7-107800791-ATCTT-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107800791
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 107800787
    reference: chr 7
allele count: 2
allele frequency: 1.658017342861406e-5
allele num: 120626
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000325269
  ensembl transcript: ENST00000351718
  gene symbol: NRCAM
  hgvsc: ENST00000351718.4:c.3235+11_3235+14delAAGA
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368308
  ensembl transcript: ENST00000379022
  gene symbol: NRCAM
  hgvsc: ENST00000379022.4:c.3598+11_3598+14delAAGA
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl transcript: ENST00000465585
  gene symbol: NRCAM
  hgvsc: ENST00000465585.1:n.434+11_434+14delAAGA
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl transcript: ENST00000415105
  gene symbol: NRCAM
  hgvsc: ENST00000415105.1:n.376+11_376+14delAAGA
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000407858
  ensembl transcript: ENST00000413765
  gene symbol: NRCAM
  hgvsc: ENST00000413765.2:c.3226+11_3226+14delAAGA
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000398174
  ensembl transcript: ENST00000445634
  gene symbol: NRCAM
  hgvsc: ENST00000445634.2:c.294+11_294+14delAAGA
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368314
  ensembl transcript: ENST00000379028
  gene symbol: NRCAM
  hgvsc: ENST00000379028.3:c.3598+11_3598+14delAAGA
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368310
  ensembl transcript: ENST00000379024
  gene symbol: NRCAM
  hgvsc: ENST00000379024.4:c.3262+11_3262+14delAAGA
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000401244
  ensembl transcript: ENST00000425651
  gene symbol: NRCAM
  hgvsc: ENST00000425651.2:c.3598+11_3598+14delAAGA
  variant of: http://identifiers.org/hgnc/7994
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6980
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5821
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12516
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3477
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14371
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2171
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8901
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1028
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1494
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 625
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 961
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 122
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7182
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: ATCTT
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ

http://identifiers.org/exac.variant/7-107800804-ACC-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107800804
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 107800802
    reference: chr 7
allele count: 1
allele frequency: 8.270751315049459e-6
allele num: 120908
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: coding_sequence_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368310
  ensembl transcript: ENST00000379024
  gene symbol: NRCAM
  hgvsc: ENST00000379024.4:c.3262_3262+1delGG
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: coding_sequence_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000401244
  ensembl transcript: ENST00000425651
  gene symbol: NRCAM
  hgvsc: ENST00000425651.2:c.3598_3598+1delGG
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: coding_sequence_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368308
  ensembl transcript: ENST00000379022
  gene symbol: NRCAM
  hgvsc: ENST00000379022.4:c.3598_3598+1delGG
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000091129
  ensembl transcript: ENST00000415105
  gene symbol: NRCAM
  hgvsc: ENST00000415105.1:n.376_376+1delGG
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: coding_sequence_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000398174
  ensembl transcript: ENST00000445634
  gene symbol: NRCAM
  hgvsc: ENST00000445634.2:c.294_294+1delGG
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: coding_sequence_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000325269
  ensembl transcript: ENST00000351718
  gene symbol: NRCAM
  hgvsc: ENST00000351718.4:c.3235_3235+1delGG
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: coding_sequence_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000407858
  ensembl transcript: ENST00000413765
  gene symbol: NRCAM
  hgvsc: ENST00000413765.2:c.3226_3226+1delGG
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: true
  consequence: splice_donor_variant
  consequence: coding_sequence_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368314
  ensembl transcript: ENST00000379028
  gene symbol: NRCAM
  hgvsc: ENST00000379028.3:c.3598_3598+1delGG
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000091129
  ensembl transcript: ENST00000465585
  gene symbol: NRCAM
  hgvsc: ENST00000465585.1:n.434_434+1delGG
  variant of: http://identifiers.org/hgnc/7994
canonical: true
consequence: splice donor
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 1494
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12556
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14485
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1028
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7152
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3478
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 961
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5821
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 625
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2171
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8904
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4622
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 287
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 5.25e1
  variant carriers: 0
hgvs: c.3598_3598+1delGG
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: ACC
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff

7-107800806-C-CAGGG
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107800806
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 107800810
    reference: chr 7
allele count: 1
allele frequency: 8.26801600687899e-6
allele num: 120948
alternate allele: CAGGG
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000091129
  ensembl transcript: ENST00000415105
  gene symbol: NRCAM
  hgvsc: ENST00000415105.1:n.375_376insCCCT
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368308
  ensembl transcript: ENST00000379022
  gene symbol: NRCAM
  hgvsc: ENST00000379022.4:c.3597_3598insCCCT
  hgvsp: ENSP00000368308.4:p.Val1200ProfsTer3
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000398174
  ensembl transcript: ENST00000445634
  gene symbol: NRCAM
  hgvsc: ENST00000445634.2:c.293_294insCCCT
  hgvsp: ENSP00000398174.2:p.Val99ProfsTer3
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000325269
  ensembl transcript: ENST00000351718
  gene symbol: NRCAM
  hgvsc: ENST00000351718.4:c.3234_3235insCCCT
  hgvsp: ENSP00000325269.6:p.Val1079ProfsTer3
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000091129
  ensembl transcript: ENST00000465585
  gene symbol: NRCAM
  hgvsc: ENST00000465585.1:n.433_434insCCCT
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000401244
  ensembl transcript: ENST00000425651
  gene symbol: NRCAM
  hgvsc: ENST00000425651.2:c.3597_3598insCCCT
  hgvsp: ENSP00000401244.2:p.Val1200ProfsTer3
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368314
  ensembl transcript: ENST00000379028
  gene symbol: NRCAM
  hgvsc: ENST00000379028.3:c.3597_3598insCCCT
  hgvsp: ENSP00000368314.3:p.Val1200ProfsTer3
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368310
  ensembl transcript: ENST00000379024
  gene symbol: NRCAM
  hgvsc: ENST00000379024.4:c.3261_3262insCCCT
  hgvsp: ENSP00000368310.4:p.Val1088ProfsTer3
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000407858
  ensembl transcript: ENST00000413765
  gene symbol: NRCAM
  hgvsc: ENST00000413765.2:c.3225_3226insCCCT
  hgvsp: ENSP00000407858.2:p.Val1076ProfsTer3
  variant of: http://identifiers.org/hgnc/7994
canonical: true
consequence: frameshift
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1028
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3478
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 961
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7173
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5821
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2171
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8905
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14510
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12559
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1494
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 625
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Val1200ProfsTer3
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: MQ

7-107800816-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107800816
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 107800816
    reference: chr 7
allele count: 1
allele frequency: 8.259275166011431e-6
allele num: 121076
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368310
  ensembl transcript: ENST00000379024
  gene symbol: NRCAM
  hgvsc: ENST00000379024.4:c.3252T>C
  hgvsp: ENST00000379024.4:c.3252T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368314
  ensembl transcript: ENST00000379028
  gene symbol: NRCAM
  hgvsc: ENST00000379028.3:c.3588T>C
  hgvsp: ENST00000379028.3:c.3588T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000407858
  ensembl transcript: ENST00000413765
  gene symbol: NRCAM
  hgvsc: ENST00000413765.2:c.3216T>C
  hgvsp: ENST00000413765.2:c.3216T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000325269
  ensembl transcript: ENST00000351718
  gene symbol: NRCAM
  hgvsc: ENST00000351718.4:c.3225T>C
  hgvsp: ENST00000351718.4:c.3225T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368308
  ensembl transcript: ENST00000379022
  gene symbol: NRCAM
  hgvsc: ENST00000379022.4:c.3588T>C
  hgvsp: ENST00000379022.4:c.3588T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000401244
  ensembl transcript: ENST00000425651
  gene symbol: NRCAM
  hgvsc: ENST00000425651.2:c.3588T>C
  hgvsp: ENST00000425651.2:c.3588T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000091129
  ensembl transcript: ENST00000465585
  gene symbol: NRCAM
  hgvsc: ENST00000465585.1:n.424T>C
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000398174
  ensembl transcript: ENST00000445634
  gene symbol: NRCAM
  hgvsc: ENST00000445634.2:c.284T>C
  hgvsp: ENST00000445634.2:c.284T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000091129
  ensembl transcript: ENST00000415105
  gene symbol: NRCAM
  hgvsc: ENST00000415105.1:n.366T>C
  variant of: http://identifiers.org/hgnc/7994
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12572
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1027
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7174
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14570
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 625
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8908
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5823
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3477
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2171
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 961
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1495
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17506
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Gly1196Gly
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Other
population: Latino
population: African
reference allele: A
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ

7-107800819-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107800819
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 107800819
    reference: chr 7
allele count: 1
allele frequency: 8.258183860205463e-6
allele num: 121092
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000401244
  ensembl transcript: ENST00000425651
  gene symbol: NRCAM
  hgvsc: ENST00000425651.2:c.3585T>C
  hgvsp: ENST00000425651.2:c.3585T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368308
  ensembl transcript: ENST00000379022
  gene symbol: NRCAM
  hgvsc: ENST00000379022.4:c.3585T>C
  hgvsp: ENST00000379022.4:c.3585T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000091129
  ensembl transcript: ENST00000415105
  gene symbol: NRCAM
  hgvsc: ENST00000415105.1:n.363T>C
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000407858
  ensembl transcript: ENST00000413765
  gene symbol: NRCAM
  hgvsc: ENST00000413765.2:c.3213T>C
  hgvsp: ENST00000413765.2:c.3213T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000091129
  ensembl transcript: ENST00000465585
  gene symbol: NRCAM
  hgvsc: ENST00000465585.1:n.421T>C
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368314
  ensembl transcript: ENST00000379028
  gene symbol: NRCAM
  hgvsc: ENST00000379028.3:c.3585T>C
  hgvsp: ENST00000379028.3:c.3585T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000325269
  ensembl transcript: ENST00000351718
  gene symbol: NRCAM
  hgvsc: ENST00000351718.4:c.3222T>C
  hgvsp: ENST00000351718.4:c.3222T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000398174
  ensembl transcript: ENST00000445634
  gene symbol: NRCAM
  hgvsc: ENST00000445634.2:c.281T>C
  hgvsp: ENST00000445634.2:c.281T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368310
  ensembl transcript: ENST00000379024
  gene symbol: NRCAM
  hgvsc: ENST00000379024.4:c.3249T>C
  hgvsp: ENST00000379024.4:c.3249T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7994
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3477
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14599
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7142
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12579
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1494
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5826
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8904
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1027
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2171
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 961
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 625
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Gly1195Gly
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
population: European (Finnish)
population: African
population: South Asian
reference allele: A
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD

7-107800836-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107800836
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 107800836
    reference: chr 7
allele count: 1
allele frequency: 8.251097395953662e-6
allele num: 121196
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000325269
  ensembl transcript: ENST00000351718
  gene symbol: NRCAM
  hgvsc: ENST00000351718.4:c.3205A>G
  hgvsp: ENSP00000325269.6:p.Ile1069Val
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000091129
  ensembl transcript: ENST00000465585
  gene symbol: NRCAM
  hgvsc: ENST00000465585.1:n.404A>G
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000407858
  ensembl transcript: ENST00000413765
  gene symbol: NRCAM
  hgvsc: ENST00000413765.2:c.3196A>G
  hgvsp: ENSP00000407858.2:p.Ile1066Val
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000401244
  ensembl transcript: ENST00000425651
  gene symbol: NRCAM
  hgvsc: ENST00000425651.2:c.3568A>G
  hgvsp: ENSP00000401244.2:p.Ile1190Val
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368310
  ensembl transcript: ENST00000379024
  gene symbol: NRCAM
  hgvsc: ENST00000379024.4:c.3232A>G
  hgvsp: ENSP00000368310.4:p.Ile1078Val
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368308
  ensembl transcript: ENST00000379022
  gene symbol: NRCAM
  hgvsc: ENST00000379022.4:c.3568A>G
  hgvsp: ENSP00000368308.4:p.Ile1190Val
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368314
  ensembl transcript: ENST00000379028
  gene symbol: NRCAM
  hgvsc: ENST00000379028.3:c.3568A>G
  hgvsp: ENSP00000368314.3:p.Ile1190Val
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000398174
  ensembl transcript: ENST00000445634
  gene symbol: NRCAM
  hgvsc: ENST00000445634.2:c.264A>G
  hgvsp: ENSP00000398174.2:p.Ile89Val
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000091129
  ensembl transcript: ENST00000415105
  gene symbol: NRCAM
  hgvsc: ENST00000415105.1:n.346A>G
  variant of: http://identifiers.org/hgnc/7994
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5826
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3478
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 961
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12599
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14650
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 625
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8905
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1495
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7104
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1027
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2172
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2653
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 160
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Ile1190Val
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: African
population: South Asian
reference allele: T
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD

http://identifiers.org/exac.variant/7-107800880-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107800880
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 107800880
    reference: chr 7
allele count: 1
allele frequency: 8.248647221855616e-6
allele num: 121232
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000401244
  ensembl transcript: ENST00000425651
  gene symbol: NRCAM
  hgvsc: ENST00000425651.2:c.3524G>T
  hgvsp: ENSP00000401244.2:p.Cys1175Phe
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000091129
  ensembl transcript: ENST00000465585
  gene symbol: NRCAM
  hgvsc: ENST00000465585.1:n.360G>T
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368314
  ensembl transcript: ENST00000379028
  gene symbol: NRCAM
  hgvsc: ENST00000379028.3:c.3524G>T
  hgvsp: ENSP00000368314.3:p.Cys1175Phe
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000091129
  ensembl transcript: ENST00000415105
  gene symbol: NRCAM
  hgvsc: ENST00000415105.1:n.302G>T
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000325269
  ensembl transcript: ENST00000351718
  gene symbol: NRCAM
  hgvsc: ENST00000351718.4:c.3161G>T
  hgvsp: ENSP00000325269.6:p.Cys1054Phe
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368308
  ensembl transcript: ENST00000379022
  gene symbol: NRCAM
  hgvsc: ENST00000379022.4:c.3524G>T
  hgvsp: ENSP00000368308.4:p.Cys1175Phe
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000407858
  ensembl transcript: ENST00000413765
  gene symbol: NRCAM
  hgvsc: ENST00000413765.2:c.3152G>T
  hgvsp: ENSP00000407858.2:p.Cys1051Phe
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368310
  ensembl transcript: ENST00000379024
  gene symbol: NRCAM
  hgvsc: ENST00000379024.4:c.3188G>T
  hgvsp: ENSP00000368310.4:p.Cys1063Phe
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000398174
  ensembl transcript: ENST00000445634
  gene symbol: NRCAM
  hgvsc: ENST00000445634.2:c.220G>T
  hgvsp: ENSP00000398174.2:p.Cys74Phe
  variant of: http://identifiers.org/hgnc/7994
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1492
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 625
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14564
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1027
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2170
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5823
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 961
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3477
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7129
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8892
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12536
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2647
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17497
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Cys1175Phe
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP

7-107800914-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107800914
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 107800914
    reference: chr 7
allele count: 8
allele frequency: 6.604365485585973e-5
allele num: 121132
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000398174
  ensembl transcript: ENST00000445634
  gene symbol: NRCAM
  hgvsc: ENST00000445634.2:c.186A>T
  hgvsp: ENSP00000398174.2:p.Ile63Phe
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000091129
  ensembl transcript: ENST00000465585
  gene symbol: NRCAM
  hgvsc: ENST00000465585.1:n.326A>T
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000407858
  ensembl transcript: ENST00000413765
  gene symbol: NRCAM
  hgvsc: ENST00000413765.2:c.3118A>T
  hgvsp: ENSP00000407858.2:p.Ile1040Phe
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000325269
  ensembl transcript: ENST00000351718
  gene symbol: NRCAM
  hgvsc: ENST00000351718.4:c.3127A>T
  hgvsp: ENSP00000325269.6:p.Ile1043Phe
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368310
  ensembl transcript: ENST00000379024
  gene symbol: NRCAM
  hgvsc: ENST00000379024.4:c.3154A>T
  hgvsp: ENSP00000368310.4:p.Ile1052Phe
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000401244
  ensembl transcript: ENST00000425651
  gene symbol: NRCAM
  hgvsc: ENST00000425651.2:c.3490A>T
  hgvsp: ENSP00000401244.2:p.Ile1164Phe
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368314
  ensembl transcript: ENST00000379028
  gene symbol: NRCAM
  hgvsc: ENST00000379028.3:c.3490A>T
  hgvsp: ENSP00000368314.3:p.Ile1164Phe
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368308
  ensembl transcript: ENST00000379022
  gene symbol: NRCAM
  hgvsc: ENST00000379022.4:c.3490A>T
  hgvsp: ENSP00000368308.4:p.Ile1164Phe
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000091129
  ensembl transcript: ENST00000415105
  gene symbol: NRCAM
  hgvsc: ENST00000415105.1:n.268A>T
  variant of: http://identifiers.org/hgnc/7994
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2169
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1495
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3469
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 961
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5791
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 625
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8880
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7057
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12386
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14302
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1027
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3711
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 201
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 174
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Ile1164Phe
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: QD

7-107800918-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107800918
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 107800918
    reference: chr 7
allele count: 1
allele frequency: 8.256820133430213e-6
allele num: 121112
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368308
  ensembl transcript: ENST00000379022
  gene symbol: NRCAM
  hgvsc: ENST00000379022.4:c.3486G>C
  hgvsp: ENST00000379022.4:c.3486G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000407858
  ensembl transcript: ENST00000413765
  gene symbol: NRCAM
  hgvsc: ENST00000413765.2:c.3114G>C
  hgvsp: ENST00000413765.2:c.3114G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000091129
  ensembl transcript: ENST00000415105
  gene symbol: NRCAM
  hgvsc: ENST00000415105.1:n.264G>C
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000325269
  ensembl transcript: ENST00000351718
  gene symbol: NRCAM
  hgvsc: ENST00000351718.4:c.3123G>C
  hgvsp: ENST00000351718.4:c.3123G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368310
  ensembl transcript: ENST00000379024
  gene symbol: NRCAM
  hgvsc: ENST00000379024.4:c.3150G>C
  hgvsp: ENST00000379024.4:c.3150G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000401244
  ensembl transcript: ENST00000425651
  gene symbol: NRCAM
  hgvsc: ENST00000425651.2:c.3486G>C
  hgvsp: ENST00000425651.2:c.3486G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000398174
  ensembl transcript: ENST00000445634
  gene symbol: NRCAM
  hgvsc: ENST00000445634.2:c.182G>C
  hgvsp: ENST00000445634.2:c.182G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368314
  ensembl transcript: ENST00000379028
  gene symbol: NRCAM
  hgvsc: ENST00000379028.3:c.3486G>C
  hgvsp: ENST00000379028.3:c.3486G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000091129
  ensembl transcript: ENST00000465585
  gene symbol: NRCAM
  hgvsc: ENST00000465585.1:n.322G>C
  variant of: http://identifiers.org/hgnc/7994
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5788
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8876
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2166
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14176
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12367
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3474
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 625
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1027
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6992
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1494
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 960
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 367
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 307
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3703
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5260
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Val1162Val
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum

7-107800919-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107800919
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 107800919
    reference: chr 7
allele count: 2
allele frequency: 1.651718613217052e-5
allele num: 121086
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000398174
  ensembl transcript: ENST00000445634
  gene symbol: NRCAM
  hgvsc: ENST00000445634.2:c.181T>C
  hgvsp: ENSP00000398174.2:p.Val61Ala
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368310
  ensembl transcript: ENST00000379024
  gene symbol: NRCAM
  hgvsc: ENST00000379024.4:c.3149T>C
  hgvsp: ENSP00000368310.4:p.Val1050Ala
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368314
  ensembl transcript: ENST00000379028
  gene symbol: NRCAM
  hgvsc: ENST00000379028.3:c.3485T>C
  hgvsp: ENSP00000368314.3:p.Val1162Ala
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000325269
  ensembl transcript: ENST00000351718
  gene symbol: NRCAM
  hgvsc: ENST00000351718.4:c.3122T>C
  hgvsp: ENSP00000325269.6:p.Val1041Ala
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368308
  ensembl transcript: ENST00000379022
  gene symbol: NRCAM
  hgvsc: ENST00000379022.4:c.3485T>C
  hgvsp: ENSP00000368308.4:p.Val1162Ala
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000407858
  ensembl transcript: ENST00000413765
  gene symbol: NRCAM
  hgvsc: ENST00000413765.2:c.3113T>C
  hgvsp: ENSP00000407858.2:p.Val1038Ala
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000401244
  ensembl transcript: ENST00000425651
  gene symbol: NRCAM
  hgvsc: ENST00000425651.2:c.3485T>C
  hgvsp: ENSP00000401244.2:p.Val1162Ala
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000091129
  ensembl transcript: ENST00000415105
  gene symbol: NRCAM
  hgvsc: ENST00000415105.1:n.263T>C
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000091129
  ensembl transcript: ENST00000465585
  gene symbol: NRCAM
  hgvsc: ENST00000465585.1:n.321T>C
  variant of: http://identifiers.org/hgnc/7994
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 7006
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8874
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5788
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12334
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 627
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1496
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3474
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2166
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 684
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 960
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14189
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1028
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 279
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 228
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3685
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Val1162Ala
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: South Asian
population: Other
reference allele: A
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP

7-107800925-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107800925
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 107800925
    reference: chr 7
allele count: 9
allele frequency: 7.433593233778247e-5
allele num: 121072
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368308
  ensembl transcript: ENST00000379022
  gene symbol: NRCAM
  hgvsc: ENST00000379022.4:c.3479G>A
  hgvsp: ENSP00000368308.4:p.Arg1160Gln
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000407858
  ensembl transcript: ENST00000413765
  gene symbol: NRCAM
  hgvsc: ENST00000413765.2:c.3107G>A
  hgvsp: ENSP00000407858.2:p.Arg1036Gln
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000091129
  ensembl transcript: ENST00000465585
  gene symbol: NRCAM
  hgvsc: ENST00000465585.1:n.315G>A
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000325269
  ensembl transcript: ENST00000351718
  gene symbol: NRCAM
  hgvsc: ENST00000351718.4:c.3116G>A
  hgvsp: ENSP00000325269.6:p.Arg1039Gln
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368310
  ensembl transcript: ENST00000379024
  gene symbol: NRCAM
  hgvsc: ENST00000379024.4:c.3143G>A
  hgvsp: ENSP00000368310.4:p.Arg1048Gln
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000398174
  ensembl transcript: ENST00000445634
  gene symbol: NRCAM
  hgvsc: ENST00000445634.2:c.175G>A
  hgvsp: ENSP00000398174.2:p.Arg59Gln
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368314
  ensembl transcript: ENST00000379028
  gene symbol: NRCAM
  hgvsc: ENST00000379028.3:c.3479G>A
  hgvsp: ENSP00000368314.3:p.Arg1160Gln
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000091129
  ensembl transcript: ENST00000415105
  gene symbol: NRCAM
  hgvsc: ENST00000415105.1:n.257G>A
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000401244
  ensembl transcript: ENST00000425651
  gene symbol: NRCAM
  hgvsc: ENST00000425651.2:c.3479G>A
  hgvsp: ENSP00000401244.2:p.Arg1160Gln
  variant of: http://identifiers.org/hgnc/7994
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 845
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 624
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1490
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14111
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6944
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1023
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2164
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12276
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3468
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5798
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 960
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8843
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5212
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 338
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17464
  bin: 9.75e1
  variant carriers: 9
genotype quality: GenotypeQuality
  all individuals: 4547
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Arg1160Gln
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
reference allele: C
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: ReadPosRankSum

