc: ENST00000483385.1:n.440G>A
  variant of: http://identifiers.org/hgnc/15522
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 814
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26166
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5845
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg36Lys
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: C
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: InbreedingCoeff

10-103588870-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103588870
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103588870
    reference: chr 10
allele count: 70
allele frequency: 5.782925499396923e-4
allele num: 121046
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000341624
  ensembl transcript: ENST00000353068
  gene symbol: KCNIP2
  hgvsc: ENST00000353068.3:c.160C>T
  hgvsp: ENSP00000341624.3:p.Arg54Cys
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000349055
  ensembl transcript: ENST00000356640
  gene symbol: KCNIP2
  hgvsc: ENST00000356640.2:c.310C>T
  hgvsp: ENSP00000349055.2:p.Arg104Cys
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000239118
  ensembl transcript: ENST00000348850
  gene symbol: KCNIP2
  hgvsc: ENST00000348850.5:c.175C>T
  hgvsp: ENSP00000239118.6:p.Arg59Cys
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000359063
  ensembl transcript: ENST00000370046
  gene symbol: KCNIP2
  hgvsc: ENST00000370046.1:c.160C>T
  hgvsp: ENSP00000359063.1:p.Arg54Cys
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000483385
  gene symbol: KCNIP2
  hgvsc: ENST00000483385.1:n.435C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000420040
  ensembl transcript: ENST00000461105
  gene symbol: KCNIP2
  hgvsc: ENST00000461105.1:c.355C>T
  hgvsp: ENSP00000420040.1:p.Arg119Cys
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000355657
  gene symbol: KCNIP2
  hgvsc: ENST00000355657.2:n.707C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000239117
  ensembl transcript: ENST00000239117
  gene symbol: KCNIP2
  hgvsc: ENST00000239117.3:c.160C>T
  hgvsp: ENSP00000239117.3:p.Arg54Cys
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000344169
  ensembl transcript: ENST00000343195
  gene symbol: KCNIP2
  hgvsc: ENST00000343195.4:c.160C>T
  hgvsp: ENSP00000344169.4:p.Arg54Cys
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000411679
  ensembl transcript: ENST00000434163
  gene symbol: KCNIP2
  hgvsc: ENST00000434163.1:c.102C>T
  hgvsp: ENST00000434163.1:c.102C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000472764
  gene symbol: KCNIP2
  hgvsc: ENST00000472764.1:n.256C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000350733
  ensembl transcript: ENST00000358038
  gene symbol: KCNIP2
  hgvsc: ENST00000358038.3:c.256C>T
  hgvsp: ENSP00000350733.3:p.Arg86Cys
  variant of: http://identifiers.org/hgnc/15522
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 26214
  bin: 2.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 5.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 813
  bin: 3.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 4.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26721
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 5.75e1
  variant carriers: 12
genotype quality: GenotypeQuality
hgvs: p.Arg119Cys
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
population: Latino
reference allele: G
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum

10-103588877-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103588877
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103588877
    reference: chr 10
allele count: 1
allele frequency: 8.261595148791329e-6
allele num: 121042
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000239117
  ensembl transcript: ENST00000239117
  gene symbol: KCNIP2
  hgvsc: ENST00000239117.3:c.153A>G
  hgvsp: ENST00000239117.3:c.153A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000341624
  ensembl transcript: ENST00000353068
  gene symbol: KCNIP2
  hgvsc: ENST00000353068.3:c.153A>G
  hgvsp: ENST00000353068.3:c.153A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000359063
  ensembl transcript: ENST00000370046
  gene symbol: KCNIP2
  hgvsc: ENST00000370046.1:c.153A>G
  hgvsp: ENST00000370046.1:c.153A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000411679
  ensembl transcript: ENST00000434163
  gene symbol: KCNIP2
  hgvsc: ENST00000434163.1:c.95A>G
  hgvsp: ENSP00000411679.1:p.Asn32Ser
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000344169
  ensembl transcript: ENST00000343195
  gene symbol: KCNIP2
  hgvsc: ENST00000343195.4:c.153A>G
  hgvsp: ENST00000343195.4:c.153A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000350733
  ensembl transcript: ENST00000358038
  gene symbol: KCNIP2
  hgvsc: ENST00000358038.3:c.249A>G
  hgvsp: ENST00000358038.3:c.249A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000355657
  gene symbol: KCNIP2
  hgvsc: ENST00000355657.2:n.700A>G
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000239118
  ensembl transcript: ENST00000348850
  gene symbol: KCNIP2
  hgvsc: ENST00000348850.5:c.168A>G
  hgvsp: ENST00000348850.5:c.168A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000349055
  ensembl transcript: ENST00000356640
  gene symbol: KCNIP2
  hgvsc: ENST00000356640.2:c.303A>G
  hgvsp: ENST00000356640.2:c.303A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000420040
  ensembl transcript: ENST00000461105
  gene symbol: KCNIP2
  hgvsc: ENST00000461105.1:c.348A>G
  hgvsp: ENST00000461105.1:c.348A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000472764
  gene symbol: KCNIP2
  hgvsc: ENST00000472764.1:n.249A>G
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000483385
  gene symbol: KCNIP2
  hgvsc: ENST00000483385.1:n.428A>G
  variant of: http://identifiers.org/hgnc/15522
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26660
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 808
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5818
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26325
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn32Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: Other
reference allele: T
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD

10-103588885-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103588885
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103588885
    reference: chr 10
allele count: 1
allele frequency: 8.265965712774223e-6
allele num: 120978
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000359063
  ensembl transcript: ENST00000370046
  gene symbol: KCNIP2
  hgvsc: ENST00000370046.1:c.145C>T
  hgvsp: ENSP00000359063.1:p.Gln49Ter
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000420040
  ensembl transcript: ENST00000461105
  gene symbol: KCNIP2
  hgvsc: ENST00000461105.1:c.340C>T
  hgvsp: ENSP00000420040.1:p.Gln114Ter
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000341624
  ensembl transcript: ENST00000353068
  gene symbol: KCNIP2
  hgvsc: ENST00000353068.3:c.145C>T
  hgvsp: ENSP00000341624.3:p.Gln49Ter
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000239118
  ensembl transcript: ENST00000348850
  gene symbol: KCNIP2
  hgvsc: ENST00000348850.5:c.160C>T
  hgvsp: ENSP00000239118.6:p.Gln54Ter
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000483385
  gene symbol: KCNIP2
  hgvsc: ENST00000483385.1:n.420C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000411679
  ensembl transcript: ENST00000434163
  gene symbol: KCNIP2
  hgvsc: ENST00000434163.1:c.87C>T
  hgvsp: ENST00000434163.1:c.87C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000349055
  ensembl transcript: ENST00000356640
  gene symbol: KCNIP2
  hgvsc: ENST00000356640.2:c.295C>T
  hgvsp: ENSP00000349055.2:p.Gln99Ter
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000239117
  ensembl transcript: ENST00000239117
  gene symbol: KCNIP2
  hgvsc: ENST00000239117.3:c.145C>T
  hgvsp: ENSP00000239117.3:p.Gln49Ter
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000344169
  ensembl transcript: ENST00000343195
  gene symbol: KCNIP2
  hgvsc: ENST00000343195.4:c.145C>T
  hgvsp: ENSP00000344169.4:p.Gln49Ter
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000350733
  ensembl transcript: ENST00000358038
  gene symbol: KCNIP2
  hgvsc: ENST00000358038.3:c.241C>T
  hgvsp: ENSP00000350733.3:p.Gln81Ter
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000472764
  gene symbol: KCNIP2
  hgvsc: ENST00000472764.1:n.241C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000355657
  gene symbol: KCNIP2
  hgvsc: ENST00000355657.2:n.692C>T
  variant of: http://identifiers.org/hgnc/15522
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 808
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26297
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5825
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln114Ter
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
population: Latino
reference allele: G
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD

10-103588900-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103588900
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103588900
    reference: chr 10
allele count: 2
allele frequency: 1.656122685568547e-5
allele num: 120764
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000411679
  ensembl transcript: ENST00000434163
  gene symbol: KCNIP2
  hgvsc: ENST00000434163.1:c.72G>C
  hgvsp: ENSP00000411679.1:p.Trp24Cys
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000420040
  ensembl transcript: ENST00000461105
  gene symbol: KCNIP2
  hgvsc: ENST00000461105.1:c.325G>C
  hgvsp: ENSP00000420040.1:p.Glu109Gln
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000350733
  ensembl transcript: ENST00000358038
  gene symbol: KCNIP2
  hgvsc: ENST00000358038.3:c.226G>C
  hgvsp: ENSP00000350733.3:p.Glu76Gln
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000359063
  ensembl transcript: ENST00000370046
  gene symbol: KCNIP2
  hgvsc: ENST00000370046.1:c.130G>C
  hgvsp: ENSP00000359063.1:p.Glu44Gln
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000344169
  ensembl transcript: ENST00000343195
  gene symbol: KCNIP2
  hgvsc: ENST00000343195.4:c.130G>C
  hgvsp: ENSP00000344169.4:p.Glu44Gln
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000355657
  gene symbol: KCNIP2
  hgvsc: ENST00000355657.2:n.677G>C
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000349055
  ensembl transcript: ENST00000356640
  gene symbol: KCNIP2
  hgvsc: ENST00000356640.2:c.280G>C
  hgvsp: ENSP00000349055.2:p.Glu94Gln
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000472764
  gene symbol: KCNIP2
  hgvsc: ENST00000472764.1:n.226G>C
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000341624
  ensembl transcript: ENST00000353068
  gene symbol: KCNIP2
  hgvsc: ENST00000353068.3:c.130G>C
  hgvsp: ENSP00000341624.3:p.Glu44Gln
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000239117
  ensembl transcript: ENST00000239117
  gene symbol: KCNIP2
  hgvsc: ENST00000239117.3:c.130G>C
  hgvsp: ENSP00000239117.3:p.Glu44Gln
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000239118
  ensembl transcript: ENST00000348850
  gene symbol: KCNIP2
  hgvsc: ENST00000348850.5:c.145G>C
  hgvsp: ENSP00000239118.6:p.Glu49Gln
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000483385
  gene symbol: KCNIP2
  hgvsc: ENST00000483385.1:n.405G>C
  variant of: http://identifiers.org/hgnc/15522
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26189
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 800
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5829
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26298
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu109Gln
num of homozygotes: 0
population: South Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
reference allele: C
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ

10-103588903-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103588903
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103588903
    reference: chr 10
allele count: 7
allele frequency: 5.799695101743223e-5
allele num: 120696
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000420040
  ensembl transcript: ENST00000461105
  gene symbol: KCNIP2
  hgvsc: ENST00000461105.1:c.322C>G
  hgvsp: ENSP00000420040.1:p.Leu108Val
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000359063
  ensembl transcript: ENST00000370046
  gene symbol: KCNIP2
  hgvsc: ENST00000370046.1:c.127C>G
  hgvsp: ENSP00000359063.1:p.Leu43Val
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000239118
  ensembl transcript: ENST00000348850
  gene symbol: KCNIP2
  hgvsc: ENST00000348850.5:c.142C>G
  hgvsp: ENSP00000239118.6:p.Leu48Val
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000411679
  ensembl transcript: ENST00000434163
  gene symbol: KCNIP2
  hgvsc: ENST00000434163.1:c.69C>G
  hgvsp: ENST00000434163.1:c.69C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000349055
  ensembl transcript: ENST00000356640
  gene symbol: KCNIP2
  hgvsc: ENST00000356640.2:c.277C>G
  hgvsp: ENSP00000349055.2:p.Leu93Val
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000344169
  ensembl transcript: ENST00000343195
  gene symbol: KCNIP2
  hgvsc: ENST00000343195.4:c.127C>G
  hgvsp: ENSP00000344169.4:p.Leu43Val
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000239117
  ensembl transcript: ENST00000239117
  gene symbol: KCNIP2
  hgvsc: ENST00000239117.3:c.127C>G
  hgvsp: ENSP00000239117.3:p.Leu43Val
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000355657
  gene symbol: KCNIP2
  hgvsc: ENST00000355657.2:n.674C>G
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000341624
  ensembl transcript: ENST00000353068
  gene symbol: KCNIP2
  hgvsc: ENST00000353068.3:c.127C>G
  hgvsp: ENSP00000341624.3:p.Leu43Val
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000483385
  gene symbol: KCNIP2
  hgvsc: ENST00000483385.1:n.402C>G
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000350733
  ensembl transcript: ENST00000358038
  gene symbol: KCNIP2
  hgvsc: ENST00000358038.3:c.223C>G
  hgvsp: ENSP00000350733.3:p.Leu75Val
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000472764
  gene symbol: KCNIP2
  hgvsc: ENST00000472764.1:n.223C>G
  variant of: http://identifiers.org/hgnc/15522
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 26291
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26079
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5812
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 801
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu108Val
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD

10-103588905-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103588905
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103588905
    reference: chr 10
allele count: 1
allele frequency: 8.289949265510494e-6
allele num: 120628
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000472764
  gene symbol: KCNIP2
  hgvsc: ENST00000472764.1:n.221G>C
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000355657
  gene symbol: KCNIP2
  hgvsc: ENST00000355657.2:n.672G>C
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000344169
  ensembl transcript: ENST00000343195
  gene symbol: KCNIP2
  hgvsc: ENST00000343195.4:c.125G>C
  hgvsp: ENSP00000344169.4:p.Gly42Ala
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000411679
  ensembl transcript: ENST00000434163
  gene symbol: KCNIP2
  hgvsc: ENST00000434163.1:c.67G>C
  hgvsp: ENSP00000411679.1:p.Val23Leu
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000483385
  gene symbol: KCNIP2
  hgvsc: ENST00000483385.1:n.400G>C
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000239117
  ensembl transcript: ENST00000239117
  gene symbol: KCNIP2
  hgvsc: ENST00000239117.3:c.125G>C
  hgvsp: ENSP00000239117.3:p.Gly42Ala
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000341624
  ensembl transcript: ENST00000353068
  gene symbol: KCNIP2
  hgvsc: ENST00000353068.3:c.125G>C
  hgvsp: ENSP00000341624.3:p.Gly42Ala
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000349055
  ensembl transcript: ENST00000356640
  gene symbol: KCNIP2
  hgvsc: ENST00000356640.2:c.275G>C
  hgvsp: ENSP00000349055.2:p.Gly92Ala
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000359063
  ensembl transcript: ENST00000370046
  gene symbol: KCNIP2
  hgvsc: ENST00000370046.1:c.125G>C
  hgvsp: ENSP00000359063.1:p.Gly42Ala
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000350733
  ensembl transcript: ENST00000358038
  gene symbol: KCNIP2
  hgvsc: ENST00000358038.3:c.221G>C
  hgvsp: ENSP00000350733.3:p.Gly74Ala
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000239118
  ensembl transcript: ENST00000348850
  gene symbol: KCNIP2
  hgvsc: ENST00000348850.5:c.140G>C
  hgvsp: ENSP00000239118.6:p.Gly47Ala
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000420040
  ensembl transcript: ENST00000461105
  gene symbol: KCNIP2
  hgvsc: ENST00000461105.1:c.320G>C
  hgvsp: ENSP00000420040.1:p.Gly107Ala
  variant of: http://identifiers.org/hgnc/15522
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 798
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26291
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25973
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5810
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly107Ala
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: DP