7-107800927-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107800927
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 107800927
    reference: chr 7
allele count: 1
allele frequency: 8.261868173631421e-6
allele num: 121038
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368308
  ensembl transcript: ENST00000379022
  gene symbol: NRCAM
  hgvsc: ENST00000379022.4:c.3477C>G
  hgvsp: ENSP00000368308.4:p.Ser1159Arg
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000398174
  ensembl transcript: ENST00000445634
  gene symbol: NRCAM
  hgvsc: ENST00000445634.2:c.173C>G
  hgvsp: ENSP00000398174.2:p.Ser58Arg
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000401244
  ensembl transcript: ENST00000425651
  gene symbol: NRCAM
  hgvsc: ENST00000425651.2:c.3477C>G
  hgvsp: ENSP00000401244.2:p.Ser1159Arg
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000091129
  ensembl transcript: ENST00000415105
  gene symbol: NRCAM
  hgvsc: ENST00000415105.1:n.255C>G
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000407858
  ensembl transcript: ENST00000413765
  gene symbol: NRCAM
  hgvsc: ENST00000413765.2:c.3105C>G
  hgvsp: ENSP00000407858.2:p.Ser1035Arg
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368310
  ensembl transcript: ENST00000379024
  gene symbol: NRCAM
  hgvsc: ENST00000379024.4:c.3141C>G
  hgvsp: ENSP00000368310.4:p.Ser1047Arg
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368314
  ensembl transcript: ENST00000379028
  gene symbol: NRCAM
  hgvsc: ENST00000379028.3:c.3477C>G
  hgvsp: ENSP00000368314.3:p.Ser1159Arg
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000325269
  ensembl transcript: ENST00000351718
  gene symbol: NRCAM
  hgvsc: ENST00000351718.4:c.3114C>G
  hgvsp: ENSP00000325269.6:p.Ser1038Arg
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000091129
  ensembl transcript: ENST00000465585
  gene symbol: NRCAM
  hgvsc: ENST00000465585.1:n.313C>G
  variant of: http://identifiers.org/hgnc/7994
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13773
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5787
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1368
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3473
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8845
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1489
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 667
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1023
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6725
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 624
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 959
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2161
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12193
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 537
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13422
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Ser1159Arg
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
population: Other
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum

7-107800936-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107800936
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 107800936
    reference: chr 7
allele count: 3920
allele frequency: 3.239615874117783e-2
allele num: 121002
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000398174
  ensembl transcript: ENST00000445634
  gene symbol: NRCAM
  hgvsc: ENST00000445634.2:c.164G>A
  hgvsp: ENST00000445634.2:c.164G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000325269
  ensembl transcript: ENST00000351718
  gene symbol: NRCAM
  hgvsc: ENST00000351718.4:c.3105G>A
  hgvsp: ENST00000351718.4:c.3105G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368314
  ensembl transcript: ENST00000379028
  gene symbol: NRCAM
  hgvsc: ENST00000379028.3:c.3468G>A
  hgvsp: ENST00000379028.3:c.3468G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000091129
  ensembl transcript: ENST00000415105
  gene symbol: NRCAM
  hgvsc: ENST00000415105.1:n.246G>A
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368308
  ensembl transcript: ENST00000379022
  gene symbol: NRCAM
  hgvsc: ENST00000379022.4:c.3468G>A
  hgvsp: ENST00000379022.4:c.3468G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000407858
  ensembl transcript: ENST00000413765
  gene symbol: NRCAM
  hgvsc: ENST00000413765.2:c.3096G>A
  hgvsp: ENST00000413765.2:c.3096G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000401244
  ensembl transcript: ENST00000425651
  gene symbol: NRCAM
  hgvsc: ENST00000425651.2:c.3468G>A
  hgvsp: ENST00000425651.2:c.3468G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368310
  ensembl transcript: ENST00000379024
  gene symbol: NRCAM
  hgvsc: ENST00000379024.4:c.3132G>A
  hgvsp: ENST00000379024.4:c.3132G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000091129
  ensembl transcript: ENST00000465585
  gene symbol: NRCAM
  hgvsc: ENST00000465585.1:n.304G>A
  variant of: http://identifiers.org/hgnc/7994
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8770
  bin: 3.75e1
  variant carriers: 544
genotype depth: GenotypeDepth
  all individuals: 2310
  bin: 5.25e1
  variant carriers: 321
genotype depth: GenotypeDepth
  all individuals: 1788
  bin: 1.75e1
  variant carriers: 86
genotype depth: GenotypeDepth
  all individuals: 1045
  bin: 6.25e1
  variant carriers: 163
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 7.25e1
  variant carriers: 73
genotype depth: GenotypeDepth
  all individuals: 11731
  bin: 3.25e1
  variant carriers: 499
genotype depth: GenotypeDepth
  all individuals: 5842
  bin: 4.25e1
  variant carriers: 496
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 9.25e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 7.75e1
  variant carriers: 46
genotype depth: GenotypeDepth
  all individuals: 741
  bin: 1.25e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 8.25e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 6805
  bin: 2.25e1
  variant carriers: 199
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 6.75e1
  variant carriers: 113
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 8.75e1
  variant carriers: 31
genotype depth: GenotypeDepth
  all individuals: 1583
  bin: 5.75e1
  variant carriers: 216
genotype depth: GenotypeDepth
  all individuals: 1093
  bin: 9.75e1
  variant carriers: 161
genotype depth: GenotypeDepth
  all individuals: 12933
  bin: 2.75e1
  variant carriers: 372
genotype depth: GenotypeDepth
  all individuals: 3624
  bin: 4.75e1
  variant carriers: 428
genotype quality: GenotypeQuality
  all individuals: 604
  bin: 4.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 2426
  bin: 8.75e1
  variant carriers: 3
hgvs: c.3468G>A
num of homozygotes: 110
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
reference allele: C
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: MQ
site quality: MQRankSum

7-107800937-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107800937
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 107800937
    reference: chr 7
allele count: 0
allele frequency: 0.0e0
allele num: 120922
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368310
  ensembl transcript: ENST00000379024
  gene symbol: NRCAM
  hgvsc: ENST00000379024.4:c.3131C>T
  hgvsp: ENSP00000368310.4:p.Ala1044Val
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000325269
  ensembl transcript: ENST00000351718
  gene symbol: NRCAM
  hgvsc: ENST00000351718.4:c.3104C>T
  hgvsp: ENSP00000325269.6:p.Ala1035Val
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000091129
  ensembl transcript: ENST00000465585
  gene symbol: NRCAM
  hgvsc: ENST00000465585.1:n.303C>T
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368314
  ensembl transcript: ENST00000379028
  gene symbol: NRCAM
  hgvsc: ENST00000379028.3:c.3467C>T
  hgvsp: ENSP00000368314.3:p.Ala1156Val
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000401244
  ensembl transcript: ENST00000425651
  gene symbol: NRCAM
  hgvsc: ENST00000425651.2:c.3467C>T
  hgvsp: ENSP00000401244.2:p.Ala1156Val
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000407858
  ensembl transcript: ENST00000413765
  gene symbol: NRCAM
  hgvsc: ENST00000413765.2:c.3095C>T
  hgvsp: ENSP00000407858.2:p.Ala1032Val
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000398174
  ensembl transcript: ENST00000445634
  gene symbol: NRCAM
  hgvsc: ENST00000445634.2:c.163C>T
  hgvsp: ENSP00000398174.2:p.Thr55Met
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368308
  ensembl transcript: ENST00000379022
  gene symbol: NRCAM
  hgvsc: ENST00000379022.4:c.3467C>T
  hgvsp: ENSP00000368308.4:p.Ala1156Val
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000091129
  ensembl transcript: ENST00000415105
  gene symbol: NRCAM
  hgvsc: ENST00000415105.1:n.245C>T
  variant of: http://identifiers.org/hgnc/7994
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 632
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2099
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3385
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8668
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1889
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 941
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11843
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13591
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1453
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5658
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7068
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1010
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 810
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13800
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Ala1156Val
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: Other
population: European (Finnish)
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQ

7-107800942-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107800942
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 107800942
    reference: chr 7
allele count: 1
allele frequency: 8.270067318347971e-6
allele num: 120918
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000398174
  ensembl transcript: ENST00000445634
  gene symbol: NRCAM
  hgvsc: ENST00000445634.2:c.163-5T>C
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl transcript: ENST00000415105
  gene symbol: NRCAM
  hgvsc: ENST00000415105.1:n.245-5T>C
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl transcript: ENST00000465585
  gene symbol: NRCAM
  hgvsc: ENST00000465585.1:n.303-5T>C
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368314
  ensembl transcript: ENST00000379028
  gene symbol: NRCAM
  hgvsc: ENST00000379028.3:c.3467-5T>C
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368310
  ensembl transcript: ENST00000379024
  gene symbol: NRCAM
  hgvsc: ENST00000379024.4:c.3131-5T>C
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000401244
  ensembl transcript: ENST00000425651
  gene symbol: NRCAM
  hgvsc: ENST00000425651.2:c.3467-5T>C
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368308
  ensembl transcript: ENST00000379022
  gene symbol: NRCAM
  hgvsc: ENST00000379022.4:c.3467-5T>C
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000407858
  ensembl transcript: ENST00000413765
  gene symbol: NRCAM
  hgvsc: ENST00000413765.2:c.3095-5T>C
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000325269
  ensembl transcript: ENST00000351718
  gene symbol: NRCAM
  hgvsc: ENST00000351718.4:c.3104-5T>C
  variant of: http://identifiers.org/hgnc/7994
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11628
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2220
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7656
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1010
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12850
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 940
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 899
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5649
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1451
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8621
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2100
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3378
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3522
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 531
  bin: 5.75e1
  variant carriers: 0
hgvs: c.3467-5T>C
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
reference allele: A
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum

7-107800951-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107800951
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 107800951
    reference: chr 7
allele count: 1
allele frequency: 8.27417299640901e-6
allele num: 120858
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000407858
  ensembl transcript: ENST00000413765
  gene symbol: NRCAM
  hgvsc: ENST00000413765.2:c.3095-14G>C
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl transcript: ENST00000465585
  gene symbol: NRCAM
  hgvsc: ENST00000465585.1:n.303-14G>C
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000401244
  ensembl transcript: ENST00000425651
  gene symbol: NRCAM
  hgvsc: ENST00000425651.2:c.3467-14G>C
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368310
  ensembl transcript: ENST00000379024
  gene symbol: NRCAM
  hgvsc: ENST00000379024.4:c.3131-14G>C
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368308
  ensembl transcript: ENST00000379022
  gene symbol: NRCAM
  hgvsc: ENST00000379022.4:c.3467-14G>C
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000325269
  ensembl transcript: ENST00000351718
  gene symbol: NRCAM
  hgvsc: ENST00000351718.4:c.3104-14G>C
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl transcript: ENST00000415105
  gene symbol: NRCAM
  hgvsc: ENST00000415105.1:n.245-14G>C
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368314
  ensembl transcript: ENST00000379028
  gene symbol: NRCAM
  hgvsc: ENST00000379028.3:c.3467-14G>C
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000398174
  ensembl transcript: ENST00000445634
  gene symbol: NRCAM
  hgvsc: ENST00000445634.2:c.163-14G>C
  variant of: http://identifiers.org/hgnc/7994
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2241
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2102
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11448
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12433
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 984
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5635
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 941
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8144
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3375
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1451
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8618
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1010
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 432
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1397
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 755
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD

7-107800953-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107800953
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 107800953
    reference: chr 7
allele count: 82320
allele frequency: 6.823720552396426e-1
allele num: 120638
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000398174
  ensembl transcript: ENST00000445634
  gene symbol: NRCAM
  hgvsc: ENST00000445634.2:c.163-16T>C
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl transcript: ENST00000465585
  gene symbol: NRCAM
  hgvsc: ENST00000465585.1:n.303-16T>C
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000325269
  ensembl transcript: ENST00000351718
  gene symbol: NRCAM
  hgvsc: ENST00000351718.4:c.3104-16T>C
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000401244
  ensembl transcript: ENST00000425651
  gene symbol: NRCAM
  hgvsc: ENST00000425651.2:c.3467-16T>C
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl transcript: ENST00000415105
  gene symbol: NRCAM
  hgvsc: ENST00000415105.1:n.245-16T>C
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368310
  ensembl transcript: ENST00000379024
  gene symbol: NRCAM
  hgvsc: ENST00000379024.4:c.3131-16T>C
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000407858
  ensembl transcript: ENST00000413765
  gene symbol: NRCAM
  hgvsc: ENST00000413765.2:c.3095-16T>C
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368314
  ensembl transcript: ENST00000379028
  gene symbol: NRCAM
  hgvsc: ENST00000379028.3:c.3467-16T>C
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368308
  ensembl transcript: ENST00000379022
  gene symbol: NRCAM
  hgvsc: ENST00000379022.4:c.3467-16T>C
  variant of: http://identifiers.org/hgnc/7994
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 8.75e1
  variant carriers: 361
genotype depth: GenotypeDepth
  all individuals: 1314
  bin: 6.25e1
  variant carriers: 1241
genotype depth: GenotypeDepth
  all individuals: 5862
  bin: 2.25e1
  variant carriers: 4525
genotype depth: GenotypeDepth
  all individuals: 8956
  bin: 3.75e1
  variant carriers: 8337
genotype depth: GenotypeDepth
  all individuals: 1509
  bin: 9.75e1
  variant carriers: 1449
genotype depth: GenotypeDepth
  all individuals: 10074
  bin: 3.25e1
  variant carriers: 8826
genotype depth: GenotypeDepth
  all individuals: 709
  bin: 7.25e1
  variant carriers: 660
genotype depth: GenotypeDepth
  all individuals: 4615
  bin: 4.75e1
  variant carriers: 4387
genotype depth: GenotypeDepth
  all individuals: 6907
  bin: 4.25e1
  variant carriers: 6542
genotype depth: GenotypeDepth
  all individuals: 978
  bin: 1.25e1
  variant carriers: 601
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 9.25e1
  variant carriers: 270
genotype depth: GenotypeDepth
  all individuals: 800
  bin: 6.75e1
  variant carriers: 738
genotype depth: GenotypeDepth
  all individuals: 9756
  bin: 2.75e1
  variant carriers: 7467
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 7.5e0
  variant carriers: 102
genotype depth: GenotypeDepth
  all individuals: 1975
  bin: 5.75e1
  variant carriers: 1849
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 7.75e1
  variant carriers: 513
genotype depth: GenotypeDepth
  all individuals: 3030
  bin: 5.25e1
  variant carriers: 2876
genotype depth: GenotypeDepth
  all individuals: 2371
  bin: 1.75e1
  variant carriers: 2107
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 8.25e1
  variant carriers: 424
genotype quality: GenotypeQuality
  all individuals: 363
  bin: 2.25e1
  variant carriers: 96
genotype quality: GenotypeQuality
  all individuals: 3767
  bin: 6.25e1
  variant carriers: 894
genotype quality: GenotypeQuality
  all individuals: 303
  bin: 4.25e1
  variant carriers: 217
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 7.5e0
  variant carriers: 35
genotype quality: GenotypeQuality
  all individuals: 1973
  bin: 8.25e1
  variant carriers: 1658
genotype quality: GenotypeQuality
  all individuals: 1165
  bin: 8.75e1
  variant carriers: 1010
num of homozygotes: 29267
population: South Asian
population: Latino
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: DP

7-107800956-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107800956
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 107800956
    reference: chr 7
allele count: 5
allele frequency: 4.172856403665437e-5
allele num: 119822
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368310
  ensembl transcript: ENST00000379024
  gene symbol: NRCAM
  hgvsc: ENST00000379024.4:c.3131-19C>A
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368314
  ensembl transcript: ENST00000379028
  gene symbol: NRCAM
  hgvsc: ENST00000379028.3:c.3467-19C>A
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl transcript: ENST00000415105
  gene symbol: NRCAM
  hgvsc: ENST00000415105.1:n.245-19C>A
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000401244
  ensembl transcript: ENST00000425651
  gene symbol: NRCAM
  hgvsc: ENST00000425651.2:c.3467-19C>A
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl transcript: ENST00000465585
  gene symbol: NRCAM
  hgvsc: ENST00000465585.1:n.303-19C>A
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000398174
  ensembl transcript: ENST00000445634
  gene symbol: NRCAM
  hgvsc: ENST00000445634.2:c.163-19C>A
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000407858
  ensembl transcript: ENST00000413765
  gene symbol: NRCAM
  hgvsc: ENST00000413765.2:c.3095-19C>A
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000325269
  ensembl transcript: ENST00000351718
  gene symbol: NRCAM
  hgvsc: ENST00000351718.4:c.3104-19C>A
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368308
  ensembl transcript: ENST00000379022
  gene symbol: NRCAM
  hgvsc: ENST00000379022.4:c.3467-19C>A
  variant of: http://identifiers.org/hgnc/7994
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1401
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3569
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10451
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2394
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1011
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 701
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2516
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10348
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 4469
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 717
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21018
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 456
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 312
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1639
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3947
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
reference allele: G
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum

7-107800960-TG-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107800960
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 107800959
    reference: chr 7
allele count: 1
allele frequency: 8.350591221858508e-6
allele num: 119752
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000398174
  ensembl transcript: ENST00000445634
  gene symbol: NRCAM
  hgvsc: ENST00000445634.2:c.163-24delC
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368314
  ensembl transcript: ENST00000379028
  gene symbol: NRCAM
  hgvsc: ENST00000379028.3:c.3467-24delC
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl transcript: ENST00000465585
  gene symbol: NRCAM
  hgvsc: ENST00000465585.1:n.303-24delC
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368310
  ensembl transcript: ENST00000379024
  gene symbol: NRCAM
  hgvsc: ENST00000379024.4:c.3131-24delC
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000325269
  ensembl transcript: ENST00000351718
  gene symbol: NRCAM
  hgvsc: ENST00000351718.4:c.3104-24delC
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000401244
  ensembl transcript: ENST00000425651
  gene symbol: NRCAM
  hgvsc: ENST00000425651.2:c.3467-24delC
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl transcript: ENST00000415105
  gene symbol: NRCAM
  hgvsc: ENST00000415105.1:n.245-24delC
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000407858
  ensembl transcript: ENST00000413765
  gene symbol: NRCAM
  hgvsc: ENST00000413765.2:c.3095-24delC
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368308
  ensembl transcript: ENST00000379022
  gene symbol: NRCAM
  hgvsc: ENST00000379022.4:c.3467-24delC
  variant of: http://identifiers.org/hgnc/7994
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20260
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 730
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4446
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1399
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2384
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4082
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10255
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3230
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 717
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10079
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1010
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1492
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2752
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7691
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 509
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: TG
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff

7-107800962-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107800962
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 107800962
    reference: chr 7
allele count: 2
allele frequency: 1.671458180116333e-5
allele num: 119656
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl transcript: ENST00000465585
  gene symbol: NRCAM
  hgvsc: ENST00000465585.1:n.303-25C>T
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368314
  ensembl transcript: ENST00000379028
  gene symbol: NRCAM
  hgvsc: ENST00000379028.3:c.3467-25C>T
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368308
  ensembl transcript: ENST00000379022
  gene symbol: NRCAM
  hgvsc: ENST00000379022.4:c.3467-25C>T
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000401244
  ensembl transcript: ENST00000425651
  gene symbol: NRCAM
  hgvsc: ENST00000425651.2:c.3467-25C>T
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl transcript: ENST00000415105
  gene symbol: NRCAM
  hgvsc: ENST00000415105.1:n.245-25C>T
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000398174
  ensembl transcript: ENST00000445634
  gene symbol: NRCAM
  hgvsc: ENST00000445634.2:c.163-25C>T
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000407858
  ensembl transcript: ENST00000413765
  gene symbol: NRCAM
  hgvsc: ENST00000413765.2:c.3095-25C>T
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368310
  ensembl transcript: ENST00000379024
  gene symbol: NRCAM
  hgvsc: ENST00000379024.4:c.3131-25C>T
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000325269
  ensembl transcript: ENST00000351718
  gene symbol: NRCAM
  hgvsc: ENST00000351718.4:c.3104-25C>T
  variant of: http://identifiers.org/hgnc/7994
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4509
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 717
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19225
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10072
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1398
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 753
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4341
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2380
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9771
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1010
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4412
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2610
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1592
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1415
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22895
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1957
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: VQSLOD

7-107800962-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107800962
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 107800962
    reference: chr 7
allele count: 1
allele frequency: 8.357290900581667e-6
allele num: 119656
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368308
  ensembl transcript: ENST00000379022
  gene symbol: NRCAM
  hgvsc: ENST00000379022.4:c.3467-25C>G
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl transcript: ENST00000465585
  gene symbol: NRCAM
  hgvsc: ENST00000465585.1:n.303-25C>G
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000407858
  ensembl transcript: ENST00000413765
  gene symbol: NRCAM
  hgvsc: ENST00000413765.2:c.3095-25C>G
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000398174
  ensembl transcript: ENST00000445634
  gene symbol: NRCAM
  hgvsc: ENST00000445634.2:c.163-25C>G
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000325269
  ensembl transcript: ENST00000351718
  gene symbol: NRCAM
  hgvsc: ENST00000351718.4:c.3104-25C>G
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000401244
  ensembl transcript: ENST00000425651
  gene symbol: NRCAM
  hgvsc: ENST00000425651.2:c.3467-25C>G
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368310
  ensembl transcript: ENST00000379024
  gene symbol: NRCAM
  hgvsc: ENST00000379024.4:c.3131-25C>G
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl transcript: ENST00000415105
  gene symbol: NRCAM
  hgvsc: ENST00000415105.1:n.245-25C>G
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368314
  ensembl transcript: ENST00000379028
  gene symbol: NRCAM
  hgvsc: ENST00000379028.3:c.3467-25C>G
  variant of: http://identifiers.org/hgnc/7994
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1010
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1398
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9771
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4509
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4412
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4341
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19225
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 753
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10072
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 717
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2380
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1415
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1957
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1161
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2722
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 743
  bin: 4.25e1
  variant carriers: 0
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: G
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff

7-107800965-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107800965
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 107800965
    reference: chr 7
allele count: 0
allele frequency: 0.0e0
allele num: 119392
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000407858
  ensembl transcript: ENST00000413765
  gene symbol: NRCAM
  hgvsc: ENST00000413765.2:c.3095-28C>T
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368308
  ensembl transcript: ENST00000379022
  gene symbol: NRCAM
  hgvsc: ENST00000379022.4:c.3467-28C>T
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl transcript: ENST00000415105
  gene symbol: NRCAM
  hgvsc: ENST00000415105.1:n.245-28C>T
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000398174
  ensembl transcript: ENST00000445634
  gene symbol: NRCAM
  hgvsc: ENST00000445634.2:c.163-28C>T
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368314
  ensembl transcript: ENST00000379028
  gene symbol: NRCAM
  hgvsc: ENST00000379028.3:c.3467-28C>T
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000325269
  ensembl transcript: ENST00000351718
  gene symbol: NRCAM
  hgvsc: ENST00000351718.4:c.3104-28C>T
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000401244
  ensembl transcript: ENST00000425651
  gene symbol: NRCAM
  hgvsc: ENST00000425651.2:c.3467-28C>T
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl transcript: ENST00000465585
  gene symbol: NRCAM
  hgvsc: ENST00000465585.1:n.303-28C>T
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368310
  ensembl transcript: ENST00000379024
  gene symbol: NRCAM
  hgvsc: ENST00000379024.4:c.3131-28C>T
  variant of: http://identifiers.org/hgnc/7994
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 717
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1399
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4395
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4650
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9534
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2370
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18822
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10172
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 772
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1010
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4750
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23065
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2529
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1484
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2685
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 1.25e1
  variant carriers: 1
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: African
reference allele: G
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP

7-107800968-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107800968
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 107800968
    reference: chr 7
allele count: 1
allele frequency: 8.368060785593547e-6
allele num: 119502
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000401244
  ensembl transcript: ENST00000425651
  gene symbol: NRCAM
  hgvsc: ENST00000425651.2:c.3467-31T>C
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl transcript: ENST00000415105
  gene symbol: NRCAM
  hgvsc: ENST00000415105.1:n.245-31T>C
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368314
  ensembl transcript: ENST00000379028
  gene symbol: NRCAM
  hgvsc: ENST00000379028.3:c.3467-31T>C
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368308
  ensembl transcript: ENST00000379022
  gene symbol: NRCAM
  hgvsc: ENST00000379022.4:c.3467-31T>C
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl transcript: ENST00000465585
  gene symbol: NRCAM
  hgvsc: ENST00000465585.1:n.303-31T>C
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000325269
  ensembl transcript: ENST00000351718
  gene symbol: NRCAM
  hgvsc: ENST00000351718.4:c.3104-31T>C
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368310
  ensembl transcript: ENST00000379024
  gene symbol: NRCAM
  hgvsc: ENST00000379024.4:c.3131-31T>C
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000407858
  ensembl transcript: ENST00000413765
  gene symbol: NRCAM
  hgvsc: ENST00000413765.2:c.3095-31T>C
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000398174
  ensembl transcript: ENST00000445634
  gene symbol: NRCAM
  hgvsc: ENST00000445634.2:c.163-31T>C
  variant of: http://identifiers.org/hgnc/7994
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18055
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5763
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2346
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 803
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1397
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10083
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4948
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 717
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1008
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9114
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4342
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2814
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6979
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3582
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2547
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 578
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: BaseQRankSum

7-107800969-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107800969
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 107800969
    reference: chr 7
allele count: 1
allele frequency: 8.369741709770836e-6
allele num: 119478
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl transcript: ENST00000465585
  gene symbol: NRCAM
  hgvsc: ENST00000465585.1:n.303-32A>G
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl transcript: ENST00000415105
  gene symbol: NRCAM
  hgvsc: ENST00000415105.1:n.245-32A>G
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368314
  ensembl transcript: ENST00000379028
  gene symbol: NRCAM
  hgvsc: ENST00000379028.3:c.3467-32A>G
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368308
  ensembl transcript: ENST00000379022
  gene symbol: NRCAM
  hgvsc: ENST00000379022.4:c.3467-32A>G
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000401244
  ensembl transcript: ENST00000425651
  gene symbol: NRCAM
  hgvsc: ENST00000425651.2:c.3467-32A>G
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368310
  ensembl transcript: ENST00000379024
  gene symbol: NRCAM
  hgvsc: ENST00000379024.4:c.3131-32A>G
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000325269
  ensembl transcript: ENST00000351718
  gene symbol: NRCAM
  hgvsc: ENST00000351718.4:c.3104-32A>G
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000407858
  ensembl transcript: ENST00000413765
  gene symbol: NRCAM
  hgvsc: ENST00000413765.2:c.3095-32A>G
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000398174
  ensembl transcript: ENST00000445634
  gene symbol: NRCAM
  hgvsc: ENST00000445634.2:c.163-32A>G
  variant of: http://identifiers.org/hgnc/7994
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4340
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17798
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5011
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9061
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6192
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1008
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 809
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9895
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2345
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 717
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1397
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1568
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1023
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22069
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6979
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1121
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2587
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: Other
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
reference allele: T
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: ReadPosRankSum

7-107800974-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107800974
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 107800974
    reference: chr 7
allele count: 2
allele frequency: 1.676755143446403e-5
allele num: 119278
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000325269
  ensembl transcript: ENST00000351718
  gene symbol: NRCAM
  hgvsc: ENST00000351718.4:c.3104-37A>T
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000407858
  ensembl transcript: ENST00000413765
  gene symbol: NRCAM
  hgvsc: ENST00000413765.2:c.3095-37A>T
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368310
  ensembl transcript: ENST00000379024
  gene symbol: NRCAM
  hgvsc: ENST00000379024.4:c.3131-37A>T
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000401244
  ensembl transcript: ENST00000425651
  gene symbol: NRCAM
  hgvsc: ENST00000425651.2:c.3467-37A>T
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl transcript: ENST00000465585
  gene symbol: NRCAM
  hgvsc: ENST00000465585.1:n.303-37A>T
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368314
  ensembl transcript: ENST00000379028
  gene symbol: NRCAM
  hgvsc: ENST00000379028.3:c.3467-37A>T
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000398174
  ensembl transcript: ENST00000445634
  gene symbol: NRCAM
  hgvsc: ENST00000445634.2:c.163-37A>T
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368308
  ensembl transcript: ENST00000379022
  gene symbol: NRCAM
  hgvsc: ENST00000379022.4:c.3467-37A>T
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl transcript: ENST00000415105
  gene symbol: NRCAM
  hgvsc: ENST00000415105.1:n.245-37A>T
  variant of: http://identifiers.org/hgnc/7994
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9040
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2340
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15883
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 866
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8611
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4306
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 717
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1394
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5159
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1008
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9234
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6410
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1560
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3473
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 897
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1115
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
reference allele: T
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum

7-107800984-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107800984
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 107800984
    reference: chr 7
allele count: 1
allele frequency: 8.430708010858751e-6
allele num: 118614
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368308
  ensembl transcript: ENST00000379022
  gene symbol: NRCAM
  hgvsc: ENST00000379022.4:c.3467-47A>G
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368314
  ensembl transcript: ENST00000379028
  gene symbol: NRCAM
  hgvsc: ENST00000379028.3:c.3467-47A>G
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000407858
  ensembl transcript: ENST00000413765
  gene symbol: NRCAM
  hgvsc: ENST00000413765.2:c.3095-47A>G
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368310
  ensembl transcript: ENST00000379024
  gene symbol: NRCAM
  hgvsc: ENST00000379024.4:c.3131-47A>G
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl transcript: ENST00000465585
  gene symbol: NRCAM
  hgvsc: ENST00000465585.1:n.303-47A>G
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000401244
  ensembl transcript: ENST00000425651
  gene symbol: NRCAM
  hgvsc: ENST00000425651.2:c.3467-47A>G
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000398174
  ensembl transcript: ENST00000445634
  gene symbol: NRCAM
  hgvsc: ENST00000445634.2:c.163-47A>G
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000325269
  ensembl transcript: ENST00000351718
  gene symbol: NRCAM
  hgvsc: ENST00000351718.4:c.3104-47A>G
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl transcript: ENST00000415105
  gene symbol: NRCAM
  hgvsc: ENST00000415105.1:n.245-47A>G
  variant of: http://identifiers.org/hgnc/7994
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2324
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4238
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12712
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5120
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11685
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7684
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1090
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1392
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 718
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10581
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1007
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3877
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3932
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 173
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1542
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2027
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: South Asian
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff

7-107800985-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107800985
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 107800985
    reference: chr 7
allele count: 1
allele frequency: 8.439958137807636e-6
allele num: 118484
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl transcript: ENST00000465585
  gene symbol: NRCAM
  hgvsc: ENST00000465585.1:n.303-48C>T
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368310
  ensembl transcript: ENST00000379024
  gene symbol: NRCAM
  hgvsc: ENST00000379024.4:c.3131-48C>T
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl transcript: ENST00000415105
  gene symbol: NRCAM
  hgvsc: ENST00000415105.1:n.245-48C>T
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368308
  ensembl transcript: ENST00000379022
  gene symbol: NRCAM
  hgvsc: ENST00000379022.4:c.3467-48C>T
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368314
  ensembl transcript: ENST00000379028
  gene symbol: NRCAM
  hgvsc: ENST00000379028.3:c.3467-48C>T
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000407858
  ensembl transcript: ENST00000413765
  gene symbol: NRCAM
  hgvsc: ENST00000413765.2:c.3095-48C>T
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000401244
  ensembl transcript: ENST00000425651
  gene symbol: NRCAM
  hgvsc: ENST00000425651.2:c.3467-48C>T
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000325269
  ensembl transcript: ENST00000351718
  gene symbol: NRCAM
  hgvsc: ENST00000351718.4:c.3104-48C>T
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000398174
  ensembl transcript: ENST00000445634
  gene symbol: NRCAM
  hgvsc: ENST00000445634.2:c.163-48C>T
  variant of: http://identifiers.org/hgnc/7994
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2324
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11695
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1391
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10574
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1092
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7657
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 718
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5129
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1007
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12724
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4240
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2777
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3924
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2335
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 2.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3881
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5281
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Latino
reference allele: G
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum

7-107807316-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107807316
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 107807316
    reference: chr 7
allele count: 497
allele frequency: 4.855222539173928e-3
allele num: 102364
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000407858
  ensembl transcript: ENST00000413765
  gene symbol: NRCAM
  hgvsc: ENST00000413765.2:c.3095-6379G>A
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368314
  ensembl transcript: ENST00000379028
  gene symbol: NRCAM
  hgvsc: ENST00000379028.3:c.3466+50G>A
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl transcript: ENST00000415105
  gene symbol: NRCAM
  hgvsc: ENST00000415105.1:n.245-6379G>A
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368310
  ensembl transcript: ENST00000379024
  gene symbol: NRCAM
  hgvsc: ENST00000379024.4:c.3131-6379G>A
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000325269
  ensembl transcript: ENST00000351718
  gene symbol: NRCAM
  hgvsc: ENST00000351718.4:c.3104-6379G>A
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000398174
  ensembl transcript: ENST00000445634
  gene symbol: NRCAM
  hgvsc: ENST00000445634.2:c.162+1406G>A
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000401244
  ensembl transcript: ENST00000425651
  gene symbol: NRCAM
  hgvsc: ENST00000425651.2:c.3466+50G>A
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368308
  ensembl transcript: ENST00000379022
  gene symbol: NRCAM
  hgvsc: ENST00000379022.4:c.3466+50G>A
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl transcript: ENST00000465585
  gene symbol: NRCAM
  hgvsc: ENST00000465585.1:n.303-6379G>A
  variant of: http://identifiers.org/hgnc/7994
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 6.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 4.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 3.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18613
  bin: 1.25e1
  variant carriers: 160
genotype depth: GenotypeDepth
  all individuals: 7419
  bin: 7.5e0
  variant carriers: 53
genotype depth: GenotypeDepth
  all individuals: 938
  bin: 3.25e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 17146
  bin: 1.75e1
  variant carriers: 162
genotype depth: GenotypeDepth
  all individuals: 9946
  bin: 2.25e1
  variant carriers: 82
genotype depth: GenotypeDepth
  all individuals: 4496
  bin: 2.75e1
  variant carriers: 36
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 752
  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 125
  bin: 9.25e1
  variant carriers: 12
genotype quality: GenotypeQuality
  all individuals: 268
  bin: 8.25e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 525
  bin: 7.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 3777
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8004
  bin: 6.25e1
  variant carriers: 3
num of homozygotes: 13
population: Other
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
reference allele: C
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD

7-107807317-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107807317
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 107807317
    reference: chr 7
allele count: 6
allele frequency: 5.779901356350185e-5
allele num: 103808
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368308
  ensembl transcript: ENST00000379022
  gene symbol: NRCAM
  hgvsc: ENST00000379022.4:c.3466+49C>T
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000325269
  ensembl transcript: ENST00000351718
  gene symbol: NRCAM
  hgvsc: ENST00000351718.4:c.3104-6380C>T
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000407858
  ensembl transcript: ENST00000413765
  gene symbol: NRCAM
  hgvsc: ENST00000413765.2:c.3095-6380C>T
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368310
  ensembl transcript: ENST00000379024
  gene symbol: NRCAM
  hgvsc: ENST00000379024.4:c.3131-6380C>T
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl transcript: ENST00000415105
  gene symbol: NRCAM
  hgvsc: ENST00000415105.1:n.245-6380C>T
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368314
  ensembl transcript: ENST00000379028
  gene symbol: NRCAM
  hgvsc: ENST00000379028.3:c.3466+49C>T
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000401244
  ensembl transcript: ENST00000425651
  gene symbol: NRCAM
  hgvsc: ENST00000425651.2:c.3466+49C>T
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl transcript: ENST00000465585
  gene symbol: NRCAM
  hgvsc: ENST00000465585.1:n.303-6380C>T
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000398174
  ensembl transcript: ENST00000445634
  gene symbol: NRCAM
  hgvsc: ENST00000445634.2:c.162+1405C>T
  variant of: http://identifiers.org/hgnc/7994
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15986
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11001
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4711
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 954
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7304
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18620
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1249
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 279
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7739
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 324
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 116
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3765
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: East Asian
reference allele: G
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: VQSLOD

7-107807325-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107807325
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 107807325
    reference: chr 7
allele count: 3
allele frequency: 2.85932138772398e-5
allele num: 104920
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000325269
  ensembl transcript: ENST00000351718
  gene symbol: NRCAM
  hgvsc: ENST00000351718.4:c.3104-6388G>A
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368310
  ensembl transcript: ENST00000379024
  gene symbol: NRCAM
  hgvsc: ENST00000379024.4:c.3131-6388G>A
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368308
  ensembl transcript: ENST00000379022
  gene symbol: NRCAM
  hgvsc: ENST00000379022.4:c.3466+41G>A
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl transcript: ENST00000465585
  gene symbol: NRCAM
  hgvsc: ENST00000465585.1:n.303-6388G>A
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000401244
  ensembl transcript: ENST00000425651
  gene symbol: NRCAM
  hgvsc: ENST00000425651.2:c.3466+41G>A
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000398174
  ensembl transcript: ENST00000445634
  gene symbol: NRCAM
  hgvsc: ENST00000445634.2:c.162+1397G>A
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl transcript: ENST00000415105
  gene symbol: NRCAM
  hgvsc: ENST00000415105.1:n.245-6388G>A
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368314
  ensembl transcript: ENST00000379028
  gene symbol: NRCAM
  hgvsc: ENST00000379028.3:c.3466+41G>A
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000407858
  ensembl transcript: ENST00000413765
  gene symbol: NRCAM
  hgvsc: ENST00000413765.2:c.3095-6388G>A
  variant of: http://identifiers.org/hgnc/7994
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1015
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5382
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7167
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17469
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 17524
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10165
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 498
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 504
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 107
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8312
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2995
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 264
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: BaseQRankSum

7-107807330-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107807330
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 107807330
    reference: chr 7
allele count: 1
allele frequency: 9.484426571569482e-6
allele num: 105436
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000398174
  ensembl transcript: ENST00000445634
  gene symbol: NRCAM
  hgvsc: ENST00000445634.2:c.162+1392C>T
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl transcript: ENST00000415105
  gene symbol: NRCAM
  hgvsc: ENST00000415105.1:n.245-6393C>T
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368310
  ensembl transcript: ENST00000379024
  gene symbol: NRCAM
  hgvsc: ENST00000379024.4:c.3131-6393C>T
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000325269
  ensembl transcript: ENST00000351718
  gene symbol: NRCAM
  hgvsc: ENST00000351718.4:c.3104-6393C>T
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000407858
  ensembl transcript: ENST00000413765
  gene symbol: NRCAM
  hgvsc: ENST00000413765.2:c.3095-6393C>T
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368314
  ensembl transcript: ENST00000379028
  gene symbol: NRCAM
  hgvsc: ENST00000379028.3:c.3466+36C>T
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000401244
  ensembl transcript: ENST00000425651
  gene symbol: NRCAM
  hgvsc: ENST00000425651.2:c.3466+36C>T
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl transcript: ENST00000465585
  gene symbol: NRCAM
  hgvsc: ENST00000465585.1:n.303-6393C>T
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368308
  ensembl transcript: ENST00000379022
  gene symbol: NRCAM
  hgvsc: ENST00000379022.4:c.3466+36C>T
  variant of: http://identifiers.org/hgnc/7994
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15998
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7011
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5879
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21272
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7556
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1080
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8288
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 239
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1082
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7029
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 393
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 491
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: DP

7-107807333-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107807333
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 107807333
    reference: chr 7
allele count: 7
allele frequency: 6.652348278942466e-5
allele num: 105226
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000401244
  ensembl transcript: ENST00000425651
  gene symbol: NRCAM
  hgvsc: ENST00000425651.2:c.3466+33G>A
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368314
  ensembl transcript: ENST00000379028
  gene symbol: NRCAM
  hgvsc: ENST00000379028.3:c.3466+33G>A
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl transcript: ENST00000415105
  gene symbol: NRCAM
  hgvsc: ENST00000415105.1:n.245-6396G>A
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000407858
  ensembl transcript: ENST00000413765
  gene symbol: NRCAM
  hgvsc: ENST00000413765.2:c.3095-6396G>A
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl transcript: ENST00000465585
  gene symbol: NRCAM
  hgvsc: ENST00000465585.1:n.303-6396G>A
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000325269
  ensembl transcript: ENST00000351718
  gene symbol: NRCAM
  hgvsc: ENST00000351718.4:c.3104-6396G>A
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000398174
  ensembl transcript: ENST00000445634
  gene symbol: NRCAM
  hgvsc: ENST00000445634.2:c.162+1389G>A
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368310
  ensembl transcript: ENST00000379024
  gene symbol: NRCAM
  hgvsc: ENST00000379024.4:c.3131-6396G>A
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368308
  ensembl transcript: ENST00000379022
  gene symbol: NRCAM
  hgvsc: ENST00000379022.4:c.3466+33G>A
  variant of: http://identifiers.org/hgnc/7994
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6445
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23043
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6559
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1226
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6805
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14736
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 393
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2079
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2082
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 525
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1083
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 273
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
reference allele: C
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

7-107807336-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107807336
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 107807336
    reference: chr 7
allele count: 1
allele frequency: 9.366453111535724e-6
allele num: 106764
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl transcript: ENST00000465585
  gene symbol: NRCAM
  hgvsc: ENST00000465585.1:n.303-6399C>A
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000407858
  ensembl transcript: ENST00000413765
  gene symbol: NRCAM
  hgvsc: ENST00000413765.2:c.3095-6399C>A
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl transcript: ENST00000415105
  gene symbol: NRCAM
  hgvsc: ENST00000415105.1:n.245-6399C>A
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368310
  ensembl transcript: ENST00000379024
  gene symbol: NRCAM
  hgvsc: ENST00000379024.4:c.3131-6399C>A
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000401244
  ensembl transcript: ENST00000425651
  gene symbol: NRCAM
  hgvsc: ENST00000425651.2:c.3466+30C>A
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368308
  ensembl transcript: ENST00000379022
  gene symbol: NRCAM
  hgvsc: ENST00000379022.4:c.3466+30C>A
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000325269
  ensembl transcript: ENST00000351718
  gene symbol: NRCAM
  hgvsc: ENST00000351718.4:c.3104-6399C>A
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000398174
  ensembl transcript: ENST00000445634
  gene symbol: NRCAM
  hgvsc: ENST00000445634.2:c.162+1386C>A
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368314
  ensembl transcript: ENST00000379028
  gene symbol: NRCAM
  hgvsc: ENST00000379028.3:c.3466+30C>A
  variant of: http://identifiers.org/hgnc/7994
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5127
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7059
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1216
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6518
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12737
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26210
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 513
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28675
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 303
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7744
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4305
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 112
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
population: African
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: QD

7-107807342-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107807342
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 107807342
    reference: chr 7
allele count: 6
allele frequency: 5.541496573507952e-5
allele num: 108274
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000398174
  ensembl transcript: ENST00000445634
  gene symbol: NRCAM
  hgvsc: ENST00000445634.2:c.162+1380C>G
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000401244
  ensembl transcript: ENST00000425651
  gene symbol: NRCAM
  hgvsc: ENST00000425651.2:c.3466+24C>G
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl transcript: ENST00000415105
  gene symbol: NRCAM
  hgvsc: ENST00000415105.1:n.245-6405C>G
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368308
  ensembl transcript: ENST00000379022
  gene symbol: NRCAM
  hgvsc: ENST00000379022.4:c.3466+24C>G
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl transcript: ENST00000465585
  gene symbol: NRCAM
  hgvsc: ENST00000465585.1:n.303-6405C>G
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000407858
  ensembl transcript: ENST00000413765
  gene symbol: NRCAM
  hgvsc: ENST00000413765.2:c.3095-6405C>G
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000325269
  ensembl transcript: ENST00000351718
  gene symbol: NRCAM
  hgvsc: ENST00000351718.4:c.3104-6405C>G
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368314
  ensembl transcript: ENST00000379028
  gene symbol: NRCAM
  hgvsc: ENST00000379028.3:c.3466+24C>G
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368310
  ensembl transcript: ENST00000379024
  gene symbol: NRCAM
  hgvsc: ENST00000379024.4:c.3131-6405C>G
  variant of: http://identifiers.org/hgnc/7994
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5908
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7901
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29848
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10142
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1333
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3783
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1141
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3177
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 167
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 300
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32547
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD

7-107807342-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107807342
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 107807342
    reference: chr 7
allele count: 3
allele frequency: 2.770748286753976e-5
allele num: 108274
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000401244
  ensembl transcript: ENST00000425651
  gene symbol: NRCAM
  hgvsc: ENST00000425651.2:c.3466+24C>A
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000398174
  ensembl transcript: ENST00000445634
  gene symbol: NRCAM
  hgvsc: ENST00000445634.2:c.162+1380C>A
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368314
  ensembl transcript: ENST00000379028
  gene symbol: NRCAM
  hgvsc: ENST00000379028.3:c.3466+24C>A
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000325269
  ensembl transcript: ENST00000351718
  gene symbol: NRCAM
  hgvsc: ENST00000351718.4:c.3104-6405C>A
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000407858
  ensembl transcript: ENST00000413765
  gene symbol: NRCAM
  hgvsc: ENST00000413765.2:c.3095-6405C>A
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl transcript: ENST00000465585
  gene symbol: NRCAM
  hgvsc: ENST00000465585.1:n.303-6405C>A
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl transcript: ENST00000415105
  gene symbol: NRCAM
  hgvsc: ENST00000415105.1:n.245-6405C>A
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368310
  ensembl transcript: ENST00000379024
  gene symbol: NRCAM
  hgvsc: ENST00000379024.4:c.3131-6405C>A
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368308
  ensembl transcript: ENST00000379022
  gene symbol: NRCAM
  hgvsc: ENST00000379022.4:c.3466+24C>A
  variant of: http://identifiers.org/hgnc/7994
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5908
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1333
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3783
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29848
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10142
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7901
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1082
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 3177
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 105
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2846
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7009
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 760
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS

7-107807345-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107807345
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 107807345
    reference: chr 7
allele count: 3
allele frequency: 2.754213947339429e-5
allele num: 108924
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368314
  ensembl transcript: ENST00000379028
  gene symbol: NRCAM
  hgvsc: ENST00000379028.3:c.3466+21G>A
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000398174
  ensembl transcript: ENST00000445634
  gene symbol: NRCAM
  hgvsc: ENST00000445634.2:c.162+1377G>A
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000401244
  ensembl transcript: ENST00000425651
  gene symbol: NRCAM
  hgvsc: ENST00000425651.2:c.3466+21G>A
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl transcript: ENST00000465585
  gene symbol: NRCAM
  hgvsc: ENST00000465585.1:n.303-6408G>A
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000407858
  ensembl transcript: ENST00000413765
  gene symbol: NRCAM
  hgvsc: ENST00000413765.2:c.3095-6408G>A
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368308
  ensembl transcript: ENST00000379022
  gene symbol: NRCAM
  hgvsc: ENST00000379022.4:c.3466+21G>A
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000325269
  ensembl transcript: ENST00000351718
  gene symbol: NRCAM
  hgvsc: ENST00000351718.4:c.3104-6408G>A
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl transcript: ENST00000415105
  gene symbol: NRCAM
  hgvsc: ENST00000415105.1:n.245-6408G>A
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368310
  ensembl transcript: ENST00000379024
  gene symbol: NRCAM
  hgvsc: ENST00000379024.4:c.3131-6408G>A
  variant of: http://identifiers.org/hgnc/7994
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1380
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5597
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8955
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31556
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8226
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3212
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 228
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 922
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34728
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 631
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 306
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 123
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
reference allele: C
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum

7-107807347-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107807347
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 107807347
    reference: chr 7
allele count: 2
allele frequency: 1.827819411442149e-5
allele num: 109420
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368310
  ensembl transcript: ENST00000379024
  gene symbol: NRCAM
  hgvsc: ENST00000379024.4:c.3131-6410C>T
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000325269
  ensembl transcript: ENST00000351718
  gene symbol: NRCAM
  hgvsc: ENST00000351718.4:c.3104-6410C>T
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000401244
  ensembl transcript: ENST00000425651
  gene symbol: NRCAM
  hgvsc: ENST00000425651.2:c.3466+19C>T
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl transcript: ENST00000465585
  gene symbol: NRCAM
  hgvsc: ENST00000465585.1:n.303-6410C>T
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000407858
  ensembl transcript: ENST00000413765
  gene symbol: NRCAM
  hgvsc: ENST00000413765.2:c.3095-6410C>T
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000398174
  ensembl transcript: ENST00000445634
  gene symbol: NRCAM
  hgvsc: ENST00000445634.2:c.162+1375C>T
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368308
  ensembl transcript: ENST00000379022
  gene symbol: NRCAM
  hgvsc: ENST00000379022.4:c.3466+19C>T
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl transcript: ENST00000415105
  gene symbol: NRCAM
  hgvsc: ENST00000415105.1:n.245-6410C>T
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368314
  ensembl transcript: ENST00000379028
  gene symbol: NRCAM
  hgvsc: ENST00000379028.3:c.3466+19C>T
  variant of: http://identifiers.org/hgnc/7994
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2961
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8476
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5388
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1391
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32483
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8243
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6351
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 126
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 126
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 964
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 226
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
population: Other
reference allele: G
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum

7-107807349-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107807349
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 107807349
    reference: chr 7
allele count: 1
allele frequency: 9.103488456776638e-6
allele num: 109848
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368310
  ensembl transcript: ENST00000379024
  gene symbol: NRCAM
  hgvsc: ENST00000379024.4:c.3131-6412A>C
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000401244
  ensembl transcript: ENST00000425651
  gene symbol: NRCAM
  hgvsc: ENST00000425651.2:c.3466+17A>C
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368308
  ensembl transcript: ENST00000379022
  gene symbol: NRCAM
  hgvsc: ENST00000379022.4:c.3466+17A>C
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl transcript: ENST00000465585
  gene symbol: NRCAM
  hgvsc: ENST00000465585.1:n.303-6412A>C
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000325269
  ensembl transcript: ENST00000351718
  gene symbol: NRCAM
  hgvsc: ENST00000351718.4:c.3104-6412A>C
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368314
  ensembl transcript: ENST00000379028
  gene symbol: NRCAM
  hgvsc: ENST00000379028.3:c.3466+17A>C
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000398174
  ensembl transcript: ENST00000445634
  gene symbol: NRCAM
  hgvsc: ENST00000445634.2:c.162+1373A>C
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl transcript: ENST00000415105
  gene symbol: NRCAM
  hgvsc: ENST00000415105.1:n.245-6412A>C
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000407858
  ensembl transcript: ENST00000413765
  gene symbol: NRCAM
  hgvsc: ENST00000413765.2:c.3095-6412A>C
  variant of: http://identifiers.org/hgnc/7994
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5162
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1412
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7713
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33104
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8736
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2813
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36310
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 886
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 621
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 853
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 129
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1073
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
reference allele: T
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff

7-107807351-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107807351
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 107807351
    reference: chr 7
allele count: 90
allele frequency: 8.150992609766701e-4
allele num: 110416
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000401244
  ensembl transcript: ENST00000425651
  gene symbol: NRCAM
  hgvsc: ENST00000425651.2:c.3466+15A>G
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000398174
  ensembl transcript: ENST00000445634
  gene symbol: NRCAM
  hgvsc: ENST00000445634.2:c.162+1371A>G
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368314
  ensembl transcript: ENST00000379028
  gene symbol: NRCAM
  hgvsc: ENST00000379028.3:c.3466+15A>G
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl transcript: ENST00000415105
  gene symbol: NRCAM
  hgvsc: ENST00000415105.1:n.245-6414A>G
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000325269
  ensembl transcript: ENST00000351718
  gene symbol: NRCAM
  hgvsc: ENST00000351718.4:c.3104-6414A>G
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl transcript: ENST00000465585
  gene symbol: NRCAM
  hgvsc: ENST00000465585.1:n.303-6414A>G
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368308
  ensembl transcript: ENST00000379022
  gene symbol: NRCAM
  hgvsc: ENST00000379022.4:c.3466+15A>G
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000407858
  ensembl transcript: ENST00000413765
  gene symbol: NRCAM
  hgvsc: ENST00000413765.2:c.3095-6414A>G
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368310
  ensembl transcript: ENST00000379024
  gene symbol: NRCAM
  hgvsc: ENST00000379024.4:c.3131-6414A>G
  variant of: http://identifiers.org/hgnc/7994
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 33898
  bin: 2.25e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4944
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2565
  bin: 1.75e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 7174
  bin: 1.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8919
  bin: 2.75e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1444
  bin: 3.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 308
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 127
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 200
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 753
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5867
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 2
population: European (Finnish)
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: T
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ

7-107807367-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107807367
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 107807367
    reference: chr 7
allele count: 1
allele frequency: 8.723719794120213e-6
allele num: 114630
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000401244
  ensembl transcript: ENST00000425651
  gene symbol: NRCAM
  hgvsc: ENST00000425651.2:c.3465A>G
  hgvsp: ENST00000425651.2:c.3465A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl transcript: ENST00000415105
  gene symbol: NRCAM
  hgvsc: ENST00000415105.1:n.245-6430A>G
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368308
  ensembl transcript: ENST00000379022
  gene symbol: NRCAM
  hgvsc: ENST00000379022.4:c.3465A>G
  hgvsp: ENST00000379022.4:c.3465A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368314
  ensembl transcript: ENST00000379028
  gene symbol: NRCAM
  hgvsc: ENST00000379028.3:c.3465A>G
  hgvsp: ENST00000379028.3:c.3465A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl transcript: ENST00000465585
  gene symbol: NRCAM
  hgvsc: ENST00000465585.1:n.303-6430A>G
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000325269
  ensembl transcript: ENST00000351718
  gene symbol: NRCAM
  hgvsc: ENST00000351718.4:c.3104-6430A>G
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368310
  ensembl transcript: ENST00000379024
  gene symbol: NRCAM
  hgvsc: ENST00000379024.4:c.3131-6430A>G
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000407858
  ensembl transcript: ENST00000413765
  gene symbol: NRCAM
  hgvsc: ENST00000413765.2:c.3095-6430A>G
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000398174
  ensembl transcript: ENST00000445634
  gene symbol: NRCAM
  hgvsc: ENST00000445634.2:c.162+1355A>G
  variant of: http://identifiers.org/hgnc/7994
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1237
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3252
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11071
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1728
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2972
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38735
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 134
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 136
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1440
  bin: 3.25e1
  variant carriers: 0
hgvs: c.3465A>G
num of homozygotes: 0
population: South Asian
population: African
population: Other
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
reference allele: T
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum

7-107807367-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107807367
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 107807367
    reference: chr 7
allele count: 3
allele frequency: 2.617115938236064e-5
allele num: 114630
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368310
  ensembl transcript: ENST00000379024
  gene symbol: NRCAM
  hgvsc: ENST00000379024.4:c.3131-6430A>C
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl transcript: ENST00000415105
  gene symbol: NRCAM
  hgvsc: ENST00000415105.1:n.245-6430A>C
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000401244
  ensembl transcript: ENST00000425651
  gene symbol: NRCAM
  hgvsc: ENST00000425651.2:c.3465A>C
  hgvsp: ENST00000425651.2:c.3465A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000407858
  ensembl transcript: ENST00000413765
  gene symbol: NRCAM
  hgvsc: ENST00000413765.2:c.3095-6430A>C
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl transcript: ENST00000465585
  gene symbol: NRCAM
  hgvsc: ENST00000465585.1:n.303-6430A>C
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368308
  ensembl transcript: ENST00000379022
  gene symbol: NRCAM
  hgvsc: ENST00000379022.4:c.3465A>C
  hgvsp: ENST00000379022.4:c.3465A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368314
  ensembl transcript: ENST00000379028
  gene symbol: NRCAM
  hgvsc: ENST00000379028.3:c.3465A>C
  hgvsp: ENST00000379028.3:c.3465A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000398174
  ensembl transcript: ENST00000445634
  gene symbol: NRCAM
  hgvsc: ENST00000445634.2:c.162+1355A>C
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000325269
  ensembl transcript: ENST00000351718
  gene symbol: NRCAM
  hgvsc: ENST00000351718.4:c.3104-6430A>C
  variant of: http://identifiers.org/hgnc/7994
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1728
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38735
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2972
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3252
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1237
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11071
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3583
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1440
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 850
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
hgvs: c.3465A>C
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: ClippingRankSum
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff

7-107807382-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107807382
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 107807382
    reference: chr 7
allele count: 3
allele frequency: 2.562569402921329e-5
allele num: 117070
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000407858
  ensembl transcript: ENST00000413765
  gene symbol: NRCAM
  hgvsc: ENST00000413765.2:c.3095-6445G>A
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl transcript: ENST00000465585
  gene symbol: NRCAM
  hgvsc: ENST00000465585.1:n.303-6445G>A
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000325269
  ensembl transcript: ENST00000351718
  gene symbol: NRCAM
  hgvsc: ENST00000351718.4:c.3104-6445G>A
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl transcript: ENST00000415105
  gene symbol: NRCAM
  hgvsc: ENST00000415105.1:n.245-6445G>A
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000401244
  ensembl transcript: ENST00000425651
  gene symbol: NRCAM
  hgvsc: ENST00000425651.2:c.3450G>A
  hgvsp: ENST00000425651.2:c.3450G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368314
  ensembl transcript: ENST00000379028
  gene symbol: NRCAM
  hgvsc: ENST00000379028.3:c.3450G>A
  hgvsp: ENST00000379028.3:c.3450G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368310
  ensembl transcript: ENST00000379024
  gene symbol: NRCAM
  hgvsc: ENST00000379024.4:c.3131-6445G>A
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000398174
  ensembl transcript: ENST00000445634
  gene symbol: NRCAM
  hgvsc: ENST00000445634.2:c.162+1340G>A
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368308
  ensembl transcript: ENST00000379022
  gene symbol: NRCAM
  hgvsc: ENST00000379022.4:c.3450G>A
  hgvsp: ENST00000379022.4:c.3450G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7994
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 979
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1683
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 40147
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1857
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12530
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1800
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4023
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2239
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 750
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Val1150Val
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
population: Other
population: East Asian
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/7-107807390-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107807390
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 107807390
    reference: chr 7
allele count: 4
allele frequency: 3.403038913749979e-5
allele num: 117542
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000325269
  ensembl transcript: ENST00000351718
  gene symbol: NRCAM
  hgvsc: ENST00000351718.4:c.3104-6453G>T
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl transcript: ENST00000415105
  gene symbol: NRCAM
  hgvsc: ENST00000415105.1:n.245-6453G>T
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000398174
  ensembl transcript: ENST00000445634
  gene symbol: NRCAM
  hgvsc: ENST00000445634.2:c.162+1332G>T
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368310
  ensembl transcript: ENST00000379024
  gene symbol: NRCAM
  hgvsc: ENST00000379024.4:c.3131-6453G>T
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000401244
  ensembl transcript: ENST00000425651
  gene symbol: NRCAM
  hgvsc: ENST00000425651.2:c.3442G>T
  hgvsp: ENSP00000401244.2:p.Glu1148Ter
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368308
  ensembl transcript: ENST00000379022
  gene symbol: NRCAM
  hgvsc: ENST00000379022.4:c.3442G>T
  hgvsp: ENSP00000368308.4:p.Glu1148Ter
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl transcript: ENST00000465585
  gene symbol: NRCAM
  hgvsc: ENST00000465585.1:n.303-6453G>T
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000407858
  ensembl transcript: ENST00000413765
  gene symbol: NRCAM
  hgvsc: ENST00000413765.2:c.3095-6453G>T
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368314
  ensembl transcript: ENST00000379028
  gene symbol: NRCAM
  hgvsc: ENST00000379028.3:c.3442G>T
  hgvsp: ENSP00000368314.3:p.Glu1148Ter
  variant of: http://identifiers.org/hgnc/7994
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13100
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1191
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 39805
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1891
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1445
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1573
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2031
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 654
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 125
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 136
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 126
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Glu1148Ter
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: African
reference allele: C
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQ

http://identifiers.org/exac.variant/7-107807399-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107807399
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 107807399
    reference: chr 7
allele count: 2
allele frequency: 1.696525515743757e-5
allele num: 117888
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000407858
  ensembl transcript: ENST00000413765
  gene symbol: NRCAM
  hgvsc: ENST00000413765.2:c.3095-6462G>T
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl transcript: ENST00000465585
  gene symbol: NRCAM
  hgvsc: ENST00000465585.1:n.303-6462G>T
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000401244
  ensembl transcript: ENST00000425651
  gene symbol: NRCAM
  hgvsc: ENST00000425651.2:c.3433G>T
  hgvsp: ENSP00000401244.2:p.Val1145Leu
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368308
  ensembl transcript: ENST00000379022
  gene symbol: NRCAM
  hgvsc: ENST00000379022.4:c.3433G>T
  hgvsp: ENSP00000368308.4:p.Val1145Leu
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000398174
  ensembl transcript: ENST00000445634
  gene symbol: NRCAM
  hgvsc: ENST00000445634.2:c.162+1323G>T
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl transcript: ENST00000415105
  gene symbol: NRCAM
  hgvsc: ENST00000415105.1:n.245-6462G>T
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368310
  ensembl transcript: ENST00000379024
  gene symbol: NRCAM
  hgvsc: ENST00000379024.4:c.3131-6462G>T
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368314
  ensembl transcript: ENST00000379028
  gene symbol: NRCAM
  hgvsc: ENST00000379028.3:c.3433G>T
  hgvsp: ENSP00000368314.3:p.Val1145Leu
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000325269
  ensembl transcript: ENST00000351718
  gene symbol: NRCAM
  hgvsc: ENST00000351718.4:c.3104-6462G>T
  variant of: http://identifiers.org/hgnc/7994
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39574
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1235
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1971
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1239
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1398
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13590
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 733
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 513
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 584
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 146
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Val1145Leu
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
population: European (Non-Finnish)
population: African
population: Latino
reference allele: C
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum

7-107807406-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107807406
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 107807406
    reference: chr 7
allele count: 1
allele frequency: 8.462527926342156e-6
allele num: 118168
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368310
  ensembl transcript: ENST00000379024
  gene symbol: NRCAM
  hgvsc: ENST00000379024.4:c.3131-6469T>C
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000407858
  ensembl transcript: ENST00000413765
  gene symbol: NRCAM
  hgvsc: ENST00000413765.2:c.3095-6469T>C
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368308
  ensembl transcript: ENST00000379022
  gene symbol: NRCAM
  hgvsc: ENST00000379022.4:c.3426T>C
  hgvsp: ENST00000379022.4:c.3426T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000401244
  ensembl transcript: ENST00000425651
  gene symbol: NRCAM
  hgvsc: ENST00000425651.2:c.3426T>C
  hgvsp: ENST00000425651.2:c.3426T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368314
  ensembl transcript: ENST00000379028
  gene symbol: NRCAM
  hgvsc: ENST00000379028.3:c.3426T>C
  hgvsp: ENST00000379028.3:c.3426T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl transcript: ENST00000465585
  gene symbol: NRCAM
  hgvsc: ENST00000465585.1:n.303-6469T>C
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000325269
  ensembl transcript: ENST00000351718
  gene symbol: NRCAM
  hgvsc: ENST00000351718.4:c.3104-6469T>C
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000398174
  ensembl transcript: ENST00000445634
  gene symbol: NRCAM
  hgvsc: ENST00000445634.2:c.162+1316T>C
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl transcript: ENST00000415105
  gene symbol: NRCAM
  hgvsc: ENST00000415105.1:n.245-6469T>C
  variant of: http://identifiers.org/hgnc/7994
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14091
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1277
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39464
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1183
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1048
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1958
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 126
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 725
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 386
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 508
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Ser1142Ser
num of homozygotes: 0
population: Latino
population: South Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
reference allele: A
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum

7-107807407-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107807407
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 107807407
    reference: chr 7
allele count: 1
allele frequency: 8.460666362082677e-6
allele num: 118194
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368310
  ensembl transcript: ENST00000379024
  gene symbol: NRCAM
  hgvsc: ENST00000379024.4:c.3131-6470C>T
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000398174
  ensembl transcript: ENST00000445634
  gene symbol: NRCAM
  hgvsc: ENST00000445634.2:c.162+1315C>T
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368308
  ensembl transcript: ENST00000379022
  gene symbol: NRCAM
  hgvsc: ENST00000379022.4:c.3425C>T
  hgvsp: ENSP00000368308.4:p.Ser1142Phe
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl transcript: ENST00000465585
  gene symbol: NRCAM
  hgvsc: ENST00000465585.1:n.303-6470C>T
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl transcript: ENST00000415105
  gene symbol: NRCAM
  hgvsc: ENST00000415105.1:n.245-6470C>T
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000407858
  ensembl transcript: ENST00000413765
  gene symbol: NRCAM
  hgvsc: ENST00000413765.2:c.3095-6470C>T
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368314
  ensembl transcript: ENST00000379028
  gene symbol: NRCAM
  hgvsc: ENST00000379028.3:c.3425C>T
  hgvsp: ENSP00000368314.3:p.Ser1142Phe
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000401244
  ensembl transcript: ENST00000425651
  gene symbol: NRCAM
  hgvsc: ENST00000425651.2:c.3425C>T
  hgvsp: ENSP00000401244.2:p.Ser1142Phe
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000325269
  ensembl transcript: ENST00000351718
  gene symbol: NRCAM
  hgvsc: ENST00000351718.4:c.3104-6470C>T
  variant of: http://identifiers.org/hgnc/7994
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39435
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1141
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14178
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1024
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1260
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1983
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 495
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 132
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 600
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 137
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 899
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Ser1142Phe
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
population: Other
population: East Asian
population: Latino
reference allele: G
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: BaseQRankSum

7-107807414-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107807414
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 107807414
    reference: chr 7
allele count: 1
allele frequency: 8.445232666159953e-6
allele num: 118410
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368314
  ensembl transcript: ENST00000379028
  gene symbol: NRCAM
  hgvsc: ENST00000379028.3:c.3418G>A
  hgvsp: ENSP00000368314.3:p.Gly1140Arg
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368310
  ensembl transcript: ENST00000379024
  gene symbol: NRCAM
  hgvsc: ENST00000379024.4:c.3131-6477G>A
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000398174
  ensembl transcript: ENST00000445634
  gene symbol: NRCAM
  hgvsc: ENST00000445634.2:c.162+1308G>A
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000407858
  ensembl transcript: ENST00000413765
  gene symbol: NRCAM
  hgvsc: ENST00000413765.2:c.3095-6477G>A
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl transcript: ENST00000415105
  gene symbol: NRCAM
  hgvsc: ENST00000415105.1:n.245-6477G>A
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl transcript: ENST00000465585
  gene symbol: NRCAM
  hgvsc: ENST00000465585.1:n.303-6477G>A
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000401244
  ensembl transcript: ENST00000425651
  gene symbol: NRCAM
  hgvsc: ENST00000425651.2:c.3418G>A
  hgvsp: ENSP00000401244.2:p.Gly1140Arg
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368308
  ensembl transcript: ENST00000379022
  gene symbol: NRCAM
  hgvsc: ENST00000379022.4:c.3418G>A
  hgvsp: ENSP00000368308.4:p.Gly1140Arg
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000325269
  ensembl transcript: ENST00000351718
  gene symbol: NRCAM
  hgvsc: ENST00000351718.4:c.3104-6477G>A
  variant of: http://identifiers.org/hgnc/7994
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2029
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14509
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39369
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 913
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1033
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1147
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 421
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 457
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 343
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Gly1140Arg
num of homozygotes: 0
population: Latino
population: South Asian
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
reference allele: C
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: QD