10-103588906-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103588906
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103588906
    reference: chr 10
allele count: 1
allele frequency: 8.292974192264313e-6
allele num: 120584
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000239117
  ensembl transcript: ENST00000239117
  gene symbol: KCNIP2
  hgvsc: ENST00000239117.3:c.124G>C
  hgvsp: ENSP00000239117.3:p.Gly42Arg
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000359063
  ensembl transcript: ENST00000370046
  gene symbol: KCNIP2
  hgvsc: ENST00000370046.1:c.124G>C
  hgvsp: ENSP00000359063.1:p.Gly42Arg
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000350733
  ensembl transcript: ENST00000358038
  gene symbol: KCNIP2
  hgvsc: ENST00000358038.3:c.220G>C
  hgvsp: ENSP00000350733.3:p.Gly74Arg
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000420040
  ensembl transcript: ENST00000461105
  gene symbol: KCNIP2
  hgvsc: ENST00000461105.1:c.319G>C
  hgvsp: ENSP00000420040.1:p.Gly107Arg
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000239118
  ensembl transcript: ENST00000348850
  gene symbol: KCNIP2
  hgvsc: ENST00000348850.5:c.139G>C
  hgvsp: ENSP00000239118.6:p.Gly47Arg
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000341624
  ensembl transcript: ENST00000353068
  gene symbol: KCNIP2
  hgvsc: ENST00000353068.3:c.124G>C
  hgvsp: ENSP00000341624.3:p.Gly42Arg
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000472764
  gene symbol: KCNIP2
  hgvsc: ENST00000472764.1:n.220G>C
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000344169
  ensembl transcript: ENST00000343195
  gene symbol: KCNIP2
  hgvsc: ENST00000343195.4:c.124G>C
  hgvsp: ENSP00000344169.4:p.Gly42Arg
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000355657
  gene symbol: KCNIP2
  hgvsc: ENST00000355657.2:n.671G>C
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000411679
  ensembl transcript: ENST00000434163
  gene symbol: KCNIP2
  hgvsc: ENST00000434163.1:c.66G>C
  hgvsp: ENSP00000411679.1:p.Arg22Ser
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000483385
  gene symbol: KCNIP2
  hgvsc: ENST00000483385.1:n.399G>C
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000349055
  ensembl transcript: ENST00000356640
  gene symbol: KCNIP2
  hgvsc: ENST00000356640.2:c.274G>C
  hgvsp: ENSP00000349055.2:p.Gly92Arg
  variant of: http://identifiers.org/hgnc/15522
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5804
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26296
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25911
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly107Arg
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: QD

10-103588913-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103588913
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103588913
    reference: chr 10
allele count: 2
allele frequency: 1.662759182587586e-5
allele num: 120282
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000239118
  ensembl transcript: ENST00000348850
  gene symbol: KCNIP2
  hgvsc: ENST00000348850.5:c.132G>A
  hgvsp: ENST00000348850.5:c.132G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000411679
  ensembl transcript: ENST00000434163
  gene symbol: KCNIP2
  hgvsc: ENST00000434163.1:c.59G>A
  hgvsp: ENSP00000411679.1:p.Gly20Asp
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000349055
  ensembl transcript: ENST00000356640
  gene symbol: KCNIP2
  hgvsc: ENST00000356640.2:c.267G>A
  hgvsp: ENST00000356640.2:c.267G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000483385
  gene symbol: KCNIP2
  hgvsc: ENST00000483385.1:n.392G>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000420040
  ensembl transcript: ENST00000461105
  gene symbol: KCNIP2
  hgvsc: ENST00000461105.1:c.312G>A
  hgvsp: ENST00000461105.1:c.312G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000350733
  ensembl transcript: ENST00000358038
  gene symbol: KCNIP2
  hgvsc: ENST00000358038.3:c.213G>A
  hgvsp: ENST00000358038.3:c.213G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000344169
  ensembl transcript: ENST00000343195
  gene symbol: KCNIP2
  hgvsc: ENST00000343195.4:c.117G>A
  hgvsp: ENST00000343195.4:c.117G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000359063
  ensembl transcript: ENST00000370046
  gene symbol: KCNIP2
  hgvsc: ENST00000370046.1:c.117G>A
  hgvsp: ENST00000370046.1:c.117G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000355657
  gene symbol: KCNIP2
  hgvsc: ENST00000355657.2:n.664G>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000341624
  ensembl transcript: ENST00000353068
  gene symbol: KCNIP2
  hgvsc: ENST00000353068.3:c.117G>A
  hgvsp: ENST00000353068.3:c.117G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000239117
  ensembl transcript: ENST00000239117
  gene symbol: KCNIP2
  hgvsc: ENST00000239117.3:c.117G>A
  hgvsp: ENST00000239117.3:c.117G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000472764
  gene symbol: KCNIP2
  hgvsc: ENST00000472764.1:n.213G>A
  variant of: http://identifiers.org/hgnc/15522
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 25422
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26249
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5800
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 800
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 818
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly20Asp
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: African
population: Other
reference allele: C
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: DP

10-103588929-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103588929
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103588929
    reference: chr 10
allele count: 1
allele frequency: 8.401666890711118e-6
allele num: 119024
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000349055
  ensembl transcript: ENST00000356640
  gene symbol: KCNIP2
  hgvsc: ENST00000356640.2:c.251C>T
  hgvsp: ENSP00000349055.2:p.Ser84Phe
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000420040
  ensembl transcript: ENST00000461105
  gene symbol: KCNIP2
  hgvsc: ENST00000461105.1:c.296C>T
  hgvsp: ENSP00000420040.1:p.Ser99Phe
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000359063
  ensembl transcript: ENST00000370046
  gene symbol: KCNIP2
  hgvsc: ENST00000370046.1:c.101C>T
  hgvsp: ENSP00000359063.1:p.Ser34Phe
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000239117
  ensembl transcript: ENST00000239117
  gene symbol: KCNIP2
  hgvsc: ENST00000239117.3:c.101C>T
  hgvsp: ENSP00000239117.3:p.Ser34Phe
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000341624
  ensembl transcript: ENST00000353068
  gene symbol: KCNIP2
  hgvsc: ENST00000353068.3:c.101C>T
  hgvsp: ENSP00000341624.3:p.Ser34Phe
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000344169
  ensembl transcript: ENST00000343195
  gene symbol: KCNIP2
  hgvsc: ENST00000343195.4:c.101C>T
  hgvsp: ENSP00000344169.4:p.Ser34Phe
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000239118
  ensembl transcript: ENST00000348850
  gene symbol: KCNIP2
  hgvsc: ENST00000348850.5:c.116C>T
  hgvsp: ENSP00000239118.6:p.Ser39Phe
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000350733
  ensembl transcript: ENST00000358038
  gene symbol: KCNIP2
  hgvsc: ENST00000358038.3:c.197C>T
  hgvsp: ENSP00000350733.3:p.Ser66Phe
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000472764
  gene symbol: KCNIP2
  hgvsc: ENST00000472764.1:n.197C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000355657
  gene symbol: KCNIP2
  hgvsc: ENST00000355657.2:n.648C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000411679
  ensembl transcript: ENST00000434163
  gene symbol: KCNIP2
  hgvsc: ENST00000434163.1:c.43C>T
  hgvsp: ENSP00000411679.1:p.Pro15Ser
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000483385
  gene symbol: KCNIP2
  hgvsc: ENST00000483385.1:n.376C>T
  variant of: http://identifiers.org/hgnc/15522
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 25601
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24625
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1762
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5552
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1156
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 776
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser99Phe
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
population: African
reference allele: G
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum

10-103588930-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103588930
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103588930
    reference: chr 10
allele count: 1
allele frequency: 8.410287463625507e-6
allele num: 118902
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000349055
  ensembl transcript: ENST00000356640
  gene symbol: KCNIP2
  hgvsc: ENST00000356640.2:c.250T>C
  hgvsp: ENSP00000349055.2:p.Ser84Pro
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000483385
  gene symbol: KCNIP2
  hgvsc: ENST00000483385.1:n.375T>C
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000344169
  ensembl transcript: ENST00000343195
  gene symbol: KCNIP2
  hgvsc: ENST00000343195.4:c.100T>C
  hgvsp: ENSP00000344169.4:p.Ser34Pro
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000355657
  gene symbol: KCNIP2
  hgvsc: ENST00000355657.2:n.647T>C
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000420040
  ensembl transcript: ENST00000461105
  gene symbol: KCNIP2
  hgvsc: ENST00000461105.1:c.295T>C
  hgvsp: ENSP00000420040.1:p.Ser99Pro
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000239118
  ensembl transcript: ENST00000348850
  gene symbol: KCNIP2
  hgvsc: ENST00000348850.5:c.115T>C
  hgvsp: ENSP00000239118.6:p.Ser39Pro
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000350733
  ensembl transcript: ENST00000358038
  gene symbol: KCNIP2
  hgvsc: ENST00000358038.3:c.196T>C
  hgvsp: ENSP00000350733.3:p.Ser66Pro
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000359063
  ensembl transcript: ENST00000370046
  gene symbol: KCNIP2
  hgvsc: ENST00000370046.1:c.100T>C
  hgvsp: ENSP00000359063.1:p.Ser34Pro
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000341624
  ensembl transcript: ENST00000353068
  gene symbol: KCNIP2
  hgvsc: ENST00000353068.3:c.100T>C
  hgvsp: ENSP00000341624.3:p.Ser34Pro
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000411679
  ensembl transcript: ENST00000434163
  gene symbol: KCNIP2
  hgvsc: ENST00000434163.1:c.42T>C
  hgvsp: ENST00000434163.1:c.42T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000239117
  ensembl transcript: ENST00000239117
  gene symbol: KCNIP2
  hgvsc: ENST00000239117.3:c.100T>C
  hgvsp: ENSP00000239117.3:p.Ser34Pro
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000472764
  gene symbol: KCNIP2
  hgvsc: ENST00000472764.1:n.196T>C
  variant of: http://identifiers.org/hgnc/15522
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1870
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 765
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1224
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24501
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25560
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser99Pro
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
reference allele: A
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum

10-103588944-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103588944
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103588944
    reference: chr 10
allele count: 2
allele frequency: 1.73331253358293e-5
allele num: 115386
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000350733
  ensembl transcript: ENST00000358038
  gene symbol: KCNIP2
  hgvsc: ENST00000358038.3:c.182A>G
  hgvsp: ENSP00000350733.3:p.Asp61Gly
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000411679
  ensembl transcript: ENST00000434163
  gene symbol: KCNIP2
  hgvsc: ENST00000434163.1:c.28A>G
  hgvsp: ENSP00000411679.1:p.Met10Val
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000344169
  ensembl transcript: ENST00000343195
  gene symbol: KCNIP2
  hgvsc: ENST00000343195.4:c.86A>G
  hgvsp: ENSP00000344169.4:p.Asp29Gly
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000239117
  ensembl transcript: ENST00000239117
  gene symbol: KCNIP2
  hgvsc: ENST00000239117.3:c.86A>G
  hgvsp: ENSP00000239117.3:p.Asp29Gly
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000341624
  ensembl transcript: ENST00000353068
  gene symbol: KCNIP2
  hgvsc: ENST00000353068.3:c.86A>G
  hgvsp: ENSP00000341624.3:p.Asp29Gly
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000349055
  ensembl transcript: ENST00000356640
  gene symbol: KCNIP2
  hgvsc: ENST00000356640.2:c.236A>G
  hgvsp: ENSP00000349055.2:p.Asp79Gly
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000483385
  gene symbol: KCNIP2
  hgvsc: ENST00000483385.1:n.361A>G
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000359063
  ensembl transcript: ENST00000370046
  gene symbol: KCNIP2
  hgvsc: ENST00000370046.1:c.86A>G
  hgvsp: ENSP00000359063.1:p.Asp29Gly
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000239118
  ensembl transcript: ENST00000348850
  gene symbol: KCNIP2
  hgvsc: ENST00000348850.5:c.101A>G
  hgvsp: ENSP00000239118.6:p.Asp34Gly
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000472764
  gene symbol: KCNIP2
  hgvsc: ENST00000472764.1:n.182A>G
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000420040
  ensembl transcript: ENST00000461105
  gene symbol: KCNIP2
  hgvsc: ENST00000461105.1:c.281A>G
  hgvsp: ENSP00000420040.1:p.Asp94Gly
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000355657
  gene symbol: KCNIP2
  hgvsc: ENST00000355657.2:n.633A>G
  variant of: http://identifiers.org/hgnc/15522
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5030
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2894
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21110
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5178
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23257
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1834
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 734
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp94Gly
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
reference allele: T
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD

10-103588946-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103588946
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103588946
    reference: chr 10
allele count: 1
allele frequency: 8.714445064138316e-6
allele num: 114752
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000483385
  gene symbol: KCNIP2
  hgvsc: ENST00000483385.1:n.359C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000344169
  ensembl transcript: ENST00000343195
  gene symbol: KCNIP2
  hgvsc: ENST00000343195.4:c.84C>T
  hgvsp: ENST00000343195.4:c.84C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000472764
  gene symbol: KCNIP2
  hgvsc: ENST00000472764.1:n.180C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000341624
  ensembl transcript: ENST00000353068
  gene symbol: KCNIP2
  hgvsc: ENST00000353068.3:c.84C>T
  hgvsp: ENST00000353068.3:c.84C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000355657
  gene symbol: KCNIP2
  hgvsc: ENST00000355657.2:n.631C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000420040
  ensembl transcript: ENST00000461105
  gene symbol: KCNIP2
  hgvsc: ENST00000461105.1:c.279C>T
  hgvsp: ENST00000461105.1:c.279C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000350733
  ensembl transcript: ENST00000358038
  gene symbol: KCNIP2
  hgvsc: ENST00000358038.3:c.180C>T
  hgvsp: ENST00000358038.3:c.180C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000239117
  ensembl transcript: ENST00000239117
  gene symbol: KCNIP2
  hgvsc: ENST00000239117.3:c.84C>T
  hgvsp: ENST00000239117.3:c.84C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000349055
  ensembl transcript: ENST00000356640
  gene symbol: KCNIP2
  hgvsc: ENST00000356640.2:c.234C>T
  hgvsp: ENST00000356640.2:c.234C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000411679
  ensembl transcript: ENST00000434163
  gene symbol: KCNIP2
  hgvsc: ENST00000434163.1:c.26C>T
  hgvsp: ENSP00000411679.1:p.Thr9Met
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000359063
  ensembl transcript: ENST00000370046
  gene symbol: KCNIP2
  hgvsc: ENST00000370046.1:c.84C>T
  hgvsp: ENST00000370046.1:c.84C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000239118
  ensembl transcript: ENST00000348850
  gene symbol: KCNIP2
  hgvsc: ENST00000348850.5:c.99C>T
  hgvsp: ENST00000348850.5:c.99C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15522
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2017
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3149
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20705
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5056
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5566
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22799
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 729
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr9Met
num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum

10-103588970-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103588970
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103588970
    reference: chr 10
allele count: 1
allele frequency: 9.31619154089808e-6
allele num: 107340
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000483385
  gene symbol: KCNIP2
  hgvsc: ENST00000483385.1:n.335C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000411679
  ensembl transcript: ENST00000434163
  gene symbol: KCNIP2
  hgvsc: ENST00000434163.1:c.16-14C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000350733
  ensembl transcript: ENST00000358038
  gene symbol: KCNIP2
  hgvsc: ENST00000358038.3:c.170-14C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000420040
  ensembl transcript: ENST00000461105
  gene symbol: KCNIP2
  hgvsc: ENST00000461105.1:c.269-14C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000349055
  ensembl transcript: ENST00000356640
  gene symbol: KCNIP2
  hgvsc: ENST00000356640.2:c.224-14C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000239117
  ensembl transcript: ENST00000239117
  gene symbol: KCNIP2
  hgvsc: ENST00000239117.3:c.74-14C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000344169
  ensembl transcript: ENST00000343195
  gene symbol: KCNIP2
  hgvsc: ENST00000343195.4:c.74-14C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000359063
  ensembl transcript: ENST00000370046
  gene symbol: KCNIP2
  hgvsc: ENST00000370046.1:c.74-14C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000341624
  ensembl transcript: ENST00000353068
  gene symbol: KCNIP2
  hgvsc: ENST00000353068.3:c.74-14C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000472764
  gene symbol: KCNIP2
  hgvsc: ENST00000472764.1:n.170-14C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000355657
  gene symbol: KCNIP2
  hgvsc: ENST00000355657.2:n.621-14C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000239118
  ensembl transcript: ENST00000348850
  gene symbol: KCNIP2
  hgvsc: ENST00000348850.5:c.89-14C>T
  variant of: http://identifiers.org/hgnc/15522
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15595
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3696
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6297
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12931
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3670
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16870
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Latino
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: G
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum

10-103588979-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103588979
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103588979
    reference: chr 10
allele count: 3
allele frequency: 2.851385773485914e-5
allele num: 105212
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000341624
  ensembl transcript: ENST00000353068
  gene symbol: KCNIP2
  hgvsc: ENST00000353068.3:c.74-23G>C
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000359063
  ensembl transcript: ENST00000370046
  gene symbol: KCNIP2
  hgvsc: ENST00000370046.1:c.74-23G>C
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000472764
  gene symbol: KCNIP2
  hgvsc: ENST00000472764.1:n.170-23G>C
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000349055
  ensembl transcript: ENST00000356640
  gene symbol: KCNIP2
  hgvsc: ENST00000356640.2:c.224-23G>C
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000483385
  gene symbol: KCNIP2
  hgvsc: ENST00000483385.1:n.326G>C
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000355657
  gene symbol: KCNIP2
  hgvsc: ENST00000355657.2:n.621-23G>C
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000344169
  ensembl transcript: ENST00000343195
  gene symbol: KCNIP2
  hgvsc: ENST00000343195.4:c.74-23G>C
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000411679
  ensembl transcript: ENST00000434163
  gene symbol: KCNIP2
  hgvsc: ENST00000434163.1:c.16-23G>C
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000239117
  ensembl transcript: ENST00000239117
  gene symbol: KCNIP2
  hgvsc: ENST00000239117.3:c.74-23G>C
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000350733
  ensembl transcript: ENST00000358038
  gene symbol: KCNIP2
  hgvsc: ENST00000358038.3:c.170-23G>C
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000239118
  ensembl transcript: ENST00000348850
  gene symbol: KCNIP2
  hgvsc: ENST00000348850.5:c.89-23G>C
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000420040
  ensembl transcript: ENST00000461105
  gene symbol: KCNIP2
  hgvsc: ENST00000461105.1:c.269-23G>C
  variant of: http://identifiers.org/hgnc/15522
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7064
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 724
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13044
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16686
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3203
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4677
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: FS

10-103588979-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103588979
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103588979
    reference: chr 10
allele count: 2
allele frequency: 1.900923848990609e-5
allele num: 105212
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000359063
  ensembl transcript: ENST00000370046
  gene symbol: KCNIP2
  hgvsc: ENST00000370046.1:c.74-23G>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000350733
  ensembl transcript: ENST00000358038
  gene symbol: KCNIP2
  hgvsc: ENST00000358038.3:c.170-23G>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000472764
  gene symbol: KCNIP2
  hgvsc: ENST00000472764.1:n.170-23G>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000341624
  ensembl transcript: ENST00000353068
  gene symbol: KCNIP2
  hgvsc: ENST00000353068.3:c.74-23G>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000349055
  ensembl transcript: ENST00000356640
  gene symbol: KCNIP2
  hgvsc: ENST00000356640.2:c.224-23G>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000239117
  ensembl transcript: ENST00000239117
  gene symbol: KCNIP2
  hgvsc: ENST00000239117.3:c.74-23G>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000344169
  ensembl transcript: ENST00000343195
  gene symbol: KCNIP2
  hgvsc: ENST00000343195.4:c.74-23G>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000483385
  gene symbol: KCNIP2
  hgvsc: ENST00000483385.1:n.326G>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000420040
  ensembl transcript: ENST00000461105
  gene symbol: KCNIP2
  hgvsc: ENST00000461105.1:c.269-23G>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000411679
  ensembl transcript: ENST00000434163
  gene symbol: KCNIP2
  hgvsc: ENST00000434163.1:c.16-23G>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000239118
  ensembl transcript: ENST00000348850
  gene symbol: KCNIP2
  hgvsc: ENST00000348850.5:c.89-23G>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000355657
  gene symbol: KCNIP2
  hgvsc: ENST00000355657.2:n.621-23G>A
  variant of: http://identifiers.org/hgnc/15522
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7064
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3203
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13044
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4677
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 724
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16686
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14218
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
population: East Asian
reference allele: C
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ

10-103588982-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103588982
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103588982
    reference: chr 10
allele count: 2
allele frequency: 1.915451950887812e-5
allele num: 104414
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000239118
  ensembl transcript: ENST00000348850
  gene symbol: KCNIP2
  hgvsc: ENST00000348850.5:c.89-26C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000239117
  ensembl transcript: ENST00000239117
  gene symbol: KCNIP2
  hgvsc: ENST00000239117.3:c.74-26C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000349055
  ensembl transcript: ENST00000356640
  gene symbol: KCNIP2
  hgvsc: ENST00000356640.2:c.224-26C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000420040
  ensembl transcript: ENST00000461105
  gene symbol: KCNIP2
  hgvsc: ENST00000461105.1:c.269-26C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000355657
  gene symbol: KCNIP2
  hgvsc: ENST00000355657.2:n.621-26C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000350733
  ensembl transcript: ENST00000358038
  gene symbol: KCNIP2
  hgvsc: ENST00000358038.3:c.170-26C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000411679
  ensembl transcript: ENST00000434163
  gene symbol: KCNIP2
  hgvsc: ENST00000434163.1:c.16-26C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000341624
  ensembl transcript: ENST00000353068
  gene symbol: KCNIP2
  hgvsc: ENST00000353068.3:c.74-26C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000483385
  gene symbol: KCNIP2
  hgvsc: ENST00000483385.1:n.323C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000472764
  gene symbol: KCNIP2
  hgvsc: ENST00000472764.1:n.170-26C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000359063
  ensembl transcript: ENST00000370046
  gene symbol: KCNIP2
  hgvsc: ENST00000370046.1:c.74-26C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000344169
  ensembl transcript: ENST00000343195
  gene symbol: KCNIP2
  hgvsc: ENST00000343195.4:c.74-26C>T
  variant of: http://identifiers.org/hgnc/15522
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17814
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13170
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2911
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5012
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7341
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 814
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
reference allele: G
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD

10-103588984-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103588984
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103588984
    reference: chr 10
allele count: 1
allele frequency: 9.609101741169235e-6
allele num: 104068
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000349055
  ensembl transcript: ENST00000356640
  gene symbol: KCNIP2
  hgvsc: ENST00000356640.2:c.224-28G>C
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000341624
  ensembl transcript: ENST00000353068
  gene symbol: KCNIP2
  hgvsc: ENST00000353068.3:c.74-28G>C
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000411679
  ensembl transcript: ENST00000434163
  gene symbol: KCNIP2
  hgvsc: ENST00000434163.1:c.16-28G>C
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000472764
  gene symbol: KCNIP2
  hgvsc: ENST00000472764.1:n.170-28G>C
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000344169
  ensembl transcript: ENST00000343195
  gene symbol: KCNIP2
  hgvsc: ENST00000343195.4:c.74-28G>C
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000239118
  ensembl transcript: ENST00000348850
  gene symbol: KCNIP2
  hgvsc: ENST00000348850.5:c.89-28G>C
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000359063
  ensembl transcript: ENST00000370046
  gene symbol: KCNIP2
  hgvsc: ENST00000370046.1:c.74-28G>C
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000355657
  gene symbol: KCNIP2
  hgvsc: ENST00000355657.2:n.621-28G>C
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000483385
  gene symbol: KCNIP2
  hgvsc: ENST00000483385.1:n.321G>C
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000420040
  ensembl transcript: ENST00000461105
  gene symbol: KCNIP2
  hgvsc: ENST00000461105.1:c.269-28G>C
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000239117
  ensembl transcript: ENST00000239117
  gene symbol: KCNIP2
  hgvsc: ENST00000239117.3:c.74-28G>C
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000350733
  ensembl transcript: ENST00000358038
  gene symbol: KCNIP2
  hgvsc: ENST00000358038.3:c.170-28G>C
  variant of: http://identifiers.org/hgnc/15522
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19018
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2834
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 929
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7445
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12511
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11262
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5663
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
population: Latino
population: East Asian
population: European (Finnish)
reference allele: C
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum

10-103588993-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103588993
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103588993
    reference: chr 10
allele count: 1
allele frequency: 1.003371327660941e-5
allele num: 99664
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000344169
  ensembl transcript: ENST00000343195
  gene symbol: KCNIP2
  hgvsc: ENST00000343195.4:c.74-37T>C
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000420040
  ensembl transcript: ENST00000461105
  gene symbol: KCNIP2
  hgvsc: ENST00000461105.1:c.269-37T>C
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000350733
  ensembl transcript: ENST00000358038
  gene symbol: KCNIP2
  hgvsc: ENST00000358038.3:c.170-37T>C
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000411679
  ensembl transcript: ENST00000434163
  gene symbol: KCNIP2
  hgvsc: ENST00000434163.1:c.16-37T>C
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000483385
  gene symbol: KCNIP2
  hgvsc: ENST00000483385.1:n.312T>C
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000349055
  ensembl transcript: ENST00000356640
  gene symbol: KCNIP2
  hgvsc: ENST00000356640.2:c.224-37T>C
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000341624
  ensembl transcript: ENST00000353068
  gene symbol: KCNIP2
  hgvsc: ENST00000353068.3:c.74-37T>C
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000472764
  gene symbol: KCNIP2
  hgvsc: ENST00000472764.1:n.170-37T>C
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000239118
  ensembl transcript: ENST00000348850
  gene symbol: KCNIP2
  hgvsc: ENST00000348850.5:c.89-37T>C
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000355657
  gene symbol: KCNIP2
  hgvsc: ENST00000355657.2:n.621-37T>C
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000239117
  ensembl transcript: ENST00000239117
  gene symbol: KCNIP2
  hgvsc: ENST00000239117.3:c.74-37T>C
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000359063
  ensembl transcript: ENST00000370046
  gene symbol: KCNIP2
  hgvsc: ENST00000370046.1:c.74-37T>C
  variant of: http://identifiers.org/hgnc/15522
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4989
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21124
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1946
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14586
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8775
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1587
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6707
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: Other
reference allele: A
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: MQ