7-107807428-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107807428
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 107807428
    reference: chr 7
allele count: 5
allele frequency: 4.217202813717717e-5
allele num: 118562
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl transcript: ENST00000415105
  gene symbol: NRCAM
  hgvsc: ENST00000415105.1:n.245-6491G>A
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000407858
  ensembl transcript: ENST00000413765
  gene symbol: NRCAM
  hgvsc: ENST00000413765.2:c.3095-6491G>A
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000398174
  ensembl transcript: ENST00000445634
  gene symbol: NRCAM
  hgvsc: ENST00000445634.2:c.162+1294G>A
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368314
  ensembl transcript: ENST00000379028
  gene symbol: NRCAM
  hgvsc: ENST00000379028.3:c.3404G>A
  hgvsp: ENSP00000368314.3:p.Arg1135Gln
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368308
  ensembl transcript: ENST00000379022
  gene symbol: NRCAM
  hgvsc: ENST00000379022.4:c.3404G>A
  hgvsp: ENSP00000368308.4:p.Arg1135Gln
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl transcript: ENST00000465585
  gene symbol: NRCAM
  hgvsc: ENST00000465585.1:n.303-6491G>A
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000401244
  ensembl transcript: ENST00000425651
  gene symbol: NRCAM
  hgvsc: ENST00000425651.2:c.3404G>A
  hgvsp: ENSP00000401244.2:p.Arg1135Gln
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368310
  ensembl transcript: ENST00000379024
  gene symbol: NRCAM
  hgvsc: ENST00000379024.4:c.3131-6491G>A
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000325269
  ensembl transcript: ENST00000351718
  gene symbol: NRCAM
  hgvsc: ENST00000351718.4:c.3104-6491G>A
  variant of: http://identifiers.org/hgnc/7994
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15157
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 803
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38995
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1062
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2153
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 469
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 395
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 304
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 222
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Arg1135Gln
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
population: African
population: South Asian
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum

7-107807429-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107807429
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 107807429
    reference: chr 7
allele count: 1
allele frequency: 8.43540169382866e-6
allele num: 118548
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368310
  ensembl transcript: ENST00000379024
  gene symbol: NRCAM
  hgvsc: ENST00000379024.4:c.3131-6492C>T
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl transcript: ENST00000415105
  gene symbol: NRCAM
  hgvsc: ENST00000415105.1:n.245-6492C>T
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368308
  ensembl transcript: ENST00000379022
  gene symbol: NRCAM
  hgvsc: ENST00000379022.4:c.3403C>T
  hgvsp: ENSP00000368308.4:p.Arg1135Ter
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl transcript: ENST00000465585
  gene symbol: NRCAM
  hgvsc: ENST00000465585.1:n.303-6492C>T
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000401244
  ensembl transcript: ENST00000425651
  gene symbol: NRCAM
  hgvsc: ENST00000425651.2:c.3403C>T
  hgvsp: ENSP00000401244.2:p.Arg1135Ter
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000325269
  ensembl transcript: ENST00000351718
  gene symbol: NRCAM
  hgvsc: ENST00000351718.4:c.3104-6492C>T
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000407858
  ensembl transcript: ENST00000413765
  gene symbol: NRCAM
  hgvsc: ENST00000413765.2:c.3095-6492C>T
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368314
  ensembl transcript: ENST00000379028
  gene symbol: NRCAM
  hgvsc: ENST00000379028.3:c.3403C>T
  hgvsp: ENSP00000368314.3:p.Arg1135Ter
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000398174
  ensembl transcript: ENST00000445634
  gene symbol: NRCAM
  hgvsc: ENST00000445634.2:c.162+1293C>T
  variant of: http://identifiers.org/hgnc/7994
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 797
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2152
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1069
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15224
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38939
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 815
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 891
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 296
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 432
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 137
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 310
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Arg1135Ter
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
population: African
population: Other
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: ReadPosRankSum

7-107807435-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107807435
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 107807435
    reference: chr 7
allele count: 1
allele frequency: 8.442238206193226e-6
allele num: 118452
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000325269
  ensembl transcript: ENST00000351718
  gene symbol: NRCAM
  hgvsc: ENST00000351718.4:c.3104-6498A>G
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000407858
  ensembl transcript: ENST00000413765
  gene symbol: NRCAM
  hgvsc: ENST00000413765.2:c.3095-6498A>G
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368308
  ensembl transcript: ENST00000379022
  gene symbol: NRCAM
  hgvsc: ENST00000379022.4:c.3397A>G
  hgvsp: ENSP00000368308.4:p.Lys1133Glu
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000398174
  ensembl transcript: ENST00000445634
  gene symbol: NRCAM
  hgvsc: ENST00000445634.2:c.162+1287A>G
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000401244
  ensembl transcript: ENST00000425651
  gene symbol: NRCAM
  hgvsc: ENST00000425651.2:c.3397A>G
  hgvsp: ENSP00000401244.2:p.Lys1133Glu
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl transcript: ENST00000465585
  gene symbol: NRCAM
  hgvsc: ENST00000465585.1:n.303-6498A>G
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368310
  ensembl transcript: ENST00000379024
  gene symbol: NRCAM
  hgvsc: ENST00000379024.4:c.3131-6498A>G
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl transcript: ENST00000415105
  gene symbol: NRCAM
  hgvsc: ENST00000415105.1:n.245-6498A>G
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368314
  ensembl transcript: ENST00000379028
  gene symbol: NRCAM
  hgvsc: ENST00000379028.3:c.3397A>G
  hgvsp: ENSP00000368314.3:p.Lys1133Glu
  variant of: http://identifiers.org/hgnc/7994
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15356
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 848
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2104
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1137
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38714
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 856
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 126
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48688
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 583
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Lys1133Glu
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
reference allele: T
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: InbreedingCoeff

7-107807465-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107807465
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 107807465
    reference: chr 7
allele count: 7
allele frequency: 5.993663841082285e-5
allele num: 116790
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl transcript: ENST00000415105
  gene symbol: NRCAM
  hgvsc: ENST00000415105.1:n.245-6528T>C
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368310
  ensembl transcript: ENST00000379024
  gene symbol: NRCAM
  hgvsc: ENST00000379024.4:c.3131-6528T>C
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000407858
  ensembl transcript: ENST00000413765
  gene symbol: NRCAM
  hgvsc: ENST00000413765.2:c.3095-6528T>C
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368308
  ensembl transcript: ENST00000379022
  gene symbol: NRCAM
  hgvsc: ENST00000379022.4:c.3367T>C
  hgvsp: ENST00000379022.4:c.3367T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000401244
  ensembl transcript: ENST00000425651
  gene symbol: NRCAM
  hgvsc: ENST00000425651.2:c.3367T>C
  hgvsp: ENST00000425651.2:c.3367T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000398174
  ensembl transcript: ENST00000445634
  gene symbol: NRCAM
  hgvsc: ENST00000445634.2:c.162+1257T>C
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000325269
  ensembl transcript: ENST00000351718
  gene symbol: NRCAM
  hgvsc: ENST00000351718.4:c.3104-6528T>C
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368314
  ensembl transcript: ENST00000379028
  gene symbol: NRCAM
  hgvsc: ENST00000379028.3:c.3367T>C
  hgvsp: ENST00000379028.3:c.3367T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl transcript: ENST00000465585
  gene symbol: NRCAM
  hgvsc: ENST00000465585.1:n.303-6528T>C
  variant of: http://identifiers.org/hgnc/7994
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1944
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2021
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1468
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37277
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15640
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 311
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3025
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 320
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 236
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 184
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Leu1123Leu
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQ

7-107807477-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107807477
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 107807477
    reference: chr 7
allele count: 3
allele frequency: 2.612011771466383e-5
allele num: 114854
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000401244
  ensembl transcript: ENST00000425651
  gene symbol: NRCAM
  hgvsc: ENST00000425651.2:c.3355A>G
  hgvsp: ENSP00000401244.2:p.Ser1119Gly
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000398174
  ensembl transcript: ENST00000445634
  gene symbol: NRCAM
  hgvsc: ENST00000445634.2:c.162+1245A>G
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl transcript: ENST00000415105
  gene symbol: NRCAM
  hgvsc: ENST00000415105.1:n.245-6540A>G
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000407858
  ensembl transcript: ENST00000413765
  gene symbol: NRCAM
  hgvsc: ENST00000413765.2:c.3095-6540A>G
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368308
  ensembl transcript: ENST00000379022
  gene symbol: NRCAM
  hgvsc: ENST00000379022.4:c.3355A>G
  hgvsp: ENSP00000368308.4:p.Ser1119Gly
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368314
  ensembl transcript: ENST00000379028
  gene symbol: NRCAM
  hgvsc: ENST00000379028.3:c.3355A>G
  hgvsp: ENSP00000368314.3:p.Ser1119Gly
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368310
  ensembl transcript: ENST00000379024
  gene symbol: NRCAM
  hgvsc: ENST00000379024.4:c.3131-6540A>G
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000325269
  ensembl transcript: ENST00000351718
  gene symbol: NRCAM
  hgvsc: ENST00000351718.4:c.3104-6540A>G
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl transcript: ENST00000465585
  gene symbol: NRCAM
  hgvsc: ENST00000465585.1:n.303-6540A>G
  variant of: http://identifiers.org/hgnc/7994
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35493
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2892
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1943
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15495
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2456
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 640
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4656
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 122
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ser1119Gly
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP

http://identifiers.org/exac.variant/7-107807479-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107807479
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 107807479
    reference: chr 7
allele count: 1
allele frequency: 8.747528823107472e-6
allele num: 114318
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000325269
  ensembl transcript: ENST00000351718
  gene symbol: NRCAM
  hgvsc: ENST00000351718.4:c.3104-6542G>T
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000398174
  ensembl transcript: ENST00000445634
  gene symbol: NRCAM
  hgvsc: ENST00000445634.2:c.162+1243G>T
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl transcript: ENST00000415105
  gene symbol: NRCAM
  hgvsc: ENST00000415105.1:n.245-6542G>T
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl transcript: ENST00000465585
  gene symbol: NRCAM
  hgvsc: ENST00000465585.1:n.303-6542G>T
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368308
  ensembl transcript: ENST00000379022
  gene symbol: NRCAM
  hgvsc: ENST00000379022.4:c.3353G>T
  hgvsp: ENSP00000368308.4:p.Arg1118Leu
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000401244
  ensembl transcript: ENST00000425651
  gene symbol: NRCAM
  hgvsc: ENST00000425651.2:c.3353G>T
  hgvsp: ENSP00000401244.2:p.Arg1118Leu
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368314
  ensembl transcript: ENST00000379028
  gene symbol: NRCAM
  hgvsc: ENST00000379028.3:c.3353G>T
  hgvsp: ENSP00000368314.3:p.Arg1118Leu
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000407858
  ensembl transcript: ENST00000413765
  gene symbol: NRCAM
  hgvsc: ENST00000413765.2:c.3095-6542G>T
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368310
  ensembl transcript: ENST00000379024
  gene symbol: NRCAM
  hgvsc: ENST00000379024.4:c.3131-6542G>T
  variant of: http://identifiers.org/hgnc/7994
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15380
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35046
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2684
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1978
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3130
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 740
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1083
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 729
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 306
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Arg1118Leu
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
population: African
reference allele: C
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: DP

7-107807479-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107807479
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 107807479
    reference: chr 7
allele count: 3
allele frequency: 2.624258646932242e-5
allele num: 114318
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368310
  ensembl transcript: ENST00000379024
  gene symbol: NRCAM
  hgvsc: ENST00000379024.4:c.3131-6542G>A
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000401244
  ensembl transcript: ENST00000425651
  gene symbol: NRCAM
  hgvsc: ENST00000425651.2:c.3353G>A
  hgvsp: ENSP00000401244.2:p.Arg1118Gln
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000325269
  ensembl transcript: ENST00000351718
  gene symbol: NRCAM
  hgvsc: ENST00000351718.4:c.3104-6542G>A
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000407858
  ensembl transcript: ENST00000413765
  gene symbol: NRCAM
  hgvsc: ENST00000413765.2:c.3095-6542G>A
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368308
  ensembl transcript: ENST00000379022
  gene symbol: NRCAM
  hgvsc: ENST00000379022.4:c.3353G>A
  hgvsp: ENSP00000368308.4:p.Arg1118Gln
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl transcript: ENST00000465585
  gene symbol: NRCAM
  hgvsc: ENST00000465585.1:n.303-6542G>A
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl transcript: ENST00000415105
  gene symbol: NRCAM
  hgvsc: ENST00000415105.1:n.245-6542G>A
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000398174
  ensembl transcript: ENST00000445634
  gene symbol: NRCAM
  hgvsc: ENST00000445634.2:c.162+1243G>A
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368314
  ensembl transcript: ENST00000379028
  gene symbol: NRCAM
  hgvsc: ENST00000379028.3:c.3353G>A
  hgvsp: ENSP00000368314.3:p.Arg1118Gln
  variant of: http://identifiers.org/hgnc/7994
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 740
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3130
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35046
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2684
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15380
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1978
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 517
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 157
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3821
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Arg1118Gln
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
population: Latino
population: Other
population: European (Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD

7-107807480-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107807480
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 107807480
    reference: chr 7
allele count: 4
allele frequency: 3.507602728914923e-5
allele num: 114038
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368314
  ensembl transcript: ENST00000379028
  gene symbol: NRCAM
  hgvsc: ENST00000379028.3:c.3352C>T
  hgvsp: ENSP00000368314.3:p.Arg1118Trp
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000401244
  ensembl transcript: ENST00000425651
  gene symbol: NRCAM
  hgvsc: ENST00000425651.2:c.3352C>T
  hgvsp: ENSP00000401244.2:p.Arg1118Trp
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000325269
  ensembl transcript: ENST00000351718
  gene symbol: NRCAM
  hgvsc: ENST00000351718.4:c.3104-6543C>T
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl transcript: ENST00000415105
  gene symbol: NRCAM
  hgvsc: ENST00000415105.1:n.245-6543C>T
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368310
  ensembl transcript: ENST00000379024
  gene symbol: NRCAM
  hgvsc: ENST00000379024.4:c.3131-6543C>T
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl transcript: ENST00000465585
  gene symbol: NRCAM
  hgvsc: ENST00000465585.1:n.303-6543C>T
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000407858
  ensembl transcript: ENST00000413765
  gene symbol: NRCAM
  hgvsc: ENST00000413765.2:c.3095-6543C>T
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368308
  ensembl transcript: ENST00000379022
  gene symbol: NRCAM
  hgvsc: ENST00000379022.4:c.3352C>T
  hgvsp: ENSP00000368308.4:p.Arg1118Trp
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000398174
  ensembl transcript: ENST00000445634
  gene symbol: NRCAM
  hgvsc: ENST00000445634.2:c.162+1242C>T
  variant of: http://identifiers.org/hgnc/7994
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 748
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 34825
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15336
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3270
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1942
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2825
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 122
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 516
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 174
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Arg1118Trp
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: Other
population: African
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: G
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum

7-107807482-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107807482
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 107807482
    reference: chr 7
allele count: 4
allele frequency: 3.525844439743319e-5
allele num: 113448
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000401244
  ensembl transcript: ENST00000425651
  gene symbol: NRCAM
  hgvsc: ENST00000425651.2:c.3350C>T
  hgvsp: ENSP00000401244.2:p.Ser1117Phe
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl transcript: ENST00000415105
  gene symbol: NRCAM
  hgvsc: ENST00000415105.1:n.245-6545C>T
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000407858
  ensembl transcript: ENST00000413765
  gene symbol: NRCAM
  hgvsc: ENST00000413765.2:c.3095-6545C>T
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000325269
  ensembl transcript: ENST00000351718
  gene symbol: NRCAM
  hgvsc: ENST00000351718.4:c.3104-6545C>T
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368308
  ensembl transcript: ENST00000379022
  gene symbol: NRCAM
  hgvsc: ENST00000379022.4:c.3350C>T
  hgvsp: ENSP00000368308.4:p.Ser1117Phe
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368314
  ensembl transcript: ENST00000379028
  gene symbol: NRCAM
  hgvsc: ENST00000379028.3:c.3350C>T
  hgvsp: ENSP00000368314.3:p.Ser1117Phe
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368310
  ensembl transcript: ENST00000379024
  gene symbol: NRCAM
  hgvsc: ENST00000379024.4:c.3131-6545C>T
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl transcript: ENST00000465585
  gene symbol: NRCAM
  hgvsc: ENST00000465585.1:n.303-6545C>T
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000398174
  ensembl transcript: ENST00000445634
  gene symbol: NRCAM
  hgvsc: ENST00000445634.2:c.162+1240C>T
  variant of: http://identifiers.org/hgnc/7994
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15243
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3575
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3128
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 778
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34325
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1918
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 498
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 720
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3748
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 604
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Ser1117Phe
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
population: Other
population: African
reference allele: G
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff

7-107807507-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107807507
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 107807507
    reference: chr 7
allele count: 1
allele frequency: 9.775935557032808e-6
allele num: 102292
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000401244
  ensembl transcript: ENST00000425651
  gene symbol: NRCAM
  hgvsc: ENST00000425651.2:c.3325T>A
  hgvsp: ENSP00000401244.2:p.Trp1109Arg
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl transcript: ENST00000415105
  gene symbol: NRCAM
  hgvsc: ENST00000415105.1:n.245-6570T>A
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368314
  ensembl transcript: ENST00000379028
  gene symbol: NRCAM
  hgvsc: ENST00000379028.3:c.3325T>A
  hgvsp: ENSP00000368314.3:p.Trp1109Arg
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368308
  ensembl transcript: ENST00000379022
  gene symbol: NRCAM
  hgvsc: ENST00000379022.4:c.3325T>A
  hgvsp: ENSP00000368308.4:p.Trp1109Arg
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl transcript: ENST00000465585
  gene symbol: NRCAM
  hgvsc: ENST00000465585.1:n.303-6570T>A
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000407858
  ensembl transcript: ENST00000413765
  gene symbol: NRCAM
  hgvsc: ENST00000413765.2:c.3095-6570T>A
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000398174
  ensembl transcript: ENST00000445634
  gene symbol: NRCAM
  hgvsc: ENST00000445634.2:c.162+1215T>A
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000325269
  ensembl transcript: ENST00000351718
  gene symbol: NRCAM
  hgvsc: ENST00000351718.4:c.3104-6570T>A
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368310
  ensembl transcript: ENST00000379024
  gene symbol: NRCAM
  hgvsc: ENST00000379024.4:c.3131-6570T>A
  variant of: http://identifiers.org/hgnc/7994
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8834
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10149
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1817
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1552
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11776
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24605
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 696
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 807
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 425
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1079
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2706
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Trp1109Arg
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: A
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: QD

7-107807522-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107807522
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 107807522
    reference: chr 7
allele count: 13
allele frequency: 1.401133840615637e-4
allele num: 92782
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368314
  ensembl transcript: ENST00000379028
  gene symbol: NRCAM
  hgvsc: ENST00000379028.3:c.3314-4A>G
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000401244
  ensembl transcript: ENST00000425651
  gene symbol: NRCAM
  hgvsc: ENST00000425651.2:c.3314-4A>G
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368308
  ensembl transcript: ENST00000379022
  gene symbol: NRCAM
  hgvsc: ENST00000379022.4:c.3314-4A>G
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000398174
  ensembl transcript: ENST00000445634
  gene symbol: NRCAM
  hgvsc: ENST00000445634.2:c.162+1200A>G
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000325269
  ensembl transcript: ENST00000351718
  gene symbol: NRCAM
  hgvsc: ENST00000351718.4:c.3104-6585A>G
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl transcript: ENST00000415105
  gene symbol: NRCAM
  hgvsc: ENST00000415105.1:n.245-6585A>G
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000407858
  ensembl transcript: ENST00000413765
  gene symbol: NRCAM
  hgvsc: ENST00000413765.2:c.3095-6585A>G
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl transcript: ENST00000465585
  gene symbol: NRCAM
  hgvsc: ENST00000465585.1:n.303-6585A>G
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368310
  ensembl transcript: ENST00000379024
  gene symbol: NRCAM
  hgvsc: ENST00000379024.4:c.3131-6585A>G
  variant of: http://identifiers.org/hgnc/7994
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12757
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1024
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1281
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2740
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18206
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7797
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 15243
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 412
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 113
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 234
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1090
  bin: 9.75e1
  variant carriers: 12
genotype quality: GenotypeQuality
  all individuals: 1413
  bin: 3.75e1
  variant carriers: 0
hgvs: c.3314-4A>G
num of homozygotes: 0
population: European (Finnish)
population: Other
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: T
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD

http://identifiers.org/exac.variant/7-107807541-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107807541
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 107807541
    reference: chr 7
allele count: 11
allele frequency: 1.304151945557584e-4
allele num: 84346
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368308
  ensembl transcript: ENST00000379022
  gene symbol: NRCAM
  hgvsc: ENST00000379022.4:c.3314-23T>G
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl transcript: ENST00000465585
  gene symbol: NRCAM
  hgvsc: ENST00000465585.1:n.303-6604T>G
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000407858
  ensembl transcript: ENST00000413765
  gene symbol: NRCAM
  hgvsc: ENST00000413765.2:c.3095-6604T>G
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl transcript: ENST00000415105
  gene symbol: NRCAM
  hgvsc: ENST00000415105.1:n.245-6604T>G
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368310
  ensembl transcript: ENST00000379024
  gene symbol: NRCAM
  hgvsc: ENST00000379024.4:c.3131-6604T>G
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368314
  ensembl transcript: ENST00000379028
  gene symbol: NRCAM
  hgvsc: ENST00000379028.3:c.3314-23T>G
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000398174
  ensembl transcript: ENST00000445634
  gene symbol: NRCAM
  hgvsc: ENST00000445634.2:c.162+1181T>G
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000325269
  ensembl transcript: ENST00000351718
  gene symbol: NRCAM
  hgvsc: ENST00000351718.4:c.3104-6604T>G
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000401244
  ensembl transcript: ENST00000425651
  gene symbol: NRCAM
  hgvsc: ENST00000425651.2:c.3314-23T>G
  variant of: http://identifiers.org/hgnc/7994
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2898
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 962
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4293
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6938
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24185
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 14970
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4762
  bin: 1.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 992
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 642
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 126
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 430
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9155
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1078
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD

7-107807546-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107807546
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 107807546
    reference: chr 7
allele count: 504
allele frequency: 6.29182063317687e-3
allele num: 80104
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000398174
  ensembl transcript: ENST00000445634
  gene symbol: NRCAM
  hgvsc: ENST00000445634.2:c.162+1176A>T
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl transcript: ENST00000465585
  gene symbol: NRCAM
  hgvsc: ENST00000465585.1:n.303-6609A>T
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000407858
  ensembl transcript: ENST00000413765
  gene symbol: NRCAM
  hgvsc: ENST00000413765.2:c.3095-6609A>T
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368308
  ensembl transcript: ENST00000379022
  gene symbol: NRCAM
  hgvsc: ENST00000379022.4:c.3314-28A>T
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000401244
  ensembl transcript: ENST00000425651
  gene symbol: NRCAM
  hgvsc: ENST00000425651.2:c.3314-28A>T
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000325269
  ensembl transcript: ENST00000351718
  gene symbol: NRCAM
  hgvsc: ENST00000351718.4:c.3104-6609A>T
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368314
  ensembl transcript: ENST00000379028
  gene symbol: NRCAM
  hgvsc: ENST00000379028.3:c.3314-28A>T
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368310
  ensembl transcript: ENST00000379024
  gene symbol: NRCAM
  hgvsc: ENST00000379024.4:c.3131-6609A>T
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl transcript: ENST00000415105
  gene symbol: NRCAM
  hgvsc: ENST00000415105.1:n.245-6609A>T
  variant of: http://identifiers.org/hgnc/7994
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 23946
  bin: 1.25e1
  variant carriers: 178
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 4.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 3.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 15887
  bin: 7.5e0
  variant carriers: 93
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6207
  bin: 1.75e1
  variant carriers: 141
genotype depth: GenotypeDepth
  all individuals: 4991
  bin: 2.25e1
  variant carriers: 70
genotype depth: GenotypeDepth
  all individuals: 3246
  bin: 2.75e1
  variant carriers: 44
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 854
  bin: 3.25e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3797
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 4.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 285
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 837
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1047
  bin: 6.75e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 3322
  bin: 3.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 335
  bin: 7.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 136
  bin: 9.25e1
  variant carriers: 13
num of homozygotes: 4
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
population: African
population: European (Finnish)
population: East Asian
reference allele: T
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum

7-107807562-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107807562
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 107807562
    reference: chr 7
allele count: 1
allele frequency: 1.43826947416868e-5
allele num: 69528
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000398174
  ensembl transcript: ENST00000445634
  gene symbol: NRCAM
  hgvsc: ENST00000445634.2:c.162+1160C>T
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368314
  ensembl transcript: ENST00000379028
  gene symbol: NRCAM
  hgvsc: ENST00000379028.3:c.3314-44C>T
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368310
  ensembl transcript: ENST00000379024
  gene symbol: NRCAM
  hgvsc: ENST00000379024.4:c.3131-6625C>T
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl transcript: ENST00000465585
  gene symbol: NRCAM
  hgvsc: ENST00000465585.1:n.303-6625C>T
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368308
  ensembl transcript: ENST00000379022
  gene symbol: NRCAM
  hgvsc: ENST00000379022.4:c.3314-44C>T
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000407858
  ensembl transcript: ENST00000413765
  gene symbol: NRCAM
  hgvsc: ENST00000413765.2:c.3095-6625C>T
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000401244
  ensembl transcript: ENST00000425651
  gene symbol: NRCAM
  hgvsc: ENST00000425651.2:c.3314-44C>T
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl transcript: ENST00000415105
  gene symbol: NRCAM
  hgvsc: ENST00000415105.1:n.245-6625C>T
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000325269
  ensembl transcript: ENST00000351718
  gene symbol: NRCAM
  hgvsc: ENST00000351718.4:c.3104-6625C>T
  variant of: http://identifiers.org/hgnc/7994
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7670
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4597
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3867
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19955
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20322
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 659
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1755
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 230
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4869
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 839
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3847
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5670
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1097
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: European (Finnish)
population: Other
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP

http://identifiers.org/exac.variant/7-107807563-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107807563
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 107807563
    reference: chr 7
allele count: 1
allele frequency: 1.476799480166583e-5
allele num: 67714
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000407858
  ensembl transcript: ENST00000413765
  gene symbol: NRCAM
  hgvsc: ENST00000413765.2:c.3095-6626T>G
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368314
  ensembl transcript: ENST00000379028
  gene symbol: NRCAM
  hgvsc: ENST00000379028.3:c.3314-45T>G
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000401244
  ensembl transcript: ENST00000425651
  gene symbol: NRCAM
  hgvsc: ENST00000425651.2:c.3314-45T>G
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl transcript: ENST00000465585
  gene symbol: NRCAM
  hgvsc: ENST00000465585.1:n.303-6626T>G
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000325269
  ensembl transcript: ENST00000351718
  gene symbol: NRCAM
  hgvsc: ENST00000351718.4:c.3104-6626T>G
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368308
  ensembl transcript: ENST00000379022
  gene symbol: NRCAM
  hgvsc: ENST00000379022.4:c.3314-45T>G
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl transcript: ENST00000415105
  gene symbol: NRCAM
  hgvsc: ENST00000415105.1:n.245-6626T>G
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368310
  ensembl transcript: ENST00000379024
  gene symbol: NRCAM
  hgvsc: ENST00000379024.4:c.3131-6626T>G
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000398174
  ensembl transcript: ENST00000445634
  gene symbol: NRCAM
  hgvsc: ENST00000445634.2:c.162+1159T>G
  variant of: http://identifiers.org/hgnc/7994
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19277
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 639
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7624
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3970
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1662
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4615
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21023
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 107
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4113
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 802
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 700
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 304
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2680
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
population: Latino
population: South Asian
population: European (Finnish)
reference allele: A
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum

http://identifiers.org/exac.variant/7-107807565-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107807565
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 107807565
    reference: chr 7
allele count: 1
allele frequency: 1.483503441727985e-5
allele num: 67408
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000407858
  ensembl transcript: ENST00000413765
  gene symbol: NRCAM
  hgvsc: ENST00000413765.2:c.3095-6628G>T
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368308
  ensembl transcript: ENST00000379022
  gene symbol: NRCAM
  hgvsc: ENST00000379022.4:c.3314-47G>T
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl transcript: ENST00000465585
  gene symbol: NRCAM
  hgvsc: ENST00000465585.1:n.303-6628G>T
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000325269
  ensembl transcript: ENST00000351718
  gene symbol: NRCAM
  hgvsc: ENST00000351718.4:c.3104-6628G>T
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368310
  ensembl transcript: ENST00000379024
  gene symbol: NRCAM
  hgvsc: ENST00000379024.4:c.3131-6628G>T
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000401244
  ensembl transcript: ENST00000425651
  gene symbol: NRCAM
  hgvsc: ENST00000425651.2:c.3314-47G>T
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368314
  ensembl transcript: ENST00000379028
  gene symbol: NRCAM
  hgvsc: ENST00000379028.3:c.3314-47G>T
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000398174
  ensembl transcript: ENST00000445634
  gene symbol: NRCAM
  hgvsc: ENST00000445634.2:c.162+1157G>T
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl transcript: ENST00000415105
  gene symbol: NRCAM
  hgvsc: ENST00000415105.1:n.245-6628G>T
  variant of: http://identifiers.org/hgnc/7994
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7577
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3958
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4613
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19293
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 636
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21065
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1667
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6234
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 673
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4034
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 295
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1619
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 897
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP

7-107808699-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107808699
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 107808699
    reference: chr 7
allele count: 11
allele frequency: 9.370793791423167e-5
allele num: 117386
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000325269
  ensembl transcript: ENST00000351718
  gene symbol: NRCAM
  hgvsc: ENST00000351718.4:c.3104-7762G>A
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000407858
  ensembl transcript: ENST00000413765
  gene symbol: NRCAM
  hgvsc: ENST00000413765.2:c.3095-7762G>A
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368308
  ensembl transcript: ENST00000379022
  gene symbol: NRCAM
  hgvsc: ENST00000379022.4:c.3313+23G>A
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368310
  ensembl transcript: ENST00000379024
  gene symbol: NRCAM
  hgvsc: ENST00000379024.4:c.3130+7068G>A
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000398174
  ensembl transcript: ENST00000445634
  gene symbol: NRCAM
  hgvsc: ENST00000445634.2:c.162+23G>A
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368314
  ensembl transcript: ENST00000379028
  gene symbol: NRCAM
  hgvsc: ENST00000379028.3:c.3313+23G>A
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl transcript: ENST00000465585
  gene symbol: NRCAM
  hgvsc: ENST00000465585.1:n.303-7762G>A
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000401244
  ensembl transcript: ENST00000425651
  gene symbol: NRCAM
  hgvsc: ENST00000425651.2:c.3313+23G>A
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl transcript: ENST00000415105
  gene symbol: NRCAM
  hgvsc: ENST00000415105.1:n.245-7762G>A
  variant of: http://identifiers.org/hgnc/7994
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1102
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1509
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 23456
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 596
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6690
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19786
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2155
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1678
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 771
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 5.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3640
  bin: 9.75e1
  variant carriers: 11
genotype quality: GenotypeQuality
  all individuals: 36707
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2503
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1373
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 550
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1561
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: Other
reference allele: C
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff

7-107808700-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107808700
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 107808700
    reference: chr 7
allele count: 2
allele frequency: 1.700275444622029e-5
allele num: 117628
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368314
  ensembl transcript: ENST00000379028
  gene symbol: NRCAM
  hgvsc: ENST00000379028.3:c.3313+22C>T
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000398174
  ensembl transcript: ENST00000445634
  gene symbol: NRCAM
  hgvsc: ENST00000445634.2:c.162+22C>T
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000325269
  ensembl transcript: ENST00000351718
  gene symbol: NRCAM
  hgvsc: ENST00000351718.4:c.3104-7763C>T
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368310
  ensembl transcript: ENST00000379024
  gene symbol: NRCAM
  hgvsc: ENST00000379024.4:c.3130+7067C>T
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000407858
  ensembl transcript: ENST00000413765
  gene symbol: NRCAM
  hgvsc: ENST00000413765.2:c.3095-7763C>T
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl transcript: ENST00000465585
  gene symbol: NRCAM
  hgvsc: ENST00000465585.1:n.303-7763C>T
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368308
  ensembl transcript: ENST00000379022
  gene symbol: NRCAM
  hgvsc: ENST00000379022.4:c.3313+22C>T
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000401244
  ensembl transcript: ENST00000425651
  gene symbol: NRCAM
  hgvsc: ENST00000425651.2:c.3313+22C>T
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl transcript: ENST00000415105
  gene symbol: NRCAM
  hgvsc: ENST00000415105.1:n.245-7763C>T
  variant of: http://identifiers.org/hgnc/7994
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1456
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1516
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 773
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1103
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19895
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23622
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6679
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2158
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 212
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 502
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2197
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37080
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: G
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: FS

7-107808717-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107808717
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 107808717
    reference: chr 7
allele count: 3
allele frequency: 2.519907267412559e-5
allele num: 119052
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000407858
  ensembl transcript: ENST00000413765
  gene symbol: NRCAM
  hgvsc: ENST00000413765.2:c.3095-7780G>A
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl transcript: ENST00000415105
  gene symbol: NRCAM
  hgvsc: ENST00000415105.1:n.245-7780G>A
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368308
  ensembl transcript: ENST00000379022
  gene symbol: NRCAM
  hgvsc: ENST00000379022.4:c.3313+5G>A
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368310
  ensembl transcript: ENST00000379024
  gene symbol: NRCAM
  hgvsc: ENST00000379024.4:c.3130+7050G>A
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000398174
  ensembl transcript: ENST00000445634
  gene symbol: NRCAM
  hgvsc: ENST00000445634.2:c.162+5G>A
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000325269
  ensembl transcript: ENST00000351718
  gene symbol: NRCAM
  hgvsc: ENST00000351718.4:c.3104-7780G>A
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl transcript: ENST00000465585
  gene symbol: NRCAM
  hgvsc: ENST00000465585.1:n.303-7780G>A
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000401244
  ensembl transcript: ENST00000425651
  gene symbol: NRCAM
  hgvsc: ENST00000425651.2:c.3313+5G>A
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368314
  ensembl transcript: ENST00000379028
  gene symbol: NRCAM
  hgvsc: ENST00000379028.3:c.3313+5G>A
  variant of: http://identifiers.org/hgnc/7994
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1096
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2155
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24870
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20601
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 798
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 577
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6700
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3629
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 858
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
hgvs: c.3313+5G>A
num of homozygotes: 0
population: South Asian
population: Latino
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum

7-107808732-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107808732
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 107808732
    reference: chr 7
allele count: 1
allele frequency: 8.330556481172942e-6
allele num: 120040
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000401244
  ensembl transcript: ENST00000425651
  gene symbol: NRCAM
  hgvsc: ENST00000425651.2:c.3303T>C
  hgvsp: ENST00000425651.2:c.3303T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl transcript: ENST00000465585
  gene symbol: NRCAM
  hgvsc: ENST00000465585.1:n.303-7795T>C
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368308
  ensembl transcript: ENST00000379022
  gene symbol: NRCAM
  hgvsc: ENST00000379022.4:c.3303T>C
  hgvsp: ENST00000379022.4:c.3303T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368314
  ensembl transcript: ENST00000379028
  gene symbol: NRCAM
  hgvsc: ENST00000379028.3:c.3303T>C
  hgvsp: ENST00000379028.3:c.3303T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl transcript: ENST00000415105
  gene symbol: NRCAM
  hgvsc: ENST00000415105.1:n.245-7795T>C
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000325269
  ensembl transcript: ENST00000351718
  gene symbol: NRCAM
  hgvsc: ENST00000351718.4:c.3104-7795T>C
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368310
  ensembl transcript: ENST00000379024
  gene symbol: NRCAM
  hgvsc: ENST00000379024.4:c.3130+7035T>C
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000398174
  ensembl transcript: ENST00000445634
  gene symbol: NRCAM
  hgvsc: ENST00000445634.2:c.152T>C
  hgvsp: ENST00000445634.2:c.152T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000407858
  ensembl transcript: ENST00000413765
  gene symbol: NRCAM
  hgvsc: ENST00000413765.2:c.3095-7795T>C
  variant of: http://identifiers.org/hgnc/7994
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6760
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1096
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2151
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21152
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25190
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8471
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 101
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3625
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Gly1101Gly
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
reference allele: A
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: QD

7-107808733-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107808733
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 107808733
    reference: chr 7
allele count: 1
allele frequency: 8.328752519447637e-6
allele num: 120066
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000407858
  ensembl transcript: ENST00000413765
  gene symbol: NRCAM
  hgvsc: ENST00000413765.2:c.3095-7796G>A
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368314
  ensembl transcript: ENST00000379028
  gene symbol: NRCAM
  hgvsc: ENST00000379028.3:c.3302G>A
  hgvsp: ENSP00000368314.3:p.Gly1101Asp
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000325269
  ensembl transcript: ENST00000351718
  gene symbol: NRCAM
  hgvsc: ENST00000351718.4:c.3104-7796G>A
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368310
  ensembl transcript: ENST00000379024
  gene symbol: NRCAM
  hgvsc: ENST00000379024.4:c.3130+7034G>A
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl transcript: ENST00000415105
  gene symbol: NRCAM
  hgvsc: ENST00000415105.1:n.245-7796G>A
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000398174
  ensembl transcript: ENST00000445634
  gene symbol: NRCAM
  hgvsc: ENST00000445634.2:c.151G>A
  hgvsp: ENSP00000398174.2:p.Gly51Asp
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368308
  ensembl transcript: ENST00000379022
  gene symbol: NRCAM
  hgvsc: ENST00000379022.4:c.3302G>A
  hgvsp: ENSP00000368308.4:p.Gly1101Asp
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl transcript: ENST00000465585
  gene symbol: NRCAM
  hgvsc: ENST00000465585.1:n.303-7796G>A
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000401244
  ensembl transcript: ENST00000425651
  gene symbol: NRCAM
  hgvsc: ENST00000425651.2:c.3302G>A
  hgvsp: ENSP00000401244.2:p.Gly1101Asp
  variant of: http://identifiers.org/hgnc/7994
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25171
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21186
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 771
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6774
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2159
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1096
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3625
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Gly1101Asp
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
reference allele: C
site quality: MQ
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum

7-107808734-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107808734
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 107808734
    reference: chr 7
allele count: 1
allele frequency: 8.327226700419692e-6
allele num: 120088
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl transcript: ENST00000415105
  gene symbol: NRCAM
  hgvsc: ENST00000415105.1:n.245-7797G>A
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl transcript: ENST00000465585
  gene symbol: NRCAM
  hgvsc: ENST00000465585.1:n.303-7797G>A
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368310
  ensembl transcript: ENST00000379024
  gene symbol: NRCAM
  hgvsc: ENST00000379024.4:c.3130+7033G>A
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000325269
  ensembl transcript: ENST00000351718
  gene symbol: NRCAM
  hgvsc: ENST00000351718.4:c.3104-7797G>A
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000398174
  ensembl transcript: ENST00000445634
  gene symbol: NRCAM
  hgvsc: ENST00000445634.2:c.150G>A
  hgvsp: ENSP00000398174.2:p.Gly51Ser
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368314
  ensembl transcript: ENST00000379028
  gene symbol: NRCAM
  hgvsc: ENST00000379028.3:c.3301G>A
  hgvsp: ENSP00000368314.3:p.Gly1101Ser
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368308
  ensembl transcript: ENST00000379022
  gene symbol: NRCAM
  hgvsc: ENST00000379022.4:c.3301G>A
  hgvsp: ENSP00000368308.4:p.Gly1101Ser
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000407858
  ensembl transcript: ENST00000413765
  gene symbol: NRCAM
  hgvsc: ENST00000413765.2:c.3095-7797G>A
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000401244
  ensembl transcript: ENST00000425651
  gene symbol: NRCAM
  hgvsc: ENST00000425651.2:c.3301G>A
  hgvsp: ENSP00000401244.2:p.Gly1101Ser
  variant of: http://identifiers.org/hgnc/7994
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2155
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25128
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 577
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21234
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 770
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1099
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6780
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2540
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39971
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 125
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Gly1101Ser
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
population: African
reference allele: C
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum

7-107808745-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107808745
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 107808745
    reference: chr 7
allele count: 1
allele frequency: 8.30827005200977e-6
allele num: 120362
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl transcript: ENST00000465585
  gene symbol: NRCAM
  hgvsc: ENST00000465585.1:n.303-7808A>G
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000325269
  ensembl transcript: ENST00000351718
  gene symbol: NRCAM
  hgvsc: ENST00000351718.4:c.3104-7808A>G
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000401244
  ensembl transcript: ENST00000425651
  gene symbol: NRCAM
  hgvsc: ENST00000425651.2:c.3290A>G
  hgvsp: ENSP00000401244.2:p.Tyr1097Cys
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368310
  ensembl transcript: ENST00000379024
  gene symbol: NRCAM
  hgvsc: ENST00000379024.4:c.3130+7022A>G
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368308
  ensembl transcript: ENST00000379022
  gene symbol: NRCAM
  hgvsc: ENST00000379022.4:c.3290A>G
  hgvsp: ENSP00000368308.4:p.Tyr1097Cys
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl transcript: ENST00000415105
  gene symbol: NRCAM
  hgvsc: ENST00000415105.1:n.245-7808A>G
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000398174
  ensembl transcript: ENST00000445634
  gene symbol: NRCAM
  hgvsc: ENST00000445634.2:c.139A>G
  hgvsp: ENSP00000398174.2:p.Tyr47Cys
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000368314
  ensembl transcript: ENST00000379028
  gene symbol: NRCAM
  hgvsc: ENST00000379028.3:c.3290A>G
  hgvsp: ENSP00000368314.3:p.Tyr1097Cys
  variant of: http://identifiers.org/hgnc/7994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000091129
  ensembl protein: ENSP00000407858
  ensembl transcript: ENST00000413765
  gene symbol: NRCAM
  hgvsc: ENST00000413765.2:c.3095-7808A>G
  variant of: http://identifiers.org/hgnc/7994
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6779
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2152
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21383
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25171
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Tyr1097Cys
num of homozygotes: 0
reference allele: T

GenotypeQuality
all individuals: 43
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3783
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5357
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 130
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 410
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3564
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2652
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 73
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17498
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 4606
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15029
bin: 6.25e1
variant carriers: 0

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

African
type: Population
allele count: 1
allele frequency: 9.723842862699339e-5
allele num: 10284
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16472
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 1
allele frequency: 1.168497312456181e-4
allele num: 8558
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66362
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.850000000000001e-1

FS
type: SiteQuality
SIO_000300: 1.803e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.29e-1

DP
type: SiteQuality
SIO_000300: 2.250241e6

QD
type: SiteQuality
SIO_000300: 1.357e1

VQSLOD
type: SiteQuality
SIO_000300: -9.157e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.86e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.51e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

MQ
type: SiteQuality
SIO_000300: 5.834e1

GenotypeQuality
all individuals: 61
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 15351
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2650
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5360
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 35
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7219
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3795
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3566
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17501
bin: 9.75e1
variant carriers: 1

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6592
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8598
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11498
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.504030802550836e-5
allele num: 66488
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10342
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16486
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -8.702999999999999e0

QD
type: SiteQuality
SIO_000300: 1.119e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.38e-1

MQ
type: SiteQuality
SIO_000300: 5.378e1

VQSLOD
type: SiteQuality
SIO_000300: -1.729e0

DP
type: SiteQuality
SIO_000300: 2.254854e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.791e0

FS
type: SiteQuality
SIO_000300: 5.212e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.44e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

GenotypeQuality
all individuals: 15378
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 3567
bin: 9.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 48
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7232
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3798
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 261
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4616
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17502
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 50
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2651
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5364
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 3.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.503668952243474e-5
allele num: 66504
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10354
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11502
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6592
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8604
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -1.148e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

DP
type: SiteQuality
SIO_000300: 2.25554e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.85e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.75e0

MQRankSum
type: SiteQuality
SIO_000300: -9.218999999999999e0

QD
type: SiteQuality
SIO_000300: 8.720000000000001e0

FS
type: SiteQuality
SIO_000300: 5.287e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.126e0

MQ
type: SiteQuality
SIO_000300: 5.331e1

GenotypeQuality
all individuals: 209
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4620
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7239
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3568
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3803
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15413
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2653
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5368
bin: 7.75e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6598
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66568
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16494
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.683570684265369e-5
allele num: 11516
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 1.95e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.039e0

DP
type: SiteQuality
SIO_000300: 2.257014e6

FS
type: SiteQuality
SIO_000300: 4.321e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.32e-1

QD
type: SiteQuality
SIO_000300: 5.92e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 2.6e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.31e0

MQ
type: SiteQuality
SIO_000300: 5.966e1

GenotypeQuality
all individuals: 5375
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 7237
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 40
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17506
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 48
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 198
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15411
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4623
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3567
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2653
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.502087902184036e-5
allele num: 66574
num of homozygotes: 0

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

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6598
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10382
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 2.257387e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.24e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 1.939e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.591e0

MQRankSum
type: SiteQuality
SIO_000300: 3.22e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.98e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.049e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

QD
type: SiteQuality
SIO_000300: 1.507e1

GenotypeQuality
all individuals: 74
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 46
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3808
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5363
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 64
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 88
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17504
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3563
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7248
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15358
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4628
bin: 8.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6598
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66630
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.676036786395974e-5
allele num: 11526
num of homozygotes: 0

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

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

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.04e-1

QD
type: SiteQuality
SIO_000300: 1.144e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.5e-1

MQRankSum
type: SiteQuality
SIO_000300: -8.42e-1

DP
type: SiteQuality
SIO_000300: 2.25849e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -4.26e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.55e-1

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

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

GenotypeQuality
all individuals: 2
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 7181
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3561
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4601
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 182
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5345
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 89
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 91
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3790
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 113
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15195
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 121
bin: 4.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11534
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: 904
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.5004651441947e-5
allele num: 66646
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

FS
type: SiteQuality
SIO_000300: 8.609999999999999e0

MQRankSum
type: SiteQuality
SIO_000300: -4.87e-1

QD
type: SiteQuality
SIO_000300: 8.9e0

MQ
type: SiteQuality
SIO_000300: 5.932e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.8e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.67e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.802e0

VQSLOD
type: SiteQuality
SIO_000300: -9.848e-1

DP
type: SiteQuality
SIO_000300: 2.256508e6

GenotypeQuality
all individuals: 245
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 14861
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2622
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 335
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 185
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 7036
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 160
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3550
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4581
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17481
bin: 9.75e1
variant carriers: 8