10-103589004-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103589004
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103589004
    reference: chr 10
allele count: 3
allele frequency: 3.218815046887406e-5
allele num: 93202
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000350733
  ensembl transcript: ENST00000358038
  gene symbol: KCNIP2
  hgvsc: ENST00000358038.3:c.170-48G>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000420040
  ensembl transcript: ENST00000461105
  gene symbol: KCNIP2
  hgvsc: ENST00000461105.1:c.269-48G>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000239118
  ensembl transcript: ENST00000348850
  gene symbol: KCNIP2
  hgvsc: ENST00000348850.5:c.89-48G>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000341624
  ensembl transcript: ENST00000353068
  gene symbol: KCNIP2
  hgvsc: ENST00000353068.3:c.74-48G>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000483385
  gene symbol: KCNIP2
  hgvsc: ENST00000483385.1:n.301G>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000355657
  gene symbol: KCNIP2
  hgvsc: ENST00000355657.2:n.621-48G>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000411679
  ensembl transcript: ENST00000434163
  gene symbol: KCNIP2
  hgvsc: ENST00000434163.1:c.16-48G>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000359063
  ensembl transcript: ENST00000370046
  gene symbol: KCNIP2
  hgvsc: ENST00000370046.1:c.74-48G>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000349055
  ensembl transcript: ENST00000356640
  gene symbol: KCNIP2
  hgvsc: ENST00000356640.2:c.224-48G>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000472764
  gene symbol: KCNIP2
  hgvsc: ENST00000472764.1:n.170-48G>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000239117
  ensembl transcript: ENST00000239117
  gene symbol: KCNIP2
  hgvsc: ENST00000239117.3:c.74-48G>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000344169
  ensembl transcript: ENST00000343195
  gene symbol: KCNIP2
  hgvsc: ENST00000343195.4:c.74-48G>A
  variant of: http://identifiers.org/hgnc/15522
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15494
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7539
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1007
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1716
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11468
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19559
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3024
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum

10-103589005-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103589005
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103589005
    reference: chr 10
allele count: 0
allele frequency: 0.0e0
allele num: 92818
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000341624
  ensembl transcript: ENST00000353068
  gene symbol: KCNIP2
  hgvsc: ENST00000353068.3:c.74-49G>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000239117
  ensembl transcript: ENST00000239117
  gene symbol: KCNIP2
  hgvsc: ENST00000239117.3:c.74-49G>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000349055
  ensembl transcript: ENST00000356640
  gene symbol: KCNIP2
  hgvsc: ENST00000356640.2:c.224-49G>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000420040
  ensembl transcript: ENST00000461105
  gene symbol: KCNIP2
  hgvsc: ENST00000461105.1:c.269-49G>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000483385
  gene symbol: KCNIP2
  hgvsc: ENST00000483385.1:n.300G>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000359063
  ensembl transcript: ENST00000370046
  gene symbol: KCNIP2
  hgvsc: ENST00000370046.1:c.74-49G>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000411679
  ensembl transcript: ENST00000434163
  gene symbol: KCNIP2
  hgvsc: ENST00000434163.1:c.16-49G>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000350733
  ensembl transcript: ENST00000358038
  gene symbol: KCNIP2
  hgvsc: ENST00000358038.3:c.170-49G>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000344169
  ensembl transcript: ENST00000343195
  gene symbol: KCNIP2
  hgvsc: ENST00000343195.4:c.74-49G>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000472764
  gene symbol: KCNIP2
  hgvsc: ENST00000472764.1:n.170-49G>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000355657
  gene symbol: KCNIP2
  hgvsc: ENST00000355657.2:n.621-49G>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000239118
  ensembl transcript: ENST00000348850
  gene symbol: KCNIP2
  hgvsc: ENST00000348850.5:c.89-49G>A
  variant of: http://identifiers.org/hgnc/15522
canonical: false
consequence: non coding transcript exon
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 7627
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1718
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 984
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11549
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2949
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19509
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15471
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
population: Other
reference allele: C
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff

10-103589550-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103589550
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103589550
    reference: chr 10
allele count: 1
allele frequency: 1.025430680885972e-4
allele num: 9752
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000239117
  ensembl transcript: ENST00000239117
  gene symbol: KCNIP2
  hgvsc: ENST00000239117.3:c.74-594C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000344169
  ensembl transcript: ENST00000343195
  gene symbol: KCNIP2
  hgvsc: ENST00000343195.4:c.74-594C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000341624
  ensembl transcript: ENST00000353068
  gene symbol: KCNIP2
  hgvsc: ENST00000353068.3:c.74-594C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000350733
  ensembl transcript: ENST00000358038
  gene symbol: KCNIP2
  hgvsc: ENST00000358038.3:c.170-594C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000359063
  ensembl transcript: ENST00000370046
  gene symbol: KCNIP2
  hgvsc: ENST00000370046.1:c.74-594C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000239118
  ensembl transcript: ENST00000348850
  gene symbol: KCNIP2
  hgvsc: ENST00000348850.5:c.89-594C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000349055
  ensembl transcript: ENST00000356640
  gene symbol: KCNIP2
  hgvsc: ENST00000356640.2:c.223+51C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000411679
  ensembl transcript: ENST00000434163
  gene symbol: KCNIP2
  hgvsc: ENST00000434163.1:c.16-594C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000472764
  gene symbol: KCNIP2
  hgvsc: ENST00000472764.1:n.170-594C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000355657
  gene symbol: KCNIP2
  hgvsc: ENST00000355657.2:n.620+51C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000420040
  ensembl transcript: ENST00000461105
  gene symbol: KCNIP2
  hgvsc: ENST00000461105.1:c.268+51C>T
  variant of: http://identifiers.org/hgnc/15522
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24631
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2835
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2543
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1612
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1414
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: African
population: Latino
reference allele: G
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum

10-103589563-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103589563
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103589563
    reference: chr 10
allele count: 14
allele frequency: 1.338944146901301e-3
allele num: 10456
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000355657
  gene symbol: KCNIP2
  hgvsc: ENST00000355657.2:n.620+38G>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000472764
  gene symbol: KCNIP2
  hgvsc: ENST00000472764.1:n.170-607G>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000341624
  ensembl transcript: ENST00000353068
  gene symbol: KCNIP2
  hgvsc: ENST00000353068.3:c.74-607G>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000359063
  ensembl transcript: ENST00000370046
  gene symbol: KCNIP2
  hgvsc: ENST00000370046.1:c.74-607G>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000239118
  ensembl transcript: ENST00000348850
  gene symbol: KCNIP2
  hgvsc: ENST00000348850.5:c.89-607G>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000420040
  ensembl transcript: ENST00000461105
  gene symbol: KCNIP2
  hgvsc: ENST00000461105.1:c.268+38G>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000350733
  ensembl transcript: ENST00000358038
  gene symbol: KCNIP2
  hgvsc: ENST00000358038.3:c.170-607G>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000349055
  ensembl transcript: ENST00000356640
  gene symbol: KCNIP2
  hgvsc: ENST00000356640.2:c.223+38G>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000344169
  ensembl transcript: ENST00000343195
  gene symbol: KCNIP2
  hgvsc: ENST00000343195.4:c.74-607G>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000411679
  ensembl transcript: ENST00000434163
  gene symbol: KCNIP2
  hgvsc: ENST00000434163.1:c.16-607G>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000239117
  ensembl transcript: ENST00000239117
  gene symbol: KCNIP2
  hgvsc: ENST00000239117.3:c.74-607G>A
  variant of: http://identifiers.org/hgnc/15522
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1845
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 2.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 1.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3287
  bin: 7.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25373
  bin: 2.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2521
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 131
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum

10-103589572-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103589572
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103589572
    reference: chr 10
allele count: 1
allele frequency: 8.241305422778968e-5
allele num: 12134
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000472764
  gene symbol: KCNIP2
  hgvsc: ENST00000472764.1:n.170-616C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000344169
  ensembl transcript: ENST00000343195
  gene symbol: KCNIP2
  hgvsc: ENST00000343195.4:c.74-616C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000411679
  ensembl transcript: ENST00000434163
  gene symbol: KCNIP2
  hgvsc: ENST00000434163.1:c.15+609C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000355657
  gene symbol: KCNIP2
  hgvsc: ENST00000355657.2:n.620+29C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000350733
  ensembl transcript: ENST00000358038
  gene symbol: KCNIP2
  hgvsc: ENST00000358038.3:c.170-616C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000239118
  ensembl transcript: ENST00000348850
  gene symbol: KCNIP2
  hgvsc: ENST00000348850.5:c.89-616C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000420040
  ensembl transcript: ENST00000461105
  gene symbol: KCNIP2
  hgvsc: ENST00000461105.1:c.268+29C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000341624
  ensembl transcript: ENST00000353068
  gene symbol: KCNIP2
  hgvsc: ENST00000353068.3:c.74-616C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000349055
  ensembl transcript: ENST00000356640
  gene symbol: KCNIP2
  hgvsc: ENST00000356640.2:c.223+29C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000239117
  ensembl transcript: ENST00000239117
  gene symbol: KCNIP2
  hgvsc: ENST00000239117.3:c.74-616C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000359063
  ensembl transcript: ENST00000370046
  gene symbol: KCNIP2
  hgvsc: ENST00000370046.1:c.74-616C>T
  variant of: http://identifiers.org/hgnc/15522
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27654
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3496
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 899
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3826
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 829
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: G
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS

http://identifiers.org/exac.variant/10-103589574-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103589574
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103589574
    reference: chr 10
allele count: 1
allele frequency: 7.930214115781126e-5
allele num: 12610
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000411679
  ensembl transcript: ENST00000434163
  gene symbol: KCNIP2
  hgvsc: ENST00000434163.1:c.15+607G>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000239117
  ensembl transcript: ENST00000239117
  gene symbol: KCNIP2
  hgvsc: ENST00000239117.3:c.74-618G>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000349055
  ensembl transcript: ENST00000356640
  gene symbol: KCNIP2
  hgvsc: ENST00000356640.2:c.223+27G>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000355657
  gene symbol: KCNIP2
  hgvsc: ENST00000355657.2:n.620+27G>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000341624
  ensembl transcript: ENST00000353068
  gene symbol: KCNIP2
  hgvsc: ENST00000353068.3:c.74-618G>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000239118
  ensembl transcript: ENST00000348850
  gene symbol: KCNIP2
  hgvsc: ENST00000348850.5:c.89-618G>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000359063
  ensembl transcript: ENST00000370046
  gene symbol: KCNIP2
  hgvsc: ENST00000370046.1:c.74-618G>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000350733
  ensembl transcript: ENST00000358038
  gene symbol: KCNIP2
  hgvsc: ENST00000358038.3:c.170-618G>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000420040
  ensembl transcript: ENST00000461105
  gene symbol: KCNIP2
  hgvsc: ENST00000461105.1:c.268+27G>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000472764
  gene symbol: KCNIP2
  hgvsc: ENST00000472764.1:n.170-618G>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000344169
  ensembl transcript: ENST00000343195
  gene symbol: KCNIP2
  hgvsc: ENST00000343195.4:c.74-618G>T
  variant of: http://identifiers.org/hgnc/15522
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28145
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 818
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3881
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3508
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 951
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
population: European (Finnish)
population: South Asian
reference allele: C
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP

http://identifiers.org/exac.variant/10-103589585-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103589585
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103589585
    reference: chr 10
allele count: 11
allele frequency: 7.399434952240011e-4
allele num: 14866
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000420040
  ensembl transcript: ENST00000461105
  gene symbol: KCNIP2
  hgvsc: ENST00000461105.1:c.268+16G>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000341624
  ensembl transcript: ENST00000353068
  gene symbol: KCNIP2
  hgvsc: ENST00000353068.3:c.74-629G>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000350733
  ensembl transcript: ENST00000358038
  gene symbol: KCNIP2
  hgvsc: ENST00000358038.3:c.170-629G>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000472764
  gene symbol: KCNIP2
  hgvsc: ENST00000472764.1:n.170-629G>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000355657
  gene symbol: KCNIP2
  hgvsc: ENST00000355657.2:n.620+16G>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000344169
  ensembl transcript: ENST00000343195
  gene symbol: KCNIP2
  hgvsc: ENST00000343195.4:c.74-629G>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000359063
  ensembl transcript: ENST00000370046
  gene symbol: KCNIP2
  hgvsc: ENST00000370046.1:c.74-629G>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000411679
  ensembl transcript: ENST00000434163
  gene symbol: KCNIP2
  hgvsc: ENST00000434163.1:c.15+596G>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000239117
  ensembl transcript: ENST00000239117
  gene symbol: KCNIP2
  hgvsc: ENST00000239117.3:c.74-629G>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000349055
  ensembl transcript: ENST00000356640
  gene symbol: KCNIP2
  hgvsc: ENST00000356640.2:c.223+16G>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000239118
  ensembl transcript: ENST00000348850
  gene symbol: KCNIP2
  hgvsc: ENST00000348850.5:c.89-629G>T
  variant of: http://identifiers.org/hgnc/15522
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 705
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1356
  bin: 2.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4078
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31470
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4320
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 295
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 1
population: Other
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP

10-103589588-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103589588
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103589588
    reference: chr 10
allele count: 1
allele frequency: 6.397134083930399e-5
allele num: 15632
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000359063
  ensembl transcript: ENST00000370046
  gene symbol: KCNIP2
  hgvsc: ENST00000370046.1:c.74-632C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000239118
  ensembl transcript: ENST00000348850
  gene symbol: KCNIP2
  hgvsc: ENST00000348850.5:c.89-632C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000344169
  ensembl transcript: ENST00000343195
  gene symbol: KCNIP2
  hgvsc: ENST00000343195.4:c.74-632C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000355657
  gene symbol: KCNIP2
  hgvsc: ENST00000355657.2:n.620+13C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000239117
  ensembl transcript: ENST00000239117
  gene symbol: KCNIP2
  hgvsc: ENST00000239117.3:c.74-632C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000349055
  ensembl transcript: ENST00000356640
  gene symbol: KCNIP2
  hgvsc: ENST00000356640.2:c.223+13C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000420040
  ensembl transcript: ENST00000461105
  gene symbol: KCNIP2
  hgvsc: ENST00000461105.1:c.268+13C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000350733
  ensembl transcript: ENST00000358038
  gene symbol: KCNIP2
  hgvsc: ENST00000358038.3:c.170-632C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000341624
  ensembl transcript: ENST00000353068
  gene symbol: KCNIP2
  hgvsc: ENST00000353068.3:c.74-632C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000411679
  ensembl transcript: ENST00000434163
  gene symbol: KCNIP2
  hgvsc: ENST00000434163.1:c.15+593C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000472764
  gene symbol: KCNIP2
  hgvsc: ENST00000472764.1:n.170-632C>T
  variant of: http://identifiers.org/hgnc/15522
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4662
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31985
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1433
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 738
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4280
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3683
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
population: African
reference allele: G
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: VQSLOD