GenotypeQuality
all individuals: 143
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5278
bin: 7.75e1
variant carriers: 0

East Asian
type: Population
allele count: 8
allele frequency: 9.263547938860583e-4
allele num: 8636
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11502
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10384
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66634
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16468
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.26e0

FS
type: SiteQuality
SIO_000300: 1.122e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.8e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.24e0

MQRankSum
type: SiteQuality
SIO_000300: -1.17e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.4e-3

MQ
type: SiteQuality
SIO_000300: 5.952e1

DP
type: SiteQuality
SIO_000300: 2.248573e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.82e-1

QD
type: SiteQuality
SIO_000300: 1.117e1

GenotypeQuality
all individuals: 14
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 126
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 278
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4571
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2621
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 182
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 13
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3550
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17475
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 217
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 208
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 252
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14544
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6993
bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10380
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8636
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11506
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66622
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.074596039363382e-5
allele num: 16462
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.15e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.8e-2

QD
type: SiteQuality
SIO_000300: 3.393e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.48e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.903e0

DP
type: SiteQuality
SIO_000300: 2.246254e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.69e-1

MQ
type: SiteQuality
SIO_000300: 5.951e1

FS
type: SiteQuality
SIO_000300: 1.477e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.84e-1

GenotypeQuality
all individuals: 5237
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6953
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14525
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 310
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 233
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3549
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17450
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 363
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4567
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2618
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 208
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 291
bin: 5.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11496
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8634
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.635767970707265e-5
allele num: 10378
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16462
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.4e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -3.64e0

QD
type: SiteQuality
SIO_000300: 1.84e0

MQ
type: SiteQuality
SIO_000300: 5.913e1

FS
type: SiteQuality
SIO_000300: 7.585899999999999e1

MQRankSum
type: SiteQuality
SIO_000300: -2.33e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.599999999999999e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -3.7e-2

VQSLOD
type: SiteQuality
SIO_000300: -2.745e1

DP
type: SiteQuality
SIO_000300: 2.246345e6

GenotypeQuality
all individuals: 15
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 173
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 365
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2618
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14584
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6937
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 403
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 227
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 173
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 249
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3677
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3540
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10382
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.080505898090721e-5
allele num: 16446
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 9.008738476322033e-5
allele num: 66602
num of homozygotes: 0

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

Latino
type: Population
allele count: 2
allele frequency: 1.73973556019485e-4
allele num: 11496
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 2.242512e6

MQRankSum
type: SiteQuality
SIO_000300: -7.199999999999999e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.299999999999999e-3

FS
type: SiteQuality
SIO_000300: 5.47e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.59e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.77e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.023e0

QD
type: SiteQuality
SIO_000300: 1.153e1

MQ
type: SiteQuality
SIO_000300: 5.962e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.08e-1

GenotypeQuality
all individuals: 495
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 307
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 592
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 485
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6636
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17457
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 316
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2616
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4532
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3535
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3595
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 485
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 454
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5153
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10374
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66598
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11488
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8634
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: 1
allele frequency: 6.084205402774397e-5
allele num: 16436
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.46e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.51e-1

MQ
type: SiteQuality
SIO_000300: 5.928e1

VQSLOD
type: SiteQuality
SIO_000300: -1.241e0

DP
type: SiteQuality
SIO_000300: 2.23579e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.5e-3

FS
type: SiteQuality
SIO_000300: 2.634e0

QD
type: SiteQuality
SIO_000300: 1.95e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.719e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.0e-2

GenotypeQuality
all individuals: 331
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 507
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 6143
bin: 6.75e1
variant carriers: 4

GenotypeQuality
all individuals: 19896
bin: 9.75e1
variant carriers: 3751

GenotypeQuality
all individuals: 12635
bin: 6.25e1
variant carriers: 6

GenotypeQuality
all individuals: 16
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 359
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 22
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3301
bin: 9.25e1
variant carriers: 8

GenotypeQuality
all individuals: 24
bin: 7.5e0
variant carriers: 3

GenotypeQuality
all individuals: 4245
bin: 8.25e1
variant carriers: 8

GenotypeQuality
all individuals: 545
bin: 3.25e1
variant carriers: 2

GenotypeQuality
all individuals: 424
bin: 4.25e1
variant carriers: 3

GenotypeQuality
all individuals: 3314
bin: 7.25e1
variant carriers: 6

GenotypeQuality
all individuals: 4802
bin: 7.75e1
variant carriers: 10

GenotypeQuality
all individuals: 658
bin: 3.75e1
variant carriers: 2

GenotypeQuality
all individuals: 27
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 426
bin: 5.25e1
variant carriers: 4

East Asian
type: Population
allele count: 59
allele frequency: 6.828703703703704e-3
allele num: 8640
num of homozygotes: 1

South Asian
type: Population
allele count: 971
allele frequency: 5.91136003896262e-2
allele num: 16426
num of homozygotes: 38

Other
type: Population
allele count: 24
allele frequency: 2.660753880266075e-2
allele num: 902
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2544
allele frequency: 3.821426425524244e-2
allele num: 66572
num of homozygotes: 67

African
type: Population
allele count: 68
allele frequency: 6.556112610875434e-3
allele num: 10372
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 37
allele frequency: 5.604362314450166e-3
allele num: 6602
num of homozygotes: 0

Latino
type: Population
allele count: 217
allele frequency: 1.888927576601671e-2
allele num: 11488
num of homozygotes: 4

ClippingRankSum
type: SiteQuality
SIO_000300: -2.03e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.65e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.84e0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.4e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.46e-2

DP
type: SiteQuality
SIO_000300: 2.25519e6

QD
type: SiteQuality
SIO_000300: 1.365e1

MQ
type: SiteQuality
SIO_000300: 5.983e1

MQRankSum
type: SiteQuality
SIO_000300: 9.2e-2

GenotypeQuality
all individuals: 5073
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 462
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 653
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 17182
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2532
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3522
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3467
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 546
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 418
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 345
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 591
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6517
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 261
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 1.25e1
variant carriers: 1

GenotypeQuality
all individuals: 4497
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 726
bin: 3.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8638
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11472
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66538
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10370
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16396
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -8.98e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.233e0

QD
type: SiteQuality
SIO_000300: 6.09e0

FS
type: SiteQuality
SIO_000300: 3.425e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.7e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.04e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.04e-1

DP
type: SiteQuality
SIO_000300: 2.213851e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.97e-1

MQ
type: SiteQuality
SIO_000300: 5.944e1

GenotypeQuality
all individuals: 852
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4492
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17174
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 16
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5050
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 702
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 892
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 569
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3432
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 407
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 626
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6355
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1129
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12328
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2534
bin: 8.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16374
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.652509652509652e-5
allele num: 10360
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66566
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8634
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 2.20366e6

BaseQRankSum
type: SiteQuality
SIO_000300: -8.58e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.3e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 1.43e0

MQRankSum
type: SiteQuality
SIO_000300: 1.4e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.38e0

QD
type: SiteQuality
SIO_000300: 1.018e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.3e-1

GenotypeQuality
all individuals: 899
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4497
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6194
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2523
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3528
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17172
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 613
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5042
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1655
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 627
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3427
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 717
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11094
bin: 6.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8638
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.663703131039814e-5
allele num: 10348
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11474
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: 16348
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 5.6e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.1e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -2.198e0

MQRankSum
type: SiteQuality
SIO_000300: -7.5e-1

QD
type: SiteQuality
SIO_000300: 2.005e1

DP
type: SiteQuality
SIO_000300: 2.198278e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.36e-1

FS
type: SiteQuality
SIO_000300: 5.163e0

VQSLOD
type: SiteQuality
SIO_000300: -1.415e0

GenotypeQuality
all individuals: 347
bin: 3.25e1
variant carriers: 144

GenotypeQuality
all individuals: 2038
bin: 6.75e1
variant carriers: 1135

GenotypeQuality
all individuals: 2122
bin: 9.25e1
variant carriers: 1924

GenotypeQuality
all individuals: 51
bin: 1.25e1
variant carriers: 39

GenotypeQuality
all individuals: 70
bin: 2.5e0
variant carriers: 26

GenotypeQuality
all individuals: 54
bin: 1.75e1
variant carriers: 40

GenotypeQuality
all individuals: 1049
bin: 7.25e1
variant carriers: 710

GenotypeQuality
all individuals: 1928
bin: 7.75e1
variant carriers: 1508

GenotypeQuality
all individuals: 541
bin: 5.75e1
variant carriers: 466

GenotypeQuality
all individuals: 683
bin: 5.25e1
variant carriers: 572

GenotypeQuality
all individuals: 454
bin: 4.75e1
variant carriers: 378

GenotypeQuality
all individuals: 364
bin: 3.75e1
variant carriers: 246

GenotypeQuality
all individuals: 43167
bin: 9.75e1
variant carriers: 42101

GenotypeQuality
all individuals: 218
bin: 2.75e1
variant carriers: 84

South Asian
type: Population
allele count: 10130
allele frequency: 6.189661493339851e-1
allele num: 16366
num of homozygotes: 3167

Latino
type: Population
allele count: 8869
allele frequency: 7.743146499039637e-1
allele num: 11454
num of homozygotes: 3448

African
type: Population
allele count: 2635
allele frequency: 2.547370456303171e-1
allele num: 10344
num of homozygotes: 337

Other
type: Population
allele count: 639
allele frequency: 7.06858407079646e-1
allele num: 904
num of homozygotes: 215

East Asian
type: Population
allele count: 7321
allele frequency: 8.483198146002318e-1
allele num: 8630
num of homozygotes: 3113

European (Non-Finnish)
type: Population
allele count: 48192
allele frequency: 7.261330761812922e-1
allele num: 66368
num of homozygotes: 17433

European (Finnish)
type: Population
allele count: 4534
allele frequency: 6.898965307364577e-1
allele num: 6572
num of homozygotes: 1554

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.59e-2

FS
type: SiteQuality
SIO_000300: 6.37e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.95e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.48e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.2e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 2.26e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.81e-1

QD
type: SiteQuality
SIO_000300: 2.651e1

DP
type: SiteQuality
SIO_000300: 2.398798e6

GenotypeQuality
all individuals: 1180
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1044
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2967
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7837
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25333
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2202
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 7023
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 580
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2791
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1170
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1606
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 476
bin: 4.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 3
allele frequency: 4.559270516717325e-4
allele num: 6580
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15952
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10312
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8602
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.024345985180705e-5
allele num: 66130
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11350
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.964e1

QD
type: SiteQuality
SIO_000300: 1.056e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

FS
type: SiteQuality
SIO_000300: 1.509e0

VQSLOD
type: SiteQuality
SIO_000300: 6.06e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.949e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.78e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.78e-1

DP
type: SiteQuality
SIO_000300: 1.816395e6

MQRankSum
type: SiteQuality
SIO_000300: -1.8e-2

GenotypeQuality
all individuals: 28
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1598
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 24605
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 550
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1986
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 213
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 558
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1210
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2419
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2917
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7010
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3865
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1166
bin: 8.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15920
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11338
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10306
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8602
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.512630464377553e-5
allele num: 66110
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6580
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.16e0

DP
type: SiteQuality
SIO_000300: 1.800001e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.96e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.321e0

MQ
type: SiteQuality
SIO_000300: 6.033e1

MQRankSum
type: SiteQuality
SIO_000300: -8.74e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 4.49e0

QD
type: SiteQuality
SIO_000300: 2.064e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

GenotypeQuality
all individuals: 77
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 7148
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 743
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 682
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2722
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2390
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3792
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 747
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2819
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 816
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7006
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1161
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.027092477675193e-5
allele num: 66070
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11316
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10300
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8594
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6578
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15902
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.0e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 5.0e-1

DP
type: SiteQuality
SIO_000300: 1.780873e6

FS
type: SiteQuality
SIO_000300: 5.36e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.07e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.37e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

QD
type: SiteQuality
SIO_000300: 1.616e1

MQ
type: SiteQuality
SIO_000300: 5.952e1

VQSLOD
type: SiteQuality
SIO_000300: 1.13e0

GenotypeQuality
all individuals: 3792
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7148
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2390
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1592
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 816
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2819
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22895
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 682
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2610
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7006
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 747
bin: 4.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6578
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66070
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8594
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11316
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.708737864077671e-5
allele num: 10300
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15902
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 5.36e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.0e-2

DP
type: SiteQuality
SIO_000300: 1.780873e6

MQ
type: SiteQuality
SIO_000300: 5.952e1

MQRankSum
type: SiteQuality
SIO_000300: 2.37e-1

QD
type: SiteQuality
SIO_000300: 1.616e1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.0e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.07e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.13e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

GenotypeQuality
all individuals: 885
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6863
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1575
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2617
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 493
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 93
bin: 7.5e0
variant carriers: 1

GenotypeQuality
all individuals: 2698
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2179
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3653
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6982
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1131
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 687
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 853
bin: 4.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15832
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8582
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 894
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65956
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11276
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10284
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.217e0

MQ
type: SiteQuality
SIO_000300: 5.878e1

MQRankSum
type: SiteQuality
SIO_000300: 1.47e-1

QD
type: SiteQuality
SIO_000300: 2.51e0

VQSLOD
type: SiteQuality
SIO_000300: -2.983e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.21e-1

FS
type: SiteQuality
SIO_000300: 2.69e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.772062e6

GenotypeQuality
all individuals: 1570
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 953
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2657
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1614
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 96
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6801
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2592
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1122
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 414
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2815
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22483
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 932
bin: 4.25e1
variant carriers: 0

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

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

African
type: Population
allele count: 1
allele frequency: 9.710623422023694e-5
allele num: 10298
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11298
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15842
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66018
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.5e-2

QD
type: SiteQuality
SIO_000300: 1.629e1

MQ
type: SiteQuality
SIO_000300: 5.97e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.05e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -2.484e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.58e0

FS
type: SiteQuality
SIO_000300: 1.154e0

DP
type: SiteQuality
SIO_000300: 1.754111e6

BaseQRankSum
type: SiteQuality
SIO_000300: 6.02e0

GenotypeQuality
all individuals: 2853
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1649
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 74
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 401
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6767
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2646
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 110
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2691
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2908
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1020
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3566
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 589
bin: 5.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15846
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10290
num of homozygotes: 0

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6574
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.515197430225158e-5
allele num: 65998
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11290
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.3742e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -2.816e0

DP
type: SiteQuality
SIO_000300: 1.749273e6

MQRankSum
type: SiteQuality
SIO_000300: 2.37e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.34e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.29e0

MQ
type: SiteQuality
SIO_000300: 5.901e1

QD
type: SiteQuality
SIO_000300: 1.449e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.3e-1

GenotypeQuality
all individuals: 3447
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1869
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18679
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2989
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 76
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1574
bin: 4.25e1
variant carriers: 1

GenotypeQuality
all individuals: 3647
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 136
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2556
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 751
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1862
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2538
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6976
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 109
bin: 1.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8576
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15748
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.77430801987225e-4
allele num: 11272
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65938
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10278
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: -2.236e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.62e-1

QD
type: SiteQuality
SIO_000300: 1.252e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.0e-1

DP
type: SiteQuality
SIO_000300: 1.718451e6

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

FS
type: SiteQuality
SIO_000300: 9.609999999999999e0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.070000000000001e-1

GenotypeQuality
all individuals: 415
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2668
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1097
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2361
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 169
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5251
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2767
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4809
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6962
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 10527
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3237
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5284
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1121
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2439
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11198
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 888
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15530
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10238
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.522672594938636e-5
allele num: 65674
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.837e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.12e-1

MQRankSum
type: SiteQuality
SIO_000300: -6.94e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.494e0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.409e0

QD
type: SiteQuality
SIO_000300: 1.013e1

DP
type: SiteQuality
SIO_000300: 1.673824e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

GenotypeQuality
all individuals: 1096
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 179
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 197
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1537
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5227
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 894
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 411
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10787
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4816
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2430
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6961
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2004
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3216
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2679
bin: 4.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8532
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.754194303550527e-5
allele num: 10252
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 880
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65594
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15496
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11180
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.673503e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.2e-3

MQRankSum
type: SiteQuality
SIO_000300: -2.41e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.15e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.14e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 2.79e0

VQSLOD
type: SiteQuality
SIO_000300: -2.827e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.428e0

GenotypeQuality
all individuals: 114
bin: 8.75e1
variant carriers: 9

GenotypeQuality
all individuals: 7647
bin: 3.75e1
variant carriers: 4

GenotypeQuality
all individuals: 6874
bin: 2.25e1
variant carriers: 3

GenotypeQuality
all individuals: 687
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 602
bin: 7.5e0
variant carriers: 1

GenotypeQuality
all individuals: 4823
bin: 5.25e1
variant carriers: 6

GenotypeQuality
all individuals: 1810
bin: 6.75e1
variant carriers: 3

GenotypeQuality
all individuals: 2125
bin: 1.75e1
variant carriers: 2

GenotypeQuality
all individuals: 505
bin: 7.25e1
variant carriers: 4

GenotypeQuality
all individuals: 6202
bin: 4.75e1
variant carriers: 4

GenotypeQuality
all individuals: 7770
bin: 3.25e1
variant carriers: 3

GenotypeQuality
all individuals: 2098
bin: 5.75e1
variant carriers: 2

GenotypeQuality
all individuals: 4237
bin: 2.75e1
variant carriers: 3

GenotypeQuality
all individuals: 1518
bin: 9.75e1
variant carriers: 471

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 756
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5934
num of homozygotes: 0

East Asian
type: Population
allele count: 8
allele frequency: 1.119507416736636e-3
allele num: 7146
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 28
allele frequency: 4.929230335891839e-4
allele num: 56804
num of homozygotes: 0

South Asian
type: Population
allele count: 4
allele frequency: 2.839698991906858e-4
allele num: 14086
num of homozygotes: 0

Latino
type: Population
allele count: 25
allele frequency: 2.593360995850622e-3
allele num: 9640
num of homozygotes: 0

African
type: Population
allele count: 432
allele frequency: 5.401350337584396e-2
allele num: 7998
num of homozygotes: 13

MQRankSum
type: SiteQuality
SIO_000300: 1.52e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 6.45e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.86e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.55e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -2.017e0

DP
type: SiteQuality
SIO_000300: 1.00645e6

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.423e1

GenotypeQuality
all individuals: 7858
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4308
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7717
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 610
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3788
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 555
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2088
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11073
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 541
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 525
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1076
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 6138
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 613
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 105
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8148
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14300
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 1.041847542976211e-4
allele num: 57590
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5966
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 770
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7248
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.58e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.19e0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.487e1

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 3.58e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.3e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.014547e6

VQSLOD
type: SiteQuality
SIO_000300: 5.6e0

GenotypeQuality
all individuals: 3690
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 502
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 538
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4192
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6986
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18706
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 181
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1072
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 1348
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 450
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 343
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 117
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2147
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7520
bin: 3.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 782
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7352
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8266
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9900
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 5.151452709664125e-5
allele num: 58236
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6014
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14370
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.6e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -7.41e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.68e-1

DP
type: SiteQuality
SIO_000300: 1.058583e6

FS
type: SiteQuality
SIO_000300: 1.7139e1

VQSLOD
type: SiteQuality
SIO_000300: -1.458e0

MQRankSum
type: SiteQuality
SIO_000300: -4.71e-1

QD
type: SiteQuality
SIO_000300: 1.183e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.852e0

GenotypeQuality
all individuals: 4026
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 355
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 158
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5962
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2475
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2331
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 495
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2256
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22825
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 119
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 516
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 106
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1067
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 260
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8312
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.914672935970129e-5
allele num: 14462
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 58488
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6062
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9942
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7384
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 786
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.43e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.445e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.53e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -4.53e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.26e-1

QD
type: SiteQuality
SIO_000300: 1.426e1

DP
type: SiteQuality
SIO_000300: 1.091127e6

GenotypeQuality
all individuals: 420
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5382
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 499
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6547
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 296
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3811
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 108
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 267
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2278
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 119
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24661
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 485
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8092
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1072
bin: 9.75e1
variant carriers: 7

Latino
type: Population
allele count: 1
allele frequency: 1.009081735620585e-4
allele num: 9910
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.962818548948615e-5
allele num: 14362
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6040
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.207146306132303e-4
allele num: 8284
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.845798391237377e-5
allele num: 58430
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 784
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7416
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.45e0

MQRankSum
type: SiteQuality
SIO_000300: -5.37e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.116917e6

FS
type: SiteQuality
SIO_000300: 4.974e0

QD
type: SiteQuality
SIO_000300: 8.76e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -2.31e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.31e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.0e-4

GenotypeQuality
all individuals: 167
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2612
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5646
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1562
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3467
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1522
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 937
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 570
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 117
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 286
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 211
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 123
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 532
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1068
bin: 9.75e1
variant carriers: 1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10050
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 59308
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7504
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14586
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6096
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.187084520417854e-4
allele num: 8424
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 796
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.51e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.686e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.59e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.175e0

DP
type: SiteQuality
SIO_000300: 1.151281e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 3.245e0

VQSLOD
type: SiteQuality
SIO_000300: 2.44e-1

QD
type: SiteQuality
SIO_000300: 1.282e1

GenotypeQuality
all individuals: 2846
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2907
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7009
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4511
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 760
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1151
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 607
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1082
bin: 9.75e1
variant carriers: 6

GenotypeQuality
all individuals: 105
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 241
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 128
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 122
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1022
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 568
bin: 7.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7640
num of homozygotes: 0

Latino
type: Population
allele count: 6
allele frequency: 5.873140172278779e-4
allele num: 10216
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14736
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 60168
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 806
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6146
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 4.89e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.303e0

DP
type: SiteQuality
SIO_000300: 1.198828e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 1.988e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.3e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.87e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.72e-1

QD
type: SiteQuality
SIO_000300: 1.239e1

VQSLOD
type: SiteQuality
SIO_000300: 1.83e0

GenotypeQuality
all individuals: 167
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 122
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32547
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2907
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1141
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 607
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4511
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 128
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 300
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1151
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 568
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1022
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 241
bin: 7.5e0
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6146
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 806
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10216
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14736
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7640
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.98603909054647e-5
allele num: 60168
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.87e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.72e-1

DP
type: SiteQuality
SIO_000300: 1.198828e6

VQSLOD
type: SiteQuality
SIO_000300: 1.83e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.303e0

MQRankSum
type: SiteQuality
SIO_000300: 4.89e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.3e-3

QD
type: SiteQuality
SIO_000300: 1.239e1

FS
type: SiteQuality
SIO_000300: 1.988e0

GenotypeQuality
all individuals: 614
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2622
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 995
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6650
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 572
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 88
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 126
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 950
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4031
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 88
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2909
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 125
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2691
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1075
bin: 9.75e1
variant carriers: 2

African
type: Population
allele count: 3
allele frequency: 3.475440222428174e-4
allele num: 8632
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10304
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 60560
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6140
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7684
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14790
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 814
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 7.847e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.73e0

DP
type: SiteQuality
SIO_000300: 1.219935e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.368e1