10-103589620-TC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103589620
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103589619
    reference: chr 10
allele count: 0
allele frequency: 0.0e0
allele num: 19006
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000350733
  ensembl transcript: ENST00000358038
  gene symbol: KCNIP2
  hgvsc: ENST00000358038.3:c.170-665delG
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000472764
  gene symbol: KCNIP2
  hgvsc: ENST00000472764.1:n.170-665delG
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000411679
  ensembl transcript: ENST00000434163
  gene symbol: KCNIP2
  hgvsc: ENST00000434163.1:c.15+560delG
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000239117
  ensembl transcript: ENST00000239117
  gene symbol: KCNIP2
  hgvsc: ENST00000239117.3:c.74-665delG
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000355657
  gene symbol: KCNIP2
  hgvsc: ENST00000355657.2:n.600delG
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000349055
  ensembl transcript: ENST00000356640
  gene symbol: KCNIP2
  hgvsc: ENST00000356640.2:c.203delG
  hgvsp: ENSP00000349055.2:p.Arg68AsnfsTer104
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000420040
  ensembl transcript: ENST00000461105
  gene symbol: KCNIP2
  hgvsc: ENST00000461105.1:c.248delG
  hgvsp: ENSP00000420040.1:p.Arg83AsnfsTer104
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000359063
  ensembl transcript: ENST00000370046
  gene symbol: KCNIP2
  hgvsc: ENST00000370046.1:c.74-665delG
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000341624
  ensembl transcript: ENST00000353068
  gene symbol: KCNIP2
  hgvsc: ENST00000353068.3:c.74-665delG
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000239118
  ensembl transcript: ENST00000348850
  gene symbol: KCNIP2
  hgvsc: ENST00000348850.5:c.89-665delG
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000344169
  ensembl transcript: ENST00000343195
  gene symbol: KCNIP2
  hgvsc: ENST00000343195.4:c.74-665delG
  variant of: http://identifiers.org/hgnc/15522
canonical: true
consequence: frameshift
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 1928
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10433
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31940
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5553
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 965
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3118
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Arg83AsnfsTer104
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Other
population: African
population: East Asian
population: Latino
reference allele: TC
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

10-103589627-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103589627
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103589627
    reference: chr 10
allele count: 0
allele frequency: 0.0e0
allele num: 19828
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000350733
  ensembl transcript: ENST00000358038
  gene symbol: KCNIP2
  hgvsc: ENST00000358038.3:c.170-671C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000344169
  ensembl transcript: ENST00000343195
  gene symbol: KCNIP2
  hgvsc: ENST00000343195.4:c.74-671C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000341624
  ensembl transcript: ENST00000353068
  gene symbol: KCNIP2
  hgvsc: ENST00000353068.3:c.74-671C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000472764
  gene symbol: KCNIP2
  hgvsc: ENST00000472764.1:n.170-671C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000239118
  ensembl transcript: ENST00000348850
  gene symbol: KCNIP2
  hgvsc: ENST00000348850.5:c.89-671C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000349055
  ensembl transcript: ENST00000356640
  gene symbol: KCNIP2
  hgvsc: ENST00000356640.2:c.197C>T
  hgvsp: ENSP00000349055.2:p.Pro66Leu
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000355657
  gene symbol: KCNIP2
  hgvsc: ENST00000355657.2:n.594C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000239117
  ensembl transcript: ENST00000239117
  gene symbol: KCNIP2
  hgvsc: ENST00000239117.3:c.74-671C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000359063
  ensembl transcript: ENST00000370046
  gene symbol: KCNIP2
  hgvsc: ENST00000370046.1:c.74-671C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000420040
  ensembl transcript: ENST00000461105
  gene symbol: KCNIP2
  hgvsc: ENST00000461105.1:c.242C>T
  hgvsp: ENSP00000420040.1:p.Pro81Leu
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000411679
  ensembl transcript: ENST00000434163
  gene symbol: KCNIP2
  hgvsc: ENST00000434163.1:c.15+554C>T
  variant of: http://identifiers.org/hgnc/15522
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2070
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1008
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31146
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5767
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12192
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 192
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Pro81Leu
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: FS

10-103589639-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103589639
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103589639
    reference: chr 10
allele count: 1
allele frequency: 4.833252779120348e-5
allele num: 20690
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000344169
  ensembl transcript: ENST00000343195
  gene symbol: KCNIP2
  hgvsc: ENST00000343195.4:c.74-683C>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000359063
  ensembl transcript: ENST00000370046
  gene symbol: KCNIP2
  hgvsc: ENST00000370046.1:c.74-683C>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000411679
  ensembl transcript: ENST00000434163
  gene symbol: KCNIP2
  hgvsc: ENST00000434163.1:c.15+542C>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000350733
  ensembl transcript: ENST00000358038
  gene symbol: KCNIP2
  hgvsc: ENST00000358038.3:c.170-683C>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000355657
  gene symbol: KCNIP2
  hgvsc: ENST00000355657.2:n.582C>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000341624
  ensembl transcript: ENST00000353068
  gene symbol: KCNIP2
  hgvsc: ENST00000353068.3:c.74-683C>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000420040
  ensembl transcript: ENST00000461105
  gene symbol: KCNIP2
  hgvsc: ENST00000461105.1:c.230C>A
  hgvsp: ENSP00000420040.1:p.Ala77Asp
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000239117
  ensembl transcript: ENST00000239117
  gene symbol: KCNIP2
  hgvsc: ENST00000239117.3:c.74-683C>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000349055
  ensembl transcript: ENST00000356640
  gene symbol: KCNIP2
  hgvsc: ENST00000356640.2:c.185C>A
  hgvsp: ENSP00000349055.2:p.Ala62Asp
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000239118
  ensembl transcript: ENST00000348850
  gene symbol: KCNIP2
  hgvsc: ENST00000348850.5:c.89-683C>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000472764
  gene symbol: KCNIP2
  hgvsc: ENST00000472764.1:n.170-683C>A
  variant of: http://identifiers.org/hgnc/15522
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1051
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5937
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13639
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30215
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2236
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10871
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Ala77Asp
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: G
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum

10-103589640-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103589640
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103589640
    reference: chr 10
allele count: 1
allele frequency: 4.820671037408407e-5
allele num: 20744
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000420040
  ensembl transcript: ENST00000461105
  gene symbol: KCNIP2
  hgvsc: ENST00000461105.1:c.229G>C
  hgvsp: ENSP00000420040.1:p.Ala77Pro
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000472764
  gene symbol: KCNIP2
  hgvsc: ENST00000472764.1:n.170-684G>C
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000350733
  ensembl transcript: ENST00000358038
  gene symbol: KCNIP2
  hgvsc: ENST00000358038.3:c.170-684G>C
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000239118
  ensembl transcript: ENST00000348850
  gene symbol: KCNIP2
  hgvsc: ENST00000348850.5:c.89-684G>C
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000349055
  ensembl transcript: ENST00000356640
  gene symbol: KCNIP2
  hgvsc: ENST00000356640.2:c.184G>C
  hgvsp: ENSP00000349055.2:p.Ala62Pro
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000411679
  ensembl transcript: ENST00000434163
  gene symbol: KCNIP2
  hgvsc: ENST00000434163.1:c.15+541G>C
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000239117
  ensembl transcript: ENST00000239117
  gene symbol: KCNIP2
  hgvsc: ENST00000239117.3:c.74-684G>C
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000355657
  gene symbol: KCNIP2
  hgvsc: ENST00000355657.2:n.581G>C
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000341624
  ensembl transcript: ENST00000353068
  gene symbol: KCNIP2
  hgvsc: ENST00000353068.3:c.74-684G>C
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000359063
  ensembl transcript: ENST00000370046
  gene symbol: KCNIP2
  hgvsc: ENST00000370046.1:c.74-684G>C
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000344169
  ensembl transcript: ENST00000343195
  gene symbol: KCNIP2
  hgvsc: ENST00000343195.4:c.74-684G>C
  variant of: http://identifiers.org/hgnc/15522
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5947
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13822
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30107
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1054
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2243
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1513
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Ala77Pro
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
population: Latino
population: East Asian
reference allele: C
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: BaseQRankSum

10-103589649-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103589649
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103589649
    reference: chr 10
allele count: 1
allele frequency: 4.721881197469072e-5
allele num: 21178
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000239117
  ensembl transcript: ENST00000239117
  gene symbol: KCNIP2
  hgvsc: ENST00000239117.3:c.74-693G>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000411679
  ensembl transcript: ENST00000434163
  gene symbol: KCNIP2
  hgvsc: ENST00000434163.1:c.15+532G>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000341624
  ensembl transcript: ENST00000353068
  gene symbol: KCNIP2
  hgvsc: ENST00000353068.3:c.74-693G>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000472764
  gene symbol: KCNIP2
  hgvsc: ENST00000472764.1:n.170-693G>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000359063
  ensembl transcript: ENST00000370046
  gene symbol: KCNIP2
  hgvsc: ENST00000370046.1:c.74-693G>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000420040
  ensembl transcript: ENST00000461105
  gene symbol: KCNIP2
  hgvsc: ENST00000461105.1:c.220G>A
  hgvsp: ENSP00000420040.1:p.Ala74Thr
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000344169
  ensembl transcript: ENST00000343195
  gene symbol: KCNIP2
  hgvsc: ENST00000343195.4:c.74-693G>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000355657
  gene symbol: KCNIP2
  hgvsc: ENST00000355657.2:n.572G>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000349055
  ensembl transcript: ENST00000356640
  gene symbol: KCNIP2
  hgvsc: ENST00000356640.2:c.175G>A
  hgvsp: ENSP00000349055.2:p.Ala59Thr
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000239118
  ensembl transcript: ENST00000348850
  gene symbol: KCNIP2
  hgvsc: ENST00000348850.5:c.89-693G>A
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000350733
  ensembl transcript: ENST00000358038
  gene symbol: KCNIP2
  hgvsc: ENST00000358038.3:c.170-693G>A
  variant of: http://identifiers.org/hgnc/15522
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2283
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29810
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14435
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6102
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1061
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Ala74Thr
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: QD

10-103589693-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103589693
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103589693
    reference: chr 10
allele count: 6
allele frequency: 2.820078962210942e-4
allele num: 21276
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000350733
  ensembl transcript: ENST00000358038
  gene symbol: KCNIP2
  hgvsc: ENST00000358038.3:c.170-737G>C
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000472764
  gene symbol: KCNIP2
  hgvsc: ENST00000472764.1:n.170-737G>C
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000239118
  ensembl transcript: ENST00000348850
  gene symbol: KCNIP2
  hgvsc: ENST00000348850.5:c.89-737G>C
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000420040
  ensembl transcript: ENST00000461105
  gene symbol: KCNIP2
  hgvsc: ENST00000461105.1:c.176G>C
  hgvsp: ENSP00000420040.1:p.Arg59Pro
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000349055
  ensembl transcript: ENST00000356640
  gene symbol: KCNIP2
  hgvsc: ENST00000356640.2:c.170-39G>C
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000355657
  gene symbol: KCNIP2
  hgvsc: ENST00000355657.2:n.528G>C
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000239117
  ensembl transcript: ENST00000239117
  gene symbol: KCNIP2
  hgvsc: ENST00000239117.3:c.74-737G>C
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000359063
  ensembl transcript: ENST00000370046
  gene symbol: KCNIP2
  hgvsc: ENST00000370046.1:c.74-737G>C
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000341624
  ensembl transcript: ENST00000353068
  gene symbol: KCNIP2
  hgvsc: ENST00000353068.3:c.74-737G>C
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000411679
  ensembl transcript: ENST00000434163
  gene symbol: KCNIP2
  hgvsc: ENST00000434163.1:c.15+488G>C
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000344169
  ensembl transcript: ENST00000343195
  gene symbol: KCNIP2
  hgvsc: ENST00000343195.4:c.74-737G>C
  variant of: http://identifiers.org/hgnc/15522
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6114
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 33218
  bin: 2.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 7367
  bin: 7.5e0
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1095
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2355
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 735
  bin: 1.25e1
  variant carriers: 1
hgvs: p.Arg59Pro
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: South Asian
population: East Asian
population: African
reference allele: C
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum

10-103589694-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103589694
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103589694
    reference: chr 10
allele count: 0
allele frequency: 0.0e0
allele num: 21302
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000411679
  ensembl transcript: ENST00000434163
  gene symbol: KCNIP2
  hgvsc: ENST00000434163.1:c.15+487C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000420040
  ensembl transcript: ENST00000461105
  gene symbol: KCNIP2
  hgvsc: ENST00000461105.1:c.175C>T
  hgvsp: ENSP00000420040.1:p.Arg59Trp
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000239118
  ensembl transcript: ENST00000348850
  gene symbol: KCNIP2
  hgvsc: ENST00000348850.5:c.89-738C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000344169
  ensembl transcript: ENST00000343195
  gene symbol: KCNIP2
  hgvsc: ENST00000343195.4:c.74-738C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000472764
  gene symbol: KCNIP2
  hgvsc: ENST00000472764.1:n.170-738C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000355657
  gene symbol: KCNIP2
  hgvsc: ENST00000355657.2:n.527C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000341624
  ensembl transcript: ENST00000353068
  gene symbol: KCNIP2
  hgvsc: ENST00000353068.3:c.74-738C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000350733
  ensembl transcript: ENST00000358038
  gene symbol: KCNIP2
  hgvsc: ENST00000358038.3:c.170-738C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000359063
  ensembl transcript: ENST00000370046
  gene symbol: KCNIP2
  hgvsc: ENST00000370046.1:c.74-738C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000239117
  ensembl transcript: ENST00000239117
  gene symbol: KCNIP2
  hgvsc: ENST00000239117.3:c.74-738C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000349055
  ensembl transcript: ENST00000356640
  gene symbol: KCNIP2
  hgvsc: ENST00000356640.2:c.170-40C>T
  variant of: http://identifiers.org/hgnc/15522
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6114
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7291
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2360
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33341
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1097
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 501
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2005
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Arg59Trp
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum

10-103589702-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103589702
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103589702
    reference: chr 10
allele count: 1
allele frequency: 4.746084480303749e-5
allele num: 21070
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000359063
  ensembl transcript: ENST00000370046
  gene symbol: KCNIP2
  hgvsc: ENST00000370046.1:c.74-746C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000239118
  ensembl transcript: ENST00000348850
  gene symbol: KCNIP2
  hgvsc: ENST00000348850.5:c.89-746C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000472764
  gene symbol: KCNIP2
  hgvsc: ENST00000472764.1:n.170-746C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000349055
  ensembl transcript: ENST00000356640
  gene symbol: KCNIP2
  hgvsc: ENST00000356640.2:c.170-48C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000420040
  ensembl transcript: ENST00000461105
  gene symbol: KCNIP2
  hgvsc: ENST00000461105.1:c.170-3C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000239117
  ensembl transcript: ENST00000239117
  gene symbol: KCNIP2
  hgvsc: ENST00000239117.3:c.74-746C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl transcript: ENST00000355657
  gene symbol: KCNIP2
  hgvsc: ENST00000355657.2:n.522-3C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000411679
  ensembl transcript: ENST00000434163
  gene symbol: KCNIP2
  hgvsc: ENST00000434163.1:c.15+479C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000341624
  ensembl transcript: ENST00000353068
  gene symbol: KCNIP2
  hgvsc: ENST00000353068.3:c.74-746C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000344169
  ensembl transcript: ENST00000343195
  gene symbol: KCNIP2
  hgvsc: ENST00000343195.4:c.74-746C>T
  variant of: http://identifiers.org/hgnc/15522
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000120049
  ensembl protein: ENSP00000350733
  ensembl transcript: ENST00000358038
  gene symbol: KCNIP2
  hgvsc: ENST00000358038.3:c.170-746C>T
  variant of: http://identifiers.org/hgnc/15522
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1088
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33580
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6099
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5459
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2369
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2425
  bin: 2.5e0
  variant carriers: 0
hgvs: c.170-3C>T
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Latino
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

GenotypeDepth
all individuals: 2
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 286
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 225
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 7903
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 332
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 343
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 959
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8603
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 177
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1047
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 782
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32040
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2711
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 527
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2122
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 236
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1745
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 73
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 252
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 8.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3778
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.521870817778404e-5
allele num: 28394
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3496
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3600
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4348
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11410
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 484
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.637e0

DP
type: SiteQuality
SIO_000300: 7.08105e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.89e-2

VQSLOD
type: SiteQuality
SIO_000300: -2.275e0

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 4.771e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.36e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 3.33e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

GenotypeDepth
all individuals: 83
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1565
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1291
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2031
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 145
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26754
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16900
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 705
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 30
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7390
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 301
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 223
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 937
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 770
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 92
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 181
bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 5.202372281760483e-5
allele num: 19222
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1820
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10096
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2900
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3006
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 400
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2064
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.45e0

VQSLOD
type: SiteQuality
SIO_000300: 3.76e0

DP
type: SiteQuality
SIO_000300: 5.84884e5

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.794e1

MQRankSum
type: SiteQuality
SIO_000300: 8.51e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.32e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -8.51e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.51e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
all individuals: 9847
bin: 1.25e1
variant carriers: 1

GenotypeQuality
all individuals: 178
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 673
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2418
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1277
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 309
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 957
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25391
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1695
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17819
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 146
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 76
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 105
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 223
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 7135
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 86
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 762
bin: 6.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 386
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 5.410669840926307e-5
allele num: 18482
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2908
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2826
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1688
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1974
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9976
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.37e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.791e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -3.581e-1

DP
type: SiteQuality
SIO_000300: 5.73222e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.48e-2

MQRankSum
type: SiteQuality
SIO_000300: -3.12e-1

QD
type: SiteQuality
SIO_000300: 1.118e1

BaseQRankSum
type: SiteQuality
SIO_000300: 9.350000000000001e-1

GenotypeDepth
all individuals: 56
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 223
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 101
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20981
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 814
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 264
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1055
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1092
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 704
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1961
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 84
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2582
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21754
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 107
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6673
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 132
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 162
bin: 7.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 334
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1464
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2530
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1224
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.055074910318633e-4
allele num: 9478
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15264
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2496
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.929e1

DP
type: SiteQuality
SIO_000300: 5.33313e5

MQRankSum
type: SiteQuality
SIO_000300: -7.95e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.78e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.13e-2

FS
type: SiteQuality
SIO_000300: 3.216e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.61e0

VQSLOD
type: SiteQuality
SIO_000300: -1.558e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.64e-1

QD
type: SiteQuality
SIO_000300: 1.455e1

GenotypeDepth
all individuals: 7
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 98
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 135
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10943
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 2947
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 136
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27283
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3833
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1101
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 335
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 124
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 407
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3309
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 918
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 91
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2996
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 219
bin: 9.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 248
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1530
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8012
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 628
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1592
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 538
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7222
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.36e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -2.318e0

QD
type: SiteQuality
SIO_000300: 1.906e1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.36e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.36e-1

DP
type: SiteQuality
SIO_000300: 3.74696e5

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.36e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.92e-2

GenotypeDepth
all individuals: 4
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 411
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 135
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1116
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11163
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3252
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 94
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2869
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2760
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 220
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 27461
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3802
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 928
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 139
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 143
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 330
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 8.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 630
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 246
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1570
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1514
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7158
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7922
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.017e0

DP
type: SiteQuality
SIO_000300: 3.71826e5

ClippingRankSum
type: SiteQuality
SIO_000300: 1.64e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.95e-2

QD
type: SiteQuality
SIO_000300: 6.67e0

VQSLOD
type: SiteQuality
SIO_000300: -3.347e0

FS
type: SiteQuality
SIO_000300: 3.68e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.638e0

MQRankSum
type: SiteQuality
SIO_000300: 9.22e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
all individuals: 19
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 996
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 221
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 257
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2868
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3266
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 151
bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2323
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 73
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3888
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11274
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 143
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27514
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 147
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 85
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1175
bin: 2.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 232
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 610
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7566
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1522
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 508
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1474
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6792
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.02e0

DP
type: SiteQuality
SIO_000300: 3.60341e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.96e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.02e0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 7.55e0

VQSLOD
type: SiteQuality
SIO_000300: -2.661e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.017e0

GenotypeDepth
all individuals: 3
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 141
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 112
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27616
bin: 7.5e0
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GenotypeQuality
all individuals: 1023
bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 447
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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bin: 9.75e1
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 7.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 490
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 594
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 234
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1458
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1518
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.3430029546065e-4
allele num: 7446
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6690
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.12e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.09e0

QD
type: SiteQuality
SIO_000300: 1.094e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.72e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.96e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.6e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -2.96e-1

FS
type: SiteQuality
SIO_000300: 1.359e0

DP
type: SiteQuality
SIO_000300: 3.56079e5

GenotypeDepth
all individuals: 7
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27990
bin: 7.5e0
variant carriers: 1

GenotypeQuality
all individuals: 133
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 220
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1209
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3721
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2178
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 84
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1027
bin: 3.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7514
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1472
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 504
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 236
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1532
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 604
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6720
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 3.56708e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.79e-2

VQSLOD
type: SiteQuality
SIO_000300: 3.04e0

QD
type: SiteQuality
SIO_000300: 1.044e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
all individuals: 7
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1386
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14806
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 482
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 66
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variant carriers: 0

GenotypeQuality
all individuals: 27653
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 94
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2859
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 139
bin: 4.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1173
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 928
bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6920
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 560
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 470
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1406
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4978
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1510
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 194
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.48e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.73e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.42e0

QD
type: SiteQuality
SIO_000300: 4.8e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.68e-2

DP
type: SiteQuality
SIO_000300: 3.42651e5

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -5.73e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.49e-1

MQ
type: SiteQuality
SIO_000300: 5.79e1

GenotypeQuality
all individuals: 22092
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 120
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
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variant carriers: 0

GenotypeQuality
all individuals: 17
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 26
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GenotypeQuality
all individuals: 8873
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variant carriers: 0

GenotypeQuality
all individuals: 101
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1910
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 158
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3077
bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8632
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66398
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10376
num of homozygotes: 0

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

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

QD
type: SiteQuality
SIO_000300: 1.321e1

DP
type: SiteQuality
SIO_000300: 2.117645e6

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.51e-1

MQ
type: SiteQuality
SIO_000300: 5.916e1

VQSLOD
type: SiteQuality
SIO_000300: 1.41e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.81e0

MQRankSum
type: SiteQuality
SIO_000300: -3.8e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.098e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

GenotypeDepth
all individuals: 3
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1933
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3141
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1055
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 31
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GenotypeQuality
all individuals: 203
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 86
bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7500
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3336
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1728
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1450
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 182
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 674
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 560
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 3.80629e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.83e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.3e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.3e0

VQSLOD
type: SiteQuality
SIO_000300: -1.116e0

FS
type: SiteQuality
SIO_000300: 8.451000000000001e0

BaseQRankSum
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.5e-1

QD
type: SiteQuality
SIO_000300: 9.69e0

GenotypeDepth
all individuals: 73
bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
all individuals: 45
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GenotypeQuality
all individuals: 103
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variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 227
bin: 9.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8254
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1518
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 176
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1840
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 720
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3300
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.34e-2

VQSLOD
type: SiteQuality
SIO_000300: 3.23e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 3.97318e5

QD
type: SiteQuality
SIO_000300: 1.056e1

GenotypeDepth
all individuals: 270
bin: 4.75e1
variant carriers: 9

GenotypeQuality
all individuals: 4500
bin: 2.5e0
variant carriers: 19

GenotypeQuality
all individuals: 429
bin: 9.75e1
variant carriers: 52

GenotypeQuality
all individuals: 2890
bin: 3.75e1
variant carriers: 44

GenotypeQuality
all individuals: 2068
bin: 4.25e1
variant carriers: 32

GenotypeQuality
all individuals: 1337
bin: 7.25e1
variant carriers: 10

GenotypeQuality
all individuals: 2721
bin: 2.75e1
variant carriers: 45

GenotypeQuality
all individuals: 1183
bin: 7.5e0
variant carriers: 19

GenotypeQuality
all individuals: 2600
bin: 4.75e1
variant carriers: 28

GenotypeQuality
all individuals: 194
bin: 9.25e1
variant carriers: 7

GenotypeQuality
all individuals: 1609
bin: 1.75e1
variant carriers: 32

GenotypeQuality
all individuals: 3657
bin: 2.25e1
variant carriers: 30

GenotypeQuality
all individuals: 1300
bin: 7.75e1
variant carriers: 12

GenotypeQuality
all individuals: 1719
bin: 5.75e1
variant carriers: 24

GenotypeQuality
all individuals: 1270
bin: 1.25e1
variant carriers: 30

GenotypeQuality
all individuals: 3090
bin: 3.25e1
variant carriers: 34

GenotypeQuality
all individuals: 4859
bin: 6.75e1
variant carriers: 22

GenotypeQuality
all individuals: 2448
bin: 5.25e1
variant carriers: 26

GenotypeQuality
all individuals: 22065
bin: 6.25e1
variant carriers: 10

GenotypeQuality
all individuals: 209
bin: 8.75e1
variant carriers: 8

GenotypeQuality
all individuals: 550
bin: 8.25e1
variant carriers: 9

South Asian
type: Population
allele count: 9
allele frequency: 7.059930969563853e-4
allele num: 12748
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 39
allele frequency: 7.897934386391251e-3
allele num: 4938
num of homozygotes: 0

Other
type: Population
allele count: 6
allele frequency: 8.403361344537815e-3
allele num: 714
num of homozygotes: 0

African
type: Population
allele count: 62
allele frequency: 7.482500603427468e-3
allele num: 8286
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 172
allele frequency: 2.954818759663288e-3
allele num: 58210
num of homozygotes: 0

Latino
type: Population
allele count: 56
allele frequency: 6.007294571980262e-3
allele num: 9322
num of homozygotes: 0

East Asian
type: Population
allele count: 46
allele frequency: 6.128430588862244e-3
allele num: 7506
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.440496e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.32e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.208e0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.53e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.85e-1

FS
type: SiteQuality
SIO_000300: 4.1346e1

MQ
type: SiteQuality
SIO_000300: 5.916e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.49e-2

VQSLOD
type: SiteQuality
SIO_000300: -9.205e0

QD
type: SiteQuality
SIO_000300: 9.1e-1

GenotypeDepth
all individuals: 5373
bin: 3.25e1
variant carriers: 1

GenotypeQuality
all individuals: 386
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 479
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variant carriers: 2

GenotypeQuality
all individuals: 30529
bin: 6.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 838
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6298
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8486
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.105107902499612e-5
allele num: 64410
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10030
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11378
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 13512
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.732e0

VQSLOD
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SIO_000300: -3.567e0

BaseQRankSum
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SIO_000300: -1.734e0

ClippingRankSum
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SIO_000300: -6.24e-1

FS
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SIO_000300: 0.0e0

MQ
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SIO_000300: 5.863e1

QD
type: SiteQuality
SIO_000300: 7.9e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.47e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.6e-3

DP
type: SiteQuality
SIO_000300: 1.380173e6

GenotypeDepth
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1658
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GenotypeQuality
all individuals: 191
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variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11410
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64620
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8528
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.323861139592794e-5
allele num: 13654
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6380
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10072
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -3.255e-1

QD
type: SiteQuality
SIO_000300: 7.9e0

MQRankSum
type: SiteQuality
SIO_000300: 2.62e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.61e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.179e0

FS
type: SiteQuality
SIO_000300: 4.961e0

DP
type: SiteQuality
SIO_000300: 1.386522e6

ClippingRankSum
type: SiteQuality
SIO_000300: -4.31e-1

MQ
type: SiteQuality
SIO_000300: 5.928e1

GenotypeDepth
all individuals: 6
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variant carriers: 0

GenotypeQuality
all individuals: 307
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variant carriers: 0

GenotypeQuality
all individuals: 2431
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GenotypeQuality
all individuals: 1625
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 33365
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GenotypeQuality
all individuals: 1423
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1194
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 474
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variant carriers: 2

GenotypeQuality
all individuals: 203
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variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13682
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11400
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 846
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 1.988466892026248e-4
allele num: 10058
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8524
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64650
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6372
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.29e0

QD
type: SiteQuality
SIO_000300: 6.87e0

FS
type: SiteQuality
SIO_000300: 1.274e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 8.76e-1

DP
type: SiteQuality
SIO_000300: 1.390092e6

ClippingRankSum
type: SiteQuality
SIO_000300: -4.33e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.17e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.336e0

GenotypeDepth
all individuals: 8
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variant carriers: 0

GenotypeQuality
all individuals: 199
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variant carriers: 0

GenotypeQuality
all individuals: 230
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variant carriers: 0

GenotypeQuality
all individuals: 1519
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GenotypeQuality
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GenotypeQuality
all individuals: 257
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GenotypeQuality
all individuals: 34514
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GenotypeQuality
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GenotypeQuality
all individuals: 2702
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GenotypeQuality
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GenotypeQuality
all individuals: 1386
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 3999
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 6136
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GenotypeQuality
all individuals: 1355
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GenotypeQuality
all individuals: 177
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GenotypeQuality
all individuals: 1080
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variant carriers: 0

GenotypeQuality
all individuals: 469
bin: 9.75e1
variant carriers: 1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11422
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6374
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.2811999417504e-5
allele num: 13734
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10106
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64724
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8542
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.01e0

QD
type: SiteQuality
SIO_000300: 1.089e1

DP
type: SiteQuality
SIO_000300: 1.404909e6

FS
type: SiteQuality
SIO_000300: 1.967e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.96e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.95e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -7.487e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.77e-1

MQ
type: SiteQuality
SIO_000300: 5.879e1

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 676
bin: 5.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10118
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8556
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11410
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 850
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6396
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.634063455775588e-5
allele num: 64738
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 7.82e-1

InbreedingCoeff
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BaseQRankSum
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FS
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SIO_000300: 1.928e0

ClippingRankSum
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SIO_000300: 4.5e-1

QD
type: SiteQuality
SIO_000300: 9.960000000000001e0

MQRankSum
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SIO_000300: 3.1e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.413787e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.15e-1

GenotypeDepth
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variant carriers: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 844
num of homozygotes: 0

African
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: 1.545499505440158e-5
allele num: 64704
num of homozygotes: 0

South Asian
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Latino
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allele frequency: 0.0e0
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European (Finnish)
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East Asian
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MQ
type: SiteQuality
SIO_000300: 5.88e1

ReadPosRankSum
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BaseQRankSum
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VQSLOD
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FS
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ClippingRankSum
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InbreedingCoeff
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QD
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MQRankSum
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DP
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1375
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GenotypeQuality
all individuals: 214
bin: 5.75e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 9.856100926473487e-5
allele num: 10146
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11444
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 856
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13876
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 64960
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8580
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6432
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 6.94e0

MQRankSum
type: SiteQuality
SIO_000300: 8.49e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.597e0

MQ
type: SiteQuality
SIO_000300: 5.931e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.43e-1

FS
type: SiteQuality
SIO_000300: 4.349e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -6.43e-1

VQSLOD
type: SiteQuality
SIO_000300: -7.144e-1

DP
type: SiteQuality
SIO_000300: 1.432661e6

GenotypeDepth
all individuals: 8
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 495
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 2.5e0
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GenotypeQuality
all individuals: 125
bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1386
bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
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: 9.25e1
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1779
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 471
bin: 9.75e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65042
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 856
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.828975820719482e-5
allele num: 10174
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11450
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6468
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8588
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13936
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 1.01e0

BaseQRankSum
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SIO_000300: -7.07e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.49e-1

FS
type: SiteQuality
SIO_000300: 9.65e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.58e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.53e-1

DP
type: SiteQuality
SIO_000300: 1.445156e6

QD
type: SiteQuality
SIO_000300: 1.277e1

GenotypeDepth
all individuals: 8
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 171
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variant carriers: 0

GenotypeQuality
all individuals: 6258
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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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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bin: 2.75e1
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GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 1.75e1
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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: 6.25e1
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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: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1312
bin: 7.75e1
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GenotypeQuality
all individuals: 677
bin: 5.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 850
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10154
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8584
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64968
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.174630506528914e-5
allele num: 13938
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11430
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6420
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.891e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.4e-3

DP
type: SiteQuality
SIO_000300: 1.449613e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.7e0

MQRankSum
type: SiteQuality
SIO_000300: -8.799999999999999e-2

VQSLOD
type: SiteQuality
SIO_000300: -1.847e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.1e-2

FS
type: SiteQuality
SIO_000300: 7.07e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.57e-1

QD
type: SiteQuality
SIO_000300: 9.82e0

GenotypeDepth
all individuals: 83
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 584
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 147
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1704
bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1249
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 200
bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 171
bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13938
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8584
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11430
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6420
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10154
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.539219307966999e-5
allele num: 64968
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 850
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.449613e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.4e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 1.7e0

QD
type: SiteQuality
SIO_000300: 9.82e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.57e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.847e-1

MQ
type: SiteQuality
SIO_000300: 5.891e1

FS
type: SiteQuality
SIO_000300: 7.07e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.1e-2

MQRankSum
type: SiteQuality
SIO_000300: -8.799999999999999e-2

GenotypeDepth
all individuals: 11
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42738
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 695
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1640
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 15
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variant carriers: 0

GenotypeQuality
all individuals: 174
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 254
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1381
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6703
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variant carriers: 0

GenotypeQuality
all individuals: 267
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 190
bin: 8.75e1
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GenotypeQuality
all individuals: 1073
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2781
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 533
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 456
bin: 9.75e1
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GenotypeQuality
all individuals: 239
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 229
bin: 5.75e1
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GenotypeQuality
all individuals: 1134
bin: 3.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10230
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11464
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.530081400330498e-5
allele num: 65356
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8610
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6526
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 860
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14226
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 8.313000000000001e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 9.119999999999999e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.083e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 3.2e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.711e0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.4e-1

DP
type: SiteQuality
SIO_000300: 1.469793e6

VQSLOD
type: SiteQuality
SIO_000300: -9.486e-1

GenotypeDepth
all individuals: 11
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
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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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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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GenotypeQuality
all individuals: 40
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 457
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 42
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1401
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6753
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 187
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11480
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10242
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6542
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14304
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65444
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 860
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.831e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.570000000000001e-1

FS
type: SiteQuality
SIO_000300: 3.41e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 6.53e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.07e-1

DP
type: SiteQuality
SIO_000300: 1.476022e6

VQSLOD
type: SiteQuality
SIO_000300: -9.985000000000001e-1

MQ
type: SiteQuality
SIO_000300: 5.558e1

QD
type: SiteQuality
SIO_000300: 1.26e1

GenotypeDepth
all individuals: 6
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2529
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

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
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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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bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 182
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 175
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1645
bin: 7.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11486
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6546
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14316
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.583511581005928e-5
allele num: 65452
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10242
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 860
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.974e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -1.642e0

VQSLOD
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DP
type: SiteQuality
SIO_000300: 1.479466e6

MQRankSum
type: SiteQuality
SIO_000300: -1.89e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.28e-1

FS
type: SiteQuality
SIO_000300: 1.6107e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.16e-1

QD
type: SiteQuality
SIO_000300: 1.281e1

GenotypeDepth
all individuals: 3
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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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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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variant carriers: 0

GenotypeQuality
all individuals: 1662
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variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 216
bin: 4.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10266
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.527090587013621e-5
allele num: 65484
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11494
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14338
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6550
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 858
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.48505e6

ReadPosRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 1.02e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -1.552e0

QD
type: SiteQuality
SIO_000300: 6.53e0

FS
type: SiteQuality
SIO_000300: 4.374e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -5.1e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.422e0

GenotypeDepth
all individuals: 80
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variant carriers: 0

GenotypeQuality
all individuals: 266
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
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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
all individuals: 1705
bin: 7.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
all individuals: 181
bin: 9.25e1
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
all individuals: 1438
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variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 559
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 187
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66082
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.499415052645263e-5
allele num: 15386
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: 10352
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8642
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11536
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.62e0

MQRankSum
type: SiteQuality
SIO_000300: 2.1e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.3e-3

FS
type: SiteQuality
SIO_000300: 3.066e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
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SIO_000300: 1.08e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.27e-1

DP
type: SiteQuality
SIO_000300: 1.520605e6

VQSLOD
type: SiteQuality
SIO_000300: -4.73e-1

QD
type: SiteQuality
SIO_000300: 1.354e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
all individuals: 6
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variant carriers: 0

GenotypeDepth
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GenotypeQuality
all individuals: 1442
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 1713
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7094
bin: 6.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6576
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11544
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.650646593321752e-5
allele num: 10362
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.508978421608571e-5
allele num: 66270
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15730
num of homozygotes: 0

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.7e-3

QD
type: SiteQuality
SIO_000300: 1.624e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.74e-1

FS
type: SiteQuality
SIO_000300: 4.766e0

DP
type: SiteQuality
SIO_000300: 1.529878e6

VQSLOD
type: SiteQuality
SIO_000300: 8.83e-1

MQ
type: SiteQuality
SIO_000300: 5.974e1

MQRankSum
type: SiteQuality
SIO_000300: -3.3e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.04e0

BaseQRankSum
type: SiteQuality
SIO_000300: -9.77e-1

GenotypeDepth
all individuals: 3
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variant carriers: 0

GenotypeDepth
all individuals: 136
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variant carriers: 0

GenotypeDepth
all individuals: 27
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variant carriers: 2

GenotypeQuality
all individuals: 27
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variant carriers: 0

GenotypeQuality
all individuals: 0
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variant carriers: 0

GenotypeQuality
all individuals: 81
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variant carriers: 0

GenotypeQuality
all individuals: 42
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variant carriers: 0

GenotypeQuality
all individuals: 74
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 51
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GenotypeQuality
all individuals: 543
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GenotypeQuality
all individuals: 1734
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GenotypeQuality
all individuals: 7178
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variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.006614552014432e-5
allele num: 66520
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16322
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11550
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10390
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8646
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 9.29e-1

MQ
type: SiteQuality
SIO_000300: 5.972e1

FS
type: SiteQuality
SIO_000300: 6.28e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.21e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.71e0

QD
type: SiteQuality
SIO_000300: 1.225e1

MQRankSum
type: SiteQuality
SIO_000300: 1.8e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 1.544793e6

BaseQRankSum
type: SiteQuality
SIO_000300: 9.1e-2

GenotypeDepth
all individuals: 9
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variant carriers: 1

GenotypeDepth
all individuals: 11
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variant carriers: 0

GenotypeDepth
all individuals: 5831
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variant carriers: 3

GenotypeQuality
all individuals: 0
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 480
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variant carriers: 32

GenotypeQuality
all individuals: 43
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variant carriers: 0

GenotypeQuality
all individuals: 45
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 76
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GenotypeQuality
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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: 28
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variant carriers: 0

GenotypeQuality
all individuals: 3
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variant carriers: 0

GenotypeQuality
all individuals: 541
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variant carriers: 0

GenotypeQuality
all individuals: 1719
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 173
bin: 9.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6568
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11552
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66546
num of homozygotes: 0

East Asian
type: Population
allele count: 30
allele frequency: 3.469812630117973e-3
allele num: 8646
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10386
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.219660934260276e-4
allele num: 16398
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 3.84e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 3.4e-1

MQ
type: SiteQuality
SIO_000300: 5.963e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.36e-1

FS
type: SiteQuality
SIO_000300: 5.2e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.7e-1

QD
type: SiteQuality
SIO_000300: 1.184e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.325e0

DP
type: SiteQuality
SIO_000300: 1.547313e6

GenotypeDepth
all individuals: 26784
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variant carriers: 0

GenotypeDepth
all individuals: 6
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variant carriers: 0

GenotypeDepth
all individuals: 11
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variant carriers: 0

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
all individuals: 3
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GenotypeQuality
all individuals: 104
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

GenotypeQuality
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GenotypeQuality
all individuals: 281
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GenotypeQuality
all individuals: 450
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GenotypeQuality
all individuals: 7163
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variant carriers: 0

GenotypeQuality
all individuals: 59
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GenotypeQuality
all individuals: 183
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variant carriers: 0

GenotypeQuality
all individuals: 541
bin: 8.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66546
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10386
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11552
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.156871818602499e-4
allele num: 8644
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6570
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.117e0

ClippingRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.943e1

BaseQRankSum
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VQSLOD
type: SiteQuality
SIO_000300: 2.59e-1

MQRankSum
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SIO_000300: 1.16e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.45e-1

DP
type: SiteQuality
SIO_000300: 1.547141e6

QD
type: SiteQuality
SIO_000300: 1.252e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

GenotypeDepth
all individuals: 141
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variant carriers: 8

GenotypeDepth
all individuals: 9
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variant carriers: 1

GenotypeDepth
all individuals: 5840
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variant carriers: 2

GenotypeQuality
all individuals: 65
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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
all individuals: 89
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 59
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GenotypeQuality
all individuals: 28
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GenotypeQuality
all individuals: 498
bin: 9.75e1
variant carriers: 70

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.523461304082876e-4
allele num: 6564
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 9.628345850182938e-5
allele num: 10386
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16442
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 64
allele frequency: 9.616251464975809e-4
allele num: 66554
num of homozygotes: 0

Latino
type: Population
allele count: 4
allele frequency: 3.462004500605851e-4
allele num: 11554
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.2e1

MQRankSum
type: SiteQuality
SIO_000300: 4.2e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 5.16e0