VQSLOD
type: SiteQuality
SIO_000300: 8.27e-1

MQRankSum
type: SiteQuality
SIO_000300: -5.36e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.1e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 6.16e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.36e-1

GenotypeQuality
all individuals: 1073
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 2463
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3013
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 630
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35598
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 79
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2425
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 918
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 129
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3717
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 803
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 595
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 300
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 873
bin: 4.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8694
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6178
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 60794
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10356
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.346438669718594e-4
allele num: 14854
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7730
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 814
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 9.66e0

MQRankSum
type: SiteQuality
SIO_000300: 5.25e-1

FS
type: SiteQuality
SIO_000300: 1.899e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.43e-1

DP
type: SiteQuality
SIO_000300: 1.23234e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.8e-3

VQSLOD
type: SiteQuality
SIO_000300: 5.39e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.135e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.6e-2

GenotypeQuality
all individuals: 224
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1071
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 298
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6116
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2252
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 576
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2313
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 129
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3020
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 128
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 862
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3467
bin: 3.25e1
variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.289656951250967e-4
allele num: 7754
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8722
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14896
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 818
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61054
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6192
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10412
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 6.889999999999999e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.01e0

QD
type: SiteQuality
SIO_000300: 1.23e1

DP
type: SiteQuality
SIO_000300: 1.243623e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.13e0

MQRankSum
type: SiteQuality
SIO_000300: 1.35e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.8e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.1e-3

GenotypeQuality
all individuals: 1157
bin: 9.75e1
variant carriers: 81

GenotypeQuality
all individuals: 760
bin: 4.25e1
variant carriers: 1

GenotypeQuality
all individuals: 2178
bin: 2.75e1
variant carriers: 2

GenotypeQuality
all individuals: 765
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3236
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 126
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 67
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 600
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 654
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3205
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 945
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 37316
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 99
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2051
bin: 3.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6222
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8794
num of homozygotes: 0

South Asian
type: Population
allele count: 10
allele frequency: 6.688068485821295e-4
allele num: 14952
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7806
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.629779327879005e-5
allele num: 61358
num of homozygotes: 0

Latino
type: Population
allele count: 79
allele frequency: 7.552581261950287e-3
allele num: 10460
num of homozygotes: 2

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 824
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.03e0

VQSLOD
type: SiteQuality
SIO_000300: 2.5e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.06e-2

FS
type: SiteQuality
SIO_000300: 1.602e0

QD
type: SiteQuality
SIO_000300: 1.268e1

DP
type: SiteQuality
SIO_000300: 1.254861e6

ClippingRankSum
type: SiteQuality
SIO_000300: -2.3e-2

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.03e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 850
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1084
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 762
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44504
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 149
bin: 7.5e0
variant carriers: 1

GenotypeQuality
all individuals: 1108
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 345
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 447
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 463
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3702
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3583
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 726
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 616
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 355
bin: 8.25e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.476683937823834e-5
allele num: 15440
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9150
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10950
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63628
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8176
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.981e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -3.606e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.382e0

MQRankSum
type: SiteQuality
SIO_000300: 2.97e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.7e-3

DP
type: SiteQuality
SIO_000300: 1.344318e6

QD
type: SiteQuality
SIO_000300: 7.77e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.17e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.71e-1

GenotypeQuality
all individuals: 3702
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 44504
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 149
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1084
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 616
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 463
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 762
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 136
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 726
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 355
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 345
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 447
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1108
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 134
bin: 8.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.714905387565223e-5
allele num: 63628
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9150
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10950
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15440
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8176
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.17e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 7.77e0

VQSLOD
type: SiteQuality
SIO_000300: -3.606e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.71e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.97e-1

DP
type: SiteQuality
SIO_000300: 1.344318e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.382e0

FS
type: SiteQuality
SIO_000300: 5.981e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.7e-3

GenotypeQuality
all individuals: 47621
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 410
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 843
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 237
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 726
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 128
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 464
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 461
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 609
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 355
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 136
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 130
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 234
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1083
bin: 9.75e1
variant carriers: 3

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64950
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 1.89897455374098e-4
allele num: 15798
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9368
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11168
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8378
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6534
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.1e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.011e0

MQRankSum
type: SiteQuality
SIO_000300: -4.2e-2

VQSLOD
type: SiteQuality
SIO_000300: 2.08e0

DP
type: SiteQuality
SIO_000300: 1.388922e6

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.26e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.77e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.8e-3

GenotypeQuality
all individuals: 1083
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 4071
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 47464
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 560
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 18
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 523
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 467
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 676
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 724
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 291
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 335
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 849
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 345
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 1.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11226
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15850
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8408
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65226
num of homozygotes: 0

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

African
type: Population
allele count: 4
allele frequency: 4.249893752656184e-4
allele num: 9412
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 3.01e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.02e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.28e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.8e-3

QD
type: SiteQuality
SIO_000300: 1.071e1

DP
type: SiteQuality
SIO_000300: 1.398084e6

ClippingRankSum
type: SiteQuality
SIO_000300: -9.5e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.36e-1

FS
type: SiteQuality
SIO_000300: 5.231e0

MQ
type: SiteQuality
SIO_000300: 5.943e1

GenotypeQuality
all individuals: 1828
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 669
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 137
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 563
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 433
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4133
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 47713
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 299
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 877
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 293
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 128
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1084
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 339
bin: 8.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8426
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15920
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 872
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65422
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.059546514091969e-4
allele num: 9438
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.888888888888889e-5
allele num: 11250
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.442e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.21e0

FS
type: SiteQuality
SIO_000300: 7.44e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.2e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -1.243e0

MQ
type: SiteQuality
SIO_000300: 5.945e1

MQRankSum
type: SiteQuality
SIO_000300: -1.8e-2

DP
type: SiteQuality
SIO_000300: 1.406678e6

VQSLOD
type: SiteQuality
SIO_000300: 1.73e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.674e0

GenotypeQuality
all individuals: 48015
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 895
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 554
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 285
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1707
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 131
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 747
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 442
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1083
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 203
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 136
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4194
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 342
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11274
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15954
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 872
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6566
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.524715640533041e-5
allele num: 65586
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8454
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9462
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -1.418e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

DP
type: SiteQuality
SIO_000300: 1.413508e6

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.8e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.154e0

QD
type: SiteQuality
SIO_000300: 7.15e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.75e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.56e-1

GenotypeQuality
all individuals: 124
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 294
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 742
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 132
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 382
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 535
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1690
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 48274
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1082
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 341
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 433
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4186
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.524390243902439e-5
allele num: 65600
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9462
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15960
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8456
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11278
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 9.154999999999999e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.65e-1

MQ
type: SiteQuality
SIO_000300: 5.944e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.17e-1

MQRankSum
type: SiteQuality
SIO_000300: -6.39e-1

VQSLOD
type: SiteQuality
SIO_000300: -4.559e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

QD
type: SiteQuality
SIO_000300: 1.253e1

DP
type: SiteQuality
SIO_000300: 1.415005e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.004e0

GenotypeQuality
all individuals: 13
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4247
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 258
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1080
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1572
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 110
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 315
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 560
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 392
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 903
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 48433
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 749
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 136
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 347
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 126
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 8.84016973125884e-5
allele num: 11312
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16022
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65684
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9478
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8468
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.421151e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.382e0

MQRankSum
type: SiteQuality
SIO_000300: 7.94e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.61e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.72e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.56e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 3.115e0

QD
type: SiteQuality
SIO_000300: 2.104e1

GenotypeQuality
all individuals: 20
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 318
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 85
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 899
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1527
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 48931
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4268
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 335
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 125
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 279
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 736
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 138
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1084
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 299
bin: 3.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.519803033526855e-5
allele num: 65798
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 872
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9452
num of homozygotes: 0

South Asian
type: Population
allele count: 4
allele frequency: 2.489729864309723e-4
allele num: 16066
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6580
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.32e-1

MQ
type: SiteQuality
SIO_000300: 5.93e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.6e-2

QD
type: SiteQuality
SIO_000300: 1.214e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

DP
type: SiteQuality
SIO_000300: 1.429978e6

FS
type: SiteQuality
SIO_000300: 1.5246e1

MQRankSum
type: SiteQuality
SIO_000300: 8.46e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.057e0

BaseQRankSum
type: SiteQuality
SIO_000300: -6.2e-2

GenotypeQuality
all individuals: 16
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4260
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 399
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 85
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 218
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1547
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 341
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 296
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 49028
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 235
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 126
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1080
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 735
bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65794
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11300
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16072
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.057753331922996e-4
allele num: 9454
num of homozygotes: 0

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -3.49e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.75e-1

DP
type: SiteQuality
SIO_000300: 1.430252e6

VQSLOD
type: SiteQuality
SIO_000300: -1.474e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -9.51e-1

MQ
type: SiteQuality
SIO_000300: 5.847e1

QD
type: SiteQuality
SIO_000300: 1.007e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.97e-1

GenotypeQuality
all individuals: 1672
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 265
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 293
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 341
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 338
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 900
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 79
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1081
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 737
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4241
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 442
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 141
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 298
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 203
bin: 4.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9438
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65744
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.863676653075696e-5
allele num: 11282
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16068
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 1.21e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.23e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.62e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.14e-1

QD
type: SiteQuality
SIO_000300: 8.279999999999999e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -5.185999999999999e-1

FS
type: SiteQuality
SIO_000300: 5.61e0

DP
type: SiteQuality
SIO_000300: 1.428701e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

GenotypeQuality
all individuals: 289
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 118
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 222
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4144
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 48227
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 138
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 10
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 414
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 126
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 664
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 825
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1089
bin: 9.75e1
variant carriers: 7

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8356
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15906
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11086
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9240
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6520
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 7
allele frequency: 1.079846970257929e-4
allele num: 64824
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 9.04e-1

FS
type: SiteQuality
SIO_000300: 4.68e-1

QD
type: SiteQuality
SIO_000300: 1.226e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.5e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.3e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 1.7e0

MQRankSum
type: SiteQuality
SIO_000300: 1.71e-1

DP
type: SiteQuality
SIO_000300: 1.413182e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.04e-1

MQ
type: SiteQuality
SIO_000300: 5.859e1

GenotypeQuality
all individuals: 253
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 145
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 460
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 46392
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 486
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 269
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3867
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 271
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 458
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 135
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 302
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 750
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1084
bin: 9.75e1
variant carriers: 3

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10856
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8156
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9094
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 3
allele frequency: 4.656938838869916e-4
allele num: 6442
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15734
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63726
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.1e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.48e-1

FS
type: SiteQuality
SIO_000300: 1.046e0

QD
type: SiteQuality
SIO_000300: 1.228e1

VQSLOD
type: SiteQuality
SIO_000300: 1.91e0

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.21e0

MQRankSum
type: SiteQuality
SIO_000300: 5.54e-1

DP
type: SiteQuality
SIO_000300: 1.388388e6

GenotypeQuality
all individuals: 133
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 284
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 157
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 362
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45804
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5054
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 467
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 517
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 123
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 496
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 87
bin: 7.5e0
variant carriers: 1

GenotypeQuality
all individuals: 297
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3821
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 622
bin: 7.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6416
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.234872808100766e-4
allele num: 8098
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10794
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15662
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63464
num of homozygotes: 0

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
allele num: 9040
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.63e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.24e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.66e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.1e-3

FS
type: SiteQuality
SIO_000300: 1.106e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.06e-1

QD
type: SiteQuality
SIO_000300: 1.176e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 4.69e-1

DP
type: SiteQuality
SIO_000300: 1.382761e6

GenotypeQuality
all individuals: 20
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 467
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 362
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 284
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5054
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45804
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 133
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 729
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 496
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 306
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 123
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1083
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 297
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 622
bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.151392915668725e-5
allele num: 63464
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8098
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.106194690265487e-4
allele num: 9040
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15662
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10794
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6416
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.06e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.24e0

MQRankSum
type: SiteQuality
SIO_000300: 4.69e-1

QD
type: SiteQuality
SIO_000300: 1.176e1

DP
type: SiteQuality
SIO_000300: 1.382761e6

FS
type: SiteQuality
SIO_000300: 1.106e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.66e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.1e-3

VQSLOD
type: SiteQuality
SIO_000300: 2.63e0

GenotypeQuality
all individuals: 86
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 535
bin: 3.25e1
variant carriers: 1

GenotypeQuality
all individuals: 20
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 313
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 295
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3797
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 346
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5299
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 715
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1081
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 613
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 288
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 459
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 133
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45568
bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.318117201074081e-5
allele num: 63310
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10758
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 840
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9004
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6408
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15642
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8076
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.947e1

DP
type: SiteQuality
SIO_000300: 1.37887e6

MQRankSum
type: SiteQuality
SIO_000300: 3.54e-1

QD
type: SiteQuality
SIO_000300: 1.222e1

FS
type: SiteQuality
SIO_000300: 3.316e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

VQSLOD
type: SiteQuality
SIO_000300: 1.75e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.8e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.44e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.15e-1

GenotypeQuality
all individuals: 33
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 575
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 93
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1082
bin: 9.75e1
variant carriers: 4

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

GenotypeQuality
all individuals: 5801
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 284
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 292
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 317
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 123
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 575
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 305
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 134
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45057
bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.175207976122436e-5
allele num: 62988
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15576
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8028
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.870207593042828e-4
allele num: 10694
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6376
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 834
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8952
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.86e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 1.935e0

QD
type: SiteQuality
SIO_000300: 1.023e1

MQRankSum
type: SiteQuality
SIO_000300: 3.98e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.919e0

DP
type: SiteQuality
SIO_000300: 1.369862e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.81e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.04e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

GenotypeQuality
all individuals: 533
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 290
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1913
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 369
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 156
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15595
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 115
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32325
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 278
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 561
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 503
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 130
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1823
bin: 3.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5890
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.905123601712471e-5
allele num: 14482
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8296
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 782
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7154
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9258
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 56430
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.93e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.2e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 2.23e0

FS
type: SiteQuality
SIO_000300: 2.017e0

DP
type: SiteQuality
SIO_000300: 1.19266e6

VQSLOD
type: SiteQuality
SIO_000300: -1.753e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.43e-1

MQ
type: SiteQuality
SIO_000300: 5.691e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.43e-1

QD
type: SiteQuality
SIO_000300: 1.193e1

GenotypeQuality
all individuals: 3564
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 476
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 456
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 23882
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2046
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1114
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 128
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 434
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 677
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19435
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 257
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 701
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 396
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3486
bin: 3.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5464
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 724
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7656
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7954
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.96093811279316e-5
allele num: 50996
num of homozygotes: 0

East Asian
type: Population
allele count: 11
allele frequency: 1.676829268292683e-3
allele num: 6560
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.447125409591897e-5
allele num: 13428
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 4.1e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.5e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.78e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.5e-2

DP
type: SiteQuality
SIO_000300: 1.014011e6

ClippingRankSum
type: SiteQuality
SIO_000300: -2.16e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.64e-1

QD
type: SiteQuality
SIO_000300: 1.048e1

GenotypeQuality
all individuals: 6037
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2707
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3217
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 255
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 110
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 397
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5290
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26499
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 133
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1087
bin: 9.75e1
variant carriers: 11

GenotypeQuality
all individuals: 1316
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 240
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 253
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 367
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 9
allele frequency: 1.271905031091012e-3
allele num: 7076
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 2.833663927458204e-4
allele num: 7058
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12384
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 650
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5916
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 46134
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.6e-3

VQSLOD
type: SiteQuality
SIO_000300: 2.05e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 2.601e0

DP
type: SiteQuality
SIO_000300: 8.53177e5

BaseQRankSum
type: SiteQuality
SIO_000300: 2.0e0

MQRankSum
type: SiteQuality
SIO_000300: 6.0e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.61e-1

QD
type: SiteQuality
SIO_000300: 1.102e1

GenotypeQuality
all individuals: 5428
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 634
bin: 4.75e1
variant carriers: 2

GenotypeQuality
all individuals: 384
bin: 7.75e1
variant carriers: 8

GenotypeQuality
all individuals: 4302
bin: 7.5e0
variant carriers: 3

GenotypeQuality
all individuals: 24427
bin: 2.25e1
variant carriers: 3

GenotypeQuality
all individuals: 2048
bin: 1.75e1
variant carriers: 4

GenotypeQuality
all individuals: 362
bin: 5.75e1
variant carriers: 6

GenotypeQuality
all individuals: 6138
bin: 6.25e1
variant carriers: 6

GenotypeQuality
all individuals: 322
bin: 5.25e1
variant carriers: 5

GenotypeQuality
all individuals: 1676
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6658
bin: 3.25e1
variant carriers: 3

GenotypeQuality
all individuals: 253
bin: 8.25e1
variant carriers: 18

GenotypeQuality
all individuals: 1564
bin: 9.75e1
variant carriers: 498

GenotypeQuality
all individuals: 120
bin: 8.75e1
variant carriers: 14

European (Non-Finnish)
type: Population
allele count: 369
allele frequency: 8.459422283356258e-3
allele num: 43620
num of homozygotes: 3

Latino
type: Population
allele count: 42
allele frequency: 6.422018348623854e-3
allele num: 6540
num of homozygotes: 0

Other
type: Population
allele count: 8
allele frequency: 1.286173633440514e-2
allele num: 622
num of homozygotes: 0

South Asian
type: Population
allele count: 24
allele frequency: 2.011397921555481e-3
allele num: 11932
num of homozygotes: 1

African
type: Population
allele count: 9
allele frequency: 1.320422535211268e-3
allele num: 6816
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 52
allele frequency: 1.049233252623083e-2
allele num: 4956
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5618
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 8.11028e5

BaseQRankSum
type: SiteQuality
SIO_000300: -6.889999999999999e-1

QD
type: SiteQuality
SIO_000300: 1.339e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.61e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.8e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 5.51e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.3e-3

MQRankSum
type: SiteQuality
SIO_000300: 2.48e-1

GenotypeQuality
all individuals: 4053
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6943
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 108
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1503
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5446
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 493
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18977
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 74
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 698
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 306
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3163
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1343
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 123
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 368
bin: 7.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4482
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10632
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4942
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6172
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.660848278431164e-5
allele num: 37582
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5190
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.03e0

VQSLOD
type: SiteQuality
SIO_000300: -2.233e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.36e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.42e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 4.68e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.769e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.78e-1

DP
type: SiteQuality
SIO_000300: 7.45027e5

GenotypeQuality
all individuals: 5399
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 184
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 232
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1629
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 721
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4082
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6966
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 123
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5605
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 16924
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 367
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1382
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1097
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 6720
bin: 1.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.737775830914965e-5
allele num: 36526
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4802
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6076
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 524
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4948
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10392
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4446
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 7.31e-1

QD
type: SiteQuality
SIO_000300: 1.445e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 7.40839e5

VQSLOD
type: SiteQuality
SIO_000300: 1.88e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.38e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 7.31e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.31e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.31e-1

GenotypeQuality
all individuals: 107
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4114
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1098
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 6901
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1380
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5643
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 99
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 231
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2788
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 803
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 123
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17372
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5363
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 364
bin: 7.75e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 2.031694433157253e-4
allele num: 4922
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4756
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4418
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 36408
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 514
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6024
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10366
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.47e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.223e1

MQRankSum
type: SiteQuality
SIO_000300: -3.77e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.77e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.01e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.016e0

DP
type: SiteQuality
SIO_000300: 7.40531e5

GenotypeQuality
all individuals: 243
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8208
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 89
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2178
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 188
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 565
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 700
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 501
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 236
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 194
bin: 5.25e1
variant carriers: 0

East Asian
type: Population
allele count: 4
allele frequency: 4.673989249824726e-4
allele num: 8558
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 9.131586156515387e-5
allele num: 65706
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6590
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.916585973163646e-5
allele num: 14458
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11496
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9710
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 868
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.081e1

MQ
type: SiteQuality
SIO_000300: 5.979e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.46e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.074e0

VQSLOD
type: SiteQuality
SIO_000300: 3.07e0

MQRankSum
type: SiteQuality
SIO_000300: 1.9e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.1e-1

FS
type: SiteQuality
SIO_000300: 7.25e-1

DP
type: SiteQuality
SIO_000300: 1.649845e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.5e-3

GenotypeQuality
all individuals: 26
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1514
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 153
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3627
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 702
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2505
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 501
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 172
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8251
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 746
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1375
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 493
bin: 3.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6588
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8568
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 868
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.52031135976648e-5
allele num: 65776
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9718
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.848376934666484e-5
allele num: 14602
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.652833e6

VQSLOD
type: SiteQuality
SIO_000300: 1.71e0

MQ
type: SiteQuality
SIO_000300: 5.967e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.6e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.52e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.04e-2

MQRankSum
type: SiteQuality
SIO_000300: 5.8e-2

QD
type: SiteQuality
SIO_000300: 1.369e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.09e-1

FS
type: SiteQuality
SIO_000300: 6.68e-1

GenotypeQuality
all individuals: 40
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2229
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 150
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 169
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 271
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 700
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 110
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 494
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1384
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 108
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2521
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8375
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 211
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 38998
bin: 6.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15474
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 2.602811035918792e-4
allele num: 11526
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 882
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8598
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9766
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66206
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.45e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.641e0

DP
type: SiteQuality
SIO_000300: 1.677643e6

VQSLOD
type: SiteQuality
SIO_000300: 7.79e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.9e-3

QD
type: SiteQuality
SIO_000300: 1.177e1

MQRankSum
type: SiteQuality
SIO_000300: -1.86e-1

FS
type: SiteQuality
SIO_000300: 6.27e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.7e-2

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

GenotypeQuality
all individuals: 53
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 700
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 493
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2244
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 389
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2547
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1377
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 97
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39987
bin: 6.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8608
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 894
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.505026789476853e-5
allele num: 66444
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16154
num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
SIO_000300: 1.2e0

FS
type: SiteQuality
SIO_000300: 5.899e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.06e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.55e-1

DP
type: SiteQuality
SIO_000300: 1.692452e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.79e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.4e-3

VQSLOD
type: SiteQuality
SIO_000300: 4.55e-1

MQ
type: SiteQuality
SIO_000300: 5.959e1

QD
type: SiteQuality
SIO_000300: 8.82e0

GenotypeQuality
all individuals: 700
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 91
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2240
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 494
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2543
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 368
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 9
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8477
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40044
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1374
bin: 8.25e1
variant carriers: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.504755025881786e-5
allele num: 66456
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16168
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 1.164e0

QD
type: SiteQuality
SIO_000300: 1.432e1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.21e-1

MQRankSum
type: SiteQuality
SIO_000300: 8.3e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.48e-1

DP
type: SiteQuality
SIO_000300: 1.693382e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.2e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.04e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.44e-1

GenotypeQuality
all individuals: 8474
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 80
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 106
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 698
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 493
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3625
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 72
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 71
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2236
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1376
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 356
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 4.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66458
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16190
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11542
num of homozygotes: 0

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

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

African
type: Population
allele count: 1
allele frequency: 1.02124183006536e-4
allele num: 9792
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.699e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.6e-2

DP
type: SiteQuality
SIO_000300: 1.693931e6

VQSLOD
type: SiteQuality
SIO_000300: 6.900000000000001e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -1.47e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.2e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -3.618e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.67e-1