DP
type: SiteQuality
SIO_000300: 1.549322e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.21e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.72e-1

MQ
type: SiteQuality
SIO_000300: 5.963e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.27e-1

GenotypeDepth
all individuals: 2
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variant carriers: 0

GenotypeDepth
all individuals: 6
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variant carriers: 0

GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 291
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GenotypeQuality
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GenotypeQuality
all individuals: 66
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GenotypeQuality
all individuals: 46
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GenotypeQuality
all individuals: 56
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GenotypeQuality
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GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 63
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variant carriers: 0

GenotypeQuality
all individuals: 170
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variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.502358703163967e-5
allele num: 66562
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16452
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6560
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8642
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11552
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 902
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DP
type: SiteQuality
SIO_000300: 1.54705e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -1.75e-1

BaseQRankSum
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InbreedingCoeff
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FS
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VQSLOD
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ClippingRankSum
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SIO_000300: -2.464e0

ReadPosRankSum
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SIO_000300: 2.59e0

QD
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SIO_000300: 1.491e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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bin: 1.75e1
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6544
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66530
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

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

Latino
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allele count: 1
allele frequency: 8.661008141347653e-5
allele num: 11546
num of homozygotes: 0

InbreedingCoeff
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SIO_000300: -1.0e-4

MQ
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SIO_000300: 5.871e1

ReadPosRankSum
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SIO_000300: 2.46e0

BaseQRankSum
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SIO_000300: -3.685e0

FS
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SIO_000300: 5.608e0

DP
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MQRankSum
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SIO_000300: -5.2e-2

VQSLOD
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SIO_000300: -1.997e0

ClippingRankSum
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SIO_000300: -1.955e0

QD
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SIO_000300: 1.293e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 0
allele frequency: 0.0e0
allele num: 16414
num of homozygotes: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6518
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66436
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8630
num of homozygotes: 0

African
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allele count: 2
allele frequency: 1.934610176049526e-4
allele num: 10338
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.77e0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.02e-1

MQRankSum
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VQSLOD
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DP
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SIO_000300: 1.542487e6

QD
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SIO_000300: 1.099e1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
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SIO_000300: 1.69e0

InbreedingCoeff
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SIO_000300: -2.0e-4

MQ
type: SiteQuality
SIO_000300: 5.953e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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variant carriers: 7

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 0
allele frequency: 0.0e0
allele num: 16396
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11522
num of homozygotes: 0

East Asian
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allele count: 7
allele frequency: 8.116883116883117e-4
allele num: 8624
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66410
num of homozygotes: 0

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

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

Other
type: Population
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allele frequency: 0.0e0
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VQSLOD
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SIO_000300: 1.54e0

InbreedingCoeff
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SIO_000300: -2.0e-4

FS
type: SiteQuality
SIO_000300: 6.25e0

BaseQRankSum
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DP
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SIO_000300: 1.541017e6

MQRankSum
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SIO_000300: 2.1e-1

ClippingRankSum
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SIO_000300: -8.599999999999999e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.79e-1

MQ
type: SiteQuality
SIO_000300: 5.958e1

QD
type: SiteQuality
SIO_000300: 1.239e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8624
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66380
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16382
num of homozygotes: 0

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

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

Other
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allele count: 0
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num of homozygotes: 0

BaseQRankSum
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SIO_000300: -5.48e-1

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

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.507113576079093e-5
allele num: 66352
num of homozygotes: 0

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

European (Finnish)
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allele frequency: 0.0e0
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Latino
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South Asian
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ClippingRankSum
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FS
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BaseQRankSum
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MQ
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MQRankSum
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ReadPosRankSum
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VQSLOD
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InbreedingCoeff
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DP
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QD
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele count: 0
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allele num: 66246
num of homozygotes: 0

European (Finnish)
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Latino
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East Asian
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South Asian
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African
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Other
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MQ
type: SiteQuality
SIO_000300: 6.0e1

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

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

Other
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East Asian
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European (Finnish)
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Latino
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South Asian
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African
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MQ
type: SiteQuality
SIO_000300: 5.919e1

QD
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InbreedingCoeff
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ReadPosRankSum
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FS
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VQSLOD
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ClippingRankSum
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DP
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SIO_000300: 1.508432e6

MQRankSum
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BaseQRankSum
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SIO_000300: -2.746e0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11428
num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 1.523554147114388e-5
allele num: 65636
num of homozygotes: 0

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

East Asian
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allele frequency: 0.0e0
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DP
type: SiteQuality
SIO_000300: 1.505399e6

VQSLOD
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MQRankSum
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InbreedingCoeff
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BaseQRankSum
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MQ
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FS
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SIO_000300: 0.0e0

ReadPosRankSum
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SIO_000300: 9.2e-2

QD
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ClippingRankSum
type: SiteQuality
SIO_000300: 1.8e-2

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

European (Non-Finnish)
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allele frequency: 3.122073056509522e-5
allele num: 64060
num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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South Asian
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East Asian
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ReadPosRankSum
type: SiteQuality
SIO_000300: 8.79e-1

DP
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MQRankSum
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BaseQRankSum
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MQ
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FS
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InbreedingCoeff
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SIO_000300: -7.0e-4

VQSLOD
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ClippingRankSum
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SIO_000300: -1.234e0

QD
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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allele frequency: 0.0e0
allele num: 834
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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East Asian
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African
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allele num: 9802
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Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 0.0e0
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ReadPosRankSum
type: SiteQuality
SIO_000300: 9.98e-1

MQRankSum
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DP
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BaseQRankSum
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MQ
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VQSLOD
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QD
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InbreedingCoeff
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SIO_000300: -7.0e-4

FS
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ClippingRankSum
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SIO_000300: -5.79e-1

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8024
num of homozygotes: 0

Latino
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Other
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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 num: 60234
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European (Finnish)
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South Asian
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MQ
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SIO_000300: 5.834e1

QD
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InbreedingCoeff
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BaseQRankSum
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VQSLOD
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DP
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MQRankSum
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FS
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ClippingRankSum
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ReadPosRankSum
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GenotypeDepth
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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GenotypeQuality
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GenotypeQuality
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East Asian
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num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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Latino
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African
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allele frequency: 0.0e0
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European (Finnish)
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Other
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European (Non-Finnish)
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allele num: 59272
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BaseQRankSum
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DP
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QD
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ClippingRankSum
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MQRankSum
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InbreedingCoeff
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VQSLOD
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MQ
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ReadPosRankSum
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FS
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.25e1
variant carriers: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5312
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 10578
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 1.68713726548792e-5
allele num: 59272
num of homozygotes: 0

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

African
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allele count: 2
allele frequency: 2.2237046920169e-4
allele num: 8994
num of homozygotes: 0

South Asian
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num of homozygotes: 0

East Asian
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Other
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European (Non-Finnish)
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European (Finnish)
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Latino
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ReadPosRankSum
type: SiteQuality
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DP
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MQRankSum
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MQ
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InbreedingCoeff
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ClippingRankSum
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FS
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BaseQRankSum
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QD
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VQSLOD
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SIO_000300: 1.13e0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 58772
num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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allele num: 12010
num of homozygotes: 0

Other
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num of homozygotes: 0

Latino
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East Asian
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num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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MQ
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SIO_000300: 5.938e1

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

European (Non-Finnish)
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allele frequency: 1.764539808018069e-5
allele num: 56672
num of homozygotes: 0

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

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

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

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

East Asian
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allele frequency: 0.0e0
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Latino
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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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Other
type: Population
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 5.613562366677894e-5
allele num: 53442
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
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SIO_000300: 8.99333e5

VQSLOD
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BaseQRankSum
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FS
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QD
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ReadPosRankSum
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ClippingRankSum
type: SiteQuality
SIO_000300: -9.3e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.1e-3

MQRankSum
type: SiteQuality
SIO_000300: 4.23e-1

GenotypeDepth
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variant carriers: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 8114
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 53264
num of homozygotes: 0

East Asian
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num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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Latino
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Other
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MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
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ReadPosRankSum
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ClippingRankSum
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VQSLOD
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FS
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DP
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BaseQRankSum
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MQRankSum
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InbreedingCoeff
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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European (Finnish)
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allele frequency: 0.0e0
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European (Non-Finnish)
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East Asian
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South Asian
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allele num: 5646
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African
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Latino
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DP
type: SiteQuality
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BaseQRankSum
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FS
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MQRankSum
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MQ
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QD
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InbreedingCoeff
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VQSLOD
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ClippingRankSum
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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African
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East Asian
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allele frequency: 2.061855670103093e-2
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Other
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European (Finnish)
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European (Non-Finnish)
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allele frequency: 0.0e0
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South Asian
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allele frequency: 1.345895020188425e-3
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InbreedingCoeff
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QD
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VQSLOD
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BaseQRankSum
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ClippingRankSum
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FS
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MQ
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DP
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MQRankSum
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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East Asian
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European (Finnish)
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Other
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European (Non-Finnish)
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Latino
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South Asian
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allele num: 6688
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MQ
type: SiteQuality
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QD
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ClippingRankSum
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DP
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MQRankSum
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InbreedingCoeff
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BaseQRankSum
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VQSLOD
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ReadPosRankSum
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FS
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 (Non-Finnish)
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African
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allele frequency: 0.0e0
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Other
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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South Asian
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QD
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MQ
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VQSLOD
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FS
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ReadPosRankSum
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MQRankSum
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InbreedingCoeff
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BaseQRankSum
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SIO_000300: -2.359e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.05e-1

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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GenotypeQuality
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Other
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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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Latino
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allele frequency: 0.0e0
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African
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European (Finnish)
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allele frequency: 0.0e0
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South Asian
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allele frequency: 1.478892175315945e-3
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European (Non-Finnish)
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FS
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QD
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ReadPosRankSum
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MQRankSum
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VQSLOD
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BaseQRankSum
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MQ
type: SiteQuality
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InbreedingCoeff
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ClippingRankSum
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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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GenotypeQuality
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Latino
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allele frequency: 0.0e0
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Other
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num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 1.710571330824495e-4
allele num: 5846
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East Asian
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European (Finnish)
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allele frequency: 0.0e0
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South Asian
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African
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InbreedingCoeff
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BaseQRankSum
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DP
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MQ
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ReadPosRankSum
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MQRankSum
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ClippingRankSum
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FS
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QD
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

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

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.621e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
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FS
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SIO_000300: 7.768e0

MQRankSum
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ClippingRankSum
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DP
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BaseQRankSum
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InbreedingCoeff
type: SiteQuality
SIO_000300: -6.98e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.495e0

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

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

East Asian
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allele frequency: 0.0e0
allele num: 640
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Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele frequency: 0.0e0
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Other
type: Population
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South Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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DP
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SIO_000300: 3.92455e5

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

European (Finnish)
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Other
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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 num: 8656
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East Asian
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South Asian
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QD
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VQSLOD
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FS
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MQRankSum
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ReadPosRankSum
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DP
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ClippingRankSum
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MQ
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InbreedingCoeff
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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European (Non-Finnish)
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African
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European (Finnish)
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Other
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Latino
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East Asian
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MQRankSum
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MQ
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VQSLOD
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ClippingRankSum
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FS
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InbreedingCoeff
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ReadPosRankSum
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DP
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QD
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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num of homozygotes: 0

European (Finnish)
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East Asian
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Latino
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South Asian
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European (Non-Finnish)
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Other
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InbreedingCoeff
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BaseQRankSum
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VQSLOD
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MQ
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FS
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ClippingRankSum
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ReadPosRankSum
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MQRankSum
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DP
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SIO_000300: 4.23478e5

QD
type: SiteQuality
SIO_000300: 7.01e0

GenotypeQuality
all individuals: 1569
bin: 6.75e1
variant carriers: 2

GenotypeQuality
all individuals: 191
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 5350
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 210
bin: 8.75e1
variant carriers: 2

GenotypeQuality
all individuals: 31697
bin: 7.5e0
variant carriers: 1

GenotypeQuality
all individuals: 2212
bin: 2.5e0
variant carriers: 1

GenotypeQuality
all individuals: 666
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 86
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 74
bin: 3.25e1
variant carriers: 2

GenotypeQuality
all individuals: 972
bin: 1.75e1
variant carriers: 2

GenotypeQuality
all individuals: 18
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 717
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 29
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 440
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 5977
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 272
bin: 9.75e1
variant carriers: 7

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 406
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 58
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9114
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 198
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.261988894497728e-4
allele num: 7924
num of homozygotes: 0

East Asian
type: Population
allele count: 5
allele frequency: 6.756756756756757e-3
allele num: 740
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2836
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 7.73e-1

FS
type: SiteQuality
SIO_000300: 2.522e0

DP
type: SiteQuality
SIO_000300: 3.88603e5

QD
type: SiteQuality
SIO_000300: 1.01e1

MQRankSum
type: SiteQuality
SIO_000300: 3.58e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.73e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.000000000000001e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 7.27e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.48e-1

GenotypeQuality
all individuals: 441
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1568
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 267
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 666
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 705
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5494
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 828
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5994
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 86
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31966
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 12
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 716
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 190
bin: 9.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2844
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 60
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 416
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9106
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7930
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 750
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 196
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.02e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.38e0

VQSLOD
type: SiteQuality
SIO_000300: -8.823e-1

QD
type: SiteQuality
SIO_000300: 8.77e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 4.21e-1

DP
type: SiteQuality
SIO_000300: 3.88281e5

ClippingRankSum
type: SiteQuality
SIO_000300: -9.22e-1

GenotypeQuality
all individuals: 21
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5981
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 190
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 686
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 617
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 665
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 74
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3749
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 76
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 54
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 713
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31831
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 441
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 266
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1564
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 4.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 196
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2838
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 46
num of homozygotes: 0

South 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: 8958
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 700
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 2.403846153846154e-3
allele num: 416
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.3e-2

FS
type: SiteQuality
SIO_000300: 3.31e0

VQSLOD
type: SiteQuality
SIO_000300: -9.821e-1

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 9.710000000000001e0

DP
type: SiteQuality
SIO_000300: 3.74253e5

BaseQRankSum
type: SiteQuality
SIO_000300: -2.383e0

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.65e-1